Phenol, a potent stimulator of adenylate cyclase in human thyroid membranes.

S M Amir, N J Mulrow, S H Ingbar
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引用次数: 9

Abstract

Among several commercial hCG preparations tested for their ability to stimulate adenylate cyclase in a human thyroid particulate fraction, only a pharmaceutical preparation (APL) was active. Activity of this preparation was lost during dialysis, but could be restored fully by the addition of phenol and partially by the addition of benzyl alcohol, the two additives present in APL. Phenol itself (0.040 - 2.0 mg/ml) induced a potent, dose-dependent stimulation of adenylate cyclase activity in a human thyroid particulate fraction and was also active in plasma membranes from rat liver and kidney cortex. Phenol exerted a biphasic effect on [125I]-bTSH binding to human thyroid membranes. Concentrations between 0.33 and 3.3 mg/ml were stimulatory to binding, while higher concentrations were inhibitory.

苯酚,人甲状腺膜腺苷酸环化酶的有效刺激物。
在测试几种商用hCG制剂刺激人甲状腺颗粒部分腺苷酸环化酶的能力时,只有一种药物制剂(APL)是有活性的。该制剂的活性在透析过程中丧失,但可以通过添加苯酚和添加苯甲醇(APL中存在的两种添加剂)来完全恢复。苯酚本身(0.040 - 2.0 mg/ml)对人甲状腺颗粒部分的腺苷酸环化酶活性产生了有效的剂量依赖性刺激,并且在大鼠肝脏和肾脏皮质的质膜中也有活性。苯酚对[125I]-bTSH与人甲状腺膜的结合具有双相作用。浓度在0.33 ~ 3.3 mg/ml之间对结合有刺激作用,而较高浓度则有抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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