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咖啡因对豚鼠肾上腺嗜铬细胞促分泌素诱导的儿茶酚胺分泌的抑制作用。

Inhibitory effects of caffeine on secretagogue-induced catecholamine secretion from adrenal chromaffin cells of the guinea-pig.

作者信息

Nakazato Y, Tani Y, Teraoka H, Sugawara T, Asano T, Ohta T, Ito S

机构信息

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

出版信息

Br J Pharmacol. 1994 Mar;111(3):935-41. doi: 10.1111/j.1476-5381.1994.tb14829.x.

Abstract
  1. The inhibitory action of caffeine on catecholamine secretion induced by secretagogues was investigated in perfused adrenal glands and dispersed chromaffin cells of the guinea-pig. 2. Caffeine (10 mM) caused a reversible inhibition of catecholamine secretion evoked by acetylcholine (ACh, 50 microM), KCl (56 mM, high K+) and veratridine (100 microM) and that induced by muscarinic receptor activation in the absence of extracellular Ca2+ in perfused adrenal glands. 3. In dispersed chromaffin cells, caffeine caused a dose-dependent inhibition of the secretory responses to 100 microM ACh and veratridine. Forskolin (30 microM), dibutyryl cyclic AMP (1 mM) and 8-bromo cyclic AMP (1 mM) did not mimic the action of caffeine. 4. In the voltage-clamp, whole-cell recording mode (at a holding potential of -60 mV or -70 mV), ACh (100 microM) evoked an inward current, and depolarizing pulses elicited inward Na+, Ca2+ and outward K+ currents. All these responses were partially inhibited by caffeine (20 mM). 5. ACh rapidly increased the intracellular concentration of Ca2+ ([Ca2+]i) in fura-2-loaded cells in either the presence or the absence of external Ca2+, though its magnitude was decreased by about 50% in Ca(2+)-free conditions. Caffeine (20 mM) inhibited these ACh-induced increases in [Ca2+]i. 6. In permeabilized chromaffin cells, caffeine (20 mM) caused an inhibition of catecholamine secretion evoked by Ca2+ (10 microM). 7. These results suggest that caffeine inhibits evoked catecholamine secretion through mechanisms such as the blockade of voltage-dependent Na+ and Ca2+ currents and ACh receptor current, and reduction of the release of intracellularly stored Ca2+ and/or Ca(2+)-sensitivity of the secretory apparatus.
摘要
  1. 在豚鼠的灌注肾上腺和分散的嗜铬细胞中研究了咖啡因对促分泌剂诱导的儿茶酚胺分泌的抑制作用。2. 咖啡因(10 mM)可可逆地抑制灌注肾上腺中乙酰胆碱(ACh,50 microM)、氯化钾(56 mM,高钾)和藜芦碱(100 microM)诱发的儿茶酚胺分泌,以及在无细胞外钙离子时毒蕈碱受体激活诱导的儿茶酚胺分泌。3. 在分散的嗜铬细胞中,咖啡因对100 microM ACh和藜芦碱的分泌反应产生剂量依赖性抑制。福斯高林(30 microM)、二丁酰环磷腺苷(1 mM)和8-溴环磷腺苷(1 mM)不能模拟咖啡因的作用。4. 在电压钳全细胞记录模式下(保持电位为-60 mV或-70 mV),ACh(100 microM)诱发内向电流,去极化脉冲诱发内向钠离子、钙离子电流和外向钾离子电流。所有这些反应均被咖啡因(20 mM)部分抑制。5. 无论有无细胞外钙离子,ACh均可迅速增加fura-2负载细胞内的钙离子浓度([Ca2+]i),尽管在无钙离子条件下其幅度降低约50%。咖啡因(20 mM)抑制这些ACh诱导的[Ca2+]i增加。6. 在透化的嗜铬细胞中,咖啡因(20 mM)可抑制钙离子(10 microM)诱发的儿茶酚胺分泌。7. 这些结果表明,咖啡因通过阻断电压依赖性钠离子和钙离子电流、ACh受体电流以及减少细胞内储存钙离子的释放和/或分泌装置的钙离子敏感性等机制抑制诱发的儿茶酚胺分泌。

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