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细胞内钠离子增加会增强血管平滑肌细胞中肌浆网释放钙离子的能力。

Increased intracellular Na+ augments mobilization of Ca2+ from SR in vascular smooth muscle cells.

作者信息

Borin M L, Tribe R M, Blaustein M P

机构信息

Department of Physiology, School of Medicine, University of Maryland, Baltimore 21201.

出版信息

Am J Physiol. 1994 Jan;266(1 Pt 1):C311-7. doi: 10.1152/ajpcell.1994.266.1.C311.

Abstract

The effect of a rise in intracellular Na+ concentration ([Na+]cyt) on the amount of Ca2+ in intracellular stores was studied in vascular smooth muscle cells from the A7r5 line. The relative amount of stored Ca2+ was estimated in fura 2-loaded cells by the rise in cytosolic free Ca2+ concentration ([Ca2+]cyt) evoked by Ca2+ release from the sarcoplasmic reticulum (SR). To improve the detection of released Ca2+, extrusion of Ca2+ from the cytosol was minimized by using nominally Na+/Ca(2+)-free medium containing 0.5 mM La3+ [for vasoconstrictor experiments, the medium contained 0.5 mM ethylene glycol-bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid and no La3+]. Ca2+ release was triggered by thapsigargin (TG), an SR Ca(2+)-ATPase inhibitor, and by the vasoconstrictors arginine vasopressin (AVP) and serotonin (5-HT). Incubation with 1-3 mM ouabain for 20 min, which raises [Na+]cyt from 4.4 to 9.0 mM, increased "resting" [Ca2+]cyt only slightly (from 87 to 122 nM). However, ouabain greatly augmented the release of Ca2+ evoked by TG [from 639 nM (control) to 1,021 nM], by AVP (from 993 to 1,597 nM), and by 5-HT (from 559 to 1,486 nM). Ouabain-induced augmentation of TG-evoked Ca2+ release was not affected by 10 microM verapamil; this implies that the effect of ouabain was not due to Ca2+ entry through voltage-gated Ca2+ channels. The response to TG was not augmented when ouabain was applied for 20 min in Na(+)-free medium (Na+ replaced by equimolar N-methyl-D-glucamine) to prevent [Na+]cyt from rising.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在源自A7r5细胞系的血管平滑肌细胞中,研究了细胞内钠离子浓度([Na⁺]cyt)升高对细胞内钙储存量的影响。通过肌浆网(SR)释放钙离子所诱发的胞质游离钙离子浓度([Ca²⁺]cyt)升高,来估算fura 2负载细胞中储存钙离子的相对量。为了提高对释放钙离子的检测,通过使用含有0.5 mM La³⁺的名义上无钠/无钙培养基(对于血管收缩实验,培养基含有0.5 mM乙二醇双(β - 氨基乙基醚)-N,N,N',N'-四乙酸且无La³⁺),将钙离子从胞质中的外排降至最低。钙离子释放由毒胡萝卜素(TG,一种SR Ca²⁺ - ATP酶抑制剂)以及血管收缩剂精氨酸加压素(AVP)和5 - 羟色胺(5 - HT)触发。用1 - 3 mM哇巴因孵育20分钟,可使[Na⁺]cyt从4.4 mM升至9.0 mM,仅使“静息”[Ca²⁺]cyt略有增加(从87 nM升至122 nM)。然而,哇巴因极大地增强了由TG(从639 nM(对照)增至1,021 nM)、AVP(从993 nM增至1,597 nM)和5 - HT(从559 nM增至1,486 nM)所诱发的钙离子释放。哇巴因诱导的TG诱发钙离子释放增强不受10 μM维拉帕米影响;这表明哇巴因的作用并非由于钙离子通过电压门控钙离子通道进入。当在无钠培养基(钠被等摩尔N - 甲基 - D - 葡糖胺替代)中应用哇巴因20分钟以防止[Na⁺]cyt升高时,对TG的反应并未增强。(摘要截取自250字)

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