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肾上腺髓质原代解离培养物中钙离子摄取与儿茶酚胺分泌之间的关系。

Relationship between Ca2+ uptake and catecholamine secretion in primary dissociated cultures of adrenal medulla.

作者信息

Holz R W, Senter R A, Frye R A

出版信息

J Neurochem. 1982 Sep;39(3):635-46. doi: 10.1111/j.1471-4159.1982.tb07940.x.

Abstract

Carbachol or elevated K+ stimulated 45Ca2+ uptake into chromaffin cells two- to fourfold. The uptake was stimulated by cholinergic drugs with nicotinic activity, but not by those with only muscarinic activity. Ca2+ uptake and catecholamine secretion induced by the mixed nicotinic-muscarinic agonist carbachol were inhibited by the nicotinic antagonist mecamylamine, but not by the muscarinic antagonist atropine. Significant Ca2+ uptake occurred within 15 s of stimulation by carbachol or elevated K+ at a time before catecholamine secretion was readily detected. At later times the time course of secretion induced by carbachol or elevated K+ was similar to that of Ca2+ uptake. There was a close correlation between Ca2+ uptake and catecholamine secretion at various concentrations of Ca2+. The concentration dependencies for inhibition of both processes by Mg2+ or Cd2+ were similar. Ca2+ uptake saturated with increasing Ca2+ concentrations, with an apparent Km for both carbachol-induced and elevated K+-induced Ca2+ uptake of approximately 2 mM. The Ca2+ dependency, however, was different for the two stimuli. The studies provide strong support for the notion that Ca2+ entry and a presumed increase in cytosolic Ca2+ concentration respectively initiates and maintains secretion. They also provide evidence for the existence of saturable, intracellular, Ca2+-dependent processes associated with catecholamine secretion. Ca2+ entry may, in addition, enhance nicotinic receptor desensitization and may cause inactivation of voltage-sensitive Ca2+ channels.

摘要

卡巴胆碱或升高的钾离子可使嗜铬细胞对45Ca2+的摄取增加2至4倍。具有烟碱活性的胆碱能药物可刺激这种摄取,但仅具有毒蕈碱活性的药物则无此作用。烟碱-毒蕈碱混合激动剂卡巴胆碱诱导的Ca2+摄取和儿茶酚胺分泌受到烟碱拮抗剂美加明的抑制,但不受毒蕈碱拮抗剂阿托品的抑制。在卡巴胆碱或升高的钾离子刺激后15秒内,即在儿茶酚胺分泌易于检测之前,就出现了显著的Ca2+摄取。在随后的时间里,卡巴胆碱或升高的钾离子诱导的分泌时间进程与Ca2+摄取相似。在不同Ca2+浓度下,Ca2+摄取与儿茶酚胺分泌之间存在密切相关性。Mg2+或Cd2+对这两个过程的抑制作用的浓度依赖性相似。随着Ca2+浓度的增加,Ca2+摄取达到饱和,卡巴胆碱诱导的和升高的钾离子诱导的Ca2+摄取的表观Km约为2 mM。然而,两种刺激的Ca2+依赖性不同。这些研究为Ca2+内流和假定的胞质Ca2+浓度增加分别启动和维持分泌这一观点提供了有力支持。它们还为与儿茶酚胺分泌相关的可饱和的、细胞内的、Ca2+依赖性过程的存在提供了证据。此外,Ca2+内流可能会增强烟碱受体脱敏,并可能导致电压敏感性Ca2+通道失活。

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