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1,8-桉叶油醇对卵清蛋白诱导的豚鼠气道反应的抑制作用涉及对机电耦联的优先作用。

Inhibitory effect of 1,8-cineole on guinea-pig airway challenged with ovalbumin involves a preferential action on electromechanical coupling.

机构信息

Department of Physiology and Pharmacology, School of Medicine, Federal University of Ceará, Fortaleza, Ceará, Brazil.

出版信息

Clin Exp Pharmacol Physiol. 2009 Nov;36(11):1120-6. doi: 10.1111/j.1440-1681.2009.05189.x. Epub 2009 Apr 27.

DOI:10.1111/j.1440-1681.2009.05189.x
PMID:19413601
Abstract
  1. 1,8-Cineole is a terpenoid constituent of essential oils with anti-inflammatory properties. It reduces the neural excitability, functions as an antinociceptive agent and has myorelaxant actions in guinea-pig airways. The aim of the present study was to investigate the mechanism underlying the myorelaxant effects of 1,8-cineole in guinea-pig isolated trachea from either naïve guinea-pigs or ovalbumin (OVA)-sensitized animals subjected to antigenic challenge. 2. Isometric recordings were made of the tone of isolated tracheal rings. Rings with an intact epithelium relaxed beyond basal tone in the presence of 1,8-cineole (6.5 x 10(-6) to 2 x 10(-2) mol/L) in a concentration-dependent manner (P < 0.001, anova) with a pD(2) value of 2.23 (95% confidence interval 2.10-2.37). Removal of the epithelium or pretreatment of intact tissue for 15 min with 50 micromol/L N(G)-nitro-l-arginine methyl ester, 5 mmol/L tetraethylammonium, 0.5 micromol/L tetrodotoxin or 5 micromol/L propranolol did not alter the potency (pD(2)) or the maximal myorelaxant effect (E(max)) of 1,8-cineole. 3. 1,8-Cineole also significantly decreased the Schultz-Dale contraction induced by OVA, mainly in preparations from OVA-sensitized animals submitted to antigen challenge. 1,8-Cineole decreased tracheal hyperresponsiveness to KCl and carbachol caused by antigen challenge and almost abolished the concentration-response curves to KCl, whereas it had little effect on the concentration-response curves to carbachol. Under Ca(2+)-free conditions and in the presence of 10(-4) mol/L acetylcholine, neither 1,8-cineole (6.5 x 10(-3) mol/L) nor verapamil (1 x 10(-5) mol/L) affected Ca(2+)-induced contractions, but they almost abolished Ba(2+)-induced contractions. 4. In conclusion, the findings of the present study show that 1,8-cineole is a tracheal myorelaxant that acts preferentially on contractile responses elicited electromechanically.
摘要
  1. 1,8-桉叶油醇是一种具有抗炎特性的萜烯类化合物。它可降低神经兴奋性,作为一种抗伤害性药物,并且在豚鼠气道中具有肌松作用。本研究的目的是探讨 1,8-桉叶油醇在正常豚鼠或卵清蛋白(OVA)致敏动物的气道中对抗原刺激引起的气道平滑肌松弛作用的机制。

  2. 对分离的气管环的张力进行等长记录。在存在 1,8-桉叶油醇(6.5×10(-6)至 2×10(-2)mol/L)的情况下,具有完整上皮的环以浓度依赖性方式(P<0.001,anova)超过基础张力而松弛,pD(2)值为 2.23(95%置信区间 2.10-2.37)。上皮去除或用 50μmol/L N(G)-硝基-L-精氨酸甲酯、5mmol/L 四乙铵、0.5μmol/L 河豚毒素或 5μmol/L 普萘洛尔预处理完整组织 15min 不会改变 1,8-桉叶油醇的效力(pD(2))或最大肌松效应(E(max))。

  3. 1,8-桉叶油醇还显著降低了 OVA 诱导的 Schultz-Dale 收缩,主要是在接受抗原刺激的 OVA 致敏动物的制剂中。1,8-桉叶油醇降低了由抗原刺激引起的 KCl 和卡巴胆碱引起的气管高反应性,并几乎消除了对 KCl 的浓度反应曲线,而对卡巴胆碱的浓度反应曲线影响较小。在无钙条件下并存在 10(-4)mol/L 乙酰胆碱的情况下,1,8-桉叶油醇(6.5×10(-3)mol/L)和维拉帕米(1×10(-5)mol/L)均不影响 Ca(2+)诱导的收缩,但它们几乎消除了 Ba(2+)诱导的收缩。

  4. 综上所述,本研究结果表明,1,8-桉叶油醇是一种气管肌松药,主要作用于电机械刺激引起的收缩反应。

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