Evidence map›Paper›PMID 31976031›Full record

ArticleOxidative medicine and cellular longevity2020

Berberine Attenuates Hyperglycemia by Inhibiting the Hepatic Glucagon Pathway in Diabetic Mice.

Ying Zhong, Jing Jin, Peiyu Liu, Yu Song, Hui Zhang, Liang Sheng, Huifang Zhou, Bijie Jiang

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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Review
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  4. Heliyon · 2024
    Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. A Review ofMolecules (Basel, Switzerland) · 2023
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Diabetes Mellitus, Mitochondrial Dysfunction and CaInternational journal of molecular sciences · 2020
    Review
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

8 authors at 3 institutions in 1 country.

Ying ZhongDepartment of Pharmacology, School of Basic Medical Science, Nanjing Medical University, 101 Longmian Rd, Nanjing, Jiangsu 211166, China.
Jing JinDepartment of Gynecology, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210029, China.
Peiyu LiuDepartment of Pharmacology, School of Basic Medical Science, Nanjing Medical University, 101 Longmian Rd, Nanjing, Jiangsu 211166, China.
Yu SongPharmacy College, Xinxiang Medical University, 601 Jinsui Avenue, Xinxiang, Henan 453003, China.
Hui ZhangPharmacy College, Xinxiang Medical University, 601 Jinsui Avenue, Xinxiang, Henan 453003, China.
Liang ShengDepartment of Pharmacology, School of Basic Medical Science, Nanjing Medical University, 101 Longmian Rd, Nanjing, Jiangsu 211166, China.ORCID https://orcid.org/0000-0003-1217-0392
Huifang ZhouDepartment of Gynecology, Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210029, China.ORCID https://orcid.org/0000-0001-5208-8727
Bijie JiangPharmacy College, Xinxiang Medical University, 601 Jinsui Avenue, Xinxiang, Henan 453003, China.ORCID https://orcid.org/0000-0002-2734-8109
Xinxiang Medical University · CNNanjing Medical University · CNNanjing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysregulated glucagon drives hyperfunction in hepatic glucose output, which is the main cause of persistent hyperglycemia in type 2 diabetes. Berberine (Zhang et al., 2010) has been used as a hypoglycemic agent, yet the mechanism by which BBR inhibits hepatic gluconeogenesis remains incompletely understood. In this study, we treated diabetic mice with BBR, tested blood glucose levels, and then performed insulin, glucose lactate, and glucagon tolerance tests. Intracellular cAMP levels in hepatocytes were determined by ELISA, hepatic gluconeogenetic genes were assayed by RT-qPCR, and the phosphorylation of CREB, which is the transcriptional factor controlling the expression of gluconeogenetic genes, was detected by western blot. BBR reduced blood glucose levels, improved insulin and glucose tolerance, and suppressed lactate- and glucagon-induced hepatic gluconeogenesis in ob/ob and STZ-induced diabetic mice. Importantly, BBR blunted glucagon-induced glucose production and gluconeogenic gene expression in hepatocytes, presumably through reducing cAMP, which resulted in the phosphorylation of CREB. By utilizing a cAMP analogue, adenylate cyclase (AC), to activate cAMP synthetase, and an inhibitor of the cAMP degradative enzyme, phosphodiesterase (PDE), we revealed that BBR accelerates intracellular cAMP degradation. BBR reduces the intracellular cAMP level by activating PDE, thus blocking activation of downstream CREB and eventually downregulating gluconeogenic genes to restrain hepatic glucose production.

Indexed as

Diabetes Mellitus, ExperimentalHyperglycemiaLiverAnimalsBerberineGlucagonMiceMice, ObeseSignal TransductionBerberineGlucagon

Identifiers

PMID31976031
PMCPMC6961611
OpenAlexW2997977632

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.