Ciriello John, Li Zhaohui, de Oliveira Cleusa V R
Department of Physiology and Pharmacology, Faculty of Medicine and Dentistry, Health Sciences Centre, University of Western Ontario, London, ON, Canada N6A 5C1.
Brain Res. 2003 Nov 21;991(1-2):84-95. doi: 10.1016/j.brainres.2003.08.008.
Intracisternal injections of hypocretin-1 (hcrt-1) have been shown to elicit sympathoexciatory responses. However, the location of central sites that may mediate these cardiovascular effects have not been clearly elucidated. This study was done in male Wistar rats to investigate the effects of microinjections of hcrt-1 into the rostral ventromedial medulla (RVMM) on mean arterial pressure (MAP), heart rate (HR) and the arterial baroreflex. An initial series of experiments was done to provide a detailed mapping of the location of hcrt-1- and hcrt-1 receptors (hcrtR-1)-like immunoreactivity (i.r.) in the RVMM region. Hcrt-1 and hcrtR-1 ir were found throughout the RVMM region, but primarily within the magnocellular reticular nucleus and the adjacent nucleus paragigantocellularis lateralis. In the second series, this region containing hcrt-1 and hcrtR-1 ir was explored for sites that elicited changes in MAP and HR in the anaesthetized rat. Microinjection of hcrt-1 (0.5-2.5 pmol) into the region of magnocellular reticular nucleus elicited a dose-dependent increase in HR, with little or no change in MAP. Administration (i.v.) of the muscarinic receptor antagonist atropine methyl bromide significantly attenuated ( approximately 62%) the HR response whereas, the total autonomic blockade abolished the HR response. Finally, unilateral or bilateral microinjection of hcrt-1 into the magnocellular reticular nucleus significantly attenuated the reflex bradycardia resulting from the activation of the baroreflex following the increase in MAP from an iv injection of phenylephrine. These data suggest that hcrt-1 in the RVMM region activates neuronal circuits that both inhibit vagal activity and increase sympathetic activity to the heart, and that it alters the excitability of central circuits that reflexly control the circulation.
脑池内注射促食欲素-1(hcrt-1)已被证明可引发交感兴奋反应。然而,可能介导这些心血管效应的中枢位点尚未明确阐明。本研究在雄性Wistar大鼠中进行,以研究向延髓头端腹内侧区(RVMM)微量注射hcrt-1对平均动脉压(MAP)、心率(HR)和动脉压力反射的影响。最初的一系列实验旨在详细描绘RVMM区域中hcrt-1和促食欲素-1受体(hcrtR-1)样免疫反应性(i.r.)的位置。在整个RVMM区域均发现了hcrt-1和hcrtR-1免疫反应性,但主要位于巨细胞网状核和相邻的外侧旁巨细胞核内。在第二个系列实验中,探索了这个含有hcrt-1和hcrtR-1免疫反应性的区域,寻找在麻醉大鼠中引发MAP和HR变化的位点。向巨细胞网状核区域微量注射hcrt-1(0.5 - 2.5 pmol)可引起HR呈剂量依赖性增加,而MAP几乎没有变化。静脉注射毒蕈碱受体拮抗剂甲基溴化阿托品可显著减弱(约62%)HR反应,而完全自主神经阻滞则消除了HR反应。最后,向巨细胞网状核单侧或双侧微量注射hcrt-1可显著减弱静脉注射去氧肾上腺素使MAP升高后激活压力反射所导致的反射性心动过缓。这些数据表明,RVMM区域中的hcrt-1激活了抑制迷走神经活动并增加心脏交感神经活动的神经回路,并且它改变了反射性控制循环的中枢回路的兴奋性。