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下丘脑腹内侧的Galnt2神经元通过脑-肝神经回路对低血糖进行反调节
作者:小柯机器人 发布时间:2025/10/15 14:34:31

近日,中国药科大学谢昊及其研究组开发出了下丘脑腹内侧的Galnt2神经元通过脑-肝神经回路对低血糖进行反调节。2025年10月14日,国际知名学术期刊《细胞—代谢》发表了这一成果。

研究组确定了长时间禁食期间血液和下丘脑葡萄糖动力学的双相模式,揭示了一个额外的阈值依赖机制。该机制由下丘脑腹内侧核(VMH)→室旁核(PVH)→外侧副巨细胞核(LPGi)→肝神经回路介导,该神经回路检测神经性糖减少并通过肝内交感神经激活传递神经信号以驱动肝糖产生。通过病毒追踪、单核RNA测序和各种无偏方法,该团队发现Galnt2既是VMH葡萄糖抑制神经元的遗传标记和分子刹车,调节低血糖感知和代谢稳态的血糖阈值。他们的研究结果强调了VMHGalnt2起源的脑-肝神经回路可以感知和反调节低血糖,并可能为针对以葡萄糖失调为特征的代谢紊乱的创新治疗策略铺平道路。

据了解,大脑严重依赖葡萄糖作为能量来源,它们对低血糖的反调节反应与葡萄糖的产生有关,这是基本的。

附:英文原文

Title: Galnt2 neurons in the ventromedial hypothalamus counterregulate hypoglycemia via a brain-liver neurocircuit

Author: Junjie Wang, Xinyuan Sun, Xiangfei Gong, Wenling Dai, Hao Hong, Li Jiang, Zhonglong Wang, Zhiyuan Tang, Xiaobo Wu, Peng Sun, Yongjie Zhang, Kun Hao, Fang Zhou, Ying Cui, Tianyu Tang, Xiao Zheng, Lanqun Mao, Guangji Wang, Haiping Hao, Hao Xie

Issue&Volume: 2025-10-14

Abstract: The brain relies heavily on glucose for energy resources, and thus prompt counterregulatory responses to hypoglycemia in connection with glucose production are fundamental. We identified a biphasic pattern in blood and hypothalamic glucose dynamics during prolonged fasting, revealing an additional threshold-dependent mechanism for counterregulation. This mechanism is mediated by a ventromedial hypothalamus (VMH)→paraventricular hypothalamic nucleus (PVH)→lateral paragigantocellular nucleus (LPGi)→liver neurocircuit that detects neuroglycopenia and transmits neural signals to drive hepatic glucose production via intrahepatic sympathetic activation. Using viral tracing, single-nucleus RNA sequencing, and various unbiased methods, we identified Galnt2 as both a genetic marker and molecular brake of VMH glucose-inhibited neurons, modulating the glycemic threshold for hypoglycemia perception and metabolic homeostasis. Our results highlight a VMHGalnt2-originated brain-liver neurocircuit that perceives and counterregulates hypoglycemia and may pave the way to innovative therapeutic strategies against metabolic disorders characterized by glucose dysregulation.

DOI: 10.1016/j.cmet.2025.09.006

Source: https://www.cell.com/cell-metabolism/abstract/S1550-4131(25)00391-2

期刊信息

Cell Metabolism:《细胞—代谢》,创刊于2005年。隶属于细胞出版社,最新IF:31.373
官方网址:https://www.cell.com/cell-metabolism/home
投稿链接:https://www.editorialmanager.com/cell-metabolism/default.aspx