Compound
aspartame
Flavoring agent sweeter than sugar, metabolized as phenylalanine and aspartic acid.
Studied for
8 endpoints · 9 findings · 5 papers · 2 null
- Total cholesterol (TC)no detected effectEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.
- ALPIlowersEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.
- Body massno detected effectEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.
- Tumour necrosis factor alpha concentrationraisesEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.
- CATraisesEvidence strength: insufficient. Mechanistic inference, no evidence found, or evidence weakened below very limited.
Structure
Loading the model…
- Class
- Organic compound
- Formula
- C14H18N2O5
- Mass
- 294.307 g/mol
- Charge
- 0
- InChIKey
- IAOZJIPTCAWIRG-QWRGUYRKSA-N
- SMILES
- COC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](N)CC(=O)O
- Look it up
- ChEBIPubChemBy InChIKey
Identity from ChEBI, geometry from PubChem. Not evidence.
What the evidence says
How to read these marks9 findings · 8 endpoints · 5 papers · 2 null · by evidence strength
What moved
7 findings
Increases tumour necrosis factor alpha concentration
Very limitedEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.Finding“In our chronic in vivo model, we found that compared with the controls, serum TNF-α was increased in both chow + ASP and HFD + ASP groups (1622.3 ± 184.1 pg/mg of protein and 2512.1 ± 251.4 pg/mg of protein, respectively), indicating a higher level of systemic inflammation in groups receiving ASP.”
Quoted verbatim from Inhibition of the gut enzyme intestinal alkaline phosphatase may explain how aspartame promotes glucose intolerance and obesity in mice.. - Study
- animal · not in humans
- Duration
- 4 months
- Dose
- 0.96 mg/mL aspartame in drinking water
- Population
- Male C57BL/6 mice on chow or high-fat diet, aspartame in drinking water versus plain water for 18 weeks; serum collected at sacrifice
Inhibition of the gut enzyme intestinal alkaline phosphatase may explain how aspartame promotes glucose intolerance and obesity in mice.2017PMID:27997218Permalink
Inhibits ALPI
Very limitedEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.Finding“In the bowel loop model, IAP activity was significantly (p = 0.02) reduced in mice that had ASP instilled into the loops compared with saline controls (0.2 ± 0.03 vs 0.4 ± 0.24).”
Quoted verbatim from Inhibition of the gut enzyme intestinal alkaline phosphatase may explain how aspartame promotes glucose intolerance and obesity in mice.. - Study
- animal · not in humans
- Dose
- 34 mg/kg instilled into the bowel loop
- Population
- Male mice, isolated 6-cm small-bowel loop injected with aspartame solution or saline, luminal contents assayed after 3 h
Inhibition of the gut enzyme intestinal alkaline phosphatase may explain how aspartame promotes glucose intolerance and obesity in mice.2017PMID:27997218Permalink
Increases triglycerides
InsufficientEvidence strength: insufficient. Mechanistic inference, no evidence found, or evidence weakened below very limited.Finding“Also, ASP 2 and ASP 3 significantly increased the levels of total cholesterol, triglycerides and low-density lipoprotein cholesterol in the rats.”
Quoted verbatim from Effects of long-term administration of aspartame on biochemical indices, lipid profile and redox status of cellular system of male rats.. - Study
- animal · not in humans
- Duration
- 2 months
- Dose
- 35 and 70 mg/kg daily by oral gavage
- Population
- Male Wistar rats given aspartame 35 mg/kg (ASP 2) and 70 mg/kg (ASP 3) daily by oral gavage for 9 weeks versus distilled water; the 15 mg/kg dose is not covered by this sentence
Effects of long-term administration of aspartame on biochemical indices, lipid profile and redox status of cellular system of male rats.2016PMID:26247507Permalink
Increases total cholesterol (TC)
InsufficientEvidence strength: insufficient. Mechanistic inference, no evidence found, or evidence weakened below very limited.Finding“Also, ASP 2 and ASP 3 significantly increased the levels of total cholesterol, triglycerides and low-density lipoprotein cholesterol in the rats.”
Quoted verbatim from Effects of long-term administration of aspartame on biochemical indices, lipid profile and redox status of cellular system of male rats.. - Study
- animal · not in humans
- Duration
- 2 months
- Dose
- 35 and 70 mg/kg daily by oral gavage
- Population
- Male Wistar rats given aspartame 35 mg/kg (ASP 2) and 70 mg/kg (ASP 3) daily by oral gavage for 9 weeks versus distilled water; the 15 mg/kg dose is not covered by this sentence
Effects of long-term administration of aspartame on biochemical indices, lipid profile and redox status of cellular system of male rats.2016PMID:26247507Permalink
Increases LDL cholesterol
InsufficientEvidence strength: insufficient. Mechanistic inference, no evidence found, or evidence weakened below very limited.Finding“Also, ASP 2 and ASP 3 significantly increased the levels of total cholesterol, triglycerides and low-density lipoprotein cholesterol in the rats.”
Quoted verbatim from Effects of long-term administration of aspartame on biochemical indices, lipid profile and redox status of cellular system of male rats.. - Study
- animal · not in humans
- Duration
- 2 months
- Dose
- 35 and 70 mg/kg daily by oral gavage
- Population
- Male Wistar rats given aspartame 35 mg/kg (ASP 2) and 70 mg/kg (ASP 3) daily by oral gavage for 9 weeks versus distilled water; the 15 mg/kg dose is not covered by this sentence
Effects of long-term administration of aspartame on biochemical indices, lipid profile and redox status of cellular system of male rats.2016PMID:26247507Permalink
Increases fasting blood glucose
InsufficientEvidence strength: insufficient. Mechanistic inference, no evidence found, or evidence weakened below very limited.Finding“At the blood metabolites level, fasting plasma glucose was significantly higher among the aspartame groups (P = 0·003) and this seems to relate to the amount of ingested aspartame (r = 0·585, P = 0·001) (Table 2).”
Quoted verbatim from The effect of aspartame and sucralose intake on body weight measures and blood metabolites: role of their form (solid and/or liquid) of ingestion.. - Study
- animal · not in humans
- Duration
- 7 weeks
- Dose
- 0.05% aspartame w/w in diet and/or drinking water
- Population
- Male Sprague Dawley rats, 7 weeks of age at start; three aspartame arms (0.05% in diet, in drinking water, or both) pooled against an unsweetened-diet, plain-water control, 7 weeks, overnight fasted at termination
The effect of aspartame and sucralose intake on body weight measures and blood metabolites: role of their form (solid and/or liquid) of ingestion.2022PMID:34420538Permalink
Show the remaining 1
Activates CAT
InsufficientEvidence strength: insufficient. Mechanistic inference, no evidence found, or evidence weakened below very limited.Finding“The activity of catalase was increased markedly in all the regions of brain (cerebral cortex (F = 27, df = 2), cerebellum(F = 34, df = 2), midbrain (F = 53, df = 2), pons-medulla (F = 14, df = 2), hippocampus (F = 25, df = 2) and hypothalamus (F = 50, df = 2)) in aspartame treated MTX animals with respect to control and MTX treated control.”
Quoted verbatim from Biochemical responses and mitochondrial mediated activation of apoptosis on long-term effect of aspartame in rat brain.. - Study
- animal · not in humans
- Population
- Male Wistar rats given methotrexate; aspartame-plus-methotrexate group versus saline control and methotrexate-only control; six brain regions, tissue assay
Biochemical responses and mitochondrial mediated activation of apoptosis on long-term effect of aspartame in rat brain.2014PMID:25009784Permalink
What did not
2 findings
No detected effect on body mass
Very limitedEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.FindingNull result“Body weight did not change after aspartame consumption compared to control (5.00 kg; 95% CI, -1.56 to 11.56) or to sucrose (3.78 kg; 95% CI, -2.18 to 9.74).”
Quoted verbatim from Metabolic effects of aspartame in adulthood: A systematic review and meta-analysis of randomized clinical trials.. - Study
- meta-analysis
- Population
- adults, pooled randomized clinical trials
Metabolic effects of aspartame in adulthood: A systematic review and meta-analysis of randomized clinical trials.2018PMID:28394643Permalink
No detected effect on total cholesterol (TC)
Very limitedEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.FindingNull result“Total cholesterol was not affected by aspartame consumption compared to control (-0.02 mmol/L; 95% CI, -0.31 to 0.27) or to sucrose (-0.24 mmol/L; 95% CI, -0.89 to 0.42).”
Quoted verbatim from Metabolic effects of aspartame in adulthood: A systematic review and meta-analysis of randomized clinical trials.. - Study
- meta-analysis
- Population
- adults, pooled randomized clinical trials
Metabolic effects of aspartame in adulthood: A systematic review and meta-analysis of randomized clinical trials.2018PMID:28394643Permalink
What it touches on the way
Mechanistic reach
2 entities
2 entities reached.
