Ichikawa T, Akimoto S, Shimazaki J
Department of Urology, School of Medicine, Chiba University, Japan.
Endocrinol Jpn. 1988 Feb;35(1):181-7. doi: 10.1507/endocrj1954.35.181.
Leuprolide, a synthetic LHRH analog, inhibited growth of the Dunning R 3327 androgen-sensitive rat prostatic tumor and induced weight loss in male accessory sex organs. The relationship between the mode of administration and efficiency of the treatment was examined. Maintenance of the drug level in vivo seemed to be one of the important factors in the suppression of tumor growth, while a decrease in the weight of the accessory sex organs was mainly dependent on the dose administered. No treatment with leuprolide surpassed the effect caused by castration. Cytosolic androgen receptor and acid phosphatase activity in the tumor tissues were not changed significantly after treatment with leuprolide.
亮丙瑞林是一种合成的促黄体生成激素释放激素(LHRH)类似物,可抑制邓宁R 3327雄激素敏感型大鼠前列腺肿瘤的生长,并导致雄性附属性器官重量减轻。研究了给药方式与治疗效果之间的关系。体内药物水平的维持似乎是抑制肿瘤生长的重要因素之一,而附属性器官重量的减轻主要取决于给药剂量。亮丙瑞林治疗未超过去势所产生的效果。亮丙瑞林治疗后,肿瘤组织中的胞质雄激素受体和酸性磷酸酶活性未发生显著变化。