Kim Sung-Hwan, Lee In-Chul, Lim Jeong-Hyeon, Moon Changjong, Bae Chun-Sik, Kim Sung-Ho, Shin Dong-Ho, Kim Hyoung-Chin, Kim Jong-Choon
College of Veterinary Medicine, Chonnam National University, Gwangju, Korea.
Lab Anim Res. 2012 Mar;28(1):11-6. doi: 10.5625/lar.2012.28.1.11. Epub 2012 Mar 21.
This study was conducted to investigate the potential effects of α-chlorohydrin (ACH) on epididymal function and antioxidant system in male rats. The test chemical was administered to male rats by gavage at doses of 0, 3, 10, and 30 mg/kg/day for 7 days. Twenty-four male rats were randomly assigned to four experimental groups, with six rats in each group. Spermatotoxicity was assessed by measurement of reproductive organ weight, testicular sperm head count, epididymal sperm motility and morphology, histopathologic examination, and oxidative damage analysis in rats. At 30 mg/kg/day, an increase in the incidence of clinical signs, epididymis weight, and gross necropsy findings of the epididymis, a decrease in the sperm motility, and an increased incidence of histopathological changes of the epididymis were observed in a dose-dependent manner. At 10 mg/kg/day, an increased incidence of clinical signs and histopathological changes and decreased sperm motility were observed. In the oxidative damage analysis, an increase in the malondialdehyde concentration and a decrease in the glutathione content and glutathione peroxidase and catalase activities in the epididymal tissue were detected at ≥3 mg/kg/day. The results show that graded doses of ACH elicit depletion of the antioxidant defense system and that the spermatotoxicity of ACH may be due to the induction of oxidative stress.
本研究旨在探讨α-氯醇(ACH)对雄性大鼠附睾功能和抗氧化系统的潜在影响。将受试化学物质以0、3、10和30mg/kg/天的剂量通过灌胃给予雄性大鼠,持续7天。将24只雄性大鼠随机分为四个实验组,每组6只大鼠。通过测量大鼠生殖器官重量、睾丸精子头部计数、附睾精子活力和形态、组织病理学检查以及氧化损伤分析来评估精子毒性。在30mg/kg/天的剂量下,观察到临床体征发生率、附睾重量以及附睾大体尸检结果增加,精子活力下降,附睾组织病理学变化发生率呈剂量依赖性增加。在10mg/kg/天的剂量下,观察到临床体征和组织病理学变化发生率增加以及精子活力下降。在氧化损伤分析中,在≥3mg/kg/天的剂量下,检测到附睾组织中丙二醛浓度增加,谷胱甘肽含量、谷胱甘肽过氧化物酶和过氧化氢酶活性下降。结果表明,不同剂量的ACH会导致抗氧化防御系统耗竭,ACH的精子毒性可能是由于氧化应激的诱导。