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钙刺激兔血管平滑肌的钠外流。

Calcium-stimulated sodium efflux from rabbit vascular smooth muscle.

作者信息

Kaplan J H, Kennedy B G, Somlyo A P

机构信息

Department of Physiology, University of Pennsylvania, Philadelphia 19104.

出版信息

J Physiol. 1987 Jul;388:245-60. doi: 10.1113/jphysiol.1987.sp016613.

Abstract
  1. The effects of the addition of Ca2+ on ouabain-resistant 22Na+ efflux from Na+-loaded strips of rabbit portal anterior mesenteric vein in Ca2+-free media have been studied. 2. Na+ efflux into Li+ media containing 5 mM-KCl is rapidly and transiently stimulated some 4- to 5-fold on the addition of Ca2+ (1.2 mM). No stimulation is observed if the Li+ medium is K+ free or if Na+ replaces Li+ ions. This Ca2+-activated Na+ efflux is not obligatorily coupled to Na+ influx. 3. The stimulation of Na+ efflux could also be triggered by the addition of 5 mM-K+ to a Ca2+-containing K+-free medium. The Ca2+-activated increase in Na+ efflux also occurred when K+ was the sole monovalent extracellular cation. Rb+ could substitute for the K+ requirement. Thus the Na+ efflux is not mediated by a system which has a specific requirement for counter-transport of Li+ or one in which Li+ but not K+ are counter-transported such as the familiar Na+-H+ exchange system. Acidification of the external medium reduced the Ca2+-stimulated Na+ efflux, in keeping with the conclusion that this efflux was not due to Na+-H+ exchange. 4. Progressive reduction of external [Ca2+] increased the time-lag to peak activation of Na+ efflux, suggesting that the effects of added Ca2+ were mediated by a rise in intracellular Ca2+. Under experimental conditions which did not result in activation of the Na+ efflux by the addition of extracellular Ca2+ alone (e.g. in Na+ media), addition of Ca2+ plus the Ca2+ ionophore, ionomycin, stimulated Na+ efflux. This further confirms that intracellular sites for Ca2+ are critical for the activation of Na+ efflux. In the absence of ionophore, in Na+ media, intracellular Ca2+ is not sufficiently increased when extracellular Ca2+ is added. A partial (40%) block of Ca2+-activated Na+ efflux by amiloride (2 X 10(-3) M) could also be overcome by the addition of ionomycin. 5. The lack of effect of a variety of inhibitors suggests that the Ca2+-stimulated Na+ efflux mechanism is not mediated via a Na+-K+-Cl- co-transport system or a Na+-H+ counter-transport system, or Na+-Ca2+ exchange. 6. The activation of Na+ efflux in smooth muscle by Ca2+ ions seems to involve Ca2+ entry partially via an extracellular Ca2+-intracellular Na+ exchange and also through other parallel pathway(s), followed by a rise in intracellular Ca2+ that activates Na+ efflux through a Ca2+-sensitive Na+ channel or other transport pathway.
摘要
  1. 研究了在无钙培养基中添加Ca2+对兔门静脉前肠系膜静脉钠负荷条带哇巴因抗性22Na+外流的影响。2. 在含5 mM-KCl的Li+培养基中,加入Ca2+(1.2 mM)后,Na+外流迅速且短暂地受到刺激,增加约4至5倍。如果Li+培养基无K+或用Na+取代Li+离子,则未观察到刺激作用。这种Ca2+激活的Na+外流并非必然与Na+内流偶联。3. 向含Ca2+的无K+培养基中添加5 mM-K+也可触发Na+外流的刺激。当K+是唯一的细胞外单价阳离子时,也会出现Ca2+激活的Na+外流增加。Rb+可替代K+的需求。因此,Na+外流不是由对Li+反向转运有特定需求的系统介导的,也不是由Li+而非K+进行反向转运的系统(如常见的Na+-H+交换系统)介导的。外部培养基酸化会降低Ca2+刺激的Na+外流,这与该外流不是由Na+-H+交换引起的结论一致。4. 外部[Ca2+]的逐渐降低增加了Na+外流达到峰值激活的时间延迟,表明添加的Ca2+的作用是由细胞内Ca2+的升高介导的。在未通过单独添加细胞外Ca2+激活Na+外流的实验条件下(如在Na+培养基中),添加Ca2+加Ca2+离子载体离子霉素可刺激Na+外流。这进一步证实细胞内Ca2+位点对Na+外流的激活至关重要。在无离子载体的情况下,在Na+培养基中添加细胞外Ca2+时,细胞内Ca2+升高不足。氨氯地平(2×10(-3) M)对Ca2+激活的Na+外流的部分(40%)阻断也可通过添加离子霉素克服。5. 多种抑制剂无效表明Ca2+刺激的Na+外流机制不是通过Na+-K+-Cl-共转运系统、Na+-H+反向转运系统或Na+-Ca2+交换介导的。6. Ca2+离子对平滑肌中Na+外流的激活似乎部分涉及Ca2+通过细胞外Ca2+-细胞内Na+交换以及其他平行途径进入,随后细胞内Ca2+升高,通过Ca2+敏感的Na+通道或其他转运途径激活Na+外流。

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