He Chao, Luo Fenlan, Chen Xingshu, Chen Fang, Li Chao, Ren Shuancheng, Qiao Qicheng, Zhang Jun, de Lecea Luis, Gao Dong, Hu Zhian
Department of Physiology, Institute of Surgery Research, Daping Hospital, Third Military Medical University, Chongqing 400042, PR China.
Department of Histology and Embryology, Institute of Surgery Research, Daping Hospital, Third Military Medical University, Chongqing 400042, PR China.
Cereb Cortex. 2016 Apr;26(4):1590-1608. doi: 10.1093/cercor/bhu322. Epub 2015 Jan 16.
The medial entorhinal cortex (MEC) plays a crucial role in spatial learning and memory. Whereas the MEC receives a dense histaminergic innervation from the tuberomamillary nucleus of the hypothalamus, the functions of histamine in this brain region remain unclear. Here, we show that histamine acts via H1Rs to directly depolarize the principal neurons in the superficial, but not deep, layers of the MEC when recording at somata. Moreover, histamine decreases the spontaneous GABA, but not glutamate, release onto principal neurons in the superficial layers by acting at presynaptic H3Rs without effect on synaptic release in the deep layers. Histamine-induced depolarization is mediated via inhibition of Kir channels and requires the activation of protein kinase C, whereas the inhibition of spontaneous GABA release by histamine depends on voltage-gated Ca(2+) channels and extracellular Ca(2+). Furthermore, microinjection of the H1R or H3R, but not H2R, antagonist respectively into the superficial, but not deep, layers of MEC impairs rat spatial learning as assessed by water maze tasks but does not affect the motor function and exploratory activity in an open field. Together, our study indicates that histamine plays an essential role in spatial learning by selectively regulating neuronal excitability and synaptic transmission in the superficial layers of the MEC.
内侧内嗅皮质(MEC)在空间学习和记忆中起着至关重要的作用。虽然MEC接受来自下丘脑结节乳头核的密集组胺能神经支配,但组胺在该脑区的功能仍不清楚。在此,我们表明,在胞体记录时,组胺通过H1受体直接使MEC浅层而非深层的主要神经元去极化。此外,组胺通过作用于突触前H3受体减少浅层主要神经元上的自发性GABA释放,但不影响谷氨酸释放,对深层的突触释放也无影响。组胺诱导的去极化是通过抑制Kir通道介导的,并且需要蛋白激酶C的激活,而组胺对自发性GABA释放的抑制取决于电压门控Ca(2+)通道和细胞外Ca(2+)。此外,分别向MEC浅层而非深层微量注射H1R或H3R拮抗剂(而非H2R拮抗剂)会损害大鼠的空间学习能力,这通过水迷宫任务评估得出,但不影响旷场中的运动功能和探索活动。总之,我们的研究表明,组胺通过选择性调节MEC浅层的神经元兴奋性和突触传递在空间学习中起着重要作用。