Kather H, Daerr W
J Cardiovasc Pharmacol. 1982;4 Suppl 2:S245-7.
The effects of prazosin on adrenergic-stimulated fat-cell lipolysis and adenylate cyclase activity were investigated. The results revealed that the antilipolytic alpha-adrenergic catecholamine effects on human fat-cell metabolism are mediated via alpha 2-receptor sites displaying extremely low affinity to prazosin, which is alpha 1-site selective. The data provide an explantation for the lack of effect of prazosin on lipid mobilization in vivo. The molecular sites mediating the lipid-lowering action of the drug, however, remain to be elucidated.
研究了哌唑嗪对肾上腺素能刺激的脂肪细胞脂解作用和腺苷酸环化酶活性的影响。结果显示,抗脂解α-肾上腺素能儿茶酚胺对人脂肪细胞代谢的作用是通过对哌唑嗪亲和力极低的α2-受体位点介导的,哌唑嗪是α1-位点选择性的。这些数据解释了哌唑嗪在体内对脂质动员缺乏作用的原因。然而,介导该药物降脂作用的分子位点仍有待阐明。