Evidence map›Paper›PMID 33062150›Full record

ArticleOxidative medicine and cellular longevity2020

Prevention of Nonalcoholic Hepatic Steatosis by Shenling Baizhu Powder: Involvement of Adiponectin-Induced Inhibition of Hepatic SREBP-1c.

Kairui Tang, Yuanjun Deng, Chuiyang Zheng, Huan Nie, Maoxing Pan, Runsen Chen, Jiqian Xie, Qinhe Yang, Yupei Zhang

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Kairui TangSchool of Traditional Chinese Medicine, Jinan University, Guangzhou 510632, China.ORCID https://orcid.org/0000-0001-9300-6329
Yuanjun DengSchool of Traditional Chinese Medicine, Jinan University, Guangzhou 510632, China.ORCID https://orcid.org/0000-0002-9048-4621
Chuiyang ZhengSchool of Traditional Chinese Medicine, Jinan University, Guangzhou 510632, China.
Huan NieSchool of Traditional Chinese Medicine, Jinan University, Guangzhou 510632, China.
Maoxing PanSchool of Traditional Chinese Medicine, Jinan University, Guangzhou 510632, China.
Runsen ChenSchool of Traditional Chinese Medicine, Jinan University, Guangzhou 510632, China.
Jiqian XieSchool of Traditional Chinese Medicine, Jinan University, Guangzhou 510632, China.
Qinhe YangSchool of Traditional Chinese Medicine, Jinan University, Guangzhou 510632, China.ORCID https://orcid.org/0000-0002-8484-6665
Yupei ZhangSchool of Traditional Chinese Medicine, Jinan University, Guangzhou 510632, China.ORCID https://orcid.org/0000-0001-8837-1313
Jinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNonalcoholic fatty liver disease (NAFLD) is a common chronic liver disease worldwide, and its incidence is increasing annually, but there is currently no specific drug for treating NAFLD. Shenling Baizhu powder (SL) is a safe herbal compound commonly used in clinical practice. Our previous research has shown that SL has the effect of preventing NAFLD, but its specific mechanism has not been determined. In this study, the potential mechanism of SL on NAFLD was explored by

methodsWistar rats fed a choline-deficient amino acid-defined diet (CDAA) were treated with SL for 8 weeks. Then, serum samples were collected to obtain biochemical indicators; adipose tissue and liver samples were collected for pathological detection; a moorFLPI-2 blood flow imager was used to measure liver microcirculation blood flow, and a rat cytokine array was used to screen potential target proteins. The expression of liver adiponectin/SREBP-1c pathway-related proteins was determined by Western blotting.

resultsSL effectively reduced the liver wet weight, as well as the levels of total cholesterol (TC) and triglyceride (TG) in the liver, and ameliorated liver injury in CDAA-fed rats. Pathological examinations showed that SL markedly reduced liver lipid droplets and improved liver lipid accumulation. In addition, the detection of liver blood flow showed that SL increased liver microcirculation in CDAA-fed rats. Through the cytokine array, a differentially expressed cytokine, namely, adiponectin, was screened in the liver. Western blotting assays showed that SL increased the expression of adiponectin and phosphoacetyl-CoA Carboxylase (p-ACC) in the liver and decreased the expression of steroid regulatory element-binding protein-1c (SREBP-1c) and fatty acid synthase (FAS).

conclusionThese results suggest that SL can increase the levels of adiponectin in the liver and serum and can inhibit the expression of SREBP-1c, thereby regulating systemic lipid metabolism and reducing liver lipid accumulation.

Indexed as

AdiponectinAnimalsCholesterolDietDisease Models, AnimalDrugs, Chinese HerbalFatty Acid SynthasesLipid MetabolismLiverMaleMicrocirculationNon-alcoholic Fatty Liver DiseasePhosphatidylcholinesRatsRats, WistarSterol Regulatory Element Binding Protein 1AdiponectinCholesterolDrugs, Chinese HerbalFatty Acid SynthasesPhosphatidylcholinespolyene phosphatidylcholineSrebf1 protein, ratSterol Regulatory Element Binding Protein 1Triglycerides

Identifiers

PMID33062150
PMCPMC7533788
OpenAlexW3034651228

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.