Magrani Janeide, de Castro e Silva Emilio, Varjão Bruno, Duarte Gleison, Ramos Ana Claudia, Athanazio Rodrigo, Barbetta Marcelo, Luz Patricia, Fregoneze Josmara B
Department of Physiology, Health Sciences Institute, Federal University of Bahia, 40110-100 Salvador-Bahia, Brazil.
Pharmacol Biochem Behav. 2004 Sep;79(1):189-98. doi: 10.1016/j.pbb.2004.07.004.
The aim of the present study was to investigate the effect of the pharmacological blockade of histamine H1 and H2 receptors located within the ventromedial hypothalamus (VMH) on overnight food and water intake and on water intake elicited by two physiological stimuli: hyperosmolarity induced by an acute intragastric salt load and water deprivation. During the overnight period, the pharmacological blockade of both H1 and H2 VMH receptors significantly increased food intake and decreased water intake. In hyperosmotic rats, the blockade of H1 VMH receptors reduced water intake, while the blockade of H2 receptors in this same region yielded no significant effect. Additionally, in water-deprived rats, the blockade of both H1 and H2 receptors located within the VMH induced a significant decrease in water intake. The inhibitory effects on drinking behavior observed in this study do not seem to be a consequence of any "illness-inducing" effect provoked by the central administration of the antihistaminergic agents employed here, because an aversion test indicated that the injection of those compounds into the VMH does not induce any "illness-like" effect. In addition, the central administration of either mepyramine or cimetidine to dehydrated and hyperosmotic rats did not produce any reduction in locomotor activity measured in an open-field arena. Injections of the antihistaminergic agents used here into the regions that circumscribe the VMH produced no significant effects on water or food intake, indicating that the actions observed here may be specifically attributed to the set of histaminergic receptors situated within the VMH.
本研究的目的是探讨对位于腹内侧下丘脑(VMH)的组胺H1和H2受体进行药理阻断,对夜间食物和水摄入量以及由两种生理刺激引发的水摄入量的影响:急性胃内盐负荷诱导的高渗和缺水。在夜间,对VMH的H1和H2受体进行药理阻断均显著增加食物摄入量并减少水摄入量。在高渗大鼠中,阻断VMH的H1受体可减少水摄入量,而在同一区域阻断H2受体则无显著影响。此外,在缺水大鼠中,阻断VMH内的H1和H2受体均导致水摄入量显著减少。本研究中观察到的对饮水行为的抑制作用似乎不是此处使用的抗组胺能药物中枢给药所引发的任何“致病”作用的结果,因为厌恶试验表明将这些化合物注射到VMH中不会诱导任何“疾病样”作用。此外,向脱水和高渗大鼠中枢给药美吡拉敏或西咪替丁,在旷场试验中测量的运动活动没有任何降低。将此处使用的抗组胺能药物注射到VMH周围区域对水或食物摄入量没有显著影响,表明此处观察到的作用可能具体归因于位于VMH内的一组组胺能受体。