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GnRH 激动剂和抗雄激素治疗对大鼠丙卡巴肼诱导的睾丸损伤的保护作用。

Protection against procarbazine-induced testicular damage by GnRH-agonist and antiandrogen treatment in the rat.

作者信息

Kangasniemi M, Wilson G, Huhtaniemi I, Meistrich M L

机构信息

Department of Experimental Radiotherapy, University of Texas, M.D. Anderson Cancer Center, Houston 77030, USA.

出版信息

Endocrinology. 1995 Aug;136(8):3677-80. doi: 10.1210/endo.136.8.7628410.

Abstract

Suppression of spermatogenesis in LBNF1 rats by treatment with the GnRH agonist Zoladex combined with the antiandrogen flutamide was evaluated in order to rapidly achieve protection of spermatogenic stem cells against procarbazine with clinically used drugs. Zoladex-flutamide treatment required 3 weeks to suppress the completion of spermatogenesis; only a small degree of suppression was observed with Zoladex alone. The suppression of spermatogenesis was reversible. In rats pretreated for 3 weeks with Zoladex-flutamide, the recovery of spermatogenesis at 9 weeks after a single injection of procarbazine as measured by testis weight, testicular sperm head counts, or a histological end point was significantly better than without hormonal pretreatment. Thus Zoladex-flutamide treatment enhanced the recovery of spermatogenesis from stem spermatogonia after procarbazine treatment in the rat and might be applicable to protect spermatogenesis in patients undergoing chemotherapy for cancer.

摘要

为了用临床使用的药物快速实现对生精干细胞的保护,使其免受丙卡巴肼的影响,研究了用促性腺激素释放激素(GnRH)激动剂戈舍瑞林联合抗雄激素氟他胺治疗对LBNF1大鼠精子发生的抑制作用。戈舍瑞林-氟他胺治疗需要3周时间来抑制精子发生的完成;单独使用戈舍瑞林时仅观察到轻微程度的抑制。精子发生的抑制是可逆的。在用戈舍瑞林-氟他胺预处理3周的大鼠中,通过睾丸重量、睾丸精子头部计数或组织学终点测量,在单次注射丙卡巴肼后9周时精子发生的恢复明显优于未进行激素预处理的情况。因此,戈舍瑞林-氟他胺治疗增强了大鼠在丙卡巴肼治疗后从精原干细胞恢复精子发生的能力,并且可能适用于保护接受癌症化疗的患者的精子发生。

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