首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Protective effects of analogs of luteinizing hormone-releasing hormone against chemotherapy-induced testicular damage in rats.
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Protective effects of analogs of luteinizing hormone-releasing hormone against chemotherapy-induced testicular damage in rats.

机译:黄体生成素释放激素类似物对化学疗法诱导的睾丸损伤的保护作用。

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摘要

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.
机译:在大鼠中研究了黄体生成素释放激素(LH-RH)类似物对各种细胞毒剂引起的睾丸损伤的可能的保护作用。激动剂[D-Trp6] LH-RH(其中Gly-6被D-色氨酸替代)和拮抗剂N-Ac- [D-Phe(pCl)1,2,D-Trp3,D-Arg6,D -Ala10] LH-RH给药12周:[D-Trp6] LH-RH以长效微胶囊的形式每月给药一次,每天释放25微克的激动剂,并以皮下注射拮抗剂的形式前三周的剂量为每天1000毫克/千克体重,此后,每天的剂量为500微克/千克体重。在3个月的恢复期之后,拮抗剂治疗组中的大多数生精小管表现出正常的形态,而激动剂治疗组中的小管斑块继续表现出对精子发生的抑制。使用白消安,顺铂或环磷酰胺只会产生可逆的睾丸损伤,用LH-RH类似物进行的预处理似乎会暂时增强肾小管的损伤。停用治疗后1个月和3个月,服用丙卡巴嗪(每周200 mg / kg体重,持续6周)可降低睾丸重量,并提高血清LH水平。组织学显示对生精小管的严重弥散性损害。生殖细胞完全消失,Sertoli细胞明显退化。即使经过5个月的恢复期,也无法恢复该损坏。一些动物用激动剂或拮抗剂预处理6周,然后在继续给予类似物的同时接受普卡巴嗪6周。在这些动物中,丙卡巴肼后睾丸重量的减少和血清LH水平的增加与未用类似物未进行过预处理的组相比没有什么明显的意义。停止治疗三个月和五个月后,接受肾上腺素和LH-RH激动剂或拮抗剂的动物中,有30%至45%的动物的大量小管显示出结构形态的完全恢复。这些结果表明,用LH-RH类似物进行预处理可以保护睾丸免受某些细胞毒性剂引起的损害。

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