Evidence map›Paper›PMID 39507870›Full record

ArticleTranslational andrology and urology2024

Quantitative proteomics reveal the protective effects of Qiang Jing decoction against oligoasthenospermia via modulating spermatogenesis related-proteins.

Desheng Wang, Haiwang Lu, Bin Bin, Siwei Lin, Jie Wang

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Article in Translational andrology and urology, 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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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Desheng Wang *Department of Andrology, Ruikang Hospital Affiliated to Guangxi University of Chinese Medicine, Nanning, China.
Haiwang Lu *Department of Andrology, The First Affiliated Hospital of Guangxi University of Chinese Medicine, Nanning, China.
Bin BinDepartment of Andrology, The First Affiliated Hospital of Guangxi University of Chinese Medicine, Nanning, China.
Siwei LinDepartment of Andrology, The First Affiliated Hospital of Guangxi University of Chinese Medicine, Nanning, China.
Jie WangDepartment of Andrology, The First Affiliated Hospital of Guangxi University of Chinese Medicine, Nanning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: According to the current situation, the treatment of oligoasthenospermia with Western medicine is still full of challenges. Qiang Jing decoction (QJD) is used for treating male infertility as a traditional Chinese medicine (TCM) prescription. In this study. we will try to uncover the molecular mechanism of QJDs in treating oligoasthenospermia based on the proteomics technology. Methods: In this study, sperm quality from oligoasthenospermia model, QJD treatment, and control rats were analyzed. Tandem mass tag (TMT) quantitative proteomics was used for the comparative analysis of protein abundance in rat testis of different treatment. Results: The therapeutic effect of QJDs on spermatogenesis function by improving sperm quality was confirmed in the present experiment. In addition, our results showed that the majority of proteins related to spermatogenesis were significantly downregulated in oligoasthenospermia model rats compared to the control group, whereas these proteins' expression levels were recovered after the QJD treatment. In the meantime, immunohistochemistry was used to determine PI3K/AKT (phosphoinositide 3 kinase/serine-threonine kinase) signaling pathway-related protein expression profiles. In brief, we think QJD improved sperm density and quality by activating spermatogenesis-related protein expression and PI3K/AKT signaling pathway. Conclusions: The results of this study may help to establish a foundation for further functional studies of key protein-mediated for improving sperm quality and alleviating oligoasthenospermia.

Indexed as

immunohistochemistryOligoasthenospermiaPI3K/AKT signaling pathwayquantitative proteomics

Identifiers

PMID39507870
PMCPMC11535736

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