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M2选择性毒蕈碱拮抗剂对麻醉豚鼠的降压作用。

Hypotensive effect of an M2-selective muscarinic antagonist in anaesthetized guinea-pigs.

作者信息

Howell R E, Kovalsky M P

机构信息

Nova Pharmaceutical Corporation, Baltimore, MD 21224, USA.

出版信息

J Auton Pharmacol. 1995 Feb;15(1):19-26. doi: 10.1111/j.1474-8673.1995.tb00344.x.

Abstract
  1. In order to determine an involvement of muscarinic M2 receptors in the regulation of systemic arterial blood pressure, we investigated the cardiovascular effects of the M2-selective antagonist methoctramine and other agents in anaesthetized guinea-pigs. 2. Intravenous injection of methoctramine, atropine, pirenzepine (an M1-selective muscarinic antagonist) or 4-DAMP (an M3-selective muscarinic antagonist) each significantly increased heart rate in comparison to vehicle controls. 3. Methoctramine produced significant, dose-dependent decreases in mean arterial blood pressure, with an ED50 of 0.1 mg kg-1. Atropine decreased blood pressure only at high doses. Pirenzepine and 4-DAMP did not alter blood pressure, indicating that M1 or M3 receptor antagonism was not responsible for the cardiovascular effects of methoctramine. 4. The hypotensive effect of methoctramine was unaltered by indomethacin pretreatment, ruling out an alteration in arachidonic acid metabolism as the mechanism of action. 5. In contrast to methoctramine, mecamylamine (a nicotinic ganglionic receptor antagonist) greatly decreased heart rate and slightly decreased blood pressure, suggesting that ganglionic blockade was not the mechanism for the cardiovascular effects of methoctramine. 6. Methoctramine (0.3 mg kg-1) pretreatment did not alter the hypertensive effect of intravenous noradrenaline, demonstrating that methoctramine did not directly inhibit vascular reactivity and indicating an indirect hypotensive of action of methoctramine. 7. In summary, the results suggest that the hypotensive action of methoctramine resulted from selective M2 receptor antagonism. Therefore, muscarinic M2 receptors appear to play a role in the regulation of systemic arterial blood pressure in guinea-pigs. However, the anatomical site(s) of action of methoctramine remains to be determined.
摘要
  1. 为了确定毒蕈碱型M2受体是否参与全身动脉血压的调节,我们研究了M2选择性拮抗剂甲溴东莨菪碱及其他药物对麻醉豚鼠的心血管效应。2. 与赋形剂对照组相比,静脉注射甲溴东莨菪碱、阿托品、哌仑西平(一种M1选择性毒蕈碱拮抗剂)或4-二甲基氨基吡啶(一种M3选择性毒蕈碱拮抗剂)均显著增加心率。3. 甲溴东莨菪碱使平均动脉血压显著降低,且呈剂量依赖性,半数有效剂量为0.1mg/kg。阿托品仅在高剂量时降低血压。哌仑西平和4-二甲基氨基吡啶未改变血压,表明M1或M3受体拮抗并非甲溴东莨菪碱心血管效应的原因。4. 吲哚美辛预处理未改变甲溴东莨菪碱的降压作用,排除了花生四烯酸代谢改变作为作用机制的可能性。5. 与甲溴东莨菪碱相反,美加明(一种烟碱型神经节受体拮抗剂)显著降低心率并轻微降低血压,提示神经节阻断并非甲溴东莨菪碱心血管效应的机制。6. 甲溴东莨菪碱(0.3mg/kg)预处理未改变静脉注射去甲肾上腺素的升压作用,表明甲溴东莨菪碱未直接抑制血管反应性,提示其降压作用为间接性。7. 总之,结果表明甲溴东莨菪碱的降压作用源于选择性M2受体拮抗。因此,毒蕈碱型M2受体似乎在豚鼠全身动脉血压调节中发挥作用。然而,甲溴东莨菪碱的作用解剖部位仍有待确定。

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