Evidence map›Paper›PMID 29138672›Full record

ArticleOxidative medicine and cellular longevity2017

Testosterone Upregulates the Expression of Mitochondrial ND1 and ND4 and Alleviates the Oxidative Damage to the Nigrostriatal Dopaminergic System in Orchiectomized Rats.

Wensheng Yan, Yunxiao Kang, Xiaoming Ji, Shuangcheng Li, Yingkun Li, Guoliang Zhang, Huixian Cui, Geming Shi

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

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

  1. Pooled it
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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 at 1 institution in 1 country.

Wensheng YanDepartment of Neurobiology, Hebei Medical University, Shijiazhuang, Hebei 050017, China.
Yunxiao KangDepartment of Neurobiology, Hebei Medical University, Shijiazhuang, Hebei 050017, China.ORCID 0000-0003-3021-8863
Xiaoming JiDepartment of Neurobiology, Hebei Medical University, Shijiazhuang, Hebei 050017, China.
Shuangcheng LiDepartment of Human Anatomy, Hebei Medical University, Shijiazhuang, Hebei 050017, China.
Yingkun LiDepartment of Human Anatomy, Hebei Medical University, Shijiazhuang, Hebei 050017, China.
Guoliang ZhangDepartment of Neurobiology, Hebei Medical University, Shijiazhuang, Hebei 050017, China.
Huixian CuiDepartment of Human Anatomy, Hebei Medical University, Shijiazhuang, Hebei 050017, China.
Geming ShiDepartment of Neurobiology, Hebei Medical University, Shijiazhuang, Hebei 050017, China.ORCID 0000-0003-2822-7576
Hebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Testosterone deficiency, as a potential risk factor for aging and aging-related neurodegenerative disorders, might induce mitochondrial dysfunction and facilitate the declines of the nigrostriatal dopaminergic system by exacerbating the mitochondrial defects and increasing the oxidative damage. Thus, how testosterone levels influence the mitochondrial function in the substantia nigra was investigated in the study. The present studies showed that testosterone deficiency impaired the mitochondrial function in the substantia nigra and induced the oxidative damage to the substantia nigra as well as the deficits in the nigrostriatal dopaminergic system. Of four mitochondrial respiratory chain complexes, castration of male rats reduced the activity of mitochondrial complex I and downregulated the expression of ND1 and ND4 of 7 mitochondrial DNA- (mtDNA-) encoded subunits of complex I in the substantia nigra. Supplements of testosterone propionate to castrated male rats ameliorated the activity of mitochondrial complex I and upregulated the expression of mitochondrial ND1 and ND4. These results suggest an important role of testosterone in maintaining the mitochondrial function in the substantia nigra and the vulnerability of mitochondrial complex I to testosterone deficiency. Mitochondrial ND1 and ND4, as potential testosterone targets, were implicated in the oxidative damage to the nigrostriatal dopaminergic system.

Indexed as

AnimalsDNA, MitochondrialDopamineDopaminergic NeuronsMaleMitochondriaMitochondrial ProteinsNADH DehydrogenaseOrchiectomyOxidative StressRatsRats, Sprague-DawleySubstantia NigraTestosteroneTestosterone PropionateUp-RegulationDNA, MitochondrialDopamineMitochondrial ProteinsNADH DehydrogenaseNADH dehydrogenase subunit 4TestosteroneTestosterone Propionate

Identifiers

PMID29138672
PMCPMC5613679
OpenAlexW2746775356

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.