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在大鼠离体肠系膜动脉中,血栓素受体刺激与SKCa活性丧失及内皮依赖性超极化因子(EDHF)反应降低相关。

Thromboxane receptor stimulation associated with loss of SKCa activity and reduced EDHF responses in the rat isolated mesenteric artery.

作者信息

Crane G J, Garland C J

机构信息

Department of Pharmacy & Pharmacology, University of Bath, Claverton Down, Bath BA2 7AY.

出版信息

Br J Pharmacol. 2004 May;142(1):43-50. doi: 10.1038/sj.bjp.0705756. Epub 2004 Mar 29.

Abstract
  1. The possibility that thromboxane (TXA(2)) receptor stimulation causes differential block of the SK(Ca) and IK(Ca) channels which underlie EDHF-mediated vascular smooth muscle hyperpolarization and relaxation was investigated in the rat isolated mesenteric artery. 2. Acetylcholine (30 nm-3 microm ACh) or cyclopiazonic acid (10 microm CPA, SERCA inhibitor) were used to stimulate EDHF-evoked smooth muscle hyperpolarization. In each case, this led to maximal hyperpolarization of around 20 mV, which was sensitive to block with 50 nm apamin and abolished by repeated stimulation of mesenteric arteries with the thromboxane mimetic, U46619 (30 nm-0.1 microm), but not the alpha(1)-adrenoceptor agonist phenylephrine (PE). 3. The ability of U46619 to abolish EDHF-evoked smooth muscle hyperpolarization was prevented by prior exposure of mesenteric arteries to the TXA(2) receptor antagonist 1 microm SQ29548. 4. Similar-sized smooth muscle hyperpolarization evoked with the SK(Ca) activator 100 microm riluzole was also abolished by prior stimulation with U46619, while direct muscle hyperpolarization in response to either levcromakalim (1 microm, K(ATP) activator) or NS1619 (40 microm, BK(Ca) activator) was unaffected. 5. During smooth muscle contraction and depolarization to either PE or U46619, ACh evoked concentration-dependent hyperpolarization (to -67 mV) and complete relaxation. These responses were well maintained during repeated stimulation with PE, but with U46619 there was a progressive decline, so that during a third exposure to U46619 maximum hyperpolarization only reached -52 mV and relaxation was reduced by 20%. This relaxation could now be blocked with charybdotoxin alone. The latter responses could be mimicked with 300 microm 1-EBIO (IK(Ca) activator), an action not modified by exposure to U46619. 6. An early consequence of TXA(2) receptor stimulation is a reduction in the arterial hyperpolarization and relaxation attributed to EDHF. This effect appears to reflect a loss of SK(Ca) activity.
摘要
  1. 在大鼠离体肠系膜动脉中,研究了血栓素(TXA₂)受体刺激是否会对小电导钙激活钾通道(SK(Ca))和大电导钙激活钾通道(IK(Ca))产生差异性阻断,这两种通道是内皮衍生超极化因子(EDHF)介导的血管平滑肌超极化和舒张的基础。2. 用乙酰胆碱(30 nM - 3 μM ACh)或环匹阿尼酸(10 μM CPA,肌浆网钙ATP酶抑制剂)刺激EDHF诱发的平滑肌超极化。在每种情况下,这都会导致约20 mV的最大超极化,该超极化对50 nM蜂毒明肽敏感,并可被血栓素类似物U46619(30 nM - 0.1 μM)反复刺激肠系膜动脉所消除,但α₁肾上腺素能受体激动剂去氧肾上腺素(PE)则不能。3. 肠系膜动脉预先暴露于TXA₂受体拮抗剂1 μM SQ29548可阻止U46619消除EDHF诱发的平滑肌超极化的能力。4. 用SK(Ca)激活剂100 μM利鲁唑诱发的类似大小的平滑肌超极化也可被U46619预先刺激所消除,而对左卡尼汀(1 μM,ATP敏感性钾通道激活剂)或NS1619(40 μM,大电导钙激活钾通道激活剂)的直接肌肉超极化则不受影响。5. 在平滑肌收缩并去极化至PE或U46619期间,ACh诱发浓度依赖性超极化(至 - 67 mV)并完全舒张。在用PE反复刺激期间,这些反应能很好地维持,但在用U46619刺激时则逐渐下降,因此在第三次暴露于U46619时,最大超极化仅达到 - 52 mV,舒张减少20%。现在单独用蝎毒素可阻断这种舒张。后一种反应可用300 μM 1 - 依布硒啉(IK(Ca)激活剂)模拟,该作用不受暴露于U46619的影响。6. TXA₂受体刺激的早期结果是归因于EDHF的动脉超极化和舒张减少。这种效应似乎反映了SK(Ca)活性的丧失。

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