Arner A, Lövgren B, Uvelius B
Acta Physiol Scand. 1983 Apr;117(4):541-5. doi: 10.1111/j.1748-1716.1983.tb07224.x.
The dependence of Ca2+ for different modes of activation has been investigated in the rat portal vein in vitro by evaluating the effects of substituting Sr2+ for Ca2+ in the extracellular fluid. For the spontaneous contractile activity as well as for contractures induced by depolarizing (high-K+) solution Sr2+ can to a large extent replace Ca2+. Sr2+ is however a poor Ca2+-substitute for the contractile response induced by alpha-stimulation (noradrenaline). The inhibition of spontaneous contractions by beta-stimulation (isoprenaline) is markedly less pronounced in Sr2+ solutions. Available data in the literature suggest that agonist interaction with alpha-receptors, in contrast to beta-receptors, is Ca2+ independent. Our results thus suggest that there exists a Ca2+ specific step between the alpha-receptor agonist occupancy and membrane excitation.
通过评估在细胞外液中用Sr2+替代Ca2+的效果,在体外对大鼠门静脉中不同激活模式下Ca2+的依赖性进行了研究。对于自发收缩活动以及由去极化(高K+)溶液诱导的挛缩,Sr2+在很大程度上可以替代Ca2+。然而,对于由α刺激(去甲肾上腺素)诱导的收缩反应,Sr2+是一种较差的Ca2+替代物。在Sr2+溶液中,β刺激(异丙肾上腺素)对自发收缩的抑制作用明显减弱。文献中的现有数据表明,与β受体相反,激动剂与α受体的相互作用不依赖Ca2+。因此,我们的结果表明,在α受体激动剂占据和膜兴奋之间存在一个Ca2+特异性步骤。