Evidence map›Paper›PMID 38853130›Full record

ArticleClinical and experimental reproductive medicine2024

Osteocalcin improves testicular morphology but does not ameliorate testosterone synthesis signaling in azoospermic mice.

Mahsa Yaghobinejad, Heidar Toolee, Somayeh Solhjoo, Elham Seifali, Soraya Parvari, Omotosho Dhulqarnain Akanji, Tayebeh Rastegar

Abstract read
In one paragraph

Article in Clinical and experimental reproductive medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Mahsa YaghobinejadAnatomy Department, Medical School, Tehran University of Medical Science, Tehran, Iran.
Heidar TooleeSchool of Allied Medical Sciences, Shahrud University of Medical Sciences, Shahrud, Iran.
Somayeh SolhjooAnatomy Department, Medical School, Kerman University of Medical Science, Tehran, Iran.
Elham SeifaliAnatomy Department, Azad Islamic University of Medical Science, Tehran, Iran.
Soraya ParvariAnatomy Department, School of Medicine, Alborz University of Medical Science, Karaj, Iran.
Omotosho Dhulqarnain AkanjiAnatomy Department, Olabisi Onabanjo University, Sagamu, Nigeria.
Tayebeh RastegarAnatomy Department, Medical School, Tehran University of Medical Science, Tehran, Iran.

Funding

Tehran University of Medical Sciences and Health Services 95-04-30-30213
6 · The paper itself

Abstract

objectiveOsteocalcin (OCN) influences spermatogenesis in conjunction with testosterone and estrogen. OCN facilitates the secretion of testosterone by engaging with G protein-coupled receptor class C group 6 member A (GPRC6A) on Leydig cells and with androgen receptors on Sertoli cells.

methodsAdult mice were assigned to the following groups: control; sham I, which received dimethyl sulfoxide for 5 weeks followed by phosphate-buffered saline for 1 month; azoospermia, which was treated with busulfan (40 mg/kg); sham II, which consisted of azoospermic animals that received phosphate-buffered saline for 1 month beginning at the 5-week mark; and the experimental group, which included azoospermic mice treated with OCN (3 ng/g/day) for 1 month.

resultsIn the mice receiving OCN treatment, immunohistochemical analysis revealed increased expression of androgen receptors and GPRC6A, indicative of enhanced spermatogenesis. Additionally, the expression levels of the cyclic adenosine monophosphate-responsive element binding protein 1, steroidogenic acute regulatory protein, and cytochrome P450 family 11 genes were elevated. However, testosterone levels exhibited no significant differences across groups. Morphometric analysis suggests that OCN may play a crucial role in spermatogenesis, as evidenced by its positive effects on germinal cells and the germinal epithelium in the azoospermia group (p<0.05).

conclusionWe conclude that OCN may serve as a beneficial therapeutic agent for male infertility.

Indexed as

Bone matrixReceptors, androgenSignal transductionTestosterone

Identifiers

PMID38853130
PMCPMC11617912

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