Head G A, Mayorov D N
Neuropharmacology Laboratory, Baker Medical Research Institute, P.O. Box 6492, St. Kilda Road Central, Melbourne, 8008, Australia.
Ann N Y Acad Sci. 2001 Jun;940:361-79. doi: 10.1111/j.1749-6632.2001.tb03691.x.
Angiotensin (Ang) receptors are located in many important central nuclei involved in the regulation of the cardiovascular system. While most interest has focused on forebrain circumventricular actions, areas of the brainstem such as the nucleus of the solitary tract and the ventrolateral medulla contain high concentrations of AT1 receptors. The present review encompasses the physiological role of Ang II in the hindbrain, particularly in relation to its influence on baroreflex control mechanisms. In rabbits there are sympatho-excitatory AT1 receptors in the rostral ventrolateral medulla (RVLM), accessible to Ang II from the cerebrospinal fluid. Activation of these receptors acutely increases renal sympathetic nerve activity (RSNA) and RSNA baroreflex responses. However, blockade of endogenous Ang receptors in the brainstem also shows sympathoexcitation, suggesting there is greater endogenous activity of a sympathoinhibitory Ang II action. Microinjections of angiotensin antagonists into the RVLM showed relatively little tonic activity of endogenous Ang II influencing sympathetic activity in conscious rabbits. However, Ang II receptors in the RVLM mediate sympathetic responses to airjet stress in conscious rabbits. Similarly with respect to heart rate baroreflexes, there appears to be little tonic effect of angiotensin in the brainstem in normal conscious animals. Chronic infusion of Ang II for two weeks into the fourth ventricle of conscious rabbits inhibits the cardiac baroreflex while infusion of losartan increases the gain of the reflex. These actions suggest that Ang II in the brainstem modulates sympathetic responses depending on specific afferent and synaptic inputs in both the short term but importantly also in the long term, thus forming an important mechanism for increasing the range of adaptive response patterns.
血管紧张素(Ang)受体位于许多参与心血管系统调节的重要中枢核团中。虽然大多数研究兴趣集中在前脑室周作用,但脑干区域如孤束核和延髓腹外侧含有高浓度的AT1受体。本综述涵盖了Ang II在后脑的生理作用,特别是其对压力反射控制机制的影响。在兔中,延髓头端腹外侧(RVLM)存在交感兴奋的AT1受体,脑脊液中的Ang II可作用于这些受体。激活这些受体可急性增加肾交感神经活动(RSNA)和RSNA压力反射反应。然而,阻断脑干中的内源性Ang受体也表现出交感兴奋,这表明存在更强的内源性交感抑制性Ang II作用。向RVLM微量注射血管紧张素拮抗剂显示,内源性Ang II对清醒兔交感神经活动的紧张性影响相对较小。然而,RVLM中的Ang II受体介导清醒兔对喷气应激的交感反应。同样,对于心率压力反射,在正常清醒动物中,脑干中的血管紧张素似乎几乎没有紧张性作用。向清醒兔的第四脑室慢性输注Ang II两周会抑制心脏压力反射,而输注氯沙坦则会增加反射增益。这些作用表明,脑干中的Ang II在短期和长期内均根据特定的传入和突触输入调节交感反应,从而形成增加适应性反应模式范围的重要机制。