The escape of cyclic AMP from dog thyroid slices exposed to positive and negative regulators.

P Cochaux, J Van Sande, S Swillens, J E Dumont
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Abstract

Incubation of dog thyroid slices with 1 mU/ml TSH resulted in enhanced intracellular and extracellular cAMP accumulation. In the absence of TSH, the intra- and extracellular cAMP concentrations remained at a constant low level. The release of cAMP from TSH-stimulated slices was inhibited by 10 microM PGA1, 1 mM probenecid or 1 mM IBMX, which are known inhibitors of cAMP escape in several tissues. Negative controls of intracellular cAMP levels are exerted in the dog thyroid by 10 microM carbamylcholine (shown to activate a Ca++- calmodulin dependent phosphodiesterase), 100 microM norepinephrine and 100 microM iodide (both inhibiting adenylate cyclase activity). The purpose of the present study was to demonstrate that these three agents do not enhance cAMP escape. The results presented here show that these agents decrease both intracellular accumulation and escape in parallel. Moreover, the escape constants obtained by numerical simulation were not greater in the presence of inhibiting concentrations of carbamylcholine, norepinephrine or iodide. Thus the inhibition by these agents of cAMP accumulation in TSH-stimulated dog thyroid slices cannot be explained by a stimulation of cAMP escape from these cells.

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暴露于正、负调节剂下的狗甲状腺片环AMP的逃逸。
以1 mU/ml TSH孵育犬甲状腺片,可增强细胞内和细胞外cAMP的积累。在缺乏TSH的情况下,细胞内和细胞外cAMP浓度保持在恒定的低水平。10微米的PGA1、1毫米的probenecid或1毫米的IBMX可以抑制tsh刺激切片中cAMP的释放,这些物质是几种组织中已知的cAMP逃逸抑制剂。在狗甲状腺细胞内cAMP水平的阴性控制是通过10微米的氨甲酰胆碱(显示激活钙调素依赖的磷酸二酯酶),100微米的去甲肾上腺素和100微米的碘化物(两者都抑制腺苷酸环化酶活性)。本研究的目的是证明这三种药物不促进cAMP的逃逸。本文的结果表明,这些药物同时减少细胞内积累和逃逸。此外,通过数值模拟得到的逸出常数在抑制浓度为氨甲酰胆碱、去甲肾上腺素或碘化物的情况下也没有增大。因此,这些药物对tsh刺激的狗甲状腺切片中cAMP积累的抑制不能通过刺激这些细胞的cAMP逃逸来解释。
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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