Department of Anesthesiology and Perioperative Medicine, Xijing Hospital, The Fourth Military Medical University, Xi'an, Shaanxi, China.
Key Laboratory of Anesthesiology (The Fourth Military Medical University), Ministry of Education of China, Xi'an, China.
CNS Neurosci Ther. 2024 Sep;30(9):e70047. doi: 10.1111/cns.70047.
The lateral hypothalamus (LHA) is an evolutionarily conserved structure that regulates basic functions of an organism, particularly wakefulness. To clarify the function of LHA neurons and their projections on regulating general anesthesia is crucial for understanding the excitatory and inhibitory effects of anesthetics on the brain. The aim of the present study is to investigate whether LHA neurons play either an inhibitory or a facilitatory role in sevoflurane-induced anesthetic arousal regulation.
We used fiber photometry and immunofluorescence staining to monitor changes in neuronal activity during sevoflurane anesthesia. Opto-/chemogenetic modulations were employed to study the effect of neurocircuit modulations during the anesthesia. Anterograde tracing was used to identify a GABAergic projection from the LHA to a periaqueductal gray (PAG) subregion.
c-Fos staining showed that LHA activity was inhibited by induction of sevoflurane anesthesia. Anterograde tracing revealed that LHA neurons project to multiple arousal-associated brain areas, with the lateral periaqueductal gray (LPAG) being one of the dense projection areas. Optogenetic experiments showed that activation of LHA neurons and their downstream target LPAG reduced the burst suppression ratio (BSR) during continuous sevoflurane anesthesia. Chemogenetic experiments showed that activation of LHA and its projection to LPAG neurons prolonged the anesthetic induction time and promoted wakefulness.
In summary, we show that an inhibitory projection from LHA to LPAG neurons promotes arousal from sevoflurane-induced loss of consciousness, suggesting a complex control of wakefulness through intimate interactions between long-range connections.
外侧下丘脑(LHA)是一个进化上保守的结构,调节着生物体的基本功能,特别是觉醒。阐明 LHA 神经元及其投射在调节全身麻醉中的作用对于理解麻醉剂对大脑的兴奋和抑制作用至关重要。本研究旨在探讨 LHA 神经元在七氟醚诱导的麻醉觉醒调节中是发挥抑制作用还是促进作用。
我们使用光纤光度法和免疫荧光染色来监测七氟醚麻醉期间神经元活动的变化。光遗传学/化学遗传学调制被用来研究麻醉期间神经回路调制的效果。顺行示踪用于鉴定来自 LHA 到中脑导水管周围灰质(PAG)亚区的 GABA 能投射。
c-Fos 染色显示,LHA 活性在七氟醚麻醉诱导时被抑制。顺行示踪显示,LHA 神经元投射到多个觉醒相关的脑区,其中外侧中脑导水管周围灰质(LPAG)是密集投射区之一。光遗传学实验表明,LHA 神经元的激活及其下游靶点 LPAG 的激活降低了连续七氟醚麻醉期间的爆发抑制比(BSR)。化学遗传学实验表明,LHA 的激活及其对 LPAG 神经元的投射延长了麻醉诱导时间并促进了觉醒。
总之,我们表明,来自 LHA 到 LPAG 神经元的抑制性投射促进了七氟醚诱导的意识丧失后的觉醒,这表明通过长程连接之间的密切相互作用,对觉醒进行了复杂的控制。