Colombari D S, Menani J V, Johnson A K
Department of Psychology, University of Iowa, Iowa City 52242-1407, USA.
Am J Physiol. 1996 Dec;271(6 Pt 2):R1470-6. doi: 10.1152/ajpregu.1996.271.6.R1470.
This study investigated the roles of serotonin (5-HT) receptors in the lateral parabrachial nucleus (LPBN) and brain angiotensin type 1 (AT1) receptors in the intake of 0.3 M NaCl and water induced by angiotensin II (ANG II). Rats were implanted with stainless steel cannulas for injections into the subfornical organ (SFO) and into the LPBN. Bilateral LPBN pretreatment with the nonselective serotonergic 5-HT1/5-HT2 receptor antagonist methysergide (4 micrograms/200 nl) markedly enhanced 0.3 M NaCl intake induced by injections of ANG II (20 ng/200 nl) into the SFO. Pretreatment of the SFO with the AT1 receptor antagonist losartan (1 microgram/200 nl) blocked the intake of 0.3 M NaCl induced by ANG II in combination with LPBN methysergide injections. These results suggest that serotonergic mechanisms associated with the LPBN inhibit the expression of salt appetite induced by ANG II injections into the SFO. In addition, the results indicate that the enhanced NaCl intake generated by central administration of ANG II in the presence of LPBN 5-HT blockade is mediated by brain AT1 receptors.
本研究调查了血清素(5-羟色胺,5-HT)受体在外侧臂旁核(LPBN)中的作用,以及脑内1型血管紧张素(AT1)受体在血管紧张素II(ANG II)诱导的0.3M NaCl和水摄入中的作用。给大鼠植入不锈钢套管,用于向穹窿下器(SFO)和LPBN注射。用非选择性血清素能5-HT1/5-HT2受体拮抗剂美西麦角(4微克/200纳升)对双侧LPBN进行预处理,可显著增强向SFO注射ANG II(20纳克/200纳升)所诱导的0.3M NaCl摄入。用AT1受体拮抗剂氯沙坦(1微克/200纳升)对SFO进行预处理,可阻断在LPBN注射美西麦角的情况下ANG II诱导的0.3M NaCl摄入。这些结果表明,与LPBN相关的血清素能机制可抑制向SFO注射ANG II所诱导的盐食欲表达。此外,结果表明,在LPBN 5-HT阻断的情况下,通过中枢给予ANG II所产生的增强的NaCl摄入是由脑内AT1受体介导的。