Studied for
4 endpoints · 4 findings · 1 paper
- HDL cholesterolraisesEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.
- LDL cholesterollowersEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.
- Total cholesterol (TC)lowersEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.
- TriglycerideslowersEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.
What the evidence says
How to read these marks4 findings · 4 endpoints · 1 paper · by evidence strength
What moved
4 findings
Decreases LDL cholesterol
Very limitedEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.Finding“Naringenin consumption significantly reduced percentages of NAFLD grades (P < .001), as well as, serum levels of triglyceride (TG) (P < .001), total cholesterol (TC) (P = .01), and low-density lipoprotein (LDL) (P = .02) and increased serum level of high-density lipoprotein (HDL) (P = .02) compared with the control group.”
Quoted verbatim from Does naringenin supplementation improve lipid profile, severity of hepatic steatosis and probability of liver fibrosis in overweight/obese patients with NAFLD? A randomised, double-blind, placebo-controlled, clinical trial.. - Study
- RCT
- Duration
- 4 weeks
- Dose
- 100 mg capsules twice a day, before lunch and dinner
- Population
- 44 overweight/obese patients with NAFLD, placebo-controlled
Does naringenin supplementation improve lipid profile, severity of hepatic steatosis and probability of liver fibrosis in overweight/obese patients with NAFLD? A randomised, double-blind, placebo-controlled, clinical trial.2021PMID:34516703Permalink
Decreases triglycerides
Very limitedEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.Finding“Naringenin consumption significantly reduced percentages of NAFLD grades (P < .001), as well as, serum levels of triglyceride (TG) (P < .001), total cholesterol (TC) (P = .01), and low-density lipoprotein (LDL) (P = .02) and increased serum level of high-density lipoprotein (HDL) (P = .02) compared with the control group.”
Quoted verbatim from Does naringenin supplementation improve lipid profile, severity of hepatic steatosis and probability of liver fibrosis in overweight/obese patients with NAFLD? A randomised, double-blind, placebo-controlled, clinical trial.. - Study
- RCT
- Duration
- 4 weeks
- Dose
- 100 mg capsules twice a day, before lunch and dinner
- Population
- 44 overweight/obese patients with NAFLD, placebo-controlled
Does naringenin supplementation improve lipid profile, severity of hepatic steatosis and probability of liver fibrosis in overweight/obese patients with NAFLD? A randomised, double-blind, placebo-controlled, clinical trial.2021PMID:34516703Permalink
Decreases total cholesterol (TC)
Very limitedEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.Finding“Naringenin consumption significantly reduced percentages of NAFLD grades (P < .001), as well as, serum levels of triglyceride (TG) (P < .001), total cholesterol (TC) (P = .01), and low-density lipoprotein (LDL) (P = .02) and increased serum level of high-density lipoprotein (HDL) (P = .02) compared with the control group.”
Quoted verbatim from Does naringenin supplementation improve lipid profile, severity of hepatic steatosis and probability of liver fibrosis in overweight/obese patients with NAFLD? A randomised, double-blind, placebo-controlled, clinical trial.. - Study
- RCT
- Duration
- 4 weeks
- Dose
- 100 mg capsules twice a day, before lunch and dinner
- Population
- 44 overweight/obese patients with NAFLD, placebo-controlled
Does naringenin supplementation improve lipid profile, severity of hepatic steatosis and probability of liver fibrosis in overweight/obese patients with NAFLD? A randomised, double-blind, placebo-controlled, clinical trial.2021PMID:34516703Permalink
Increases HDL cholesterol
Very limitedEvidence strength: very limited. Human evidence with major recorded weaknesses, or non-human, uncontrolled or unverified evidence.Finding“Naringenin consumption significantly reduced percentages of NAFLD grades (P < .001), as well as, serum levels of triglyceride (TG) (P < .001), total cholesterol (TC) (P = .01), and low-density lipoprotein (LDL) (P = .02) and increased serum level of high-density lipoprotein (HDL) (P = .02) compared with the control group.”
