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The effects of extracellular pH and calcium change on force and intracellular calcium in rat vascular smooth muscle.

机译:细胞外pH和钙变化对大鼠血管平滑肌力和细胞内钙的影响。

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摘要

1. In order to investigate the mechanism whereby changes in external pH (pHo) alter tone in rat mesenteric resistance vessels, we have made simultaneous measurements of tension and intracellular Ca2+ [Ca2+]i. Strips of mesenteric artery were loaded with the Ca(2+)-sensitive indicator indo-1 and superfused with physiological salt solution at pH 7.4 and 37 degrees C. 2. An increase of pHo from 7.4 to 7.9 produced an increase in tension. This was accompanied by an increase in [Ca2+]i in resting and high-K(+)-depolarized vessels. Acidification to 6.9 reduced tension and was associated with a fall in [Ca2+]i. Over the pHi range examined, 6.6-7.9, parallel changes in [Ca2+]i and tension were found in K(+)-activated vessels. 3. In contrast to the relatively slow change in [Ca2+]i, pHi and tension with change of pHo, depolarization produced rapid changes in [Ca2+]i and tension, consistent with a more direct action on Ca2+ mobilization. 4. Reducing the external [Ca2+] below 1 mM produced a pronounced fall in [Ca2+]i and force. Changes in [Ca2+]i, produced by alteration of external [Ca2+] (Cao2+) were used to examine the relation between [Ca2+]i and tension. A linear relation was found. Alteration of pHo to 6.9 or 7.9 did not significantly change this relation. When the tension data were normalized to their own maxima, no shift in the tension-Ca2+ relation occurred, suggesting little or no effect of pH on the Ca2+ sensitivity of force production by the contractile proteins. 5. To determine further whether the changes in [Ca2+]i produced by alteration of pHo could account for all the changes observed in tension, [Ca2+]i was restored to control levels while maintaining an altered pHo. When this was done, restoration of [Ca2+]i led to restoration of force. Thus, in this preparation, the changes in [Ca2+]i produced by altering pHo in depolarized vessels can account for the changes in vascular tone.
机译:1.为了研究外部pH(pHo)的变化改变大鼠肠系膜阻力血管张力的机制,我们同时测量了张力和细胞内Ca2 + [Ca2 +] i。肠系膜动脉条上装有Ca(2+)敏感指示剂indo-1,并在pH 7.4和37摄氏度下与生理盐水混合。2. pHo从7.4增加到7.9导致张力增加。这伴随着静止和高K(+)去极化血管中[Ca2 +] i的增加。酸化至6.9可降低张力,并与[Ca2 +] i降低有关。在检查的pHi范围内(6.6-7.9),在K(+)激活的容器中发现[Ca2 +] i和张力的平行变化。 3.与[Ca2 +] i,pHi和张力随pHo的变化相对缓慢变化相反,去极化产生[Ca2 +] i和张力的快速变化,这与对Ca2 +动员的更直接作用相一致。 4.将外部[Ca2 +]降低到1 mM以下会导致[Ca2 +] i和作用力明显下降。通过改变外部[Ca2 +](Cao2 +)产生的[Ca2 +] i变化来检查[Ca2 +] i与张力之间的关系。发现线性关系。 pHo更改为6.9或7.9不会显着改变这种关系。当将张力数据归一化到其最大值时,张力与Ca2 +的关系就不会发生变化,这表明pH值对收缩蛋白对Ca2 +敏感性产生力的影响几乎没有或没有影响。 5.为了进一步确定通过改变pHo产生的[Ca2 +] i的变化是否可以解释张力中观察到的所有变化,将[Ca2 +] i恢复到对照水平,同时保持pHo的变化。完成此操作后,[Ca2 +] i的恢复导致力的恢复。因此,在该制剂中,通过改变去极化血管中pHo产生的[Ca2 +] i的变化可以解释血管张力的变化。

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