Karashima T, Zalatnai A, Schally A V
Endocrine, Polypeptide and Cancer Institute, Veterans Administration Medical Center, New Orleans, LA 70146.
Proc Natl Acad Sci U S A. 1988 Apr;85(7):2329-33. doi: 10.1073/pnas.85.7.2329.
Possible protective effects of analogs of luteinizing hormone-releasing hormone (LH-RH) against testicular damage caused by various cytotoxic agents were investigated in rats. The agonist [D-Trp6]LH-RH (in which Gly-6 is replaced by D-tryptophan) and the antagonist N-Ac-[D-Phe(pCl)1,2,D-Trp3,D-Arg6,D-Ala10]LH-RH were administered for 12 weeks: [D-Trp6]LH-RH was given once a month in the form of long-acting microcapsules liberating 25 micrograms of agonist per day, and the antagonist was injected s.c. at a dose of 1000 micrograms per kg of body weight per day for the first 3 weeks and, thereafter, at a dose of 500 micrograms per kg of body weight per day. After a recovery period of 3 months, most seminiferous tubules in the antagonist-treated group showed a normal morphology, while patches of tubules in the agonist-treated group continued to show some suppression of spermatogenesis. Administration of busulfan, cisplatin, or cyclophosphamide produced only a reversible testicular injury, and pretreatment with LH-RH analogs seemed to temporarily enhance the tubular damage. Administration of procarbazine (200 mg per kg of body weight per week for 6 weeks) resulted in decreased testicular weights and increased serum LH levels 1 and 3 months after the discontinuation of treatment. The histology showed severe diffuse damage to seminiferous tubules. The germinal cells completely disappeared and the Sertoli cells were markedly degenerated. This damage was not restored even after a recovery period of 5 months. Some animals were pretreated for 6 weeks with the agonist or antagonist and then received procarbazine for 6 weeks while administration of analogs was continued. In these animals, the decrease in testicular weights and increase in serum LH levels after procarbazine were less marked than in the group not pretreated with the analogs. Three and 5 months after cessation of treatment, a large number of tubules showed a complete restoration of structural morphology in 30-45% of the animals that received procarbazine and the LH-RH agonist or antagonist. These results indicate that pretreatment with LH-RH analogs may protect testes against damage caused by some cytotoxic agents.
在大鼠中研究了促黄体生成激素释放激素(LH-RH)类似物对各种细胞毒性药物所致睾丸损伤的可能保护作用。给予激动剂[D-色氨酸6]LH-RH(其中甘氨酸-6被D-色氨酸取代)和拮抗剂N-乙酰-[D-苯丙氨酸(对氯)1,2,D-色氨酸3,D-精氨酸6,D-丙氨酸10]LH-RH 12周:[D-色氨酸6]LH-RH以长效微胶囊形式每月给药一次,每天释放25微克激动剂,拮抗剂在最初3周内以每天每千克体重1000微克的剂量皮下注射,此后以每天每千克体重500微克的剂量注射。经过3个月的恢复期后,拮抗剂治疗组的大多数生精小管形态正常,而激动剂治疗组的部分小管仍表现出一定程度的精子发生抑制。给予白消安、顺铂或环磷酰胺仅产生可逆性睾丸损伤,用LH-RH类似物预处理似乎会暂时加重小管损伤。给予丙卡巴肼(每周每千克体重200毫克,共6周)导致治疗停止后1个月和3个月睾丸重量减轻,血清LH水平升高。组织学显示生精小管严重弥漫性损伤。生殖细胞完全消失,支持细胞明显退化。即使经过5个月的恢复期,这种损伤也未恢复。一些动物先用激动剂或拮抗剂预处理6周,然后接受丙卡巴肼治疗6周,同时继续给予类似物。在这些动物中,丙卡巴肼后睾丸重量的减轻和血清LH水平的升高不如未用类似物预处理的组明显。治疗停止后3个月和5个月,在接受丙卡巴肼和LH-RH激动剂或拮抗剂的动物中,30%-45%的动物大量小管显示结构形态完全恢复。这些结果表明,用LH-RH类似物预处理可能保护睾丸免受某些细胞毒性药物所致的损伤。