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Multiple omics integration analysis reveals the regulatory effect of chitosan oligosaccharide on testicular development. | LitMetric

AI Article Synopsis

  • Infertility is a widespread issue affecting many people globally, with about 50% of cases linked to male factors, and the effects of chitosan oligosaccharide (COS) on male fertility remain underexplored.
  • A comprehensive study using RNA-seq, serum metabolomics, and gut microbiome analysis found that COS could potentially treat oligospermia by boosting the expression of important proteins for sperm production and testicular growth.
  • The research indicates that COS enhances male reproductive health by modifying gut bacteria, influencing serum metabolites, activating the PI3K-Akt signaling pathway, and improving antioxidant levels in the testes.

Article Abstract

Infertility is a global health problem affecting millions of people of reproductive age worldwide, with approximately half caused by males. Chitosan oligosaccharide (COS) has strong antioxidant capacity, but its impact on the male reproductive system has not been effectively evaluated. To address this, we integrated RNA-seq, serum metabolomics and intestinal 16 S rDNA analysis to conduct a comprehensive investigation on the male reproductive system. The results showed that COS has potential targets for the treatment of oligospermia, which can promote the expression of meiotic proteins DDX4, DAZL and SYCP1, benefit germ cell proliferation and testicular development, enhance antioxidant capacity, and increase the expression of testicular steroid proteins STAR and CYP11A1. At the same time, COS can activate PI3K-Akt signaling pathway in testis and TM3 cells. Microbiome and metabolomics analysis suggested that COS alters gut microbial community composition and cooperates with serum metabolites to regulate spermatogenesis. Therefore, COS promotes male reproduction by regulating intestinal microorganisms and serum metabolism, activating PI3K-Akt signaling pathway, improving testicular antioxidant capacity and steroid regulation.

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Source
http://dx.doi.org/10.1016/j.ecoenv.2024.116802DOI Listing

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