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首页> 外文期刊>Fundamental & clinical pharmacology. >Inhibitory effect of Zataria multiflora Boiss and carvacrol on histamine (H 1) receptors of guinea-pig tracheal chains
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Inhibitory effect of Zataria multiflora Boiss and carvacrol on histamine (H 1) receptors of guinea-pig tracheal chains

机译:百日草和香芹酚对豚鼠气管链中组胺(H 1)受体的抑制作用

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The inhibitory effect of aqueous-ethanolic extract of Zataria multiflora Boiss (Labiatae) and carvacrol on histamine (H 1) receptors was examined on tracheal chains of guinea-pigs. The effects of three concentrations of aqueous-ethanolic extract, carvacrol, 10nm chlorpheniramine, and saline on histamine (H 1) receptors were tested on three groups of guinea-pig tracheal chains as follows: incubated trachea with (i) indomethacin (n=9), (ii) indomethacin, propranolol, and atropine (n=7), and (iii) indomethacin and propranolol (n=6). The EC 50 (effective concentration of histamine causing 50% of maximum response) obtained in the presence of chlorpheniramine for all concentrations of the extract and carvacrol in all three groups was significantly higher than that of saline (P0.001 for all cases). The EC 50 obtained in the presence of all concentrations of extract in groups 2 and 3 was lower than group 1 and in group 3 lower than group 2 (P0.01 to P0.001). However, EC 50 obtained in the presence of all concentrations of carvacrol in group 3 and two higher concentrations in group 2 was higher than that of group 1 (P0.01 to P0.001). There was no significant difference in the maximum response obtained in the presence of different concentrations of extract and carvacrol between three groups. There was a parallel rightward shift in concentration-response curves obtained in the presence of all concentrations of the extract and carvacrol in all three groups. These results indicated an inhibitory effect of Z. multiflora and its constituent carvacrol on histamine H 1 receptors.
机译:研究了豚鼠气管链上的百日草(Labiatae)和香芹酚的乙醇水溶液对组胺(H 1)受体的抑制作用。在三组豚鼠气管链上测试了三种浓度的乙醇提取物,香芹酚,10nm氯苯那敏和生理盐水的浓度对组胺(H 1)受体的影响:将气管与(i)消炎痛(n = 9)孵育),(ii)消炎痛,普萘洛尔和阿托品(n = 7),以及(iii)消炎痛和普萘洛尔(n = 6)。在三组所有浓度的提取物和香芹酚中,在扑尔敏存在下获得的EC 50(有效浓度的组胺引起最大响应的50%)显着高于生理盐水(所有情况下P <0.001)。第2组和第3组在所有浓度的提取物存在下获得的EC 50均低于第1组,而第3组的EC 50低于第2组(P <0.01至P <0.001)。然而,第3组在所有浓度香芹酚存在下和第2组两个较高浓度下获得的EC 50均高于第1组(P <0.01至P <0.001)。在三组中存在不同浓度的提取物和香芹酚的情况下,获得的最大反应无显着差异。在所有浓度的所有三组提取物和香芹酚的存在下,浓度-响应曲线均发生平行向右移动。这些结果表明,何首乌及其组成香芹酚对组胺H 1受体具有抑制作用。

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