Cheng Juan, Wu Fang, Zhang Mingrui, Ding Ding, Fan Sumei, Chen Guihai, Zhang Jin, Wang Liecheng
Department of Physiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, China.
Teaching and Research Office of Physiology, School of Basic Medical Sciences, Anhui Medical College, Hefei, China.
Front Neurosci. 2020 Dec 14;14:615854. doi: 10.3389/fnins.2020.615854. eCollection 2020.
The ventrolateral preoptic nucleus (VLPO) in the anterior hypothalamus and the tuberomammillary nucleus (TMN) in the posterior hypothalamus are critical regions which involve the regulation of sleep-wakefulness flip-flop in the central nervous system. Most of the VLPO neurons are sleep-promoting neurons, which co-express γ-aminobutyric acid (GABA) and galanin, while TMN neurons express histamine (HA), a key wake-promoting neurotransmitter. Previous studies have shown that the two regions are innervated between each other, but how to regulate the sleep-wake cycle are not yet clear. Here, bicuculline (Bic), a GABA -receptor antagonist, L-glutamate (L-Glu), an excitatory neurotransmitter, and triprolidine (Trip), a HA receptor (HRH) inhibitor, were bilaterally microinjected into TMN or VLPO after surgically implanting the electroencephalogram (EEG) and electromyography (EMG) electrode recording system. Microinjecting L-Glu into VLPO during the night significantly increased the NREM sleep time, and this phenomenon was weakened after selectively blocking GABA receptors with Bic microinjected into TMN. Those results reveal that VLPO neurons activated, which may inhibit TMN neurons inducing sleep via GABA receptors. On the contrary, exciting TMN neurons by L-Glu during the day, the wakefulness time was significantly increased. These phenomena were reversed by blocking HRH with Trip microinjected into VLPO. Those results reveal that TMN neuron activating may manipulate VLPO neurons via HRH, and induce wakefulness. In conclusion, VLPO GABAergic neurons and TMN histaminergic neurons may interact with each other in regulating the sleep-wake cycle.
下丘脑前部的腹外侧视前核(VLPO)和下丘脑后部的结节乳头体核(TMN)是中枢神经系统中涉及调节睡眠-觉醒转换的关键区域。大多数VLPO神经元是促进睡眠的神经元,它们共同表达γ-氨基丁酸(GABA)和甘丙肽,而TMN神经元表达组胺(HA),一种促进觉醒的关键神经递质。先前的研究表明,这两个区域相互支配,但它们如何调节睡眠-觉醒周期尚不清楚。在此,在手术植入脑电图(EEG)和肌电图(EMG)电极记录系统后,将GABA受体拮抗剂荷包牡丹碱(Bic)、兴奋性神经递质L-谷氨酸(L-Glu)和HA受体(HRH)抑制剂曲普利啶(Trip)双侧微量注射到TMN或VLPO中。夜间向VLPO微量注射L-Glu可显著增加非快速眼动睡眠时间,而在向TMN微量注射Bic选择性阻断GABA受体后,这种现象减弱。这些结果表明,VLPO神经元被激活,可能通过GABA受体抑制诱导睡眠的TMN神经元。相反,白天用L-Glu刺激TMN神经元,觉醒时间显著增加。向VLPO微量注射Trip阻断HRH可逆转这些现象。这些结果表明,激活TMN神经元可能通过HRH操纵VLPO神经元并诱导觉醒。总之,VLPO的GABA能神经元和TMN的组胺能神经元可能在调节睡眠-觉醒周期中相互作用。