Quoted verbatim from Does naringenin supplementation improve lipid profile, severity of hepatic steatosis and probability of liver fibrosis in overweight/obese patients with NAFLD? A randomised, double-blind, placebo-controlled, clinical trial.. - Study
- RCT
- Duration
- 4 weeks
- Dose
- 100 mg capsules twice a day, before lunch and dinner
- Population
- 44 overweight/obese patients with NAFLD, placebo-controlled
Does naringenin supplementation improve lipid profile, severity of hepatic steatosis and probability of liver fibrosis in overweight/obese patients with NAFLD? A randomised, double-blind, placebo-controlled, clinical trial.2021PMID:34516703Permalink
On the label
Labelled products
6 products
Source: NIH DSLD · Ingredient: naringenin · 6 products · Declared amount per serving: 36–300 mg (5 products)
6 labels state an amount0 do not
- BioGenesis NutraceuticalsAdrenal Support Plus36 mgper 2 Capsule(s)DSLD:20760
- Centurion LabzOut of Rage XXX50 mgper 11.7 Gram(s)DSLD:201411
- Designs for HealthThermo-EFx300 mgper 1 Capsule(s)DSLD:23265
- i-Prevail SupplementsA.M.P.'D UP200 mgper 1 Capsule(s)DSLD:228497
- Redcon1Total War Pineapple JuiceNaringin Note: 98%0.17 Gram(s)per 6.45 Gram(s)DSLD:237008
- SuperSmartNatural Anti Aromatase SupportGrapefruit extract · standardized to 99% naringin200 mgper 2 Tablet(s)DSLD:332400
Label record: NIH Office of Dietary Supplements · CC0
Papers screened
10 papers
- Compound
- naringenin
- Screened
- 10
- Admitted
- 1
- Discarded
- 8
- Not read
- 1
Produced a finding1 paper
- PMID:345167032026-10-11
Discarded: no extractable result3 papers
- PMID:32879962no claim extracted — narrated_not_pooled2026-10-11
- PMID:34860705claims extracted but the two passes did not agree2026-10-11
- NCT03582553declared_contrast×7 — no posted analysis compares a naringenin arm with a placebo/no-intervention arm and carries a p-value (150 mg Dose=EXPERIMENTAL+subject, 300 mg Dose=EXPERIMENTAL+subject, 600 mg Dose=EXPERIMENTAL+subject, 900 mg Dose=EXPERIMENTAL+subject, Placebo=PLACEBO_COMPARATOR)2026-10-06
Discarded: another reason, stated per paper3 papers
- PMID:31468636no claim extracted — cause not determined (one pass only) — measured: serum naringenin concentration-time pharmacokinetics (Cmax, AUC over 24 h, half-life, apparent oral clearance), LC-based serum assay2026-10-11
- PMID:35804246no claim extracted — instrument_not_stated2026-10-11
- PMID:40996618no claim extracted — instrument_not_stated2026-10-11
Discarded: no comparator2 papers
- PMID:20100371no claim extracted — comparator_not_absence2026-10-11
- PMID:34310866no claim extracted — comparator_not_absence2026-10-11
Not read yet1 paper
- PMID:303914642026-09-29
Measured, not recorded
- Compound
- naringenin
- Endpoints measured
- 76 endpoints
- Recorded as a finding
- No
Show what was measured
hesperetin conjugate profile in urine
no effect, n = 16
the profile of the conjugates of flavanones formed and excreted in urine is neither affected by the absorption site nor by a 3-fold change in dose
PMID:20100371 · one of two readings recorded this
plasma naringenin AUC
increases, p = 0.0001, n = 16
The area under the plasma-time curve of naringenin from (2) alpha-rhamnosidase-treated orange juice was increased about 4-fold (P < 0.0001)
PMID:20100371 · one of two readings recorded this
plasma naringenin Cmax
increases, p = 0.0001, n = 16
peak plasma concentration (Cmax) was 5.4-fold higher (P < 0.0001)
PMID:20100371 · one of two readings recorded this
plasma naringenin Tmax
decreases, p = 0.002, n = 16
Tmax was decreased from 311 to 92 min (P = 0.002)
PMID:20100371 · one of two readings recorded this
urinary excretion of naringenin, percent of dose
