Magrani Janeide, de Castro e Silva Emilio, Ramos Ana Claudia, Athanazio Rodrigo, Barbetta Marcelo, Fregoneze Josmara B
Department of Physiology, Health Sciences Institute, Federal University of Bahia, 40110-100 Salvador, Bahia, Brazil.
Physiol Behav. 2005 Feb 15;84(2):233-43. doi: 10.1016/j.physbeh.2004.11.010. Epub 2005 Jan 25.
The aim of the present study was to evaluate the participation of brain H1 and H2 histaminergic receptors on water and salt intake induced by water deprivation (24 h), furosemide-induced sodium depletion and central angiotensinergic pharmacological stimulation in rats. Third ventricle injections of the H1 and H2 receptor antagonists, mepyramine (50, 100, 200 and 400 nmol) and cimetidine (100, 200 and 400 nmol), were unable to modify water intake induced by water deprivation and sodium depletion. Salt intake elicited by water deprivation and sodium depletion was reduced by the central administration of mepyramine, while intracerebroventricular administration of cimetidine had no effect. Water and salt intake evoked by central angiotensinergic stimulation (10 ng) was diminished by third ventricle injections of both mepyramine and cimetidine. Inhibition of the ingestive behaviors observed here is not a result of any illness-like effect produced by the intracerebroventricular injections of the histaminergic antagonists used, as demonstrated by an avoidance test. It was also shown that third ventricle injections of these compounds were unable to modify the hedonic behavior that leads rats to drink a tasty saccharin solution. We conclude that central histaminergic receptors participate in the control of salt intake induced by distinct physiological and pharmacological stimuli.
本研究的目的是评估脑内H1和H2组胺能受体在大鼠因禁水(24小时)、速尿诱导的钠缺乏以及中枢血管紧张素能药理刺激所引起的水和盐摄入过程中的作用。向第三脑室注射H1和H2受体拮抗剂,即美吡拉敏(50、100、200和400纳摩尔)和西咪替丁(100、200和400纳摩尔),无法改变因禁水和钠缺乏所引起的水摄入。美吡拉敏中枢给药可减少因禁水和钠缺乏所引起的盐摄入,而脑室内注射西咪替丁则无此作用。第三脑室注射美吡拉敏和西咪替丁均可减少中枢血管紧张素能刺激(10纳克)所引起的水和盐摄入。如回避试验所示,此处观察到的摄食行为抑制并非是由脑室内注射所用组胺能拮抗剂产生的任何类似疾病的效应所致。研究还表明,第三脑室注射这些化合物无法改变使大鼠饮用美味糖精溶液的享乐行为。我们得出结论,中枢组胺能受体参与了由不同生理和药理刺激所诱导的盐摄入控制。