Pousette A, Carlström K, Stege R
Department of Clinical Chemistry, Karolinska Institutet, Huddinge University Hospital, Sweden.
Urol Res. 1989;17(2):95-8. doi: 10.1007/BF00262027.
Serum levels of testosterone (T), 17 alpha-hydroxyprogesterone (17OHP), 4-androstene-3,17-dione (A-4), dehydroepiandrosterone (DHA), dehydroepiandrosterone sulfate (DHAS) and cortisol were measured before and after 6 months of treatment in prostatic cancer patients treated by orchidectomy (ORX) or with oral + parenteral estrogens (OE), single parenteral estrogens (PE; 160 or 320 mg polyestradiol phosphate i.m. every fourth week), estramustine phosphate (ECYT) or LHRH agonist without (LHRH) or with (LHRH-F) flutamide. Castration values of T and 170HP were reached in all types of treatment (PE at the higher dose). A-4 levels were suppressed by all treatment regimens except ECYT; DHA by OE and LHRH-F and DHAS by ORX, OE and LHRH-F. The most pronounced suppression was found in the LHRH-F group. Cortisol levels were markedly increased by OE and ECYT. The observed effects on the adrenal androgens A4, DHA and DHAS and on cortisol probably reflect different degrees of liver interaction rather than interaction with adrenocortical steroid synthesis.
对接受睾丸切除术(ORX)或口服加胃肠外雌激素(OE)、单一胃肠外雌激素(PE;每四周肌肉注射160或320毫克磷酸聚雌二醇)、磷酸雌莫司汀(ECYT)或无氟他胺(LHRH)或有氟他胺(LHRH-F)的促性腺激素释放激素(LHRH)激动剂治疗的前列腺癌患者,在治疗6个月前后测量血清睾酮(T)、17α-羟孕酮(17OHP)、4-雄烯-3,17-二酮(A-4)、脱氢表雄酮(DHA)、硫酸脱氢表雄酮(DHAS)和皮质醇水平。所有类型的治疗(较高剂量的PE)均达到了T和170HP的去势值。除ECYT外,所有治疗方案均抑制A-4水平;OE和LHRH-F抑制DHA水平,ORX、OE和LHRH-F抑制DHAS水平。在LHRH-F组中发现抑制作用最为明显。OE和ECYT使皮质醇水平显著升高。观察到的对肾上腺雄激素A4、DHA和DHAS以及对皮质醇的影响可能反映了不同程度的肝脏相互作用,而非与肾上腺皮质类固醇合成的相互作用。