Hajós M, Siok C J, Hoffmann W E, Li S, Kocsis B
Department of Neuroscience, Pfizer Global Research and Development, Eastern Point Road, Groton, CT 06340, USA.
J Pharmacol Exp Ther. 2008 Jan;324(1):391-8. doi: 10.1124/jpet.107.130070. Epub 2007 Oct 16.
Preclinical findings demonstrate procognitive actions of histamine 3 (H3) receptor antagonists/inverse agonists. Since a prominent role of neuronal network oscillations of the hippocampus, such as theta band oscillation, has been recognized in numerous cognitive functions, in the present study, the potential involvement of H3 receptors in modulation of hippocampal theta activity has been investigated using various recording paradigms. Systemic administration of the selective H3 receptor antagonists/inverse agonists, thioperamide and ciproxifan (0.1 mg/kg to 1 mg/kg i.v.), dose dependently increased hippocampal theta power, similarly to methylphenidate (0.1-1 mg/kg i.v.), in chloral hydrate anesthetized rats. When hippocampal theta oscillation was elicited by electrical brainstem (nucleus pontis oralis) stimulation, ciproxifan (1 mg/kg i.v.) augmented the power of stimulation-induced theta. In contrast, systemic administration of methylphenidate (1 mg/kg i.v.) did not modify elicited theta. To analyze the role of H3 receptors on stage- and behavior-dependent hippocampal theta activity, polysomnographic recordings were carried out together with field potential recordings at the hippocampal fissure in freely moving rats for 8 h during the light phase of the circadian cycle. Systemic administration of ciproxifan (3.0 mg/kg, i.p.) promoted wakefulness with a concomitant reduction in cortical delta power and augmented novelty-induced hippocampal theta activity. These findings provide evidence that H3 receptors play an important role in regulation of hippocampal theta oscillation, representing one of the probable mechanisms involved in histamine-induced modulation of higher brain functions, such as attention and learning.
临床前研究结果表明组胺3(H3)受体拮抗剂/反向激动剂具有促认知作用。由于海马体神经元网络振荡(如θ波段振荡)在众多认知功能中发挥着重要作用,因此在本研究中,使用各种记录范式研究了H3受体在调节海马体θ活动中的潜在作用。在水合氯醛麻醉的大鼠中,选择性H3受体拮抗剂/反向激动剂硫代哌酰胺和西普罗芬(静脉注射0.1mg/kg至1mg/kg)的全身给药剂量依赖性地增加了海马体θ功率,与哌醋甲酯(静脉注射0.1 - 1mg/kg)相似。当通过脑干电刺激(脑桥嘴侧核)诱发海马体θ振荡时,西普罗芬(静脉注射1mg/kg)增强了刺激诱发的θ功率。相比之下,哌醋甲酯(静脉注射1mg/kg)的全身给药并未改变诱发的θ。为了分析H3受体在依赖阶段和行为的海马体θ活动中的作用,在昼夜节律周期的光照阶段,对自由活动的大鼠进行了8小时的多导睡眠图记录,并在海马裂处进行场电位记录。西普罗芬(腹腔注射3.0mg/kg)的全身给药促进了清醒,同时皮质δ功率降低,并增强了新奇诱导的海马体θ活动。这些发现提供了证据,表明H3受体在调节海马体θ振荡中起重要作用,这是组胺诱导的高级脑功能(如注意力和学习)调节所涉及的可能机制之一。