Department of Physiology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Applied Biomedical Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Clin Exp Hypertens. 2022 May 19;44(4):297-305. doi: 10.1080/10641963.2021.2007944. Epub 2022 Mar 10.
The cardiovascular effects of nicotinic receptors of cholinergic system in the pedunculopontine tegmental nucleus (PPT) were shown.
In the following, the cardiovascular effects of the muscarinic receptor, another receptor in this system, were examined.
Rats were divided into eight groups: 1) control; 2 and 3) Ach (acetylcholine, an agonist) 90 and 150 nmol; 4 and 5) Atr (atropine; a muscarinic antagonist) 3 and 9 nmol; 6) Atr 3 + Ach 150; 7) Atr 9 + Ach 150; and 8) Atr 3 + hexamethonium (Hexa; 300 nmol) + Ach 150. After anesthesia, cannulation of the femoral artery was performed, and then the mean arterial pressure (MAP), systolic blood pressure (SBP), and heart rate (HR) were recorded using a power lab apparatus.
Following drug microinjection, the maximum change (Δ) in MAP, SBP, and HR was calculated and analyzed. Both doses of Ach (90 and 150) significantly decreased ΔMAP and ΔSBP but could not change ΔHR. Neither of the doses of Atr significantly affected ΔMAP, ΔSBP, and ΔHR. Co-injection of Atr 3 + Ach 150 only increased ΔHR, but Atr 9 + Ach 150 decreased ΔMAP and ΔSBP than Ach 150 alone. The effect of the co-injection of Atr 9 + Hexa 300 + Ach 150 was also the same as the Atr 9 + Ach 150 group.
The present results revealed that cholinergic muscarinic receptors in the PPT have an inhibitory effect on MAP and SBP with no important effect on HR.
已经证明了胆碱能系统的烟碱受体在脑桥被盖脚核(PPT)中的心血管效应。
在下面,将检查该系统中的另一种受体——毒蕈碱受体的心血管效应。
将大鼠分为 8 组:1)对照组;2 和 3)Ach(乙酰胆碱,激动剂)90 和 150 nmol;4 和 5)Atr(阿托品;毒蕈碱拮抗剂)3 和 9 nmol;6)Atr 3 + Ach 150;7)Atr 9 + Ach 150;和 8)Atr 3 + 六烃季铵(Hexa;300 nmol)+Ach 150。麻醉后,进行股动脉插管,然后使用功率实验室仪器记录平均动脉压(MAP)、收缩压(SBP)和心率(HR)。
药物微注射后,计算并分析 MAP、SBP 和 HR 的最大变化(Δ)。两种剂量的 Ach(90 和 150)均显著降低了 ΔMAP 和 ΔSBP,但不能改变 ΔHR。两种剂量的 Atr 均未显著影响 ΔMAP、ΔSBP 和 ΔHR。Atr 3 + Ach 150 的共同注射仅增加了 ΔHR,但 Atr 9 + Ach 150 降低了 ΔMAP 和 ΔSBP,与 Ach 150 单独使用相比。Atr 9 + Hexa 300 + Ach 150 的共同注射的效果也与 Atr 9 + Ach 150 组相同。
本研究结果表明,PPT 中的胆碱能毒蕈碱受体对 MAP 和 SBP 具有抑制作用,对 HR 没有重要影响。