0 reported hops2 assembled from the scaffold
Registered, and not reported
- Source
- ClinicalTrials.gov
- Intervention
- aspartame
- Status
- Completed, terminated or suspended
- Results posted
- No
Trials without posted results
47 trials
47 registered trials without posted results · Overdue (FDAAA 801): 46
46 past the window1 within it, or no actual date
- NCT04567108completed2026-05-21a university or hospital
- NCT07764367completed2025-09-30a university or hospitalpast the reporting window
- NCT07242066completed2025-08-01a university or hospitalpast the reporting window
- NCT06374641completed2025-06-06a university or hospitalpast the reporting window
- NCT07506564completed2025-03-05a university or hospitalpast the reporting window
- NCT03596788terminated— Insufficient recruitment2025-02-17a university or hospitalpast the reporting window
- NCT04066569completed2024-10-30a university or hospitalpast the reporting window
- NCT04208256completed2024-09-30a university or hospitalpast the reporting window
- NCT05592951completed2023-07-14a university or hospitalpast the reporting window
- NCT05680064completed2023-07-01a university or hospitalpast the reporting window
- NCT04671043completed2023-02-02a university or hospitalpast the reporting window
- NCT04474002completed2022-12-31a university or hospitalpast the reporting window
Show the remaining 35
- NCT04330196completed2020-12-03a university or hospitalpast the reporting window
- NCT03708939completed2020-08-01a university or hospitalpast the reporting window
- NCT02548767completed2020-03-13a university or hospitalpast the reporting window
- NCT05645991completed2020-02-28a university or hospitalpast the reporting window
- NCT03954418completed2020-02-01a university or hospitalpast the reporting window
- NCT03525184completed2019-12-10US federal agencypast the reporting window
- NCT03992365completed2019-10-15industrypast the reporting window
- NCT02934321completed2019-08-23a university or hospitalpast the reporting window
- NCT02520258completed2019-06-25a university or hospitalpast the reporting window
- NCT04904133completed2019-05-12a university or hospitalpast the reporting window
- NCT05437874completed2019-01-31a university or hospitalpast the reporting window
- NCT02928653completed2018-02a university or hospitalpast the reporting window
- NCT02569762completed2018-01a university or hospitalpast the reporting window
- NCT02459535completed2017-06a university or hospitalpast the reporting window
- NCT02999321completed2017-05-05a university or hospitalpast the reporting window
- NCT02448667completed2017-04-17a university or hospitalpast the reporting window
- NCT01200940completed2017-03-02NIHpast the reporting window
- NCT03200197completed2017-03a university or hospitalpast the reporting window
- NCT05654285completed2016-05-27a university or hospitalpast the reporting window
- NCT03668015completed2015-06-04a university or hospitalpast the reporting window
- NCT01683929completed2014-06a university or hospitalpast the reporting window
- NCT01103921completed2014-01a university or hospitalpast the reporting window
- NCT04804397completed2013-06a university or hospitalpast the reporting window
- NCT02128516completed2012-04a university or hospitalpast the reporting window
- NCT01529281completed2011-09a university or hospitalpast the reporting window
- NCT00777647completed2010-12a university or hospitalpast the reporting window
- NCT00654108completed2010-05-30NIHpast the reporting window
- NCT01115088completed2010-04a university or hospitalpast the reporting window
- NCT01122082completed2009-08a university or hospitalpast the reporting window
- NCT00978900completed2009-03a university or hospitalpast the reporting window
- NCT00731510completed2008-10a university or hospitalpast the reporting window
- NCT01799096completed2008-10a university or hospitalpast the reporting window
- NCT00776971completed2008-09a university or hospitalpast the reporting window
- NCT00350350completed2004-11industrypast the reporting window
- NCT07175740completed2004-05-28a university or hospitalpast the reporting window
Papers screened
739 papers
- Compound
- aspartame
- Screened
- 739
- Admitted
- 5
- Discarded
- 547
- Not read
- 187
- Showing
- 200 of 739
Produced a finding5 papers
- PMID:262475072026-10-12
- PMID:250097842026-10-05
- PMID:279972182026-10-05
and 2 more.
Discarded: the wrong intervention437 papers
- PMID:16448051cited by PMID:25786106; not about the subject it would be filed under2026-10-17
- PMID:18183564cited by PMID:25786106; not about the subject it would be filed under2026-10-17
- PMID:18288723cited by PMID:25786106; not about the subject it would be filed under2026-10-17
- PMID:18667148cited by PMID:25786106; not about the subject it would be filed under2026-10-17
- PMID:21526840cited by PMID:25786106; not about the subject it would be filed under2026-10-17
- PMID:21533907cited by PMID:25786106; not about the subject it would be filed under2026-10-17
- PMID:22972297cited by PMID:25313461; not about the subject it would be filed under2026-10-17
- PMID:22980325cited by PMID:25313461; not about the subject it would be filed under2026-10-17
- PMID:23526699cited by PMID:25313461; not about the subject it would be filed under2026-10-17
- PMID:23652017cited by PMID:25313461; not about the subject it would be filed under2026-10-17
- PMID:23844011cited by PMID:25313461; not about the subject it would be filed under2026-10-17
- PMID:23850261cited by PMID:25313461; not about the subject it would be filed under2026-10-17
and 425 more.
Discarded: not retrievable64 papers
- PMID:10390691no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-17
- PMID:10406399no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-17
- PMID:15459030no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-17
- PMID:1676993no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-17
- PMID:1941798no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-17
- PMID:3277925no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-17
- PMID:8624169no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-17
- PMID:24182455no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-17
- PMID:4200872no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-17
- PMID:13549594no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-16
- PMID:14474846no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-16
- PMID:1978225no PMID parsed, abstract under 200 characters, or no record returned by efetch2026-10-16
and 52 more.
Discarded: an endpoint this vocabulary does not hold20 papers
- PMID:16507461no claim extracted — no_outcome_node — measured: tumour incidence in a lifetime rodent bioassay (malignant-tumor-bearing animals, lymphoma/leukemia, renal pelvis carcinoma), histopathology at necropsy | tumour incidence in rats (malignant-tumor-bearing animals; lymphomas and leukemias; renal pelvis/ureter carcinomas), histopathology at necropsy2026-10-12
- PMID:24925367no claim extracted — no_outcome_node — measured: angiogenesis, vessel proliferation in chick chorioallantoic membrane assay; wound healing in rat skin | angiogenesis, chick chorioallantoic membrane vessel proliferation2026-10-12
- PMID:24961835no claim extracted — no_outcome_node — measured: adipocyte differentiation, lipid accumulation by Oil Red O staining in 3T3-L1 cells; adipogenic transcription factor expression by qRT-PCR and Western blot | adipocyte lipid accumulation in 3T3-L1 cells, Oil Red O staining2026-10-12
- PMID:28446800no claim extracted — no_outcome_node — measured: epididymal sperm function (count, viability, motility) and sperm antioxidant enzyme activities in rat; existing antioxidant-enzyme nodes are blood-matrix | antioxidant enzyme activity and GSH in rat epididymal sperm; sperm function (count, viability, morphology, motility), method not stated2026-10-12
- PMID:31108189no claim extracted — no_outcome_node — measured: placental weight in rat, weighed after gavage on gestation days 9-11; placental zone thickness by histology | placental weight in rats, and placental zone thickness by histomorphometry2026-10-12
- PMID:29561882no claim extracted — no_outcome_node — measured: serum growth hormone concentration by multiplex bead immunoassay (Luminex); tissue differentially expressed genes by microarray | serum growth hormone, Luminex bead assay; hypothalamic and adrenal differentially expressed genes, Affymetrix Mouse Gene 1.0 ST microarray2026-10-05
- PMID:29567262claims extracted but the object named resolved to no node — recorded in candidate_nodes (ADR-0070)2026-10-05
and 13 more.
Discarded: no extractable result16 papers
- PMID:25543075no claim extracted — no_quantitative_result2026-10-12
- PMID:27565676claims extracted but refused by the deterministic validators2026-10-12
- PMID:30547285claims extracted but refused by the deterministic validators2026-10-12
- PMID:38499183claims extracted but the two passes did not agree2026-10-12
- PMID:17805418claims extracted but the two passes did not agree2026-10-05
- PMID:22509243claims extracted but the two passes did not agree2026-10-05
- PMID:25313461claims extracted but the two passes did not agree2026-10-05
and 9 more.
Discarded: another reason, stated per paper9 papers
- PMID:27640132no claim extracted — cause not determined (one pass only) — measured: insulin tolerance test glucose disposal in mice; blood glucose fasting state not stated2026-10-12
- PMID:37323037no claim extracted — cause not determined (one pass only) — measured: cancer risk pooled across colorectal, breast, prostate, stomach cancer and CLL (not all-site), case-control OR by FFQ-assessed aspartame intake2026-10-12
and 7 more.
Discarded: the wrong population1 paper
and 1 more.
Not read yet187 papers
- PMID:240636142026-10-08
- PMID:107772542026-10-08
- PMID:24200322026-10-08
- PMID:20466252026-10-06
- PMID:27925962026-10-06
- PMID:27968972026-10-06
- PMID:62045222026-10-06
- PMID:72812052026-10-06
- PMID:74410892026-10-06
- PMID:8276192026-10-06
and 177 more.
Measured, not recorded
- Compound
- aspartame
- Endpoints measured
- 639 endpoints
- Recorded as a finding
- No
Show what was measured
Ames/Salmonella/microsome mutagenicity test, TA98 and TA100 strains
no effect
ASP was not mutagenic for Salmonella typhimurium TA98 and TA100 strains in the absence and presence of S9 mix.
PMID:15478947 · one of two readings recorded this
Ames/Salmonella/microsome mutagenicity test
no effect
ASP was not mutagenic for Salmonella typhimurium TA98 and TA100 strains in the absence and presence of S9 mix.
PMID:15478947 · one of two readings recorded this
chromosome aberration (CA) test, human lymphocytes
increases
ASP induced CAs at all concentrations (500, 1000 and 2000 microg/ml) and treatment periods (24 and 48 h) dose-dependently, while it did not induce SCEs.
