Effects of Selective Estrogen Receptor Modulators on Plasma Membrane Estrogen Receptors and Catecholamine Synthesis and Secretion in Cultured Bovine Adrenal Medullary Cells

Journal of Pharmacological Sciences

Toru Hachisuga³  Nobuyuki Yanagihara²  Susumu Ueno¹  Yumiko Toyohira²  Go Obara⁴  Toshinori Kawagoe³  Hirohide Inagaki²  Keita Takahashi²  Masato Tsutsui⁵ 

[1] Department of Occupational Toxicology, Institute of Industrial Ecological Sciences, University of Occupational and Environmental Health, Japan;Department of Pharmacology, School of Medicine, University of Occupational and Environmental Health, Japan;Department of Obstetrics and Gynecology, School of Medicine, University of Occupational and Environmental Health, Japan;Department of Anesthesiology, School of Medicine, University of Occupational and Environmental Health, Japan;Department of Pharmacology, Graduate School of Medicine, University of The Ryukyus, Japan

关键词: adrenal medulla;    catecholamine synthesis and secretion;    plasma membrane estrogen receptor;    raloxifene;    selective estrogen receptor modulator;   

DOI  :  10.1254/jphs.13155FP

学科分类：药学

来源: Nihon Yakuri Gakkai Henshuubu / Japanese Pharmacological Society

【 摘 要 】

References(28)Cited-By(1)We previously reported the occurrence and function of plasma membrane estrogen receptors in cultured bovine adrenal medullary cells. Here we report the effects of raloxifene and tamoxifen, selective estrogen receptor modulators, on plasma membrane estrogen receptors and catecholamine synthesis and secretion in these cells. Raloxifene caused dual effects on the specific binding of [3H]17β-estradiol to the plasma membranes isolated from bovine adrenal medulla; that is, it had a stimulatory effect at 1.0 �? 10 nM but an inhibitory effect at 1.0 �? 10 μM, whereas tamoxifen (1.0 nM �? 10 μM) increased binding at all concentrations (except for 100 nM). Tamoxifen at 100 nM caused a significant increase in basal 14C-catecholamine synthesis from [14C]tyrosine, whereas tamoxifen and raloxifene at higher concentrations attenuated basal and acetylcholine-induced 14C-catecholamine synthesis. Raloxifene (0.3, 1.0, and 3 �? 100 μM) and tamoxifen (10 �? 100 μM) also suppressed catecholamine secretion and 45Ca2+ and 22Na+ influx, respectively, induced by acetylcholine. Raloxifene (1.0 μM) inhibited Na+ current evoked by acetylcholine in Xenopus oocytes expressing α4β2 neuronal nicotinic acetylcholine receptors. The present findings suggest that raloxifene and tamoxifen at low concentrations allosterically modulate plasma membrane estrogen receptors and at high concentrations inhibit acetylcholine-induced catecholamine synthesis and secretion by inhibiting Na+ and Ca2+ influx in bovine adrenal medulla.

【 授权许可】

Unknown