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兰尼碱抑制咖啡因诱发的培养牛肾上腺嗜铬细胞的钙离子动员和儿茶酚胺分泌。

Ryanodine inhibits caffeine-evoked Ca2+ mobilization and catecholamine secretion from cultured bovine adrenal chromaffin cells.

作者信息

Teraoka H, Nakazato Y, Ohga A

机构信息

Department of Pharmacology, Faculty of Veterinary Medicine, Hokkaido University, Sapporo, Japan.

出版信息

J Neurochem. 1991 Dec;57(6):1884-90. doi: 10.1111/j.1471-4159.1991.tb06399.x.

Abstract

The effects of ryanodine, a selective inhibitor of the Ca(2+)-induced Ca2+ release mechanism, on caffeine-evoked changes in cytosolic Ca2+ concentration ([Ca2+]i) and catecholamine secretion were investigated using cultured bovine adrenal chromaffin cells. Caffeine (5-40 mM) caused a concentration-dependent transient rise in [Ca2+]i and catecholamine secretion in Ca2+/Mg(2+)-free medium containing 0.2 mM EGTA. Ryanodine (5 x 10(-5) M) alone had no effect on either [Ca2+]i or catecholamine secretion. Although the application of ryanodine plus caffeine caused the same increase in both [Ca2+]i and catecholamine secretion as those induced by caffeine alone, ryanodine (4 x 10(-7) - 5 x 10(-5) M) irreversibly prevented the increase in both [Ca2+]i and catecholamine secretion resulting from subsequent caffeine application over a range of concentrations. The secretory response to caffeine was markedly enhanced by replacement of Na+ with sucrose in Ca2+/Mg(2+)-free medium, and this enhanced response was also blocked by ryanodine. Caffeine was found to decrease the susceptibility of the secretory apparatus to Ca2+ in digitonin-permeabilized cells. These results indicate that caffeine mobilizes Ca2+ from intracellular stores, the function of which is irreversibly blocked by ryanodine, resulting in the increase in catecholamine secretion in the bovine adrenal chromaffin cell.

摘要

利用培养的牛肾上腺嗜铬细胞,研究了ryanodine(一种Ca(2+)诱导的Ca2+释放机制的选择性抑制剂)对咖啡因诱发的胞质Ca2+浓度([Ca2+]i)变化和儿茶酚胺分泌的影响。在含有0.2 mM EGTA的无Ca2+/Mg(2+)培养基中,咖啡因(5 - 40 mM)引起[Ca2+]i和儿茶酚胺分泌呈浓度依赖性的短暂升高。单独使用ryanodine(5×10(-5) M)对[Ca2+]i或儿茶酚胺分泌均无影响。虽然同时应用ryanodine和咖啡因引起的[Ca2+]i和儿茶酚胺分泌增加与单独使用咖啡因时相同,但ryanodine(4×10(-7) - 5×10(-5) M)在一系列浓度范围内不可逆地阻止了随后应用咖啡因所导致的[Ca2+]i和儿茶酚胺分泌增加。在无Ca2+/Mg(2+)培养基中用蔗糖替代Na+可显著增强对咖啡因的分泌反应,且这种增强的反应也被ryanodine阻断。发现在洋地黄皂苷通透的细胞中,咖啡因可降低分泌装置对Ca2+的敏感性。这些结果表明,咖啡因从细胞内储存库中动员Ca2+,其功能被ryanodine不可逆地阻断,从而导致牛肾上腺嗜铬细胞中儿茶酚胺分泌增加。

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