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氯氮平和佛波酯对肾上腺嗜铬细胞儿茶酚胺分泌的影响。

Effect of calmidazolium and phorbol ester on catecholamine secretion from adrenal chromaffin cells.

作者信息

Burgoyne R D, Norman K M

出版信息

Biochim Biophys Acta. 1984 Sep 14;805(1):37-43. doi: 10.1016/0167-4889(84)90034-x.

Abstract

Carbamylcholine-stimulated catecholamine release from adrenal chromaffin cells was completely inhibited by pretreatment of the cells for 10 min with 1 microM calmidazolium. Catecholamine release due to 55 mM K+ and ionophore A23187 was also inhibited by calmidazolium but less effectively than release due to carbamylcholine. Inhibition of release appeared to be due to an effect of calmidazolium on a step distal to Ca2+ entry, since the carbamylcholine-stimulated rise in the concentration of intracellular free calcium, monitored using quin-2, was unaffected by calmidazolium. The possibility was considered that calmidazolium inhibited secretion through an effect on protein kinase C rather than calmodulin. However, the phorbol ester, 12-O-tetradecanoylphorbol 13-acetate (TPA), had no demonstrable effect on catecholamine release, arguing against a significant role for protein kinase C in secretion from adrenal chromaffin cells. These results give further support to the notion that calmodulin plays a role in the secretory process in chromaffin cells.

摘要

用1微摩尔/升的氯米帕明预处理肾上腺嗜铬细胞10分钟,可完全抑制氨甲酰胆碱刺激的儿茶酚胺释放。氯米帕明也可抑制由55毫摩尔/升钾离子和离子载体A23187引起的儿茶酚胺释放,但效果不如对氨甲酰胆碱引起的释放抑制明显。释放的抑制似乎是由于氯米帕明对钙离子进入后的一个步骤产生影响,因为用喹啉-2监测到的氨甲酰胆碱刺激引起的细胞内游离钙浓度升高不受氯米帕明影响。曾考虑过氯米帕明通过对蛋白激酶C而非钙调蛋白的作用来抑制分泌的可能性。然而,佛波酯12-O-十四酰佛波醇13-乙酸酯(TPA)对儿茶酚胺释放没有明显影响,这表明蛋白激酶C在肾上腺嗜铬细胞分泌中不起重要作用。这些结果进一步支持了钙调蛋白在嗜铬细胞分泌过程中起作用的观点。

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