Kholkute S D, Patil R K, Sharma S, Elger W A, Puri C P
Institute for Research in Reproduction (ICMR)3 Parel, Bombay, India.
Biol Reprod. 1990 May-Jun;42(5-6):808-14. doi: 10.1095/biolreprod42.5.808.
The effects of a progesterone antagonist ZK 98.734 on release of bioactive luteinizing hormone (LH) and testosterone were studied in adult male common marmosets by using the following experimental protocols: (1) the blocking of the nocturnal rise in testosterone levels by ZK 98.734, (2) the pharmacodynamic effects of ZK 98.734 on testosterone and LH levels, (3) the reversal of ZK 98.734-induced decrease in testosterone by treatment with human chorionic gonadotropin (hCG), and (4) the blocking of estradiol-induced positive feedback release of LH by ZK 98.734. Sixteen adult male common marmosets were used for different experiments after resting them for at least 4 wk between experiments. Testosterone and bioactive LH levels were measured by specific radioimmunoassay and in vitro bioassay methods, respectively. Treatment (i.m.) of male common marmosets (n = 6/group) with ZK 98.734 (1 mg or 5 mg/day) at 1700 h for 3 consecutive days significantly (p less than 0.05) suppressed the nocturnal (2200 h) rise in testosterone levels. The effects of the two doses were not dose-related; however, the decrease on the first day of treatment was more pronounced with the 5-mg dose than with the 1-mg dose. Diurnal rhythms were restored during the post-treatment period. Similarly, treatment with ZK 98.734 (5 mg, n = 8/group) at 1000 h caused a decrease in testosterone and LH levels. The levels were significantly (p less than 0.05) lower at 3 and 6 h after treatment compared to pretreatment levels.(ABSTRACT TRUNCATED AT 250 WORDS)
通过以下实验方案,研究了孕酮拮抗剂ZK 98.734对成年雄性普通狨猴生物活性促黄体生成素(LH)和睾酮释放的影响:(1)ZK 98.734对睾酮水平夜间升高的阻断作用;(2)ZK 98.734对睾酮和LH水平的药效学作用;(3)用人绒毛膜促性腺激素(hCG)治疗逆转ZK 98.734引起的睾酮降低;(4)ZK 98.734对雌二醇诱导的LH正反馈释放的阻断作用。16只成年雄性普通狨猴在实验之间至少休息4周后用于不同实验。分别通过特异性放射免疫测定法和体外生物测定法测量睾酮和生物活性LH水平。在1700 h给雄性普通狨猴(每组n = 6)连续3天肌肉注射ZK 98.734(1 mg或5 mg/天),显著(p < 0.05)抑制了夜间(2200 h)睾酮水平的升高。两种剂量的作用与剂量无关;然而,治疗第一天5 mg剂量组的降低比1 mg剂量组更明显。治疗后阶段昼夜节律恢复。同样,在1000 h用ZK 98.734(5 mg,每组n = 8)治疗导致睾酮和LH水平降低。与治疗前水平相比,治疗后3小时和6小时水平显著(p < 0.05)降低。(摘要截断于250字)