Dysregulation of lncRNA and circRNA Expression in Mouse Testes after Exposure to Triptolide

Suping Xiong1, Yanting Li1, Yang Xiang1

  • 1Institute of Life Science and School of Life Science, Nanchang University, Nanchang, China.

Abstract

Insights

Triptolide causes male reproductive toxicity by affecting sperm and altering noncoding RNA expression. This study reveals potential RNA markers for triptolide-induced male infertility.

Area of Science:

  • Reproductive toxicology
  • Transcriptomics
  • Male infertility

Background:

  • Triptolide shows therapeutic potential but has severe reproductive toxicity, limiting clinical use.
  • Noncoding RNAs (lncRNAs, circRNAs) are vital for spermatogenesis; their dysregulation can cause male infertility.
  • The role of noncoding RNAs in triptolide-induced reproductive toxicity is unknown.

Purpose of the Study:

  • To investigate the molecular mechanisms of triptolide-induced male reproductive toxicity.
  • To explore the involvement of noncoding RNAs (lncRNAs, circRNAs) in this toxicity.
  • To identify potential RNA biomarkers for triptolide-induced male infertility.

Main Methods:

  • Mice were exposed to triptolide.
  • Strand-specific RNA sequencing was performed on total RNA to analyze lncRNA, circRNA, and mRNA expression profiles.
  • Bioinformatic analyses (Gene Ontology, pathway analysis) were used to interpret the functional implications of altered gene expression.

Main Results:

  • Triptolide exposure significantly reduced testicular weight, sperm count, and motility, and caused sperm morphology defects.
  • Aberrant expression profiles of lncRNAs, circRNAs, and mRNAs were observed in triptolide-treated mice.
  • Differentially expressed RNAs were functionally linked to spermatogenesis processes; some RNAs showed potential as toxicity markers.

Conclusions:

  • This study provides a transcriptomic database for triptolide-induced toxicity.
  • It enhances understanding of triptolide's adverse effects on male reproduction.
  • Further research is needed to improve triptolide's therapeutic index by mitigating its toxicity.

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