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毒蕈碱受体的刺激会提高大鼠心室肌细胞内游离钙离子的浓度。

Stimulation of muscarinic receptors raises free intracellular Ca2+ concentration in rat ventricular myocytes.

作者信息

Korth M, Sharma V K, Sheu S S

机构信息

Institut für Pharmakologie und Toxikologie der Technischen Universität München, Federal Republic of Germany.

出版信息

Circ Res. 1988 Jun;62(6):1080-7. doi: 10.1161/01.res.62.6.1080.

Abstract

The effect of carbachol on free intracellular calcium concentration, ([Ca2+]i) and on intracellular hydrogen concentration (pHi) was determined from fluorescence signals obtained from rat ventricular myocytes. Application of carbachol (300 mumol/l) to quin2-loaded myocytes bathed in 2 mmol/l Ca2+-containing solution caused [Ca2+]i to increase within 7-10 minutes from 182 +/- 9 to 212 +/- 11 nmol/l (n = 4). Carbachol acted via stimulation of muscarinic receptors because atropine (1 mumol/l) either prevented or abolished the increase in [Ca2+]i. Carbachol also produced a positive inotropic effect in rat papillary muscles contracting isometrically at a frequency of 0.5 Hz and enhanced contracture in resting preparations in the presence of high extracellular Ca2+ concentration ([Ca2+]o) (20 mmol/l). The effect of carbachol on [Ca2+]i was dependent on [Ca2+]o. In the presence of 10 mmol/l [Ca2+]o, the increase in [Ca2+]i was about two times that elicited by carbachol when bath [Ca2+]o was 2 mmol/l. Reduction of [Ca2+]o to 50 mumol/l abolished the carbachol effect but did not prevent caffeine-induced Ca2+ release. The carbachol-induced rise in [Ca2+]i remained unchanged in the presence of either 10 mmol/l caffeine or 1 mumol/l ryanodine. In the absence of extracellular Na+ concentration [( Na+]o), carbachol no longer produced an increase in [Ca2+]i of cardiomyocytes and failed to enhance Na+-withdrawal contracture of the rat papillary muscle. In contrast to the effect on [Ca2+]i, carbachol did not produce any change in pHi as determined from fluorescence signals obtained from rat ventricular myocytes loaded with 2',7'-bis(carboxyethyl)-5,6-carboxyfluorescein.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过从大鼠心室肌细胞获得的荧光信号,测定了卡巴胆碱对细胞内游离钙浓度([Ca2+]i)和细胞内氢离子浓度(pHi)的影响。将卡巴胆碱(300μmol/L)应用于浸浴在含2mmol/L Ca2+溶液中的喹啉2负载的肌细胞,导致[Ca2+]i在7 - 10分钟内从182±9增加到212±11nmol/L(n = 4)。卡巴胆碱通过刺激毒蕈碱受体起作用,因为阿托品(1μmol/L)可预防或消除[Ca2+]i的增加。卡巴胆碱还对以0.5Hz频率等长收缩的大鼠乳头肌产生正性肌力作用,并在高细胞外钙浓度([Ca2+]o)(20mmol/L)存在时增强静息标本中的挛缩。卡巴胆碱对[Ca2+]i的影响取决于[Ca2+]o。在存在10mmol/L [Ca2+]o时,[Ca2+]i的增加约为浴液[Ca2+]o为2mmol/L时卡巴胆碱引起的增加的两倍。将[Ca2+]o降低至50μmol/L可消除卡巴胆碱的作用,但不阻止咖啡因诱导的Ca2+释放。在存在10mmol/L咖啡因或1μmol/L Ryanodine的情况下,卡巴胆碱诱导的[Ca2+]i升高保持不变。在不存在细胞外钠浓度[(Na+)o]的情况下,卡巴胆碱不再使心肌细胞的[Ca2+]i增加,并且不能增强大鼠乳头肌的钠-撤离挛缩。与对[Ca2+]i的影响相反,根据从负载有2',7'-双(羧乙基)-5,6-羧基荧光素的大鼠心室肌细胞获得的荧光信号测定,卡巴胆碱对pHi没有产生任何变化。(摘要截断于250字)

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