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Different sensitivities to dihydropyridines of catecholamine release from cat and ox adrenals.

作者信息

Gandía L, Michelena P, de Pascual R, López M G, García A G

机构信息

Departamento de Farmacología y Terapéutica, Universidad Autónoma de Madrid, Facultad de Medicina, Spain.

出版信息

Neuroreport. 1990 Oct;1(2):119-22. doi: 10.1097/00001756-199010000-00009.

DOI:10.1097/00001756-199010000-00009
PMID:1717038
Abstract

Catecholamine release evoked by quick pulses of Ca2+ (2.5 mM) given sequentially at 30 min intervals to cat and ox adrenal glands perfused continuously with Ca2+ free Krebs-Tris solutions containing 35 or 118 mM K+, was studied. In the feline, the secretory response was highly sensitive to various dihydropyridine (DHP) derivatives. For instance, secretion was completely blocked by nM concentrations of (+)isradipine (IC50 between 3 and 4 nM) and markedly potentiated by (-)Bay-K-8644. In contrast, the bovine secretory responses were resistant to blockade by nitrendipine or (+)isradipine, as well as to potentiation by Bay-K-8644, even at microM concentrations. From these experiments, it seems clear that distinct subtypes of Ca2+ channels might mediate a similar secretory response in ox and cat adrenal chromaffin cells, at least in the present experimental conditions.

摘要

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引用本文的文献

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R56865 inhibits catecholamine release from bovine chromaffin cells by blocking calcium channels.R56865通过阻断钙通道抑制牛嗜铬细胞释放儿茶酚胺。
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Dotarizine versus flunarizine as calcium antagonists in chromaffin cells.多他利嗪与氟桂利嗪作为嗜铬细胞中钙拮抗剂的比较
Br J Pharmacol. 1995 Jan;114(2):369-76. doi: 10.1111/j.1476-5381.1995.tb13236.x.
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Multiple calcium channel subtypes in isolated rat chromaffin cells.分离的大鼠嗜铬细胞中的多种钙通道亚型。
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Calcium channel subtypes in cat chromaffin cells.猫嗜铬细胞中的钙通道亚型。
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