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去甲肾上腺素、生长抑素和阿片类物质对豚鼠黏膜下神经元钙电流的抑制作用

Inhibition of calcium currents by noradrenaline, somatostatin and opioids in guinea-pig submucosal neurones.

作者信息

Surprenant A, Shen K Z, North R A, Tatsumi H

机构信息

Vollum Institute, Oregon Health Sciences University, Portland 97201.

出版信息

J Physiol. 1990 Dec;431:585-608. doi: 10.1113/jphysiol.1990.sp018349.

Abstract
  1. Whole-cell recordings were made from submucosal neurones acutely dissociated from guinea-pigs. The actions of noradrenaline, somatostatin and [Met5]enkephalin on currents carried by calcium ions were studied. 2. On depolarization from a holding potential of -70 mV, an inward current activated at -40 mV, reached its peak amplitude at 10 mV and reversed to outward at 72 mV (with external calcium of 5 mM and internal caesium of 160 mM). 3. Cadmium, nickel and cobalt reversibly blocked the calcium current; concentrations causing 50% block were 2.5, 500 and 2000 microM respectively. The calcium current (holding at -70 or -30 mV) was reversibly blocked by omega-conotoxin (100 nM), and unaffected by Bay K 8644 (0.1-10 microM) and nifedipine (1 microM). Cadmium caused an outward shift in holding current at -30 mV, implying that there was a persistent inward calcium current at this potential. 4. Noradrenaline, somatostatin and [Met5]enkephalin decreased the calcium current. The maximal inhibition observed with any one agonist, or with a combination of two agonists, did not exceed 50%; concentrations giving half-maximal inhibition were 5.5 microM for noradrenaline, 4 nM for somatostatin and 1 microM for [Met5]enkephalin. The inhibition was independent of membrane potential. All three agonists also reduced the persistent calcium current at -30 mV. 5. Inhibition of the calcium current by noradrenaline occurred with a latency of not less than 175 ms; cadmium applied by the same method depressed the current within 5-45 ms. 6. Experiments with selective agonists and antagonists indicated that the receptor types involved in calcium current inhibition were alpha 2-adrenoceptors and delta-opioid receptors. Somatostatin acted at a distinct receptor. 7. Calcium currents were also inhibited by intracellular dialysis with guanosine 5'-O-(3-thiotriphosphate) (GTP-gamma-S). Agonists were ineffective in cells pre-treated with pertussis toxin, but their action was restored when purified GTP-binding proteins (Go or Gi) were included in the intracellular recording solution. 8. It is concluded that noradrenaline, somatostatin and [Met5]enkephalin act at their respective receptors on guinea-pig submucosal neurones to inhibit a voltage-dependent calcium current. Activation of the same receptors also increases a potassium conductance in these cells: in both cases a pertussis-sensitive G protein is involved.
摘要
  1. 全细胞记录是在急性分离的豚鼠黏膜下神经元上进行的。研究了去甲肾上腺素、生长抑素和[Met5]脑啡肽对钙离子携带电流的作用。2. 从-70 mV的钳制电位去极化时,内向电流在-40 mV时激活,在10 mV时达到峰值幅度,并在72 mV时反转向外(细胞外钙浓度为5 mM,细胞内铯浓度为160 mM)。3. 镉、镍和钴可逆性阻断钙电流;引起50%阻断的浓度分别为2.5、500和2000 microM。钙电流(钳制在-70或-30 mV)被ω-芋螺毒素(100 nM)可逆性阻断,不受Bay K 8644(0.1 - 10 microM)和硝苯地平(1 microM)影响。镉在-30 mV时使钳制电流向外偏移,这意味着在此电位存在持续性内向钙电流。4.去甲肾上腺素、生长抑素和[Met5]脑啡肽降低钙电流。任何一种激动剂或两种激动剂组合所观察到的最大抑制不超过50%;产生半数最大抑制的浓度,去甲肾上腺素为5.5 microM,生长抑素为4 nM,[Met5]脑啡肽为1 microM。抑制作用与膜电位无关。这三种激动剂也降低了-30 mV时的持续性钙电流。5. 去甲肾上腺素对钙电流的抑制潜伏期不少于175 ms;用相同方法施加的镉在5 - 45 ms内使电流降低。6. 选择性激动剂和拮抗剂实验表明,参与钙电流抑制的受体类型是α2 -肾上腺素能受体和δ -阿片受体。生长抑素作用于不同的受体。7. 用鸟苷5'-O-(3 -硫代三磷酸)(GTP -γ - S)进行细胞内透析也可抑制钙电流。在百日咳毒素预处理的细胞中激动剂无效,但当细胞内记录溶液中加入纯化的GTP结合蛋白(Go或Gi)时,其作用恢复。8. 得出结论,去甲肾上腺素、生长抑素和[Met5]脑啡肽作用于豚鼠黏膜下神经元各自的受体,抑制电压依赖性钙电流。相同受体的激活也增加了这些细胞中的钾电导:在这两种情况下都涉及百日咳敏感的G蛋白。

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