Van Eldere J, Raeymaekers L, Casteels R
Pflugers Arch. 1982 Oct;395(1):81-3. doi: 10.1007/BF00584974.
We have investigated the effect of isoprenaline on the amplitude of the transient contraction of isolated arteries induced by releasing the intracellular Ca with an agonist during incubation in a Ca-free solution. Under some conditions this force development is an indication of the amount of Ca in the intracellular store. Loading the store in high K+ solution in the presence of isoprenaline increases the amplitude of the subsequent contraction in Ca-free solution by 6 to 16% as compared to the control. The presence of isoprenaline during the loading procedure in the control solution with 5.9 mM K+ does not affect the amplitude of the subsequent contraction of the rabbit ear artery. In the rabbit coronary artery such pretreatment with isoprenaline inhibits the contraction to 40% of the control. These results indicate that beta-agonists may stimulate the Ca uptake in the intracellular store and, depending on the tissue, inhibit the influx of Ca.
我们研究了在无钙溶液中孵育期间,通过用激动剂释放细胞内钙来诱导离体动脉产生瞬时收缩时,异丙肾上腺素对其收缩幅度的影响。在某些情况下,这种力量的产生表明细胞内储存钙的量。与对照组相比,在存在异丙肾上腺素的情况下,于高钾溶液中加载储存钙会使随后在无钙溶液中的收缩幅度增加6%至16%。在含有5.9 mM钾的对照溶液中加载过程中存在异丙肾上腺素,并不影响兔耳动脉随后的收缩幅度。在兔冠状动脉中,用异丙肾上腺素进行这种预处理会使收缩抑制至对照的40%。这些结果表明,β-激动剂可能会刺激细胞内储存钙的摄取,并根据组织的不同,抑制钙的内流。