Evidence map›Paper›PMID 34139672›Full record

ArticleAging2021

Testosterone ameliorates age-related brain mitochondrial dysfunction.

Wensheng Yan, Tianyun Zhang, Yunxiao Kang, Guoliang Zhang, Xiaoming Ji, Xu Feng, Geming Shi

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 29% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

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  16. Male reproductive ageing: a radical road to ruin.Human reproduction (Oxford, England) · 2023
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  17. Cocaine perturbs mitovesicle biology in the brain.Journal of extracellular vesicles · 2023
    Article
  18. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Wensheng YanDepartment of Neurobiology, Hebei Medical University, Shijiazhuang, China.
Tianyun ZhangDepartment of Neurobiology, Hebei Medical University, Shijiazhuang, China.
Yunxiao KangDepartment of Neurobiology, Hebei Medical University, Shijiazhuang, China.
Guoliang ZhangNeuroscience Research Center, Hebei Medical University, Shijiazhuang, China.
Xiaoming JiDepartment of Neurobiology, Hebei Medical University, Shijiazhuang, China.
Xu FengHebei Laboratory Animal Center, Hebei Medical University, Shijiazhuang, China.
Geming ShiDepartment of Neurobiology, Hebei Medical University, Shijiazhuang, China.
Hebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brain mitochondrial dysfunction and reduced testosterone levels are common features of aging in men. Although evidence suggests that the two phenomena are interrelated, it is unclear whether testosterone supplementation ameliorates mitochondrial dysfunction in the aging male brain. Here, we show that testosterone supplementation significantly alleviates exploratory behavioral deficits and oxidative damage in the substantia nigra and hippocampus of aging male rats. These effects were consistent with improved mitochondrial function, reflected by testosterone-induced increases in mitochondrial membrane potential (MMP), antioxidant enzyme (GSH-PX, catalase, and Mn-SOD) expression/activity, and mitochondrial respiratory complex activities in both brain regions. Furthermore, elevated PGC-1α, NRF-1, and TFAM expression (suggestive of enhanced mitochondrial biogenesis), increased citrate synthase activity, mtDNA copy number, and ND1, COX1, and ATP6 expression (indicative of increased mitochondrial content), as well as increased PINK1/Parkin and decreased P62 expression (suggesting mitophagy activation), were detected in the substantial nigra and hippocampus of aged male rats after testosterone supplementation. These findings suggest that testosterone supplementation may be a viable approach to ameliorating brain mitochondrial dysfunction and thus prevent or treat cognitive-behavioral deficits and neurodegenerative conditions associated with aging.

Indexed as

AgingAnimalsAntioxidantsBehavior, AnimalBody WeightBrainDopamine Plasma Membrane Transport ProteinsElectron TransportExploratory BehaviorHippocampusMaleMembrane Potential, MitochondrialMitochondriaNeuronsProtein KinasesPTEN-Induced Putative KinaseAntioxidantsDopamine Plasma Membrane Transport Proteinsparkin proteinProtein KinasesPTEN-Induced Putative KinaseTestosteroneTyrosine 3-MonooxygenaseUbiquitin-Protein Ligasesaged male ratsantioxidative capacitymitochondrial biogenesismitochondrial functiontestosterone

Identifiers

PMID34139672
PMCPMC8266321
OpenAlexW3168962813

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.