Evidence map›Paper›PMID 27075663›Full record

ArticleBMC pharmacology & toxicology2016

Salidroside alleviates oxidative stress in the liver with non- alcoholic steatohepatitis in rats.

Ze-ran Yang, Hui-fang Wang, Tie-cheng Zuo, Li-li Guan, Ning Dai

Open access · goldAbstract read
In one paragraph

Article in BMC pharmacology & toxicology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
  2. Review
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  6. Nutrients · 2023
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  11. Protective Effects of Salidroside against Carbon Tetrachloride (CClInternational journal of molecular sciences · 2019
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Ze-ran YangDepartment of Gastroenterology, the first Affiliated Hospital of Dalian Medical University, 222, Zhongshan Road, Dalian, 116011, Liaoning Province, China.
Hui-fang WangDepartment of Gastroenterology, the first Affiliated Hospital of Dalian Medical University, 222, Zhongshan Road, Dalian, 116011, Liaoning Province, China.
Tie-cheng ZuoDepartment of Gastroenterology, the first Affiliated Hospital of Dalian Medical University, 222, Zhongshan Road, Dalian, 116011, Liaoning Province, China.
Li-li GuanDepartment of Digestive Physiology, Dalian Medical University, Dalian, Liaoning Province, China.
Ning DaiDepartment of Gastroenterology, the first Affiliated Hospital of Dalian Medical University, 222, Zhongshan Road, Dalian, 116011, Liaoning Province, China. dainingdn@live.com.
Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNonalcoholic steatohepatitis (NASH) is characterized by fat accumulation in the hepatocyte, inflammation, liver cell injury, and varying degrees of fibrosis, and can lead to oxidative stress in liver. Here, we investigated whether Salidroside, a natural phenolic antioxidant product, can protect rat from liver injury during NASH.

methodsNASH model was established by feeding the male SD rats with high-fat and high-cholesterol diet for 14 weeks. Four groups of male SD rats including, normal diet control group, NASH model group, and Salidroside treatment group with150mg/kg and 300 mg/kg respectively, were studied. Salidroside was given by oral administration to NASH in rats from 9 weeks to 14 weeks. At the end of 14 weeks, liver and serum were harvested, and the liver injury, oxidative stress and histological features were evaluated.

resultsNASH rats exhibited significant increases in the following parameters as compared to normal diet control rats: fat droplets with foci of inflammatory cell infiltration in the liver. ALT, AST in serum and TG, TC in hepatocyte elevated. Oxidative responsive genes including CYP2E1 and Nox2 increased. Additionally, NASH model decreased antioxidant enzymes SOD, GSH, GPX, and CAT in the liver due to their rapid depletion after battling against oxidative stress. Compared to NASH model group, treatment rats with Salidroside effectively reduced lipid accumulation, inhibited liver injury in a does-dependent manner. Salidroside treatment restored antioxidant enzyme levels, inhibited expression of CYP2E1 and Nox2 mRNA in liver, which prevented the initial step of generating free radicals from NASH.

conclusionThe data presented here show that oral administration of Salidroside prevented liver injury in the NASH model, likely through exerting antioxidant actions to suppress oxidative stress and the free radical-generating CYP2E1 enzyme, Nox2 in liver.

Indexed as

Administration, OralAnimalsAntioxidantsCytochrome P-450 CYP2E1Diet, High-FatDose-Response Relationship, DrugEnzyme RepressionGlucosidesLipid DropletsLipid MetabolismLipid PeroxidationLiverMaleMembrane GlycoproteinsNADPH Oxidase 2NADPH OxidasesAntioxidantsCybb protein, ratCytochrome P-450 CYP2E1GlucosidesMembrane GlycoproteinsNADPH Oxidase 2NADPH OxidasesOxidoreductasesPhenolsrhodiolosideCYP2E1Non-alcoholic steatohepatitisNox2Oxidative stressSalidroside

Identifiers

PMID27075663
PMCPMC4831194
OpenAlexW2339813221

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.