PMID:15478947 · one of two readings recorded this
chromosome aberration (CA) test in human lymphocytes
increases
ASP induced CAs at all concentrations (500, 1000 and 2000 microg/ml) and treatment periods (24 and 48 h) dose-dependently, while it did not induce SCEs.
PMID:15478947 · one of two readings recorded this
chromosome aberration frequency in human lymphocytes, chromosome aberration (CA) test
increases
Not recorded as a finding: this platform holds no node for the endpoint
ASP induced CAs at all concentrations (500, 1000 and 2000 microg/ml) and treatment periods (24 and 48 h) dose-dependently, while it did not induce SCEs.
PMID:15478947 · one of two readings recorded this
genotoxicity of aspartame in human lymphocytes (chromosome aberration, sister chromatid exchange, micronucleus, mitotic and replication indices) and mutagenicity in the Ames Salmonella/microsome test
increases
Not recorded as a finding: this platform holds no node for the endpoint
ASP induced CAs at all concentrations (500, 1000 and 2000 microg/ml) and treatment periods (24 and 48 h) dose-dependently, while it did not induce SCEs.
PMID:15478947 · one of two readings recorded this
micronucleus test, human lymphocytes
increases
In addition, ASP induced micronuclei at the highest concentrations only.
PMID:15478947 · one of two readings recorded this
micronucleus test in human lymphocytes
increases
In addition, ASP induced micronuclei at the highest concentrations only.
PMID:15478947 · one of two readings recorded this
mitotic index (MI), human lymphocytes
decreases
However, ASP decreased the mitotic index (MI) at all concentrations and treatment periods dose-dependently.
PMID:15478947 · one of two readings recorded this
mitotic index (MI) in human lymphocytes
decreases
However, ASP decreased the mitotic index (MI) at all concentrations and treatment periods dose-dependently.
PMID:15478947 · one of two readings recorded this
replication index (RI), human lymphocytes
decreases
On the other hand, ASP decreased the replication index (RI) only at the highest concentration for 48 h treatment period.
PMID:15478947 · one of two readings recorded this
replication index (RI) in human lymphocytes
decreases
ASP decreased the replication index (RI) only at the highest concentration for 48 h treatment period.
PMID:15478947 · one of two readings recorded this
sister chromatid exchange (SCE) test, human lymphocytes
no effect
ASP induced CAs at all concentrations (500, 1000 and 2000 microg/ml) and treatment periods (24 and 48 h) dose-dependently, while it did not induce SCEs.
PMID:15478947 · one of two readings recorded this
sister chromatid exchange (SCE) test in human lymphocytes
no effect
ASP induced CAs at all concentrations (500, 1000 and 2000 microg/ml) and treatment periods (24 and 48 h) dose-dependently, while it did not induce SCEs.
PMID:15478947 · one of two readings recorded this
incidence of malignant-tumor-bearing animals, positive trend
increases, p = 0.01
an increased incidence of malignant-tumor-bearing animals with a positive significant trend in males (p < or = 0.05) and in females (p < or = 0.01)
PMID:16507461 · one of two readings recorded this
incidence of malignant-tumor-bearing animals, positive trend
increases, p = 0.05
an increased incidence of malignant-tumor-bearing animals with a positive significant trend in males (p < or = 0.05) and in females (p < or = 0.01)
PMID:16507461 · one of two readings recorded this
incidence of malignant-tumor-bearing animals
increases, p = 0.01
in particular those females treated at 50,000 ppm (p < or = 0.01)
PMID:16507461 · one of two readings recorded this
lymphomas and leukemias incidence, positive trend
increases, p = 0.01
an increase in lymphomas and leukemias with a positive significant trend in both males (p < or = 0.05) and females (p < or = 0.01)
PMID:16507461 · one of two readings recorded this
lymphomas and leukemias incidence, positive trend
increases, p = 0.05
an increase in lymphomas and leukemias with a positive significant trend in both males (p < or = 0.05) and females (p < or = 0.01)
PMID:16507461 · one of two readings recorded this
lymphomas and leukemias incidence
increases, p = 0.05
in particular in females treated at doses of 100,000 (p < or = 0.01), 50,000 (p < or = 0.01), 10,000 (p < or = 0.05), 2,000 (p < or = 0.05), or 400 ppm (p < or = 0.01)
PMID:16507461 · one of two readings recorded this
lymphomas and leukemias incidence
increases, p = 0.01
in particular in females treated at doses of 100,000 (p < or = 0.01), 50,000 (p < or = 0.01), 10,000 (p < or = 0.05), 2,000 (p < or = 0.05), or 400 ppm (p < or = 0.01)
PMID:16507461 · one of two readings recorded this
lymphomas and leukemias incidence
increases, p = 0.05
in particular in females treated at doses of 100,000 (p < or = 0.01), 50,000 (p < or = 0.01), 10,000 (p < or = 0.05), 2,000 (p < or = 0.05), or 400 ppm (p < or = 0.01)
PMID:16507461 · one of two readings recorded this
lymphomas and leukemias incidence
increases, p = 0.01
in particular in females treated at doses of 100,000 (p < or = 0.01), 50,000 (p < or = 0.01), 10,000 (p < or = 0.05), 2,000 (p < or = 0.05), or 400 ppm (p < or = 0.01)
PMID:16507461 · one of two readings recorded this
lymphomas and leukemias incidence
increases, p = 0.01
in particular in females treated at doses of 100,000 (p < or = 0.01), 50,000 (p < or = 0.01), 10,000 (p < or = 0.05), 2,000 (p < or = 0.05), or 400 ppm (p < or = 0.01)
PMID:16507461 · one of two readings recorded this
malignant schwannomas of peripheral nerves, positive trend
increases, p = 0.05
an increased incidence of malignant schwannomas of peripheral nerves with a positive trend (p < or = 0.05) in males
PMID:16507461 · one of two readings recorded this
transitional cell carcinomas of renal pelvis and ureter and precursors (dysplasias), positive trend
increases, p = 0.01
with a positive significant trend (p < or = 0.01), of transitional cell carcinomas of the renal pelvis and ureter
PMID:16507461 · one of two readings recorded this
transitional cell carcinomas of renal pelvis and ureter and precursors (dysplasias)
increases, p = 0.01
in females treated at 100,000 (p < or = 0.01), 50,000 (p < or = 0.01), 10,000 (p < or = 0.01), 2,000 (p < or = 0.05), or 400 ppm (p < or = 0.05)
PMID:16507461 · one of two readings recorded this
transitional cell carcinomas of renal pelvis and ureter and precursors (dysplasias)
increases, p = 0.01
in females treated at 100,000 (p < or = 0.01), 50,000 (p < or = 0.01), 10,000 (p < or = 0.01), 2,000 (p < or = 0.05), or 400 ppm (p < or = 0.05)
PMID:16507461 · one of two readings recorded this
transitional cell carcinomas of renal pelvis and ureter and precursors (dysplasias)
increases, p = 0.05
in females treated at 100,000 (p < or = 0.01), 50,000 (p < or = 0.01), 10,000 (p < or = 0.01), 2,000 (p < or = 0.05), or 400 ppm (p < or = 0.05)
PMID:16507461 · one of two readings recorded this
transitional cell carcinomas of renal pelvis and ureter and precursors (dysplasias)
increases, p = 0.05
in females treated at 100,000 (p < or = 0.01), 50,000 (p < or = 0.01), 10,000 (p < or = 0.01), 2,000 (p < or = 0.05), or 400 ppm (p < or = 0.05)
PMID:16507461 · one of two readings recorded this
transitional cell carcinomas of renal pelvis and ureter and precursors (dysplasias)
increases, p = 0.01
in females treated at 100,000 (p < or = 0.01), 50,000 (p < or = 0.01), 10,000 (p < or = 0.01), 2,000 (p < or = 0.05), or 400 ppm (p < or = 0.05)
PMID:16507461 · one of two readings recorded this
feed and water consumption
no effect
We observed no relevant differences in feed consumption between treated and untreated groups, in either males or females
PMID:17805418 · one of two readings recorded this
historical control incidence of lymphomas/leukemias, female rats
n = 2274
the overall incidence of lymphomas/leukemias was 20.6% (range, 8.0–30.9%) among 2,265 male rats and 13.3% (range, 4.0–25.0%) among 2,274 female rats
PMID:17805418 · one of two readings recorded this
historical control incidence of lymphomas/leukemias, male rats
n = 2265
the overall incidence of lymphomas/leukemias was 20.6% (range, 8.0–30.9%) among 2,265 male rats and 13.3% (range, 4.0–25.0%) among 2,274 female rats
PMID:17805418 · one of two readings recorded this
historical control incidence of mammary cancers, female rats
The overall incidence of mammary cancers in the same group of female rats was 9.2% (range, 4.0–14.2%)
PMID:17805418 · one of two readings recorded this
incidence of lymphomas/leukemias, histopathology at necropsy
increases, significant at 2,000 ppm in males and females; dose-related in females
Not recorded as a finding: no outcome node for lymphoma/leukaemia incidence
When compared with the untreated control group, the increased incidence of lymphomas/ leukemias in treated males and females was significant at 2,000 ppm APM (p ≤ 0.05 and p ≤ 0.01, respectively).
