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细胞内钙离子参与胆碱能和α-肾上腺素能激动剂从大鼠腮腺腺泡细胞释放荧光染料钙黄绿素的过程。

Involvement of intracellular calcium ions in the release of the fluorescent dye calcein by cholinergic and alpha-adrenergic agonists from rat parotid acinar cells.

作者信息

Sugita M, Shiba Y, Furuya K, Yamagishi S, Kanno Y

机构信息

Department of Oral Physiology, Hiroshima University School of Dentistry, Japan.

出版信息

Pflugers Arch. 1995 Feb;429(4):555-60. doi: 10.1007/BF00704161.

Abstract

Effects of cholinergic and adrenergic agonists on the secretion of the fluorescent dye calcein were examined to clarify the involvement of calcium ions in the secretion of calcein from acinar cells dispersed from the rat parotid gland. Addition of carbachol (CCh) and noradrenalin (NA), but not isoproterenol (IPR), enhanced the net release of calcein from acinar cells during the subsequent 10 min in a dose range from 10(-8) M to 10(-6) M. The net release of calcein reached a maximum 7 min after the addition of CCh. The release of calcein was suppressed by the simultaneous additions of atropine with CCh, or phenoxybenzamine with NA. Addition of CCh induced a sustained dose-dependent increase in the intracellular levels of calcium ions, ([Ca2+]i). Addition of NA at 10(-6) M increased [Ca2+]i. Phenoxybenzamine completely inhibited the NA-induced increase, but propranolol did not. The removal of extracellular calcium ions did not influence the release of calcein induced by 10(-6) M CCh, but it abolished the sustained increase in [Ca2+]i. The transient increase in [Ca2+]i induced by CCh was observed in the absence of extracellular calcium ions. A calcium ion chelator, 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid (BAPTA) inhibited the CCh-induced release of calcein. The calcium ionophore, A23187 (2.5 x 10(-6) M), but not 10(-3) M dibutyryl cAMP, evoked the release of calcein. It also increased [Ca2+]i. Removal of extracellular calcium ions suppressed the A23187-induced release of calcein.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了胆碱能和肾上腺素能激动剂对荧光染料钙黄绿素分泌的影响,以阐明钙离子在大鼠腮腺分散腺泡细胞分泌钙黄绿素过程中的作用。在随后10分钟内,加入卡巴胆碱(CCh)和去甲肾上腺素(NA)而非异丙肾上腺素(IPR),在10⁻⁸M至10⁻⁶M剂量范围内增强了钙黄绿素从腺泡细胞的净释放。加入CCh后7分钟,钙黄绿素的净释放达到最大值。同时加入阿托品与CCh或苯氧苄胺与NA可抑制钙黄绿素的释放。加入CCh可导致细胞内钙离子水平([Ca²⁺]i)持续剂量依赖性增加。加入10⁻⁶M NA可增加[Ca²⁺]i。苯氧苄胺完全抑制NA诱导的增加,但普萘洛尔无此作用。去除细胞外钙离子不影响10⁻⁶M CCh诱导的钙黄绿素释放,但消除了[Ca²⁺]i 的持续增加。在无细胞外钙离子的情况下观察到CCh诱导的[Ca²⁺]i 短暂增加。钙离子螯合剂1,2-双(2-氨基苯氧基)乙烷-N,N,N',N'-四乙酸(BAPTA)抑制CCh诱导的钙黄绿素释放。钙离子载体A23187(2.5×10⁻⁶M)而非10⁻³M二丁酰环磷腺苷(dbcAMP)可引发钙黄绿素释放。它也增加[Ca²⁺]i。去除细胞外钙离子可抑制A23187诱导的钙黄绿素释放。(摘要截短于250字)

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