Evidence map›Paper›PMID 38706874›Full record

ArticleFrontiers in molecular neuroscience2024

Rotenone-induced PINK1/Parkin-mediated mitophagy: establishing a silkworm model for Parkinson's disease potential.

Hantao Zhang, Jinyue Yang, Yinglu Guo, Peng Lü, Xun Gong, Keping Chen, Xiubin Li, Min Tang

Abstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
  2. Article
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  5. Review
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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

8 authors.

Hantao Zhang *School of Life Sciences, Jiangsu University, Zhenjiang, Jiangsu, China.
Jinyue Yang *Department of Neurology, The Second Affiliated Hospital of Shandong First Medical University, Taian, Shandong, China.
Yinglu GuoSchool of Life Sciences, Jiangsu University, Zhenjiang, Jiangsu, China.
Peng LüSchool of Life Sciences, Jiangsu University, Zhenjiang, Jiangsu, China.
Xun GongAffiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, China.
Keping ChenSchool of Life Sciences, Jiangsu University, Zhenjiang, Jiangsu, China.
Xiubin LiDepartment of Neurology, The Second Affiliated Hospital of Shandong First Medical University, Taian, Shandong, China.
Min TangSchool of Life Sciences, Jiangsu University, Zhenjiang, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD), ranking as the second most prevalent neurodegenerative disorder globally, presents a pressing need for innovative animal models to deepen our understanding of its pathophysiology and explore potential therapeutic interventions. The development of such animal models plays a pivotal role in unraveling the complexities of PD and investigating promising treatment avenues. In this study, we employed transcriptome sequencing on BmN cells treated with 1 μg/ml rotenone, aiming to elucidate the underlying toxicological mechanisms. The investigation brought to light a significant reduction in mitochondrial membrane potential induced by rotenone, subsequently triggering mitophagy. Notably, the PTEN induced putative kinase 1 (PINK1)/Parkin pathway emerged as a key player in the cascade leading to rotenone-induced mitophagy. Furthermore, our exploration extended to silkworms exposed to 50 μg/ml rotenone, revealing distinctive motor dysfunction as well as inhibition of

Indexed as

animal modelmitophagyParkinson’s diseaserotenonesilkworm

Identifiers

PMID38706874
PMCPMC11066238

What OpenQuestion holds

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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.