PMID:17805418 · one of two readings recorded this
incidence of lymphomas/leukemias
increases, p = 0.01
the increased incidence of lymphomas/ leukemias in treated males and females was significant at 2,000 ppm APM (p ≤ 0.05 and p ≤ 0.01, respectively)
PMID:17805418 · one of two readings recorded this
incidence of lymphomas/leukemias
increases, p = 0.05
the increased incidence of lymphomas/ leukemias in treated males and females was significant at 2,000 ppm APM (p ≤ 0.05 and p ≤ 0.01, respectively)
PMID:17805418 · one of two readings recorded this
incidence of lymphomas/leukemias
increases, p = 0.01
The data show that APM causes a significant, dose-related increased incidence in females (p ≤ 0.01)
PMID:17805418 · one of two readings recorded this
incidence of malignant tumor-bearing animals, lymphomas/leukemias and mammary carcinomas by histopathology at natural death, in Sprague-Dawley rats given aspartame in feed at 2,000 or 400 ppm from fetal day 12 for life, with Cox regression for dose-response
increases, malignant tumor incidence significantly increased in males at 2,000 ppm aspartame; the numeric rise in females was not significant
Not recorded as a finding: every result is a subgroup, with no whole-population estimate
The incidence of malignant tumors was significantly increased in males treated with 2,000 ppm APM (p ≤ 0.01) compared with controls (Table 1).
PMID:17805418 · one of two readings recorded this
incidence of malignant tumor-bearing animals
increases
Albeit not significant, a numeric increase of the incidence of animals bearing malignant tumors was also observed among females exposed to 2,000 ppm APM compared with controls (Table 2)
PMID:17805418 · one of two readings recorded this
incidence of malignant tumor-bearing animals
increases, p = 0.01
The incidence of malignant tumors was significantly increased in males treated with 2,000 ppm APM (p ≤ 0.01) compared with controls (Table 1)
PMID:17805418 · one of two readings recorded this
incidence of malignant tumor-bearing animals
increases, p = 0.01
The incidence of malignant tumor–bearing animals occurred with a significant, dose-related increase in males (p ≤ 0.01)
PMID:17805418 · one of two readings recorded this
incidence of mammary gland carcinomas in females, histopathology at necropsy
increases, females at 2,000 ppm APM significantly higher than controls
Not recorded as a finding: the sentences that carry the finding do not name the compound as subject (agentless), and breast-cancer-incidence node is registry or pathology diagnosis in people
The incidence of lesions in females exposed to 2,000 ppm APM was significantly higher (p ≤ 0.05) compared with the controls.
PMID:17805418 · one of two readings recorded this
incidence of mammary gland carcinomas
increases, p = 0.05
The incidence of lesions in females exposed to 2,000 ppm APM was significantly higher (p ≤ 0.05) compared with the controls
PMID:17805418 · one of two readings recorded this
incidence of mammary gland carcinomas
increases, p = 0.05
A dose-related increase in the incidence of carcinomas was observed in females (p ≤ 0.05)
PMID:17805418 · one of two readings recorded this
mammary carcinomas in males
unclear
Two carcinomas were also observed among males treated with 2,000 ppm APM
PMID:17805418 · one of two readings recorded this
mean body weight, weekly then fortnightly
no effect, no difference in mean body weight between treated groups and controls
Not recorded as a finding: agentless sentence naming 'the treated groups' with no compound; absence is stated one-way only for survival
No difference in mean body weight was observed in the treated groups compared with the controls.
PMID:17805418 · one of two readings recorded this
mean body weight
no effect
No difference in mean body weight was observed in the treated groups compared with the controls
PMID:17805418 · one of two readings recorded this
survival
decreases
We observed a slight decrease, seemingly dose related, in survival in the treated groups compared with the control group in both males and females
PMID:17805418 · one of two readings recorded this
HDL cholesterol
decreases
HDL-C (mg/dL) | 77.13 | ± | 3.55 | 63.25** | ± | 3.04 | 54.47§§ | ± | 2.73 | 41.45**§§ | ± | 2.23
PMID:22509243 · one of two readings recorded this
HOMA-IR
no effect
HOMA-IR | 2.36 | ± | 0.35 | 3.19 | ± | 0.24 | 1.35§ | ± | 0.11 | 1.29§§ | ± | 0.1
PMID:22509243 · one of two readings recorded this
LDL cholesterol
increases
LDL (mg/dL) | 23.54 | ± | 3.10 | 36.34* | ± | 3.42 | 42.80 | ± | 2.63 | 60.89**§§ | ± | 2.41
PMID:22509243 · one of two readings recorded this
annulus crossing index, probe test
decreases, p = 0.01
male aspartame-fed mice crossed the former location of the platform significantly less frequently than controls (<0.01), and had a lower Annulus Crossing Index (<0.01)
PMID:22509243 · one of two readings recorded this
aspartame ingestion
Averaged aspartame ingestion in the drinking water was 55.14±4.74 mg/Kg body weight
PMID:22509243 · one of two readings recorded this
body length and visceral fat deposition
increases, p = 0.01
Body length and visceral fat deposition were both increased in aspartame-fed mice of both sexes (Table 1, P<0.01)
PMID:22509243 · one of two readings recorded this
body length
increases
Length (cm) | 9.65 | ± | 0.08 | 10.04** | ± | 0.08 | 9.21 | ± | 0.07 | 9.52**§§ | ± | 0.06
PMID:22509243 · one of two readings recorded this
body weight at 17 weeks
no effect
Body Weight (17 weeks) | 24.02 | ± | 0.48 | 24.96 | ± | 0.4 | 18.91§§ | ± | 0.21 | 19.42§§ | ± | 0.27
PMID:22509243 · one of two readings recorded this
body weight at 6 weeks
no effect
Body Weight (6 weeks) | 17.6 | ± | 0.13 | 17.22 | ± | 0.35 | 14.31§§ | ± | 0.17 | 14.34§§ | ± | 0.22
PMID:22509243 · one of two readings recorded this
correlation of body weight at 6 weeks with body weight at 17 weeks
p = 0.001
body weight at six weeks of age strongly correlated with weight at 17 weeks (Table 2, r = 0.888, P<0.001)
PMID:22509243 · one of two readings recorded this
correlation of visceral fat with probe-test annulus crossing index
decreases
Probe Test | −0.213 | −0.027 | −0.359* | −0.004 | −0.074 | −0.052 | 0.048 | 0.317* | −0.303*
PMID:22509243 · one of two readings recorded this
correlation of visceral fat with probe-test floating time
increases
Probe Test | 0.258 | 0.188 | 0.457** | −0.077 | 0.433** | 0.177 | 0.202 | 0.012 | 0.074
PMID:22509243 · one of two readings recorded this
correlation of visceral fat with probe-test latency
increases
Probe Test | 0.211 | 0.076 | 0.431** | 0.017 | 0.207 | 0.150 | −0.116 | −0.257 | 0.281*
PMID:22509243 · one of two readings recorded this
correlation of visceral fat with probe-test platform crosses
decreases
Probe Test | −0.265 | −0.120 | −0.401** | 0.023 | −0.157 | −0.080 | −0.005 | 0.223 | −0.221
PMID:22509243 · one of two readings recorded this
correlation of visceral fat with probe-test thigmotaxis
increases
Probe Test | −0.010 | 0.211 | 0.356* | 0.001 | 0.259 | 0.133 | 0.061 | 0.123 | −0.097
PMID:22509243 · one of two readings recorded this
escape latency, acquisition
increases, p = 0.05
latencies of male aspartame-treated mice were higher than control latencies on the last 2 days of the 4-day trial (<0.05)
PMID:22509243 · one of two readings recorded this
fasting blood glucose, both sexes
increases, p = 0.01
aspartame-fed mice had elevated fasting blood glucose levels compared to non-consumers of both sexes, although females had lower levels than males (Table 1, P<0.01)
PMID:22509243 · one of two readings recorded this
fasting glucose
increases
Fasting Glucose (mM) | 3.1 | ± | 0.18 | 4.61** | ± | 0.43 | 2.93 | ± | 0.13 | 3.65**§ | ± | 0.17
PMID:22509243 · one of two readings recorded this
fasting insulin
decreases
Fasting Insulin (uIU/ml) | 17.32 | ± | 2.54 | 16.67 | ± | 1.86 | 10.37§ | ± | 0.8 | 8*§§ | ± | 0.58
PMID:22509243 · one of two readings recorded this
floating time, acquisition
increases, p = 0.001
with male aspartame-fed mice exhibiting increased floating behavior on days 2,3 and 4 compared to controls (<0.001)
PMID:22509243 · one of two readings recorded this
GLM p-value: annulus crossing index, probe test
no effect, p = 0.199
Annulus Crossing Index | 0.263 | 0.536 | 0.290 | 0.619 | 0.199
PMID:22509243 · one of two readings recorded this
GLM p-value: annulus crossing index, probe test
decreases, p = 0.001
Annulus Crossing Index | 0.781 | 0.569 | <.01 | 0.553 | <.001
PMID:22509243 · one of two readings recorded this
GLM p-value: floating time, probe test
no effect, p = 0.175
Floating (% time) | 0.191 | 0.347 | 0.640 | <.01 | 0.175
PMID:22509243 · one of two readings recorded this
GLM p-value: floating time, probe test
increases, p = 0.05
Floating time (%) | 0.348 | <.01 | <.001 | <.001 | <.05
PMID:22509243 · one of two readings recorded this
GLM p-value: latency, probe test
no effect, p = 0.474
Latency | 0.817 | 0.359 | 0.644 | 0.090 | 0.474