increases, p = 0.0001, n = 16
the amount in urine was increased from 7 to 47 % (P < 0.0001) of the dose
PMID:20100371 · one of two readings recorded this
relevant adverse events and blood safety markers
no effect, n = 18
There were no relevant AEs or changes in blood safety markers following ingestion of any of the naringenin doses
PMID:31468636 · one of two readings recorded this
NAFLD-related biological processes (energy balance, lipid and glucose metabolism, inflammation, oxidative stress)
modulates, n = 36
Of 1217 full-text articles assessed, 36 studies met the inclusion criteria
PMID:32879962 · one of two readings recorded this
antipyretic time
decreases, p = 0.02, n = 180
Antipyretic time (day) | 1.5 ± 0.2 | 3.8 ± 0.4 |.02
PMID:34310866 · one of two readings recorded this
baseline age
no effect, p = 0.56, n = 180
Age (years) | 2.7 ± 1.2 | 2.6 ± 1.0 |.56
PMID:34310866 · one of two readings recorded this
baseline body temperature
no effect, p = 0.81, n = 180
Temperature (℃) | 38.2 ± 2.5 | 38.4 ± 2.2 |.81
PMID:34310866 · one of two readings recorded this
baseline heart rate
no effect, p = 0.64, n = 180
Heart rate, number/min | 94 ± 6 | 95 ± 8 |.64
PMID:34310866 · one of two readings recorded this
bullae of lung (complication)
decreases, p = 0.04, n = 180
Bullae of lung | 2 (2.2) | 9 (10) |.04
PMID:34310866 · one of two readings recorded this
cough disappearance time
decreases, p = 0.03, n = 180
Cough disappearance time (day) | 3.7 ± 0.5 | 5.6 ± 0.6 |.03
PMID:34310866 · one of two readings recorded this
gastrointestinal bleed (complication)
decreases, p = 0.03, n = 180
Gastrointestinal bleed | 1 (1.1) | 11 (12.2) |.03
PMID:34310866 · one of two readings recorded this
lung rale disappearance time
decreases, p = 0.04, n = 180
Lung rale disappearance time (day) | 4.3 ± 1.2 | 6.5 ± 1.4 |.04
PMID:34310866 · one of two readings recorded this
proteinuria (complication)
decreases, p = 0.01, n = 180
Proteinuria | 3 (3.3) | 15 (16.7) |.01
PMID:34310866 · one of two readings recorded this
serum IL‐10
no effect, p = 0.33, n = 180
IL‐10 (ng/ml) | T0 | 14.0 ± 1.8 | 12.9 ± 3.2 |.33
PMID:34310866 · one of two readings recorded this
serum IL‐10
increases, p = 0.05, n = 180
T1 | 31.9 ± 4.6 * | 24.6 ± 8.4 * |.05
PMID:34310866 · one of two readings recorded this
serum IL‐10
increases, p = 0.04, n = 180
T2 | 43.7 ± 9.0 ** | 27.5 ± 8.9 * |.04
PMID:34310866 · one of two readings recorded this
serum IL‐10
increases, p = 0.03, n = 180
T3 | 51.2 ± 15.4 *** | 32.4 ± 6.7 ** |.03
PMID:34310866 · one of two readings recorded this
serum IL-6, IL-8, IL-10 and TNF-α by ELISA at T0-T3, symptom disappearance times and complication incidence in children with bronchial pneumonia
decreases, serum IL-6, IL-8 and TNF-α reduced more in the naringenin group than the azithromycin group at T1, T2 and T3 (p <.05)
Not recorded as a finding: the comparison was against another active treatment
Moreover, the serum levels of IL‐6, IL‐8, and TNF‐α in the NAR group showed more significant reduction at T1, T2, and T3 (p <.05), especially at T2 and T3, compared to the AZI group.
PMID:34310866 · one of two readings recorded this
serum IL-6, IL-8, IL-10 and TNF-α by ELISA at T0-T3; symptom disappearance times; complication and adverse reaction incidence, naringenin 5 mg/kg/day versus azithromycin 10 mg/kg/day for 5 days in children with bronchial pneumonia
decreases, serum IL-6, IL-8 and TNF-α reduced more in NAR group than AZI group
Not recorded as a finding: the comparison was against another active treatment
Moreover, the serum levels of IL‐6, IL‐8, and TNF‐α in the NAR group showed more significant reduction at T1, T2, and T3 (p <.05), especially at T2 and T3, compared to the AZI group.
