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β2肾上腺素能受体激动剂丙卡特罗对犬气管平滑肌细胞的舒张作用。

Relaxing actions of procaterol, a beta 2-adrenoceptor stimulant, on smooth muscle cells of the dog trachea.

作者信息

Fujiwara T, Sumimoto K, Itoh T, Suzuki H, Kuriyama H

机构信息

Department of Pharmacology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

Br J Pharmacol. 1988 Jan;93(1):199-209. doi: 10.1111/j.1476-5381.1988.tb11422.x.

Abstract
  1. The effects of procaterol, a beta 2-adrenoceptor agonist, on smooth muscle cells of the dog trachea were investigated by use of microelectrode and isometric tension recording methods, and by measurement of Ca transients as estimated from the fura-2 fluorescence, adenosine 3':5'-cyclic monophosphate (cyclic AMP) and breakdown of phosphatidylinositols. 2. Procaterol hyperpolarized the membrane and increased the ionic conductance (above 10 nM) in a dose-dependent manner. These actions were inhibited by propranolol. 3. Procaterol inhibited the mechanical responses evoked by acetylcholine (ACh), histamine or 5-hydroxytryptamine (5-HT), in the presence or absence of Ca2+ in the bath solution, but not that evoked by high concentrations of ACh (1 microM). The ID50 value of procaterol for the peak amplitude of the ACh-induced contraction (30 nM) was 0.3 nM. The equivalent values for the histamine-induced phasic and tonic responses (10 microM) were 0.15 and 0.01 nM), respectively. 4. Procaterol (over 1 nM) increased the amount of cyclic AMP in a dose-dependent manner which was blocked by prior application of propranolol. 5. Procaterol did not alter the changes in the amounts of phosphatidylinositol 4,5-bisphosphate (PI-P2) and phosphatidic acid (PA) induced by ACh, histamine or 5-HT. Thus, the synthesis of inositol 1,4,5-trisphosphate is not affected by stimulation of the beta 2-adrenoceptor. 6. ACh increased the free Ca2+ concentration to a greater extent than that produced by histamine or 5-HT. These changes were reduced by procaterol, except for those induced by high concentrations of ACh (over 1 microM). 7. It is concluded that procaterol relaxes tissues precontracted by various agonists due to a reduction in the free Ca2+. This inhibitory action may be due to an increase in the amount of cyclic AMP but does not result from an inhibition of the hydrolysis of phosphatidyl inositols. The hyperpolarization induced by procaterol may partly contribute to the observed relaxation.
摘要
  1. 采用微电极和等长张力记录方法,并通过测量基于fura - 2荧光、腺苷3':5'-环磷酸(环磷酸腺苷)和磷脂酰肌醇分解估算的钙瞬变,研究了β2肾上腺素能受体激动剂丙卡特罗对犬气管平滑肌细胞的作用。2. 丙卡特罗使细胞膜超极化,并以剂量依赖方式增加离子电导(高于10 nM)。这些作用被普萘洛尔抑制。3. 在浴液中存在或不存在Ca2+的情况下,丙卡特罗均抑制乙酰胆碱(ACh)、组胺或5 - 羟色胺(5 - HT)诱发的机械反应,但不抑制高浓度ACh(1 μM)诱发的反应。丙卡特罗对ACh诱导收缩峰值幅度(30 nM)的ID50值为0.3 nM。组胺诱导的相性和强直性反应(10 μM)的等效值分别为0.15和0.01 nM。4. 丙卡特罗(超过1 nM)以剂量依赖方式增加环磷酸腺苷的量,这被预先应用普萘洛尔所阻断。5. 丙卡特罗不改变ACh、组胺或5 - HT诱导的磷脂酰肌醇4,5 - 二磷酸(PI - P2)和磷脂酸(PA)量的变化。因此,肌醇1,4,5 - 三磷酸的合成不受β2肾上腺素能受体刺激的影响。6. ACh比组胺或5 - HT更大程度地增加游离Ca2+浓度。除高浓度ACh(超过1 μM)诱导的变化外,这些变化被丙卡特罗减少。7. 得出结论,丙卡特罗通过降低游离Ca2+使由各种激动剂预收缩的组织松弛。这种抑制作用可能归因于环磷酸腺苷量的增加,但不是由于磷脂酰肌醇水解的抑制。丙卡特罗诱导的超极化可能部分有助于观察到的松弛。

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