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Cyproterone acetate displaces opiate binding in mouse brain.

作者信息

Gutiérrez M, Menéndez L, Ruiz-Gayo M, Hidalgo A, Baamonde A

机构信息

Departamento de Medicina, Facultad de Medicina, Oviedo, Spain.

出版信息

Eur J Pharmacol. 1997 Jun 5;328(1):99-102. doi: 10.1016/s0014-2999(97)83034-8.

Abstract

Drugs acting on androgen receptors modify opioid transmission in the central nervous system. To investigate a direct interaction, we studied whether the binding of [3H]diprenorphine to mouse brain membranes was modified by cyproterone acetate (progesterone derivative with antiandrogen activity), flutamide (non-steroidal antiandrogen), 5alpha-dihydrotestosterone and progesterone. Only cyproterone acetate inhibited [3H]diprenorphine binding (IC50 = (1.62 +/- 0.33) x 10(-6) M) without modifying its association rate. These results suggest that cyproterone acetate binds to opiate receptors independently of its classical androgenic intracellular receptor effect.

摘要

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