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

机译:选择性雌激素受体调节剂对培养牛肾上腺髓质细胞血浆膜雌激素受体和儿茶胺合成及分泌的影响

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摘要

Abstract.: 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. Keywords:: adrenal medulla, catecholamine synthesis and secretion, plasma membrane estrogen receptor, raloxifene, selective estrogen receptor modulator
机译:摘要.:我们之前报道了培养牛肾上腺髓质细胞中血浆膜雌激素受体的发生和功能。在这里,我们报告了雷洛昔芬和他莫昔芬,选择性雌激素受体调节剂,在这些细胞中对血浆膜雌激素受体和儿茶酚胺合成和分泌的影响。雷洛昔芬对从牛肾上腺髓质中分离的血浆膜的血浆膜的特异性结合引起了双重影响;也就是说,它具有1.0-10nm的刺激作用,但抑制效果为1.0-10μm,而Tamoxifen(1.0nm-10μm)在所有浓度下增加结合(除100nm之外)。 Tamoxifen在100nm处导致[14C]酪氨酸的基础14C-儿茶酚胺合成显着增加,而Tamoxifen和Raloxifenes在较高浓度下减弱基础和乙酰胆碱诱导的14C-儿茶酚胺合成。雷洛昔芬(0.3,1.0和3-100μm)和他莫昔芬(10-100μm)还抑制了乙酰胆碱诱导的儿茶酚胺分泌和45cA2 +和22NA +流入。雷洛昔芬(1.0μm)抑制乙酰胆碱在表达α4β2神经元氰基乙酰胆碱受体的Xenopus卵母细胞中引起的Na +电流。本研究结果表明,通过抑制牛肾上腺髓质中的Na +和Ca2 +流入,在低浓度下,在低浓度下的雷洛昔芬和三莫昔芬抑制乙酰胆碱诱导的儿茶胺合成和分泌。关键词::肾上腺髓质,儿茶酚胺合成和分泌,血浆膜雌激素受体,雷洛昔芬,选择性雌激素受体调节剂

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