Evidence map›Paper›PMID 25411028›Full record

ArticleMolecular bioSystems2015

A metabolomic and pharmacokinetic study on the mechanism underlying the lipid-lowering effect of orally administered berberine.

Shenghua Gu, Bei Cao, Runbin Sun, Yueqing Tang, Janice L Paletta, Xiaolei Wu, Xiao-Lei Wu, Linsheng Liu, Weibin Zha, Chunyan Zhao and 7 more

Erratum issuedAbstract read
In one paragraph

Article in Molecular bioSystems, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 18% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 86 citations in OpenAlex.

  1. Pooled it
  2. Berberine alleviates soybean meal-induced enteritis in hybrid yellow catfish (Animal nutrition (Zhongguo xu mu shou yi xue hui) · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Pharmacokinetic-Pharmacodynamic Correlation Analysis ofPharmaceuticals (Basel, Switzerland) · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 7 institutions in 2 countries.

Shenghua GuState Key Laboratory of Natural Medicines, Key Laboratory of Drug Metabolism and Pharmacokinetics, Jiangsu Key laboratory of drug design and optimization, China Pharmaceutical University, Nanjing 210009, China. jiyea@cpu.edu.cn.
Bei Cao
Runbin Sun
Yueqing Tang
Janice L Paletta
Xiaolei Wu
Xiao-Lei Wu
Linsheng Liu
Weibin Zha
Chunyan Zhao
Yan Li
Jason M Ridlon
Jason M Radlon
Phillip B Hylemon
Huiping Zhou
Jiye Aa
Guangji Wang
State Key Laboratory of Natural MedicinePeking University · CNChina Pharmaceutical University · CNShanghai University of Traditional Chinese Medicine · CNVirginia Commonwealth University · USNanjing Drum Tower Hospital · CNUniversity of Richmond · US

Funding

Prevent HIV protease inhibitor-induced atherosclerosis by BerberineR01AT004148 · NCCIH · VIRGINIA COMMONWEALTH UNIVERSITY · PI ZHOU, HUIPING ROSE · 2007 to 2010
$1.4M
NCCIH NIH HHS R01 AT004148
6 · The paper itself

Abstract

Clinical and animal studies demonstrated that orally administered berberine had a distinct lipid-lowering effect. However, pharmacokinetic studies showed that berberine was poorly absorbed into the body so the levels of berberine in the blood and target tissues were far below the effective concentrations revealed. To probe the underlying mechanism, the effect of berberine on the biological system was studied on a high-fat-diet-induced hamster hyperlipidemia model. Our results showed that intragastrically-administered berberine was poorly absorbed into circulation and most berberine accumulated in gut content. Although the bioavailability of intragastrically administered berberine was much lower than that of intraperitoneally administered berberine, it had a stronger lipid-lowing effect, indicating that the gastrointestinal tract is a potential target for the hypolipidemic effect of berberine. A metabolomic study on both serum and gut content showed that orally administered berberine significantly regulated molecules involved in lipid metabolism, and increased the generation of bile acids in the hyperlipidemic model. DNA analysis revealed that the orally administered berberine modulated the gut microbiota, and berberine showed a significant inhibition of the 7α-dehydroxylation conversion of cholic acid to deoxycholic acid, indicating a decreased elimination of bile acids in the gut. However, in model hamsters, elevated bile acids failed to downregulate the expression and function of CYP7A1 in a negative feedback loop. It was suggested that the hypocholesterolemic effect of orally administered berberine involves modulating the turnover of bile acids and the farnesoid X receptor signal pathway.

Indexed as

MetabolomicsAdministration, OralAnimalsBerberineBody WeightCholestanetriol 26-MonooxygenaseCholesterol 7-alpha-HydroxylaseCholic AcidChromatography, GasDiet, High-FatGallbladderGastrointestinal TractGene Expression Regulation, EnzymologicHep G2 CellsHumansHyperlipidemiasBerberineCholestanetriol 26-MonooxygenaseCholesterol 7-alpha-HydroxylaseCholic AcidHypolipidemic AgentsLipidsRNA, Messenger

Identifiers

PMID25411028
PMCPMC4302037
OpenAlexW4230869250

What OpenQuestion holds

Textmetadata
LicenceTDM
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.