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Effects of Qilin pills on spermatogenesis, reproductive hormones, oxidative stress, and the TSSK2 gene in a rat model of oligoasthenospermia. | LitMetric

AI Article Synopsis

  • A study on Qilin pills (QLPs) evaluates their impact on male fertility by examining spermatogenesis, reproductive hormones, and oxidative stress in rats with oligoasthenospermia.
  • QLPs were administered to rats for 60 days after inducing infertility, measuring various sperm parameters and hormonal levels.
  • Results show that QLPs significantly enhance semen quality, restore hormone levels, reduce oxidative stress, and regulate a gene linked to spermatogenesis, indicating their potential as a therapeutic option for male infertility.

Article Abstract

Background: Qilin pills (QLPs), a classic Traditional Chinese Medicine (TCM) formula for treating male infertility, effectively improve semen quality in clinical trials. This study was designed to evaluate the effects of QLPs on spermatogenesis, reproductive hormones, oxidative stress, and the testis-specific serinekinase-2 (TSSK2) gene in a rat model of oligoasthenospermia.

Methods: Forty adult male Sprague-Dawley (SD) rats were randomly divided into four groups. The rat model with oligoasthenospermia was generated by intragastric administration of tripterygium glycosides (TGs) once daily for 4 weeks. Then, two treatment groups were given different doses (1.62 g/kg and 3.24 g/kg) of QLPs once daily for 60 days. Sperm parameters, testicular histology and reproductive hormone measurements, oxidative stress tests, and TSSK2 expression tests were carried out.

Results: QLPs effectively improved semen parameters and testicular histology; restored the levels of FSH, LH, PRL, fT, and SHBG; reduced the levels of oxidative stress products (ROS and MDA); increased testicular SOD activity; and restored the expression of spermatogenesis-related gene TSSK2.

Conclusion: QLPs have a therapeutic effect on a rat model of oligoasthenospermia, and this effect is manifested as improvement of semen quality and testis histology, gonadal axis stability, decreased oxidative stress, and the regulation of testis-specific spermatogenesis-related gene TSSK2.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076898PMC
http://dx.doi.org/10.1186/s12906-019-2799-7DOI Listing

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