受体占用和地塞米松对晶状体-肾上腺素能受体的调节。

M E Ireland, D M Richiert, K Tran
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引用次数: 5

摘要

鸡晶状体环垫(CLAP)细胞原代培养中β -肾上腺素能结合位点用二氢丙烯诺尔(DHAP)进行了表征。结合位点亲和力和密度与先前在新分离细胞的粗膜上表征的β -肾上腺素能受体(bar)相似。在竞争性置换研究中,β受体阻滞剂心得安被证明以浓度依赖的方式增加可用结合位点的数量。在与dhp结合之前,急性暴露于心得安的淋病细胞也会导致可用结合位点的数量增加。最后,地塞米松治疗可调节晶状体β -肾上腺素能结合位点水平。这些结果表明晶状体bar受到共同的调节机制的影响,并进一步暗示眼科药物可能是白内障的诱发因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulation of lens beta-adrenergic receptors by receptor occupancy and dexamethasone.

Beta-adrenergic binding sites in primary cultures of chick lens annular pad (CLAP) cells were characterized with dihydroalprenolol (DHAP). Binding site affinities and densities were similar to beta-adrenergic receptors (BARs) previously characterized on crude membranes from freshly isolated cells. In competitive displacement studies, the beta-blocker propranolol was shown to increase the number of available binding sites in a concentration dependent manner. Acute exposure of CLAP cells to propranolol prior to DHAP binding also resulted in an increase in the number of available binding sites. Finally, lens beta-adrenergic binding site levels could be modulated by dexamethasone treatment. These results indicate that lens BARs are subject to common regulatory mechanisms and further implicate ophthalmic pharmaceuticals as possible cataractogenic agents.

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