PMID:34310866 · one of two readings recorded this
serum IL‐6
no effect, p = 0.87, n = 180
IL‐6 (ng/ml) | T0 | 78.4 ± 12.3 | 78.9 ± 11.7 |.87
PMID:34310866 · one of two readings recorded this
serum IL‐6
no effect, p = 0.14, n = 180
T1 | 64.9 ± 11.8 * | 72.1 ± 10.2 |.14
PMID:34310866 · one of two readings recorded this
serum IL‐6
decreases, p = 0.04, n = 180
T2 | 45.3 ± 9.1 ** | 68.3 ± 9.4 |.04
PMID:34310866 · one of two readings recorded this
serum IL‐6
decreases, p = 0.03, n = 180
T3 | 34.9 ± 8.2 *** | 53.5 ± 7.8 * |.03
PMID:34310866 · one of two readings recorded this
serum IL‐8
no effect, p = 0.69, n = 180
IL‐8 (ng/ml) | T0 | 62.4 ± 10.3 | 61.7 ± 10.3 |.69
PMID:34310866 · one of two readings recorded this
serum IL‐8
no effect, p = 0.28, n = 180
T1 | 42.9 ± 8.6 * | 57.1 ± 11.6 |.28
PMID:34310866 · one of two readings recorded this
serum IL‐8
decreases, p = 0.02, n = 180
T2 | 17.4 ± 3.3 *** | 50.4 ± 10.9 * |.02
PMID:34310866 · one of two readings recorded this
serum IL‐8
decreases, p = 0.04, n = 180
T3 | 15.3 ± 2.7 *** | 32.7 ± 10.9 ** |.04
PMID:34310866 · one of two readings recorded this
serum TNF‐α
no effect, p = 0.73, n = 180
TNF‐α (ng/ml) | T0 | 74.7 ± 16.3 | 73.9 ± 11.5 |.73
PMID:34310866 · one of two readings recorded this
serum TNF‐α
decreases, p = 0.04, n = 180
T1 | 42.9 ± 8.6 ** | 67.2 ± 12.3 |.04
PMID:34310866 · one of two readings recorded this
serum TNF‐α
decreases, p = 0.02, n = 180
T2 | 35.8 ± 5.1 ** | 55.7 ± 8.9 * |.02
PMID:34310866 · one of two readings recorded this
serum TNF‐α
decreases, p = 0.01, n = 180
T3 | 26.4 ± 3.6 *** | 51.6 ± 10.2 * |.01
PMID:34310866 · one of two readings recorded this
AST, ALT and NAFLD fibrosis score (NFS)
no effect, n = 44
However, there were no significant changes in AST, ALT and NFS
PMID:34516703 · one of two readings recorded this
AST, ALT and NAFLD fibrosis score
no effect, no significant changes
Not recorded as a finding: agentless sentence does not name the compound
However, there were no significant changes in AST, ALT and NFS.
PMID:34516703 · one of two readings recorded this
percentage of NAFLD grades (hepatic steatosis severity)
decreases, P < .001
Not recorded as a finding: no outcome node for ultrasound steatosis grade
Naringenin consumption significantly reduced percentages of NAFLD grades (P < .001), as well as, serum levels of triglyceride (TG) (P < .001), total cholesterol (TC) (P = .01), and low-density lipoprotein (LDL) (P = .02) and increased serum level of high-density lipoprotein (HDL) (P = .02) compared with the control group.
PMID:34516703 · both readings recorded this
percentages of NAFLD grades (hepatic steatosis severity)
decreases, p = 0.001, n = 44
Naringenin consumption significantly reduced percentages of NAFLD grades (P < .001)
PMID:34516703 · one of two readings recorded this
serum HDL
increases, p = 0.02, n = 44
increased serum level of high-density lipoprotein (HDL) (P = .02) compared with the control group
PMID:34516703 · one of two readings recorded this
serum LDL
decreases, p = 0.02, n = 44
low-density lipoprotein (LDL) (P = .02)
PMID:34516703 · one of two readings recorded this
serum total cholesterol
decreases, p = 0.01, n = 44
total cholesterol (TC) (P = .01)
PMID:34516703 · one of two readings recorded this
serum triglyceride
decreases, p = 0.001, n = 44
serum levels of triglyceride (TG) (P < .001)
PMID:34516703 · one of two readings recorded this
atherogenic index of plasma, non-HDL-C, TC/HDL-C, TG/HDL-C, LDL-C/HDL-C and non-HDL-C/HDL-C ratio
decreases, p = 0.05, n = 44
were significantly reduced in the intervention group, compared to the placebo group post intervention (P < 0.05)
PMID:34860705 · one of two readings recorded this
BMI and visceral fat level, naringenin versus placebo for 4 weeks in overweight/obese NAFLD patients
decreases, BMI reduced versus placebo, P = 0.001, p = 0.001
Not recorded as a finding: the supporting sentence never names the compound
Moreover, there was a significant reduction in BMI and visceral fat level in the intervention group when compared with the placebo group (P = 0.001 and P = 0.039, respectively).
