Evidence map›Paper›PMID 37869512›Full record

ReviewFrontiers in neuroscience2023

Targeting mitophagy for depression amelioration: a novel therapeutic strategy.

Wangjun Xu, Weiping Gao, Yukun Guo, Feng Xue, Lulu Di, Shaojie Fang, Linlin Fan, Yangyang He, Yunfeng Zhou, Xinmei Xie and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

9 citing papers in PubMed, 24 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

11 authors at 1 institution in 1 country.

Wangjun XuSchool of Pharmacy, Henan University, Kaifeng, China.
Weiping GaoSchool of Pharmacy, Henan University, Kaifeng, China.
Yukun GuoSchool of Pharmacy, Henan University, Kaifeng, China.
Feng XueSchool of Pharmacy, Henan University, Kaifeng, China.
Lulu DiSchool of Pharmacy, Henan University, Kaifeng, China.
Shaojie FangSchool of Pharmacy, Henan University, Kaifeng, China.
Linlin FanHenan Key Laboratory of Brain Targeted Bio-nanomedicine, School of Pharmacy, Henan University, Kaifeng, China.
Yangyang HeSchool of Pharmacy, Henan University, Kaifeng, China.
Yunfeng ZhouSchool of Pharmacy, Henan University, Kaifeng, China.
Xinmei XieSchool of Pharmacy, Henan University, Kaifeng, China.
Xiaobin PangSchool of Pharmacy, Henan University, Kaifeng, China.
Henan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Major depressive disorder is a global psychiatric condition characterized by persistent low mood and anhedonia, which seriously jeopardizes the physical and mental well-being of affected individuals. While various hypotheses have been proposed to explicate the etiology of depression, the precise pathogenesis and effective treatment of this disorder remain elusive. Mitochondria, as the primary organelles responsible for cellular energy production, possess the ability to meet the essential energy demands of the brain. Research indicated that the accumulation of damaged mitochondria is associated with the onset of depression. Mitophagy, a type of cellular autophagy, specifically targets and removes excess or damaged mitochondria. Emerging evidence demonstrated that mitophagy dysfunction was involved in the progression of depression, and several pharmacological interventions that stimulating mitophagy exerted excellent antidepressant actions. We provided an overview of updated advancements on the regulatory mechanism of mitophagy and the mitophagy abnormality in depressed patients and animals, as well as in cell models of depression. Meanwhile, various therapeutic strategies to restore mitophagy for depression alleviation were also discussed in this review.

Indexed as

depressiondrug therapymitochondriamitophagyregulatory mechanism

Identifiers

PMID37869512
PMCPMC10587558
OpenAlexW4387403938

What OpenQuestion holds

Textmetadata
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.