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Pharmacological characterization of β_2-adrenoceptor in PGT-β mouse pineal gland tumour cells

机译:小鼠松果体PGT-β肿瘤细胞中β_2-肾上腺素受体的药理特性

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摘要

1. The adrenoceptor in a mouse pineal gland tumour cell line (PGT-β) was identified and characterized using pharmacological and physiological approaches. 2. Adrenaline and noradrenaline, adrenoceptor agonists, stimulated cyclic AMP generation in a concentration-dependent manner, adrenoceptor agonists, stimulated cyclic AMP generation in a concentration-dependent manner, but had no effect on inositol 1, 4, 5-trisphosphate production. Adrenaline was a more potent activator of cyclic AMP generation than noradrenaline, with half Maximal-effective concentrations (EC_50) seen at 175 ± 22 nM and 18 ± 2 μM for adrenaline and Noiradrenaline, respectively.
机译:1.使用药理和生理学方法鉴定并表征了小鼠松果体腺癌细胞系(PGT-β)中的肾上腺素能受体。 2.肾上腺素和去甲肾上腺素,肾上腺素受体激动剂,以浓度依赖性方式刺激环状AMP的产生,肾上腺素受体激动剂,以浓度依赖性方式刺激环状AMP的产生,但对肌醇1、4、5-三磷酸的产生没有影响。肾上腺素比去甲肾上腺素是更有效的环AMP生成激活剂,肾上腺素和去甲肾上腺素的最大有效浓度(EC_50)分别为175±22 nM和18±2μM。

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