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ORIGINAL RESEARCH article

Front. Cell Dev. Biol.

Sec. Molecular and Cellular Reproduction

Volume 13 - 2025 | doi: 10.3389/fcell.2025.1679330

This article is part of the Research TopicRedox Regulation in Sperm and Oocyte from Gametogenesis to Fertilization for Reproductive HealthView all 4 articles

L-cysteine Mitigates Busulfan-Induced Testicular Injury through Modulation of CBS/H2S Axis

Provisionally accepted
Song  LiuSong Liu1,2Bin  WeiBin Wei1,2Huijun  YangHuijun Yang2,3*Han  WeiHan Wei4Anran  XuAnran Xu2,3Lianbing  ShengLianbing Sheng1,2Xiangyang  SunXiangyang Sun2,3Yunling  DongYunling Dong1,2
  • 1Shandong Provincial Maternal and Child Health Care Hospital Affiliated to Qingdao University, Jinan, China
  • 2Key Laboratory of Birth Regulation and Control Technology of National Health Commission of China, Jinan, China
  • 3Shandong Province Maternal and Child Health Care Hospital Key Laboratory of Birth Regulation and Control Technology of National Health Commission, Jinan, China
  • 4Dalian Women and Children's Medical Group, Dalian, China

The final, formatted version of the article will be published soon.

Global male infertility, characterized by decreased spermatogenesis and sperm quality, is a significant concern. L-cysteine, essential for hydrogen sulfide (H2S) synthesis, offers numerous biological advantages. However, the protective mechanisms of L-cysteine in treating spermatogenic dysfunction need further exploration. This study aims to examine L-cysteine's protective effects on busulfan-induced testicular toxicity. Results show that administering L-cysteine at different doses (2.5, 5.0, and 10 mg/kg) led to notable improvements in final body weight, testis weight, sperm count, sperm motility, testosterone levels, and seminiferous tubule architecture. At a 5.0 mg/kg dosage, L-cysteine mitigated testicular injury by activating the CBS/H2S axis. Moreover, L-cysteine effectively reduced apoptosis and oxidative stress through Nrf2/HO-1 pathway activation. Various analyses demonstrated that L-cysteine enhanced the repair of the blood-testis barrier (BTB) disrupted by busulfan. Mechanistically, L-cysteine activated the PI3K/Akt/mTOR pathway in the testes. Notably, the CBS inhibitor AOAA reversed L-cysteine's protective effects on busulfan-induced testicular damage. In summary, the study suggests that L-cysteine can safeguard against busulfan-induced spermatogenic dysfunction, apoptosis, oxidative stress, and BTB disruption by modulating the PI3K/Akt/mTOR pathway, hinging on CBS/H2S axis activation. These findings propose L-cysteine as a potential treatment for male infertility, particularly in individuals undergoing busulfan chemotherapy.

Keywords: L-cysteine, CBS/H2S, Oxidative Stress, Blood-Testis Barrier, PI3K/Akt/mTOR pathway

Received: 04 Aug 2025; Accepted: 16 Sep 2025.

Copyright: © 2025 Liu, Wei, Yang, Wei, Xu, Sheng, Sun and Dong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Huijun Yang, sdsfyyhj123@163.com

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