PMID:22509243 · one of two readings recorded this
GLM p-value: latency, probe test
unclear, p = 0.001
Latency | 0.862 | 0.061 | <.001 | <.01 | <.001
PMID:22509243 · one of two readings recorded this
GLM p-value: mean distance to goal, probe test
increases, p = 0.05
Mean distance to goal (m) | 0.626 | 0.822 | 0.291 | <.05 | <.05
PMID:22509243 · one of two readings recorded this
GLM p-value: mean distance to goal, probe test
increases, p = 0.05
Mean distance to goal (m) | <.05 | <.05 | <.001 | <.001 | <.05
PMID:22509243 · one of two readings recorded this
GLM p-value: platform crosses, probe test
no effect, p = 0.277
Platform Crosses | 0.225 | 0.339 | 0.650 | 0.153 | 0.277
PMID:22509243 · one of two readings recorded this
GLM p-value: platform crosses, probe test
decreases, p = 0.001
Platform Crosses | 0.715 | 0.547 | <.001 | 0.800 | <.001
PMID:22509243 · one of two readings recorded this
GLM p-value: thigmotaxis time, probe test
no effect, p = 0.818
Thigmotaxis (% time) | 0.623 | 0.957 | 0.452 | <.05 | 0.818
PMID:22509243 · one of two readings recorded this
GLM p-value: thigmotaxis time, probe test
no effect, p = 0.236
Thigmotaxis time (%) | <.01 | <.01 | <.0001 | <.0001 | 0.236
PMID:22509243 · one of two readings recorded this
GLM p-value: time in non-target quadrants, probe test
increases, p = 0.05
Time in non-target quadrants (%) | 0.321 | 0.895 | 0.602 | 0.175 | <.05
PMID:22509243 · one of two readings recorded this
GLM p-value: time in non-target quadrants, probe test
no effect, p = 0.111
Time in non-target quadrants (%) | <.01 | 0.076 | <.05 | 0.112 | 0.111
PMID:22509243 · one of two readings recorded this
GLM p-value: time in target quadrant, probe test
decreases, p = 0.05
Time in target quadrant (%) | 0.321 | 0.897 | 0.605 | 0.176 | <.05
PMID:22509243 · one of two readings recorded this
GLM p-value: time in target quadrant, probe test
no effect, p = 0.112
Time in target quadrant (%) | <.01 | 0.076 | <.05 | 0.112 | 0.112
PMID:22509243 · one of two readings recorded this
glucose after insulin challenge, random-fed ITT
increases, p = 0.001
glucose levels in male aspartame-fed mice were 120.2% higher than control mice following insulin challenge (= 0.001)
PMID:22509243 · one of two readings recorded this
ITT AUCtotal
no effect, p = 0.19
AUCtotal (mM x min) | 4819.93 | ± | 190.36 | 5194.63 | ± | 208.04 | 0.19
PMID:22509243 · one of two readings recorded this
ITT AUCtotal
increases, p = 0.001
AUCtotal (mM x min) | 4829.58 | ± | 131.96 | 5829.79 | ± | 197.07 | <.001
PMID:22509243 · one of two readings recorded this
ITT glucose half-life T½
no effect, p = 0.31
T½ (min) | 34.19 | ± | 4.4 | 23.28 | ± | 9.59 | 0.31
PMID:22509243 · one of two readings recorded this
ITT glucose half-life T½
no effect, p = 0.59
T½ (min) | 39.69 | ± | 14.05 | 51.61 | ± | 16.63 | 0.59
PMID:22509243 · one of two readings recorded this
ITT Kglucose
no effect, p = 0.31
Kglucose (%/min) | 2.71 | ± | 0.37 | 2.24 | ± | 0.26 | 0.31
PMID:22509243 · one of two readings recorded this
ITT Kglucose
no effect, p = 0.15
Kglucose (%/min) | 2.92 | ± | 0.28 | 2.32 | ± | 0.29 | 0.15
PMID:22509243 · one of two readings recorded this
liver weight
increases
Liver Weight (g) | 0.89 | ± | 0.02 | 1.03* | ± | 0.06 | 0.76 | ± | 0.03 | 0.71§§ | ± | 0.02
PMID:22509243 · one of two readings recorded this
mean distance to goal, acquisition
increases, p = 0.05
aspartame-fed mice were farther from their goal than controls on all four days of acquisition training, suggestive of impaired learning (<0.05)
PMID:22509243 · one of two readings recorded this
percent weight gain between 6 and 17 weeks of age
increases, weight gain significantly higher in male aspartame group; female weight gain unaffected, p = 0.024
Not recorded as a finding: Reported as significant in males only (P = 0.024) with females unaffected, so the whole-population contrast is not a single estimate; gain from baseline is not total body mass
Weight gain was significantly higher in the male aspartame diet group compared to controls (Table 1, P = 0.024), but female weight gain was unaffected by diet.
PMID:22509243 · one of two readings recorded this
platform crossings, probe test
decreases, p = 0.01
male aspartame-fed mice crossed the former location of the platform significantly less frequently than controls (<0.01), and had a lower Annulus Crossing Index (<0.01)
PMID:22509243 · one of two readings recorded this
relative weight of liver
modulates
RW of Liver (g/20g BW) | 0.75 | ± | 0.02 | 0.82 | ± | 0.04 | 0.81 | ± | 0.03 | 0.736* | ± | 0.02
PMID:22509243 · one of two readings recorded this
relative weight of visceral fat
increases
RW of Visceral Fat (g/20g BW) | 0.08 | ± | 0.01 | 0.192** | ± | 0.02 | 0.09 | ± | 0.01 | 0.13**§§ | ± | 0.01
PMID:22509243 · one of two readings recorded this
serum triglycerides
modulates
TG (mg/dL) | 104.17 | ± | 7.42 | 107.41 | ± | 5.88 | 123.25 | ± | 6.67 | 98.24* | ± | 6.32
PMID:22509243 · one of two readings recorded this
spatial and directional search strategies, acquisition
decreases, p = 0.05
compared to control, aspartame-fed mice exhibited significantly less time acquiring spatial and directional strategies to find the hidden platform during the acquisition training (<0.05)
PMID:22509243 · one of two readings recorded this
spatial learning and reference memory in the Morris water maze (probe-test time swimming at the former platform location, acquisition latency, thigmotaxis, floating); also fasting blood glucose by Ascensia Contour glucometer and percent weight gain
decreases, aspartame-fed mice of both genders spent significantly less time swimming towards the former platform position than control, P < 0.05
Not recorded as a finding: this platform holds no node for the endpoint
Once the platform had been removed, aspartame-fed mice of both genders spent significantly less time swimming towards the former position of the hidden platform compared to control, (<0.05).
PMID:22509243 · one of two readings recorded this
thigmotaxis, acquisition
increases, p = 0.01
Thigmotaxis, defined as percentage of time spent swimming within 16cm of the pool wall, was greatly increased in aspartame-treated males throughout the whole experiment (<0.01)
PMID:22509243 · one of two readings recorded this
time in target quadrant, acquisition
decreases, p = 0.05
aspartame-fed males spent significantly less time searching for the platform in the target quadrant (<0.05)
PMID:22509243 · one of two readings recorded this
time swimming toward former platform position, probe test
decreases, p = 0.05
aspartame-fed mice of both genders spent significantly less time swimming towards the former position of the hidden platform compared to control, (<0.05)
PMID:22509243 · one of two readings recorded this
total cholesterol
no effect
T-CHOL (mg/dL) | 121.5 | ± | 1.08 | 121.08 | ± | 1.4 | 121.92 | ± | 0.91 | 122 | ± | 0.46
PMID:22509243 · one of two readings recorded this
visceral fat
increases
Visceral Fat (g) | 0.09 | ± | 0.02 | 0.24** | ± | 0.02 | 0.08 | ± | 0.01 | 0.13**§§ | ± | 0.01
PMID:22509243 · one of two readings recorded this
% weight gain (6-17 weeks)
increases
% Weight Gain | 36.42 | ± | 2.44 | 45.31* | ± | 2.71 | 32.3 | ± | 1.45 | 35.63§§ | ± | 1.5
PMID:22509243 · one of two readings recorded this
weight gain, males
increases, p = 0.024
Weight gain was significantly higher in the male aspartame diet group compared to controls (Table 1, P = 0.024)
PMID:22509243 · one of two readings recorded this
Angiogenesis, CAM assay
increases
In CAM assay, aspartame increased angiogenesis in a concentration-dependent manner
PMID:24925367 · one of two readings recorded this
Antiangiogenic effect, tube formation assay
no effect
there was no antiangiogenic effect of aspartame on tube formation assay in vitro
PMID:24925367 · one of two readings recorded this
HUVEC proliferation, XTT assay
no effect
There was a slight proliferative effect of aspartame on human umbilical vein endothelial cells on XTT assay in vitro, but it was not statistically significant
PMID:24925367 · one of two readings recorded this
Skin wound healing, rat model
increases, p = 0.05
in vivo rat model of skin wound-healing study showed that aspartame group had better healing than control group, and this was statistically significant at p < 0.05
PMID:24925367 · one of two readings recorded this
Vessel proliferation, CAM assay
increases, p = 0.001
Compared with the control group, aspartame has significantly increased vessel proliferation (p < 0.001)
PMID:24925367 · one of two readings recorded this
vessel proliferation in the chick chorioallantoic membrane assay, skin wound healing in rats, XTT proliferation and tube formation in human umbilical vein endothelial cells
increases
Not recorded as a finding: this platform holds no node for the endpoint
Compared with the control group, aspartame has significantly increased vessel proliferation (p < 0.001).
