Department of Animal Science, Bharathidasan University, Tiruchirappalli, 620024, Tamil Nadu, India.
Research Coordinator & Department of Biotechnology, Bioinformatics and Microbiology, National College (Autonomous), Tiruchirappalli, 620001, Tamil Nadu, India.
Reprod Sci. 2024 Oct;31(10):3228-3239. doi: 10.1007/s43032-024-01627-3. Epub 2024 Jun 28.
Atrazine (ATZ, CHClN) is a widely used synthetic herbicide that contaminates drinking water. It is a known endocrine disruptor that disrupts various molecular pathways involved in hormone signaling, and DNA damage, and can cause reproductive disorders, including decreased fertility, and abnormal development of reproductive organs, as revealed in animal model studies. However, the effect of ATZ on steroidogenesis in the male reproductive system, especially reduction of ketosteroids to hydroxysteroids, remains unclear. This study investigated the toxicity of ATZ on the male reproductive system in the Wistar rat model, with an emphasis on its adverse effect on aldo-ketoreductase family 1 member C2 (AKR1C2). Male Wistar rats were administered ATZ for 56 days (duration of one spermatogenic cycle) through oral route, at 20, 40 and 60 mg/kg body weight (bw) doses. The results indicate that ATZ exposure affects the body weight, impairs sperm production, and decrease FSH, LH, and testosterone levels. Additionally, the down-regulation of key steroidogenic enzymes by ATZ disrupted the synthesis of testosterone, leading to decreased levels of this essential male hormone. On the other hand, the expression of AKR1C2 (mRNA and protein) in the testis was upregulated. The findings suggest that AKR1C2 plays a role in androgen metabolism. Furthermore, its overexpression may lead to alteration in the expression of genes in the connected pathway, causing an increase in the breakdown or inactivation of androgens, which would result in lower androgen levels and, thereby, lead to hypoandrogenism, as the combined effects of down-regulation of steroidogenic genes and up-regulation of AKR1C2. These findings reveal direct implication of disrupted AKR1C2 in male reproductive health and highlight the need for further research on the impact of environmental toxins on human fertility, ultimately providing for better patient care.
莠去津(ATZ,CHClN)是一种广泛使用的合成除草剂,会污染饮用水。它是一种已知的内分泌干扰物,会破坏参与激素信号传递和 DNA 损伤的各种分子途径,并可能导致生殖障碍,包括生育力下降和生殖器官发育异常,这在动物模型研究中已有揭示。然而,莠去津对雄性生殖系统甾体生成的影响,特别是将酮甾转化为羟甾,仍不清楚。本研究在 Wistar 大鼠模型中调查了莠去津对雄性生殖系统的毒性,重点研究其对醛酮还原酶家族 1 成员 C2(AKR1C2)的不良影响。雄性 Wistar 大鼠通过口服途径连续 56 天(一个精子发生周期的持续时间)给予莠去津,剂量分别为 20、40 和 60mg/kg 体重。结果表明,莠去津暴露会影响体重,损害精子生成,并降低 FSH、LH 和睾酮水平。此外,莠去津下调关键甾体生成酶会破坏睾酮的合成,导致这种重要雄性激素水平降低。另一方面,睾丸中 AKR1C2(mRNA 和蛋白质)的表达上调。研究结果表明,AKR1C2 在雄激素代谢中发挥作用。此外,其过表达可能导致相关途径中基因表达的改变,导致雄激素的分解或失活增加,从而导致雄激素水平降低,进而导致低雄激素血症,这是甾体生成基因下调和 AKR1C2 上调的综合作用。这些发现揭示了 AKR1C2 对雄性生殖健康的直接影响,并强调需要进一步研究环境毒素对人类生育能力的影响,最终为更好的患者护理提供依据。