Evidence map›Paper›PMID 31828466›Full record

ArticleCellular and molecular neurobiology2020

Berberine attenuated the cytotoxicity induced by t-BHP via inhibiting oxidative stress and mitochondria dysfunction in PC-12 cells.

Zhengmao Li, Ting Jiang, Qi Lu, Ke Xu, Jianping He, Lei Xie, Zaifeng Chen, Zhilong Zheng, Luxia Ye, Kebin Xu and 2 more

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular neurobiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Molecular landscape of Berberine's therapeutic potential in gastrointestinal disorders.Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Autophagy and apoptosis cascade: which is more prominent in neuronal death?Cellular and molecular life sciences : CMLS · 2021
    Review
  17. Article
  18. Article
  19. Review
  20. Article
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

12 authors at 3 institutions in 1 country.

Zhengmao LiSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Ting JiangSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Qi LuSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Ke XuInstitute of Life Sciences, Wenzhou University, Wenzhou, Zhejiang, China.
Jianping HeDepartment of Pharmacy, Shaoxing No. 2 Hospital, Shaoxing, Zhejiang, China.
Lei XieDepartment of Orthopaedics, Shaoxing No. 2 Hospital, Shaoxing, Zhejiang, China.
Zaifeng ChenDepartment of Neurosurgery, Cixi People's Hospital, Wenzhou Medical Uinversity, Ninbo, Zhejiang, China.
Zhilong ZhengSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Luxia YeSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Kebin XuDepartment of Pharmacy, Ningbo No. 2 Hospital, Ningbo, Zhejiang, China.
Hongyu ZhangSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China. hyzhang@wmu.edu.cn.ORCID http://orcid.org/0000-0003-1946-5468
Aiping HuSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China. hap@wmu.edu.cn.
Wenzhou Medical University · CNShaoxing Second Hospital · CNWenzhou University · CN

Funding

National Natural Science Foundation of China 81501953National Natural Science Foundation of China 81572237National Natural Science Foundation of China 81722028National Natural Science Foundation of China 81772450Natural Science Foundation of Ningbo 2018A610309Natural Science Foundation of Zhejiang Province LQ16H090007Natural Science Foundation of Zhejiang Province LQ18H090008Natural Science Foundation of Zhejiang Province LQ18H150003Natural Science Foundation of Zhejiang Province LY14H090013Natural Science Foundation of Zhejiang Province R18H50001
6 · The paper itself

Abstract

Neurodegenerative diseases all share several common features such as involvement of oxidative damage and mitochondrial dysfunction in pathogenesis. Oxidative stress induced by overproduction of mitochondrial reactive oxygen species (ROS) or impairment of the antioxidant deficiency results in mitochondrial dysfunction and initiation of the cell death cascade. Berberine (BBR), a traditional Chinese medicine, has been reported to exert anti-oxidative stress and anti-apoptosis effect in CNS diseases. However, the mechanism of BBR on regulating mitophagy and protecting mitochondrial function under oxidative stress remains unclear. In present study, we evaluated the beneficial effects of BBR on the tert-butyl hydroperoxide (t-BHP)-induced cytotoxicity. Furthermore, we explored the protective role of BBR in mitochondrial function and mitophagy under oxidative stress in PC-12 cells. Our results demonstrated that BBR effectively inhibited t-BHP-induced apoptosis which is associated with the decreased leakage of lactate dehydrogenase (LDH) and ROS overproduction. Moreover, BBR significantly suppressed cytochrome c expression, upregulated the ratio of Bcl-2/Bax, and ameliorated mitochondrial dysfunction by optimizing mitochondria membrane potential (ΔΨm) status and ATP production. In addition, BBR reduced the expression of autophagy-specific marker LC3, SQTM1/p62, and maintained lysosome normal function which involved the restoration of upstream signaling pathway AKT and mTOR phosphorylation level. Collectively, these findings suggested that BBR protects PC-12 cells from oxidative injury through inhibiting ROS level, mitochondria dysfunction, and mitophagy via PI3K/AKT/mTOR signaling pathways, which suggest a potential therapeutic strategy for oxidative stress and neurotoxic damages.

Indexed as

AnimalsBerberineCell DeathChromonesCytochromes cLysosomesMembrane Potential, MitochondrialMicrotubule-Associated ProteinsMitochondriaMitophagyMorpholinesOxidative StressPC12 CellsRatsSignal Transductiontert-Butylhydroperoxide2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-oneAnxa3 protein, ratBerberineChromonesCytochromes cMicrotubule-Associated ProteinsMorpholinestert-ButylhydroperoxideBerberine (BBR)MitophagyNeurotoxicity Analysis of varianceOxidative stressPI3K/AKT/mTOR

Identifiers

PMID31828466
PMCPMC11448801
OpenAlexW2995739131

What OpenQuestion holds

Textmetadata
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.