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大鼠尾动脉中α-肾上腺素能受体激活引起的细胞内游离钙离子浓度变化

Changes in intracellular free Ca2+ concentration by activation of alpha-adrenoceptors in rat tail artery.

作者信息

Abe K, Saito H, Matsuki N

机构信息

Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, University of Tokyo, Japan.

出版信息

Jpn J Pharmacol. 1990 Feb;52(2):337-44. doi: 10.1254/jjp.52.337.

Abstract

Changes in intracellular free Ca2+ concentration ([Ca2+]i) by activation of alpha 1- and alpha 2-adrenoceptors were microfluorometrically measured in rat tail arteries loaded with the Ca2(+)-sensitive fluorescent dye fura-2. Under the normal condition (1.8 mM Ca2+), stimulation with the selective alpha 1-adrenoceptor agonist phenylephrine very rapidly raised [Ca2+]i to the peak concentration, plateauing at this level, whereas the stimulation with the selective alpha 2-adrenoceptor agonist UK-14,304 gradually increased [Ca2+]i. In Ca2(+)-free solution, the stimulation of alpha 1-adrenoceptors caused a transient increase in [Ca2+]i, whereas the stimulation of alpha 2-adrenoceptors had no effect. These results directly prove that alpha 1-adrenoceptor activation induces both the release of intracellular Ca2+ and the influx of extracellular Ca2+, whereas activation of alpha 2-adrenoceptors evokes only the influx of extracellular Ca2+. Plotting the increase in [Ca2+]i against the developed contraction revealed that it was always linearly related regardless of the type of alpha-adrenoceptor stimulated. Therefore, the intracellular mechanisms after the increase in [Ca2+]i are probably common to the vasocontractile responses mediated by alpha 1- and alpha 2-adrenoceptors.

摘要

利用负载Ca2+敏感荧光染料fura-2的大鼠尾动脉,通过显微荧光测定法测量了α1和α2肾上腺素能受体激活引起的细胞内游离Ca2+浓度([Ca2+]i)变化。在正常条件下(1.8 mM Ca2+),用选择性α1肾上腺素能受体激动剂去氧肾上腺素刺激可使[Ca2+]i非常迅速地升高至峰值浓度,并在此水平保持平稳,而用选择性α2肾上腺素能受体激动剂UK-14,304刺激则使[Ca2+]i逐渐升高。在无Ca2+溶液中,刺激α1肾上腺素能受体导致[Ca2+]i短暂升高,而刺激α2肾上腺素能受体则无作用。这些结果直接证明,α1肾上腺素能受体激活可诱导细胞内Ca2+释放和细胞外Ca2+内流,而α2肾上腺素能受体激活仅引起细胞外Ca2+内流。将[Ca2+]i的升高与所产生的收缩进行绘图显示,无论刺激的α肾上腺素能受体类型如何,二者始终呈线性相关。因此,[Ca2+]i升高后的细胞内机制可能是α1和α2肾上腺素能受体介导的血管收缩反应所共有的。

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