Jacobi G H, Kurth K H, Altwein J E
Urologe A. 1979 Mar;18(2):91-8.
Since Prolactin has intra- and extrapostatic effects on growth and function of the prostate, the influence of the anti-prolactin bromocriptine (PRAVIDEL) was investigated in 15 patients with untreated prostatic carcinoma of various grades of differentiation in vivo. A five-days treatment with 15 mg Pravidel daily significantly suppressed prostatic androgen uptake, unrelated to tumor grading. 5 alpha-Reductase was favored in poorly differentiated lesions with a decreased testosterone/dihydrotestosterone ratio. The pretherapeutic accumulation of 5 alpha-androstanediol was diminished after Pravidel and the tissue/plasma ratio decreased. The 17 beta-hydroxy-pathway of testosterone is predominant as compared to the 17-keto pathway; both pathways are favored after Pravidel in poorly differentiated tumors. Intraprostatic metabolic effects of Pravidel are not related to peripheral androgen levels nor are they dependent on altered prostatic hormone uptake. In the poorly differentiated prostatic tumors Pravidel initiates a metabolic situation as observed in prostate cancer responding to androgen depletion or estrogen therapy.
由于催乳素对前列腺的生长和功能具有体内和体外作用,因此在15例未经治疗的不同分化程度前列腺癌患者体内研究了抗催乳素药物溴隐亭(帕罗西汀)的影响。每天15毫克帕罗西汀进行为期五天的治疗可显著抑制前列腺雄激素摄取,与肿瘤分级无关。在分化差的病变中,5α-还原酶受青睐,睾酮/双氢睾酮比值降低。帕罗西汀治疗后,5α-雄甾二醇的治疗前蓄积减少,组织/血浆比值降低。与17-酮途径相比,睾酮的17β-羟基途径占主导地位;在分化差的肿瘤中,帕罗西汀治疗后这两条途径均受青睐。帕罗西汀的前列腺内代谢作用与外周雄激素水平无关,也不依赖于前列腺激素摄取的改变。在分化差的前列腺肿瘤中,帕罗西汀引发的代谢情况与对雄激素耗竭或雌激素治疗有反应的前列腺癌中观察到的情况相同。