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磷脂酶A2和蛋白激酶C促成家兔肠系膜动脉中肌丝对5-羟色胺的致敏作用。

Phospholipase A2 and protein kinase C contribute to myofilament sensitization to 5-HT in the rabbit mesenteric artery.

作者信息

Parsons S J, Sumner M J, Garland C J

机构信息

Department of Pharmacology, University of Bristol, UK.

出版信息

J Physiol. 1996 Mar 1;491 ( Pt 2)(Pt 2):447-53. doi: 10.1113/jphysiol.1996.sp021228.

DOI:10.1113/jphysiol.1996.sp021228
PMID:8866867
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1158738/
Abstract
  1. Calcium (Ca2+, 0.1-100 microM) stimulated concentration-dependent contractions in small strips from the rabbit mesenteric artery in which the smooth muscle cells had been permeabilized with Staphylococcus aureus alpha-toxin. 2. 5-Hydroxytryptamine (5-HT) and phenylephrine, each in the presence of 10 microM guanosine 5'-triphosphate (GTP), concentration-dependently stimulated additional contractions in strips sub-maximally contracted by the presence of a buffered concentration of calcium (0.3 microM). All the additional contraction was abolished with the selective inhibitor of protein kinase C, Ro 31-8220 (10 microM). 3. Quinacrine (10-50 microM), an inhibitor of phospholipase A2, selectively inhibited the sensitization to 5-HT, but did not alter the sensitization to either phenylephrine or GTP. 4. Myofilament sensitization to calcium was mimicked by exogenous arachidonic acid (300 microM, in the presence of indomethacin, miconazole and BW755c) and the stable analogue of arachidonic acid, 5,8,11,14-eicosatetrayonic acid (ETYA, 100 microM), and in both cases did not require the additional presence of GTP. Ro 31-8220, but not quinacrine, reduced the sensitization to arachidonic acid by around 30%. 5. These results indicate that G protein-linked myofilament sensitization to calcium in the mesenteric artery that follows the activation of 5-HT receptors, but not alpha 1-receptors, involves phospholipase A2. The sensitization stimulated by each of these different receptors, and a component of the response to arachidonic acid, also appears to involve the activation of protein kinase C.
摘要
  1. 钙(Ca2+,0.1 - 100微摩尔)刺激了经金黄色葡萄球菌α毒素使平滑肌细胞通透的兔肠系膜动脉小条带产生浓度依赖性收缩。2. 5-羟色胺(5-HT)和去氧肾上腺素,在各自存在10微摩尔鸟苷5'-三磷酸(GTP)的情况下,浓度依赖性地刺激了由缓冲浓度的钙(0.3微摩尔)引起的亚最大收缩条带产生额外收缩。蛋白激酶C的选择性抑制剂Ro 31 - 8220(10微摩尔)消除了所有额外收缩。3. 磷脂酶A2抑制剂喹吖因(10 - 50微摩尔)选择性地抑制了对5-HT的致敏作用,但不改变对去氧肾上腺素或GTP的致敏作用。4. 外源性花生四烯酸(300微摩尔,在吲哚美辛、咪康唑和BW755c存在的情况下)和花生四烯酸的稳定类似物5,8,11,14-二十碳四烯酸(ETYA,100微摩尔)模拟了肌丝对钙的致敏作用,并且在这两种情况下都不需要额外存在GTP。Ro 31 - 8220,但不是喹吖因,将对花生四烯酸的致敏作用降低了约30%。5. 这些结果表明,5-HT受体而非α1受体激活后,肠系膜动脉中G蛋白偶联的肌丝对钙的致敏作用涉及磷脂酶A2。这些不同受体各自刺激的致敏作用以及对花生四烯酸反应的一个成分,似乎也涉及蛋白激酶C的激活。

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A divergence in the MAP kinase regulatory network defined by MEK kinase and Raf.由MEK激酶和Raf定义的MAP激酶调节网络中的差异。
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Importance of inositol (1,4,5)-trisphosphate, intracellular Ca2+ release and myofilament Ca2+ sensitization in 5-hydroxytryptamine-evoked contraction of rabbit mesenteric artery.肌醇(1,4,5)-三磷酸、细胞内钙离子释放及肌丝钙离子致敏在5-羟色胺诱发兔肠系膜动脉收缩中的重要性
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Augmented agonist-induced Ca(2+)-sensitization of coronary artery contraction in genetically hypertensive rats. Evidence for altered signal transduction in the coronary smooth muscle cells.增强激动剂诱导的遗传性高血压大鼠冠状动脉收缩的钙敏化作用。冠状动脉平滑肌细胞信号转导改变的证据。
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How is the level of free arachidonic acid controlled in mammalian cells?哺乳动物细胞中游离花生四烯酸的水平是如何控制的?
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