Evidence map›Paper›PMID 31301005›Full record

ArticleThe journal of physiological sciences : JPS2019

Effects of testosterone on circadian rhythmicity in old mice.

Atsuyoshi Hashimoto, Shingo Fujiki, Wataru Nakamura, Takahiro J Nakamura

Open access · goldAbstract read
In one paragraph

Article in The journal of physiological sciences : JPS, 2019. 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
0.6field-weighted citation impact, top 38% 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, 11 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

4 authors at 2 institutions in 1 country.

Atsuyoshi HashimotoLaboratory of Animal Physiology, School of Agriculture, Meiji University, 1-1-1 Hgashimita, Tama-ku, Kawasaki, Kanagawa, 214-8571, Japan.
Shingo FujikiLaboratory of Animal Physiology, School of Agriculture, Meiji University, 1-1-1 Hgashimita, Tama-ku, Kawasaki, Kanagawa, 214-8571, Japan.
Wataru NakamuraDepartment of Oral-Chrono Physiology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Nagasaki, 852-8588, Japan.
Takahiro J NakamuraLaboratory of Animal Physiology, School of Agriculture, Meiji University, 1-1-1 Hgashimita, Tama-ku, Kawasaki, Kanagawa, 214-8571, Japan. takahiro@meiji.ac.jp.ORCID http://orcid.org/0000-0002-1702-9278
Meiji University · JPNagasaki University · JP

Funding

Japan Society for the Promotion of Science 17H04022
6 · The paper itself

Abstract

Serum testosterone concentration decreases with age in humans and rodents. Accordingly, old male mice show changes in locomotor activity rhythms: a lengthened free-running period and decreased activity levels among others. To investigate whether testosterone replacement improves the age-related decline in circadian rhythmicity, we examined the effects of testosterone on the circadian rhythms of wheel running activity in old male mice. Intact male C57BL/6J mice (18-22 months old) were subcutaneously implanted with silicone tubes packed with testosterone propionate (TP) or cholesterol. TP treatment significantly decreased the daily wheel running revolutions in a normal light/dark (LD) cycle and in constant darkness (DD), but did not affect the free-running period. The same experiment performed on young male gonadectomized mice (3-5 months old) demonstrated that TP treatment significantly increased activity levels in both LD and DD. These results suggest that testosterone replacement exacerbates the age-related decline in circadian rhythmicity.

Indexed as

AnimalsCircadian RhythmDarknessLightMaleMiceMice, Inbred C57BLMotor ActivityPhotoperiodTestosteroneTestosteroneCircadian rhythmFree-running periodPER2::LUCTestosteroneWheel running

Identifiers

PMID31301005
PMCPMC10717400
OpenAlexW2960313089

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.