Nilsson H, Jensen P E, Mulvany M J
Department of Pharmacology, University of Aarhus, Denmark.
J Vasc Res. 1994 Nov-Dec;31(6):314-21. doi: 10.1159/000159059.
The role of membrane potential-dependent and independent regulation of the intracellular free calcium concentration ([Ca2+]i) was assessed in the mesenteric small arteries of Wistar rats. [Ca2+]i was determined by Fura-2 fluorescence. Membrane potential measurements were made using intracellular microelectrodes. Depolarization with a high-potassium solution (K-PSS) elevated [Ca2+]i and induced contraction. Further addition of 10 microM noradrenaline (NA) did not elevate [Ca2+]i further but enhanced tone. Addition of calcium channel inhibitors (felodipine or D-600) inhibited the maintained rise in [Ca2+]i with K-PSS, but NA still elevated [Ca2+]i and force to about half the previous level. Further addition of either ryanodine or thapsigargin eliminated the rise in [Ca2+]i with NA, although 10-20% of the contraction remained. Simultaneous measurements of membrane potential, [Ca2+]i, and force during cumulative additions of NA or K-PSS in the absence of inhibitors showed similar relations between membrane potential and [Ca2+]i for each means of activation. The results indicate that membrane potential and [Ca2+]i are strongly correlated in mesenteric small arteries. A small part of the [Ca2+]i increase to NA can be attributed to release from intracellular stores. Membrane potential-independent calcium channels that are directly operated by adrenoceptors appear to play a minor role in the regulation of [Ca2+]i in these vessels.
在Wistar大鼠的肠系膜小动脉中评估了膜电位依赖性和非依赖性对细胞内游离钙浓度([Ca2+]i)的调节作用。通过Fura-2荧光法测定[Ca2+]i。使用细胞内微电极进行膜电位测量。用高钾溶液(K-PSS)使膜去极化可升高[Ca2+]i并诱导收缩。进一步添加10微摩尔去甲肾上腺素(NA)不会使[Ca2+]i进一步升高,但会增强张力。添加钙通道抑制剂(非洛地平或D-600)可抑制K-PSS引起的[Ca2+]i持续升高,但NA仍可使[Ca2+]i和张力升高至先前水平的约一半。进一步添加ryanodine或毒胡萝卜素可消除NA引起的[Ca2+]i升高,尽管仍有10%-20%的收缩存在。在无抑制剂的情况下,在累积添加NA或K-PSS期间同时测量膜电位、[Ca2+]i和张力,结果表明每种激活方式下膜电位与[Ca2+]i之间存在相似的关系。结果表明,肠系膜小动脉中膜电位与[Ca2+]i密切相关。NA引起的[Ca2+]i升高的一小部分可归因于细胞内钙库的释放。由肾上腺素能受体直接调控的膜电位非依赖性钙通道在这些血管的[Ca2+]i调节中似乎起次要作用。