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异丙肾上腺素对猪冠状动脉主动张力及钙调蛋白敏感磷酸二酯酶活性的影响。

Effects of isoproterenol on active force and Ca2+ X calmodulin-sensitive phosphodiesterase activity in porcine coronary artery.

作者信息

Miller J R, Wells J N

出版信息

Biochem Pharmacol. 1987 Jun 1;36(11):1819-24. doi: 10.1016/0006-2952(87)90244-9.

Abstract

Relaxation of vascular smooth muscle following beta-adrenergic stimulation may result from reduction of the cytoplasmic Ca2+ concentration, reduction in the sensitivity of the contractile apparatus to Ca2+, or both. To help resolve these possibilities, we measured the extent of activation of Ca2+ X calmodulin-sensitive phosphodiesterase in intact porcine coronary artery strips as a functional indicator of the cytoplasmic Ca2+ concentration. Both calmodulin-stimulated phosphodiesterase activity and active force increased during K+ stimulation of coronary artery strips. Relaxation of K+-contracted artery strips following stimulus withdrawal was accompanied by rapid inactivation of Ca2+ X calmodulin-sensitive phosphodiesterase. The temporal relationship between isoproterenol-induced relaxation and inactivation of Ca2+ X calmodulin-sensitive phosphodiesterase was studied in both histamine- and K+-contracted tissues. Stimulation of strips with 10 microM histamine or with 44 mM K+ led to comparable increases both in active force and in calmodulin-stimulated phosphodiesterase activity. Thereafter, sustained contraction elicited by histamine was accompanied by a decrease in calmodulin-stimulated phosphodiesterase activity. Isoproterenol rapidly relaxed histamine-contracted strips and accelerated the decrease in phosphodiesterase activity. In contrast, sustained contraction in response to K+ was accompanied by a sustained elevation of calmodulin-stimulated phosphodiesterase activity. Isoproterenol treatment of K+-contracted tissues led to relaxation that was slow and incomplete, and it had very little effect on calmodulin-stimulated phosphodiesterase activity. We conclude that reduction of the cytoplasmic Ca2+ concentration is important for rapid relaxation of the coronary artery following beta-adrenergic stimulation. We cannot disallow the possibility that a decrease in the sensitivity of the contractile apparatus to Ca2+ is involved to some degree.

摘要

β-肾上腺素能刺激后血管平滑肌的舒张可能是由于细胞质Ca2+浓度降低、收缩装置对Ca2+的敏感性降低,或两者兼而有之。为了帮助确定这些可能性,我们测量了完整猪冠状动脉条带中Ca2+·钙调蛋白敏感磷酸二酯酶的激活程度,作为细胞质Ca2+浓度的功能指标。在冠状动脉条带的K+刺激过程中,钙调蛋白刺激的磷酸二酯酶活性和主动张力均增加。刺激撤除后,K+收缩的动脉条带的舒张伴随着Ca2+·钙调蛋白敏感磷酸二酯酶的快速失活。在组胺和K+收缩的组织中研究了异丙肾上腺素诱导的舒张与Ca2+·钙调蛋白敏感磷酸二酯酶失活之间的时间关系。用10μM组胺或44mM K+刺激条带导致主动张力和钙调蛋白刺激的磷酸二酯酶活性均有相当程度的增加。此后,组胺引起的持续收缩伴随着钙调蛋白刺激的磷酸二酯酶活性的降低。异丙肾上腺素迅速舒张组胺收缩的条带并加速磷酸二酯酶活性的降低。相比之下,对K+的持续收缩伴随着钙调蛋白刺激的磷酸二酯酶活性的持续升高。用异丙肾上腺素处理K+收缩的组织导致舒张缓慢且不完全,并且对钙调蛋白刺激的磷酸二酯酶活性影响很小。我们得出结论,细胞质Ca2+浓度的降低对于β-肾上腺素能刺激后冠状动脉的快速舒张很重要。我们不能排除收缩装置对Ca2+的敏感性在某种程度上降低也参与其中的可能性。

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