PMID:34860705 · one of two readings recorded this
BMI
decreases, p = 0.001, n = 44
there was a significant reduction in BMI and visceral fat level in the intervention group when compared with the placebo group (P = 0.001 and P = 0.039, respectively)
PMID:34860705 · one of two readings recorded this
mean corpuscular hemoglobin concentration
increases, p = 0.05, n = 44
a marginally significant increase in the mean corpuscular hemoglobin concentration when compared with the placebo group (P = 0.050)
PMID:34860705 · one of two readings recorded this
mean corpuscular hemoglobin
increases, P = 0.023, p = 0.023
Not recorded as a finding: no outcome node for mean corpuscular hemoglobin
Mean corpuscular hemoglobin increased significantly in the naringenin group compared to the placebo group at the endpoint (P = 0.023).
PMID:34860705 · one of two readings recorded this
mean corpuscular hemoglobin
increases, p = 0.023, n = 44
Mean corpuscular hemoglobin increased significantly in the naringenin group compared to the placebo group at the endpoint (P = 0.023)
PMID:34860705 · one of two readings recorded this
systolic blood pressure, blood pressure
p = 0.055
Not recorded as a finding: marginal result (P = 0.055) with no significant direction; setting unspecified node would also be unbound
Furthermore, naringenin supplementation could marginally reduce systolic blood pressure (P = 0.055).
PMID:34860705 · one of two readings recorded this
systolic blood pressure
no effect, p = 0.055, n = 44
naringenin supplementation could marginally reduce systolic blood pressure (P = 0.055)
PMID:34860705 · one of two readings recorded this
visceral fat level, obesity-related parameter
decreases, P = 0.039, p = 0.039
Not recorded as a finding: no outcome node for visceral fat level
Moreover, there was a significant reduction in BMI and visceral fat level in the intervention group when compared with the placebo group (P = 0.001 and P = 0.039, respectively).
PMID:34860705 · one of two readings recorded this
visceral fat level
decreases, p = 0.039, n = 44
there was a significant reduction in BMI and visceral fat level in the intervention group when compared with the placebo group (P = 0.001 and P = 0.039, respectively)
PMID:34860705 · one of two readings recorded this
nitric oxide
decreases
NO (SMD - 3.97, 95% CI [- 5.50 to - 2.45]; I2 = 73.4%, p = 0.005)
PMID:35804246 · one of two readings recorded this
GSH
increases
GSH (SMD 4.58, 95% CI [1.64 to 7.51]; I2 = 90.5%, p < 0.001)
PMID:35804246 · one of two readings recorded this
MDA
decreases
MDA (SMD - 3.65, 95% CI [- 4.80 to - 2.51]; I2 = 69.4%, p = 0.001)
PMID:35804246 · one of two readings recorded this
TNF-α
decreases
TNF-α (SMD - 5.10, 95% CI [- 6.34 to - 3.86]; I2 = 74.7%, p < 0.001)
PMID:35804246 · one of two readings recorded this
IFN-γ
decreases
IFN-γ (SMD - 6.18, 95% CI [- 8.73 to - 3.62]; I2 = 53.7%, p = 0.115)
PMID:35804246 · one of two readings recorded this
IL-6
decreases
IL-6 (SMD - 5.84, 95% CI [- 7.83 to - 3.85]; I2 = 86.5%, p < 0.001)
PMID:35804246 · one of two readings recorded this
CAT
increases
CAT (SMD 4.19, 95% CI [1.33 to 7.06]; I2 = 79.9%, p = 0.007)
PMID:35804246 · one of two readings recorded this
GPx
increases
GPx (SMD 9.65, 95% CI [2.56 to 16.74]; I2 = 86.6%, p = 0.001)
PMID:35804246 · one of two readings recorded this
IL-1β
decreases
IL-1β (SMD - 4.23, 95% CI [- 5.09 to - 3.37]; I2 = 0.0%, p = 0.462)
PMID:35804246 · one of two readings recorded this
inflammatory and oxidative-stress markers (TNF-α, IL-6, IL-1β, IFN-γ, NF-κB, NO, CAT, SOD, GPx, GSH, MDA) pooled as SMD in animal autoimmune-disease models; sample matrix and assay not stated in abstract
no effect, SOD activity SMD 1.89, 95% CI [- 1.11 to 4.89]
Not recorded as a finding: the paper never states the instrument the node requires
However, treatment with naringenin showed no statistically difference in SOD activity (SMD 1.89, 95% CI [- 1.11 to 4.89]; I2 = 93.6%, p < 0.001).
