Scheucher A, Pirola C J, Balda M S, Dabsys S M, Alvarez A L, Finkielman S, Nahmod V E
Neuropharmacology. 1987 Feb-Mar;26(2-3):181-5. doi: 10.1016/0028-3908(87)90207-3.
The infusion of pilocarpine, acetylcholine, bradykinin and the selective M1 muscarinic agonist McNeil-A-343 into the lateral septal area produced a dose-dependent increase of arterial blood pressure and heart rate. The M1 muscarinic agonist carbamylcholine that causes a rise in arterial blood pressure when injected into the anterior lateral ventricles did not produce any cardiovascular effects when infused into the lateral septal area. Chronic treatment with atropine induced supersensitivity to the muscarinic agonists and a significant increase in the number of muscarinic receptors. In this study bradykinin failed to produce any significant change in cardiovascular activity. Pirenzepine, a M1 muscarinic blocking agent, inhibited completely the effect of both muscarinic agonists and bradykinin on cardiovascular activity. In fact, in vitro studies shows that the displacement of the binding of [3H]QNB by pirenzepine is compatible with the presence of the M1 subtype of muscarinic receptor in the lateral septal area, where it may play a major role on cardiovascular regulation.
将毛果芸香碱、乙酰胆碱、缓激肽以及选择性M1毒蕈碱激动剂麦克尼尔-A-343注入外侧隔区,可使动脉血压和心率呈剂量依赖性升高。当注入前外侧脑室时会引起动脉血压升高的M1毒蕈碱激动剂氨甲酰胆碱,注入外侧隔区时未产生任何心血管效应。用阿托品进行慢性治疗可诱导对毒蕈碱激动剂超敏,并使毒蕈碱受体数量显著增加。在本研究中,缓激肽未能使心血管活动产生任何显著变化。M1毒蕈碱阻断剂哌仑西平完全抑制了毒蕈碱激动剂和缓激肽对心血管活动的作用。事实上,体外研究表明,哌仑西平对[3H]QNB结合的置换与外侧隔区存在M1亚型毒蕈碱受体相符,该受体可能在心血管调节中起主要作用。