PMID:24925367 · one of two readings recorded this
lipid accumulation in differentiated 3T3-L1 adipocytes by Oil Red O staining; PPARgamma, FABP4, C/EBPalpha mRNA by qRT-PCR; PPARgamma, SREBP1, adipsin protein by Western blot
decreases
Not recorded as a finding: this platform holds no node for the endpoint
Aspartame reduced lipid accumulation in differentiated adipocytes as evidenced by Oil Red O staining.
PMID:24961835 · one of two readings recorded this
Lipid accumulation in differentiated adipocytes
decreases
Aspartame reduced lipid accumulation in differentiated adipocytes as evidenced by Oil Red O staining
PMID:24961835 · one of two readings recorded this
p-PPARγ, PPARγ, SREBP1 and adipsin protein induction
decreases
Western blot analysis showed that the induction of p-PPARγ, PPARγ, SREBP1, and adipsin was markedly reduced in the aspartame-treated adipocytes
PMID:24961835 · one of two readings recorded this
PPARγ, FABP4 and C/EBPα mRNA expression
decreases
qRT-PCR analysis showed that the PPARγ, FABP4, and C/EBPα mRNA expression was significantly reduced in the aspartame-treated adipocytes
PMID:24961835 · one of two readings recorded this
catalase activity
increases
cerebral cortex (F = 27, df = 2), cerebellum(F = 34, df = 2), midbrain (F = 53, df = 2), pons-medulla (F = 14, df = 2), hippocampus (F = 25, df = 2) and hypothalamus (F = 50, df = 2)
PMID:25009784 · one of two readings recorded this
catalase activity
increases
cerebral cortex (F = 27, df = 2), cerebellum(F = 34, df = 2), midbrain (F = 53, df = 2), pons-medulla (F = 14, df = 2), hippocampus (F = 25, df = 2) and hypothalamus (F = 50, df = 2)
PMID:25009784 · one of two readings recorded this
catalase activity
increases
cerebral cortex (F = 27, df = 2), cerebellum(F = 34, df = 2), midbrain (F = 53, df = 2), pons-medulla (F = 14, df = 2), hippocampus (F = 25, df = 2) and hypothalamus (F = 50, df = 2)
PMID:25009784 · one of two readings recorded this
catalase activity
increases
cerebral cortex (F = 27, df = 2), cerebellum(F = 34, df = 2), midbrain (F = 53, df = 2), pons-medulla (F = 14, df = 2), hippocampus (F = 25, df = 2) and hypothalamus (F = 50, df = 2)
PMID:25009784 · one of two readings recorded this
catalase activity
increases
cerebral cortex (F = 27, df = 2), cerebellum(F = 34, df = 2), midbrain (F = 53, df = 2), pons-medulla (F = 14, df = 2), hippocampus (F = 25, df = 2) and hypothalamus (F = 50, df = 2)
PMID:25009784 · one of two readings recorded this
catalase activity
increases
cerebral cortex (F = 27, df = 2), cerebellum(F = 34, df = 2), midbrain (F = 53, df = 2), pons-medulla (F = 14, df = 2), hippocampus (F = 25, df = 2) and hypothalamus (F = 50, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione peroxidase activity
increases
cerebral cortex (F = 153, df = 2), cerebellum (F = 151, df = 2), midbrain (F = 43, df = 2), pons-medulla (F = 152, df = 2), hippocampus (F = 150, df = 2) and hypothalamus (F = 237, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione peroxidase activity
increases
cerebral cortex (F = 153, df = 2), cerebellum (F = 151, df = 2), midbrain (F = 43, df = 2), pons-medulla (F = 152, df = 2), hippocampus (F = 150, df = 2) and hypothalamus (F = 237, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione peroxidase activity
increases
cerebral cortex (F = 153, df = 2), cerebellum (F = 151, df = 2), midbrain (F = 43, df = 2), pons-medulla (F = 152, df = 2), hippocampus (F = 150, df = 2) and hypothalamus (F = 237, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione peroxidase activity
increases
cerebral cortex (F = 153, df = 2), cerebellum (F = 151, df = 2), midbrain (F = 43, df = 2), pons-medulla (F = 152, df = 2), hippocampus (F = 150, df = 2) and hypothalamus (F = 237, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione peroxidase activity
increases
cerebral cortex (F = 153, df = 2), cerebellum (F = 151, df = 2), midbrain (F = 43, df = 2), pons-medulla (F = 152, df = 2), hippocampus (F = 150, df = 2) and hypothalamus (F = 237, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione peroxidase activity
increases
cerebral cortex (F = 153, df = 2), cerebellum (F = 151, df = 2), midbrain (F = 43, df = 2), pons-medulla (F = 152, df = 2), hippocampus (F = 150, df = 2) and hypothalamus (F = 237, df = 2)
PMID:25009784 · one of two readings recorded this
reduced glutathione
decreases
cerebral cortex (F = 62, df = 2), cerebellum (F = 39, df = 2), midbrain (F = 40, df = 2), pons-medulla (F = 38, df = 2), hippocampus (F = 33, df = 2) and hypothalamus (F = 50, df = 2)
PMID:25009784 · one of two readings recorded this
reduced glutathione
decreases
cerebral cortex (F = 62, df = 2), cerebellum (F = 39, df = 2), midbrain (F = 40, df = 2), pons-medulla (F = 38, df = 2), hippocampus (F = 33, df = 2) and hypothalamus (F = 50, df = 2)
PMID:25009784 · one of two readings recorded this
reduced glutathione
decreases
cerebral cortex (F = 62, df = 2), cerebellum (F = 39, df = 2), midbrain (F = 40, df = 2), pons-medulla (F = 38, df = 2), hippocampus (F = 33, df = 2) and hypothalamus (F = 50, df = 2)
PMID:25009784 · one of two readings recorded this
reduced glutathione
decreases
cerebral cortex (F = 62, df = 2), cerebellum (F = 39, df = 2), midbrain (F = 40, df = 2), pons-medulla (F = 38, df = 2), hippocampus (F = 33, df = 2) and hypothalamus (F = 50, df = 2)
PMID:25009784 · one of two readings recorded this
reduced glutathione
decreases
cerebral cortex (F = 62, df = 2), cerebellum (F = 39, df = 2), midbrain (F = 40, df = 2), pons-medulla (F = 38, df = 2), hippocampus (F = 33, df = 2) and hypothalamus (F = 50, df = 2)
PMID:25009784 · one of two readings recorded this
reduced glutathione
decreases
cerebral cortex (F = 62, df = 2), cerebellum (F = 39, df = 2), midbrain (F = 40, df = 2), pons-medulla (F = 38, df = 2), hippocampus (F = 33, df = 2) and hypothalamus (F = 50, df = 2)
PMID:25009784 · one of two readings recorded this
activated caspase 3 mRNA expression
increases
cerebral cortex (F = 174.98, df = 2), cerebellum (F = 71.51, df = 2), hippocampus (F = 167.36, df = 2) and hypothalamus (F = 5.08, df = 2)
PMID:25009784 · one of two readings recorded this
activated caspase 3 mRNA expression
increases
cerebral cortex (F = 174.98, df = 2), cerebellum (F = 71.51, df = 2), hippocampus (F = 167.36, df = 2) and hypothalamus (F = 5.08, df = 2)
PMID:25009784 · one of two readings recorded this
activated caspase 3 mRNA expression
increases
cerebral cortex (F = 174.98, df = 2), cerebellum (F = 71.51, df = 2), hippocampus (F = 167.36, df = 2) and hypothalamus (F = 5.08, df = 2)
PMID:25009784 · one of two readings recorded this
activated caspase 3 mRNA expression
increases
cerebral cortex (F = 174.98, df = 2), cerebellum (F = 71.51, df = 2), hippocampus (F = 167.36, df = 2) and hypothalamus (F = 5.08, df = 2)
PMID:25009784 · one of two readings recorded this
Bax mRNA expression
increases
cerebral cortex (F = 57.62, df = 2), cerebellum (F = 48.83, df = 2), hippocampus (F = 97.80, df = 2) and hypothalamus (F = 27.74, df = 2)
PMID:25009784 · one of two readings recorded this
Bax mRNA expression
increases
cerebral cortex (F = 57.62, df = 2), cerebellum (F = 48.83, df = 2), hippocampus (F = 97.80, df = 2) and hypothalamus (F = 27.74, df = 2)
PMID:25009784 · one of two readings recorded this
Bax mRNA expression
increases
cerebral cortex (F = 57.62, df = 2), cerebellum (F = 48.83, df = 2), hippocampus (F = 97.80, df = 2) and hypothalamus (F = 27.74, df = 2)
PMID:25009784 · one of two readings recorded this
Bax mRNA expression
increases
cerebral cortex (F = 57.62, df = 2), cerebellum (F = 48.83, df = 2), hippocampus (F = 97.80, df = 2) and hypothalamus (F = 27.74, df = 2)
PMID:25009784 · one of two readings recorded this
Bax protein expression and activated caspase 3
increases
cerebral cortex (F = 23.59, df = 2), cerebellum (F = 5.78, df = 2), and hippocampus (F = 6.14, df = 2)
PMID:25009784 · one of two readings recorded this
Bax protein expression and activated caspase 3
increases
cerebral cortex (F = 23.59, df = 2), cerebellum (F = 5.78, df = 2), and hippocampus (F = 6.14, df = 2)