PMID:35804246 · one of two readings recorded this
NF-κB
decreases
NF-κB (SMD - 3.77, 95% CI [- 6.03 to - 1.51]; I2 = 80.1%, p = 0.002)
PMID:35804246 · one of two readings recorded this
SOD activity
no effect
SOD activity (SMD 1.89, 95% CI [- 1.11 to 4.89]; I2 = 93.6%, p < 0.001)
PMID:35804246 · one of two readings recorded this
MDA
decreases
while improving antioxidant defenses (SOD, GSH) and reducing oxidative stress (MDA)
PMID:40996618 · one of two readings recorded this
TNF-α
decreases
levels of TNF-α (SMD = - 4.94), IL-6 (SMD = - 2.97), IL-1β (SMD = - 5.55), and IL-17 (SMD = - 1.22)
PMID:40996618 · one of two readings recorded this
IL-6
decreases
levels of TNF-α (SMD = - 4.94), IL-6 (SMD = - 2.97), IL-1β (SMD = - 5.55), and IL-17 (SMD = - 1.22)
PMID:40996618 · one of two readings recorded this
IL-17
decreases
levels of TNF-α (SMD = - 4.94), IL-6 (SMD = - 2.97), IL-1β (SMD = - 5.55), and IL-17 (SMD = - 1.22)
PMID:40996618 · one of two readings recorded this
arthritis severity score
decreases
Naringenin significantly reduced arthritis severity (SMD = - 3.50), paw volume (SMD = - 1.78)
PMID:40996618 · one of two readings recorded this
cartilage-degrading enzymes MMP-3, MMP-9
decreases
It also improved histopathology and body weight, and decreased cartilage-degrading enzymes (MMP-3, MMP-9)
PMID:40996618 · one of two readings recorded this
cytokine levels (TNF-α, IL-6, IL-1β, IL-17), arthritis score, paw volume, oxidative stress markers (SOD, GSH, MDA) pooled as SMD in rodent arthritis models; sample matrix and assay not stated in abstract
decreases, TNF-α SMD = - 4.94
Not recorded as a finding: the paper never states the instrument the node requires
Naringenin significantly reduced arthritis severity (SMD = - 3.50), paw volume (SMD = - 1.78), and levels of TNF-α (SMD = - 4.94), IL-6 (SMD = - 2.97), IL-1β (SMD = - 5.55), and IL-17 (SMD = - 1.22), while improving antioxidant defenses (SOD, GSH) and reducing oxidative stress (MDA).
PMID:40996618 · one of two readings recorded this
histopathology and body weight
increases
It also improved histopathology and body weight, and decreased cartilage-degrading enzymes (MMP-3, MMP-9)
PMID:40996618 · one of two readings recorded this
IL-1β
decreases
levels of TNF-α (SMD = - 4.94), IL-6 (SMD = - 2.97), IL-1β (SMD = - 5.55), and IL-17 (SMD = - 1.22)
PMID:40996618 · one of two readings recorded this
paw volume
decreases
Naringenin significantly reduced arthritis severity (SMD = - 3.50), paw volume (SMD = - 1.78)
PMID:40996618 · one of two readings recorded this
SOD and GSH (antioxidant defenses)
increases
while improving antioxidant defenses (SOD, GSH) and reducing oxidative stress (MDA)
PMID:40996618 · one of two readings recorded this
TNF-α, IL-6, IL-1β and IL-17 levels, SOD, GSH and MDA, arthritis score and paw volume in rodent rheumatoid arthritis models, pooled SMD
decreases, TNF-α SMD = - 4.94
Not recorded as a finding: the paper never states the instrument the node requires
Naringenin significantly reduced arthritis severity (SMD = - 3.50), paw volume (SMD = - 1.78), and levels of TNF-α (SMD = - 4.94), IL-6 (SMD = - 2.97), IL-1β (SMD = - 5.55), and IL-17 (SMD = - 1.22), while improving antioxidant defenses (SOD, GSH) and reducing oxidative stress (MDA).
PMID:40996618 · one of two readings recorded this
Sources cited
1 paper
- Subject
- naringenin
- Findings
- 4
- Papers
- 1