Applied Biomedical Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Pharmacology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Clin Exp Hypertens. 2022 May 19;44(4):366-371. doi: 10.1080/10641963.2022.2050744. Epub 2022 Mar 9.
The pedunculopontine tegmental nucleus (PPT) is involved in cardiovascular regulation. The presence of mu (μ) opioid receptors in the PPT nucleus has been determined. In the present study, the role of this nucleus in normotensive conditions and then the role of these receptors on cardiovascular function in hypotension induced by hemorrhage (HEM) were investigated.
Animals were divided into the following groups: Group 1: control, Group 2: HEM, Group 3: morphine at dose 100 nmol (a general opioid receptor agonist), Group 4: naloxone at dose 100 nmol (a general opioid receptor antagonist), Group 5: morphine + HEM, and Group 6: naloxone + HEM. After anesthesia, two femoral arteries were cannulated to record the cardiovascular parameters and blood withdrawal. Two minutes after induction of HEM, drugs were injected into the nucleus, and cardiovascular parameters were measured. Changes (Δ) in cardiovascular responses due to drug injection and HEM were calculated and compared to control and HEM groups.
HEM significantly reduced changes in systolic and mean arterial pressures and increased heart rate changes compared to control. Morphine microinjection in normotensive and HEM rats significantly decreased systolic blood pressure, mean arterial pressure, and heart rate, and naloxone significantly increased all these parameters.
This study showed that the PPT nucleus plays a role in modulating the cardiovascular responses induced by HEM. The µ opioid receptor of the PPT nucleus in the normotensive and HEM rats have inhibitory effects on blood pressure and heart rate mainly, and these effects are eliminated by naloxone microinjection.
被盖脚桥核(PPT)参与心血管调节。现已确定 PPT 核内存在μ阿片受体。本研究旨在探讨该核在正常血压条件下的作用,以及其在出血性低血压(HEM)诱导下对心血管功能的作用。
动物分为以下几组:第 1 组:对照组;第 2 组:HEM 组;第 3 组:吗啡 100nmol(一种通用阿片受体激动剂);第 4 组:纳洛酮 100nmol(一种通用阿片受体拮抗剂);第 5 组:吗啡+HEM 组;第 6 组:纳洛酮+HEM 组。麻醉后,经两侧股动脉插管记录心血管参数和采血。在 HEM 诱导后 2 分钟,将药物注入核内,并测量心血管参数。计算药物注射和 HEM 引起的心血管反应变化(Δ),并与对照组和 HEM 组进行比较。
与对照组相比,HEM 显著降低了收缩压和平均动脉压的变化,并增加了心率的变化。在正常血压和 HEM 大鼠中,吗啡微注射显著降低了收缩压、平均动脉压和心率,而纳洛酮显著增加了所有这些参数。
本研究表明,PPT 核在调节 HEM 诱导的心血管反应中起作用。正常血压和 HEM 大鼠 PPT 核内的μ阿片受体对血压和心率主要具有抑制作用,这些作用可被纳洛酮微注射消除。