PMID:25009784 · one of two readings recorded this
Bax protein expression and activated caspase 3
increases
cerebral cortex (F = 23.59, df = 2), cerebellum (F = 5.78, df = 2), and hippocampus (F = 6.14, df = 2)
PMID:25009784 · one of two readings recorded this
Bcl2 mRNA expression
decreases
cerebral cortex (F = 243.29, df = 2), cerebellum (F = 58.96, df = 2), hippocampus (F = 114.14, df = 2) and hypothalamus (F = 222.61, df = 2)
PMID:25009784 · one of two readings recorded this
Bcl2 mRNA expression
decreases
cerebral cortex (F = 243.29, df = 2), cerebellum (F = 58.96, df = 2), hippocampus (F = 114.14, df = 2) and hypothalamus (F = 222.61, df = 2)
PMID:25009784 · one of two readings recorded this
Bcl2 mRNA expression
decreases
cerebral cortex (F = 243.29, df = 2), cerebellum (F = 58.96, df = 2), hippocampus (F = 114.14, df = 2) and hypothalamus (F = 222.61, df = 2)
PMID:25009784 · one of two readings recorded this
Bcl2 mRNA expression
decreases
cerebral cortex (F = 243.29, df = 2), cerebellum (F = 58.96, df = 2), hippocampus (F = 114.14, df = 2) and hypothalamus (F = 222.61, df = 2)
PMID:25009784 · one of two readings recorded this
Bcl2 protein expression
decreases
cerebral cortex (F = 34.07, df = 2), cerebellum (F = 81.03, df = 2), and hippocampus (F = 60.35, df = 2)
PMID:25009784 · one of two readings recorded this
Bcl2 protein expression
decreases
cerebral cortex (F = 34.07, df = 2), cerebellum (F = 81.03, df = 2), and hippocampus (F = 60.35, df = 2)
PMID:25009784 · one of two readings recorded this
Bcl2 protein expression
decreases
cerebral cortex (F = 34.07, df = 2), cerebellum (F = 81.03, df = 2), and hippocampus (F = 60.35, df = 2)
PMID:25009784 · one of two readings recorded this
brain reduced glutathione by region
decreases, decreased in all brain regions studied versus control and MTX control
Not recorded as a finding: reduced-glutathione node is erythrocyte, whole blood or plasma; this is brain tissue
The activity of reduced glutathione was decreased in the entire brain regions studied such as cerebral cortex (F = 62, df = 2), cerebellum (F = 39, df = 2), midbrain (F = 40, df = 2), pons-medulla (F = 38, df = 2), hippocampus (F = 33, df = 2) and hypothalamus (F = 50, df = 2) in aspartame treated MTX animals when compared to control and MTX treated control.
PMID:25009784 · one of two readings recorded this
brain-region superoxide dismutase, catalase, glutathione peroxidase and reduced glutathione in tissue homogenate
increases, SOD activity increased significantly in aspartame-treated MTX animals in all six brain regions versus control and MTX control
Not recorded as a finding: Outcome nodes superoxide-dismutase-activity, catalase-activity, glutathione-peroxidase-activity and reduced-glutathione are defined on erythrocyte lysate, whole blood, plasma or serum; these are brain-region homogenates, so they are near misses and are recorded in the mechanism lane instead
Activity of SOD increased significantly in aspartame treated MTX animals in the regions cerebral cortex (F = 8.7, df = 2), cerebellum (F = 8.9, df = 2), midbrain (F = 25, df = 2), pons-medulla (F = 21, df = 2), hippocampus (F = 119, df = 2) and hypothalamus (F = 11, df = 2) when compared to control and MTX treated control.
PMID:25009784 · one of two readings recorded this
glutathione reductase activity
decreases
cerebral cortex (F = 4.11, df = 2), cerebellum (F = 6.67, df = 2), midbrain (F = 8.42, df = 2), pons-medulla (F = 19, df = 2), hippocampus (F = 172, df = 2) and hypothalamus (F = 20, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione reductase activity
decreases
cerebral cortex (F = 4.11, df = 2), cerebellum (F = 6.67, df = 2), midbrain (F = 8.42, df = 2), pons-medulla (F = 19, df = 2), hippocampus (F = 172, df = 2) and hypothalamus (F = 20, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione reductase activity
decreases
cerebral cortex (F = 4.11, df = 2), cerebellum (F = 6.67, df = 2), midbrain (F = 8.42, df = 2), pons-medulla (F = 19, df = 2), hippocampus (F = 172, df = 2) and hypothalamus (F = 20, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione reductase activity
decreases
cerebral cortex (F = 4.11, df = 2), cerebellum (F = 6.67, df = 2), midbrain (F = 8.42, df = 2), pons-medulla (F = 19, df = 2), hippocampus (F = 172, df = 2) and hypothalamus (F = 20, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione reductase activity
decreases
cerebral cortex (F = 4.11, df = 2), cerebellum (F = 6.67, df = 2), midbrain (F = 8.42, df = 2), pons-medulla (F = 19, df = 2), hippocampus (F = 172, df = 2) and hypothalamus (F = 20, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione reductase activity
decreases
cerebral cortex (F = 4.11, df = 2), cerebellum (F = 6.67, df = 2), midbrain (F = 8.42, df = 2), pons-medulla (F = 19, df = 2), hippocampus (F = 172, df = 2) and hypothalamus (F = 20, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione-S-transferase activity
increases
cerebral cortex (F = 71, df = 2), cerebellum (F = 33, df = 2), midbrain (F = 87, df = 2), pons-medulla (F = 19, df = 2), hippocampus (F = 32, df = 2) and hypothalamus (F = 72, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione-S-transferase activity
increases
cerebral cortex (F = 71, df = 2), cerebellum (F = 33, df = 2), midbrain (F = 87, df = 2), pons-medulla (F = 19, df = 2), hippocampus (F = 32, df = 2) and hypothalamus (F = 72, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione-S-transferase activity
increases
cerebral cortex (F = 71, df = 2), cerebellum (F = 33, df = 2), midbrain (F = 87, df = 2), pons-medulla (F = 19, df = 2), hippocampus (F = 32, df = 2) and hypothalamus (F = 72, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione-S-transferase activity
increases
cerebral cortex (F = 71, df = 2), cerebellum (F = 33, df = 2), midbrain (F = 87, df = 2), pons-medulla (F = 19, df = 2), hippocampus (F = 32, df = 2) and hypothalamus (F = 72, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione-S-transferase activity
increases
cerebral cortex (F = 71, df = 2), cerebellum (F = 33, df = 2), midbrain (F = 87, df = 2), pons-medulla (F = 19, df = 2), hippocampus (F = 32, df = 2) and hypothalamus (F = 72, df = 2)
PMID:25009784 · one of two readings recorded this
glutathione-S-transferase activity
increases
cerebral cortex (F = 71, df = 2), cerebellum (F = 33, df = 2), midbrain (F = 87, df = 2), pons-medulla (F = 19, df = 2), hippocampus (F = 32, df = 2) and hypothalamus (F = 72, df = 2)
PMID:25009784 · one of two readings recorded this
hippocampal neuronal morphology (H&E)
decreases
Aspartame + MTX treated animal’s shows the neuronal shrinkage of hippocampal layer due to degeneration of pyramidal cells, as visualized by H&E, when compared to control and MTX controls
PMID:25009784 · one of two readings recorded this
lipid peroxidation
increases
cerebral cortex (F = 73, df = 2), cerebellum (F = 313, df = 2), midbrain (F = 206, df = 2), pons-medulla (F = 362, df = 2), hippocampus (F = 135, df = 2) and hypothalamus(F = 811, df = 2)
PMID:25009784 · one of two readings recorded this
lipid peroxidation
increases
cerebral cortex (F = 73, df = 2), cerebellum (F = 313, df = 2), midbrain (F = 206, df = 2), pons-medulla (F = 362, df = 2), hippocampus (F = 135, df = 2) and hypothalamus(F = 811, df = 2)
PMID:25009784 · one of two readings recorded this
lipid peroxidation
increases
cerebral cortex (F = 73, df = 2), cerebellum (F = 313, df = 2), midbrain (F = 206, df = 2), pons-medulla (F = 362, df = 2), hippocampus (F = 135, df = 2) and hypothalamus(F = 811, df = 2)
PMID:25009784 · one of two readings recorded this
lipid peroxidation
increases
cerebral cortex (F = 73, df = 2), cerebellum (F = 313, df = 2), midbrain (F = 206, df = 2), pons-medulla (F = 362, df = 2), hippocampus (F = 135, df = 2) and hypothalamus(F = 811, df = 2)
PMID:25009784 · one of two readings recorded this
lipid peroxidation
increases
cerebral cortex (F = 73, df = 2), cerebellum (F = 313, df = 2), midbrain (F = 206, df = 2), pons-medulla (F = 362, df = 2), hippocampus (F = 135, df = 2) and hypothalamus(F = 811, df = 2)
