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电压门控钙通道活性调节仓鼠提睾肌小动脉平滑肌细胞钙波。

Voltage-gated Ca channel activity modulates smooth muscle cell calcium waves in hamster cremaster arterioles.

机构信息

Department of Pharmacology and Toxicology, Michigan State University , East Lansing, Michigan.

出版信息

Am J Physiol Heart Circ Physiol. 2018 Oct 1;315(4):H871-H878. doi: 10.1152/ajpheart.00292.2018. Epub 2018 Jun 29.

Abstract

Cremaster muscle arteriolar smooth muscle cells (SMCs) display inositol 1,4,5-trisphosphate receptor-dependent Ca waves that contribute to global myoplasmic Ca concentration and myogenic tone. However, the contribution made by voltage-gated Ca channels (VGCCs) to arteriolar SMC Ca waves is unknown. We tested the hypothesis that VGCC activity modulates SMC Ca waves in pressurized (80 cmHO/59 mmHg, 34°C) hamster cremaster muscle arterioles loaded with Fluo-4 and imaged by confocal microscopy. Removal of extracellular Ca dilated arterioles (32 ± 3 to 45 ± 3 μm, n = 15, P < 0.05) and inhibited the occurrence, amplitude, and frequency of Ca waves ( n = 15, P < 0.05), indicating dependence of Ca waves on Ca influx. Blockade of VGCCs with nifedipine (1 μM) or diltiazem (10 μM) or deactivation of VGCCs by hyperpolarization of smooth muscle with the K channel agonist cromakalim (10 μM) produced similar inhibition of Ca waves ( P < 0.05). Conversely, depolarization of SMCs with the K channel blocker tetraethylammonium (1 mM) constricted arterioles from 26 ± 3 to 14 ± 2 μm ( n = 11, P < 0.05) and increased wave occurrence (9 ± 3 to 16 ± 3 waves/SMC), amplitude (1.6 ± 0.07 to 1.9 ± 0.1), and frequency (0.5 ± 0.1 to 0.9 ± 0.2 Hz, n = 10, P < 0.05), effects that were blocked by nifedipine (1 μM, P < 0.05). Similarly, the VGCC agonist Bay K8644 (5 nM) constricted arterioles from 14 ± 1 to 8 ± 1 μm and increased wave occurrence (3 ± 1 to 10 ± 1 waves/SMC) and frequency (0.2 ± 0.1 to 0.6 ± 0.1 Hz, n = 6, P < 0.05), effects that were unaltered by ryanodine (50 μM, n = 6, P > 0.05). These data support the hypothesis that Ca waves in arteriolar SMCs depend, in part, on the activity of VGCCs. NEW & NOTEWORTHY Arterioles that control blood flow to and within skeletal muscle depend on Ca influx through voltage-gated Ca channels and release of Ca from internal stores through inositol 1,4,5-trisphosphate receptors in the form of Ca waves to maintain pressure-induced smooth muscle tone.

摘要

提睾肌肌动脉平滑肌细胞 (SMCs) 显示肌醇 1,4,5-三磷酸受体依赖性 Ca 波,有助于整体肌浆 Ca 浓度和肌原性张力。然而,电压门控钙通道 (VGCC) 对动脉 SMC Ca 波的贡献尚不清楚。我们测试了以下假设:VGCC 活性调节加压 (80 cmHO/59 mmHg,34°C) 仓鼠提睾肌肌动脉中的 SMC Ca 波,并用共聚焦显微镜对 Fluo-4 加载的血管进行成像。去除细胞外 Ca 会扩张血管 (32±3 至 45±3 μm,n=15,P<0.05) 并抑制 Ca 波的发生、幅度和频率 (n=15,P<0.05),表明 Ca 波依赖于 Ca 内流。用硝苯地平 (1 μM) 或地尔硫卓 (10 μM) 阻断 VGCC 或用平滑肌超极化的 K 通道激动剂克罗卡林 (10 μM) 使 VGCC 失活产生类似的 Ca 波抑制 (P<0.05)。相反,用 K 通道阻断剂四乙铵 (1 mM) 去极化 SMC 会使血管从 26±3 收缩到 14±2 μm(n=11,P<0.05),并增加波的发生 (9±3 到 16±3 波/ SMC),幅度 (1.6±0.07 至 1.9±0.1) 和频率 (0.5±0.1 至 0.9±0.2 Hz,n=10,P<0.05),这些作用被硝苯地平 (1 μM,P<0.05) 阻断。同样,VGCC 激动剂 Bay K8644(5 nM) 使血管从 14±1 收缩到 8±1 μm,并增加波的发生 (3±1 到 10±1 波/ SMC) 和频率 (0.2±0.1 到 0.6±0.1 Hz,n=6,P<0.05),这些作用不受肌醇 1,4,5-三磷酸受体拮抗剂ryanodine (50 μM,n=6,P>0.05) 的影响。这些数据支持以下假设:动脉 SMC 中的 Ca 波部分依赖于 VGCC 的活性。

新的和值得注意的是

控制骨骼肌血流的小动脉依赖于通过电压门控钙通道的 Ca 内流和通过肌醇 1,4,5-三磷酸受体从内部储存库释放 Ca 形成 Ca 波,以维持压力诱导的平滑肌张力。

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