Toxicology Division, CSIR-Central Drug Research Institute, Lucknow, India.
PLoS One. 2013 Jul 1;8(7):e69086. doi: 10.1371/journal.pone.0069086. Print 2013.
Salinomycin is used as an antibiotic in animal husbandry. Its implication in cancer therapy has recently been proposed. Present study evaluated the toxic effects of Salinomycin on male reproductive system of mice. Doses of 1, 3 or 5 mg/kg of Salinomycin were administered daily for 28 days. Half of the mice were sacrificed after 24 h of the last treatment and other half were sacrificed 28 days after withdrawal of treatment. Effects of SAL on body and reproductive organ weights were studied. Histoarchitecture of testis and epididymis was evaluated along with ultrastructural changes in Leydig cells. Serum and testicular testosterone and luteinizing hormones were estimated. Superoxide dismutase, reduced glutathione, lipid peroxidation, catalase and lactate dehydrogenase activities were measured. Spermatozoa count, morphology, motility and fertility were evaluated. Expression patterns of steroidogenic acute regulatory protein (StAR) and cytochrome P450 side chain cleavage proteins (CYP11A1) were assessed by Western blotting. Salinomycin treatment was lethal to few mice and retarded body growth in others with decreased weight of testes and seminal vesicles in a dose dependent manner. Seminiferous tubules in testes were disrupted and the epithelium of epididymis showed frequent occurrence of vacuolization and necrosis. Leydig cells showed hypertrophied cytoplasm with shrunken nuclei, condensed mitochondria, proliferated endoplasmic reticulum and increased number of lipid droplets. Salinomycin decreased motility and spermatozoa count with increased number of abnormal spermatozoa leading to infertility. The testosterone and luteinizing hormone levels were decreased in testis but increased in serum at higher doses. Depletion of superoxide dismutase and reduced glutathione with increased lipid peroxidation in both testis and epididymis indicated generation of oxidative stress. Suppressed expression of StAR and CYP11A1 proteins indicates inhibition of steroidogenesis. Spermatogenesis was however observed in testis 28 days after Salinomycin withdrawal. The results indicate reversible dose-dependent adverse effects of Salinomycin on male reproductive system of mice.
硫酸黏菌素被用作畜牧业中的抗生素。最近有人提出,它可能对癌症治疗有作用。本研究评估了硫酸黏菌素对雄性小鼠生殖系统的毒性作用。每天给予 1、3 或 5mg/kg 的硫酸黏菌素,连续 28 天。一半的小鼠在最后一次治疗后 24 小时处死,另一半在治疗停止 28 天后处死。研究了 SAL 对体重和生殖器官重量的影响。评估了睾丸和附睾的组织学结构以及睾丸间质细胞的超微结构变化。估计了血清和睾丸中的睾酮和促黄体生成激素。测量了超氧化物歧化酶、还原型谷胱甘肽、脂质过氧化、过氧化氢酶和乳酸脱氢酶的活性。评估了精子计数、形态、活力和生育力。通过 Western 印迹评估了类固醇急性调节蛋白(StAR)和细胞色素 P450 侧链裂解蛋白(CYP11A1)的表达模式。硫酸黏菌素处理对少数小鼠致死,对其他小鼠的体重增长产生延迟作用,导致睾丸和精囊重量呈剂量依赖性下降。睾丸的生精小管受损,附睾上皮常出现空泡化和坏死。睾丸间质细胞的细胞质肥大,细胞核皱缩,线粒体浓缩,内质网增生,脂滴数量增加。硫酸黏菌素降低了精子的活力和计数,增加了畸形精子的数量,导致不育。睾丸中的睾酮和黄体生成素水平降低,但在较高剂量时血清中的水平增加。睾丸和附睾中超氧化物歧化酶和还原型谷胱甘肽的耗竭以及脂质过氧化的增加表明氧化应激的产生。StAR 和 CYP11A1 蛋白的表达抑制表明类固醇生成受到抑制。然而,在硫酸黏菌素停药 28 天后,睾丸中仍观察到精子发生。结果表明,硫酸黏菌素对雄性小鼠生殖系统具有可逆的、剂量依赖性的不良影响。