PMID:25009784 · one of two readings recorded this
lipid peroxidation
increases
cerebral cortex (F = 73, df = 2), cerebellum (F = 313, df = 2), midbrain (F = 206, df = 2), pons-medulla (F = 362, df = 2), hippocampus (F = 135, df = 2) and hypothalamus(F = 811, df = 2)
PMID:25009784 · one of two readings recorded this
plasma methanol level
increases
the aspartame treated MTX animals showed a marked increase (F = 140, df = 2) in the plasma methanol level from control and MTX treated control animals
PMID:25009784 · one of two readings recorded this
protein carbonyl
increases
cerebral cortex (F = 143, df = 2), cerebellum (F = 23, df = 2), midbrain (F = 24, df = 2), pons-medulla (F = 14, df = 2), hippocampus (F = 64, df = 2) and hypothalamus (F = 132, df = 2)
PMID:25009784 · one of two readings recorded this
protein carbonyl
increases
cerebral cortex (F = 143, df = 2), cerebellum (F = 23, df = 2), midbrain (F = 24, df = 2), pons-medulla (F = 14, df = 2), hippocampus (F = 64, df = 2) and hypothalamus (F = 132, df = 2)
PMID:25009784 · one of two readings recorded this
protein carbonyl
increases
cerebral cortex (F = 143, df = 2), cerebellum (F = 23, df = 2), midbrain (F = 24, df = 2), pons-medulla (F = 14, df = 2), hippocampus (F = 64, df = 2) and hypothalamus (F = 132, df = 2)
PMID:25009784 · one of two readings recorded this
protein carbonyl
increases
cerebral cortex (F = 143, df = 2), cerebellum (F = 23, df = 2), midbrain (F = 24, df = 2), pons-medulla (F = 14, df = 2), hippocampus (F = 64, df = 2) and hypothalamus (F = 132, df = 2)
PMID:25009784 · one of two readings recorded this
protein carbonyl
increases
cerebral cortex (F = 143, df = 2), cerebellum (F = 23, df = 2), midbrain (F = 24, df = 2), pons-medulla (F = 14, df = 2), hippocampus (F = 64, df = 2) and hypothalamus (F = 132, df = 2)
PMID:25009784 · one of two readings recorded this
protein carbonyl
increases
cerebral cortex (F = 143, df = 2), cerebellum (F = 23, df = 2), midbrain (F = 24, df = 2), pons-medulla (F = 14, df = 2), hippocampus (F = 64, df = 2) and hypothalamus (F = 132, df = 2)
PMID:25009784 · one of two readings recorded this
protein thiol (sulfhydryl) content
decreases
cerebral cortex (F = 78, df = 2), cerebellum (F = 129, df = 2), midbrain (F = 53, df = 2), pons-medulla (F = 275, df = 2), hippocampus (F = 17, df = 2) and hypothalamus (F = 239, df = 2)
PMID:25009784 · one of two readings recorded this
protein thiol (sulfhydryl) content
decreases
cerebral cortex (F = 78, df = 2), cerebellum (F = 129, df = 2), midbrain (F = 53, df = 2), pons-medulla (F = 275, df = 2), hippocampus (F = 17, df = 2) and hypothalamus (F = 239, df = 2)
PMID:25009784 · one of two readings recorded this
protein thiol (sulfhydryl) content
decreases
cerebral cortex (F = 78, df = 2), cerebellum (F = 129, df = 2), midbrain (F = 53, df = 2), pons-medulla (F = 275, df = 2), hippocampus (F = 17, df = 2) and hypothalamus (F = 239, df = 2)
PMID:25009784 · one of two readings recorded this
protein thiol (sulfhydryl) content
decreases
cerebral cortex (F = 78, df = 2), cerebellum (F = 129, df = 2), midbrain (F = 53, df = 2), pons-medulla (F = 275, df = 2), hippocampus (F = 17, df = 2) and hypothalamus (F = 239, df = 2)
PMID:25009784 · one of two readings recorded this
protein thiol (sulfhydryl) content
decreases
cerebral cortex (F = 78, df = 2), cerebellum (F = 129, df = 2), midbrain (F = 53, df = 2), pons-medulla (F = 275, df = 2), hippocampus (F = 17, df = 2) and hypothalamus (F = 239, df = 2)
PMID:25009784 · one of two readings recorded this
protein thiol (sulfhydryl) content
decreases
cerebral cortex (F = 78, df = 2), cerebellum (F = 129, df = 2), midbrain (F = 53, df = 2), pons-medulla (F = 275, df = 2), hippocampus (F = 17, df = 2) and hypothalamus (F = 239, df = 2)
PMID:25009784 · one of two readings recorded this
superoxide dismutase (SOD) activity
increases
cerebral cortex (F = 8.7, df = 2), cerebellum (F = 8.9, df = 2), midbrain (F = 25, df = 2), pons-medulla (F = 21, df = 2), hippocampus (F = 119, df = 2) and hypothalamus (F = 11, df = 2)
PMID:25009784 · one of two readings recorded this
superoxide dismutase (SOD) activity
increases
cerebral cortex (F = 8.7, df = 2), cerebellum (F = 8.9, df = 2), midbrain (F = 25, df = 2), pons-medulla (F = 21, df = 2), hippocampus (F = 119, df = 2) and hypothalamus (F = 11, df = 2)
PMID:25009784 · one of two readings recorded this
superoxide dismutase (SOD) activity
increases
cerebral cortex (F = 8.7, df = 2), cerebellum (F = 8.9, df = 2), midbrain (F = 25, df = 2), pons-medulla (F = 21, df = 2), hippocampus (F = 119, df = 2) and hypothalamus (F = 11, df = 2)
PMID:25009784 · one of two readings recorded this
superoxide dismutase (SOD) activity
increases
cerebral cortex (F = 8.7, df = 2), cerebellum (F = 8.9, df = 2), midbrain (F = 25, df = 2), pons-medulla (F = 21, df = 2), hippocampus (F = 119, df = 2) and hypothalamus (F = 11, df = 2)
PMID:25009784 · one of two readings recorded this
superoxide dismutase (SOD) activity
increases
cerebral cortex (F = 8.7, df = 2), cerebellum (F = 8.9, df = 2), midbrain (F = 25, df = 2), pons-medulla (F = 21, df = 2), hippocampus (F = 119, df = 2) and hypothalamus (F = 11, df = 2)
PMID:25009784 · one of two readings recorded this
superoxide dismutase (SOD) activity
increases
cerebral cortex (F = 8.7, df = 2), cerebellum (F = 8.9, df = 2), midbrain (F = 25, df = 2), pons-medulla (F = 21, df = 2), hippocampus (F = 119, df = 2) and hypothalamus (F = 11, df = 2)
PMID:25009784 · one of two readings recorded this
fasting blood glucose
increases
Fasting blood glucose (mM) | 5.4±0.2 | 6.9±0.4† | 5.6±0.2 | 7.4±0.6†
PMID:25313461 · one of two readings recorded this
Bacteroides/Prevotella spp. (log scale, fecal qPCR)
no effect, p = 0.244
Bacteroides/Prevotella spp. | 7.47±0.092 | 7.25±0.142 | 6.46±0.076* | 6.62±0.069* | <0.001 | 0.244 | 0.153
PMID:25313461 · one of two readings recorded this
Bifidobacterium spp. (log scale, fecal qPCR)
no effect, p = 0.062
Bifidobacterium spp. | 5.51±0.199 | 4.55±0.114 | 6.57±0.313* | 5.97±0.316† | 0.011 | 0.062 | 0.126
PMID:25313461 · one of two readings recorded this
blood glucose AUC in OGTT, main effect of APM
no effect, p = 0.05
No main effect of APM on blood glucose AUC was observed (p>0.05)
PMID:25313461 · one of two readings recorded this
blood glucose AUC in OGTT, main effect of diet
increases, p = 0.05
There was a significant main effect of diet for blood glucose AUC wherein HF was higher than CH (p<0.05)
PMID:25313461 · one of two readings recorded this
Sources cited
5 papers
- Subject
- aspartame
- Findings
- 9
- Papers
- 5
The effect of aspartame and sucralose intake on body weight measures and blood metabolites: role of their form (solid and/or liquid) of ingestion.record2022PMID:344205381 finding
Metabolic effects of aspartame in adulthood: A systematic review and meta-analysis of randomized clinical trials.record2018PMID:283946432 findings
Inhibition of the gut enzyme intestinal alkaline phosphatase may explain how aspartame promotes glucose intolerance and obesity in mice.record2017PMID:279972182 findings
Effects of long-term administration of aspartame on biochemical indices, lipid profile and redox status of cellular system of male rats.record2016PMID:262475073 findings
Biochemical responses and mitochondrial mediated activation of apoptosis on long-term effect of aspartame in rat brain.record2014PMID:250097841 finding
Other names
15 names
Resolves to: aspartame
- Also called
- 1-methyl N-L-alpha-aspartyl-L-phenylalanate1-methyl N-L-α-aspartyl-L-phenylalanate3-Amino-N-(alpha-carboxyphenethyl)succinamic acid N-methyl ester3-Amino-N-(alpha-methoxycarbonylphenethyl) succinamic acid3-Amino-N-(α-carboxyphenethyl)succinamic acid N-methyl ester3-Amino-N-(α-methoxycarbonylphenethyl) succinamic acidAsp-phe-omeAspartylphenylalanine methyl esterE 951L-Aspartyl-L-phenylalanine methyl esterNutraSweet
- Systematic name
- methyl L-alpha-aspartyl-L-phenylalaninatemethyl L-α-aspartyl-L-phenylalaninate
- Sold as
- AminoSweetSanecta