Neuronal Oscillations Laboratory, Department of Neuroscience, Karolinska Institute, SE-17177 Stockholm, Sweden.
J Physiol. 2010 Apr 15;588(Pt 8):1241-9. doi: 10.1113/jphysiol.2009.180984. Epub 2010 Feb 15.
The study of rhythmic electrical activity in slice preparations has generated important insights into neural network function. While the synaptic mechanisms involved in the generation of in vitro network oscillations have been studied widely, little is known about the modulatory influence exerted on rhythmic activity in neuronal networks by neuropeptides and biogenic amines. Gamma oscillations play an important role in cognitive processes and are altered or disrupted in disorders such as Alzheimer's disease (AD) and schizophrenia. Given the importance of gamma oscillations for learning, memory and cognition processes as well as the recent interest in histamine H(3) receptors in the development of pro-cognitive drugs to treat disorders such as AD and schizophrenia, it is relevant to study the impact of histaminergic mechanisms on network gamma oscillations. Here we show for the first time a modulation of gamma oscillation by histaminergic mechanisms. Selective activation of the H(3) receptor by R-alpha-methylhistamine significantly reduces the power of kainate-induced gamma oscillations, but not carbachol-induced gamma oscillations, in the rat hippocampal slice preparation without affecting oscillation frequency. This effect is neither caused by a decrease in excitatory or inhibitory postsynaptic currents, nor a decrease in cellular excitability. Instead, we find that the decrease in oscillation power following H(3) receptor activation results from a desynchronization of pyramidal neuron action potential firing with regard to the local field potential oscillation cycle. Our data provide a possible mechanism of action for histamine in regulating gamma oscillations in the hippocampal network.
在切片制剂中研究节律性电活动为神经网络功能提供了重要的见解。虽然已经广泛研究了体外网络振荡产生中涉及的突触机制,但对于神经肽和生物胺对神经元网络节律性活动的调制影响知之甚少。γ 振荡在认知过程中起着重要作用,并且在阿尔茨海默病(AD)和精神分裂症等疾病中发生改变或中断。鉴于 γ 振荡对学习、记忆和认知过程的重要性,以及组胺 H(3)受体在开发治疗 AD 和精神分裂症等疾病的认知增强药物方面的最新兴趣,研究组胺能机制对网络 γ 振荡的影响是相关的。在这里,我们首次展示了组胺能机制对 γ 振荡的调制。通过 R-α-甲基组胺选择性激活 H(3)受体,可显著降低大鼠海马切片制剂中由海人藻酸诱导的 γ 振荡的功率,但不影响由卡巴胆碱诱导的 γ 振荡的功率,而不影响振荡频率。这种作用既不是由兴奋性或抑制性突触后电流减少引起的,也不是由细胞兴奋性降低引起的。相反,我们发现,H(3)受体激活后,振荡功率降低是由于锥体神经元动作电位放电相对于局部场电位振荡周期的去同步化。我们的数据为组胺在调节海马网络中的 γ 振荡提供了一种可能的作用机制。