Brain Cognition and Brain Disease Institute, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences (CAS).
CAS Key Laboratory of Brain Connectome and Manipulation.
J Clin Invest. 2020 Dec 1;130(12):6539-6554. doi: 10.1172/JCI136105.
Homeostasis of bone metabolism is regulated by the central nervous system, and mood disorders such as anxiety are associated with bone metabolism abnormalities, yet our understanding of the central neural circuits regulating bone metabolism is limited. Here, we demonstrate that chronic stress in crewmembers resulted in decreased bone density and elevated anxiety in an isolated habitat mimicking a space station. We then used a mouse model to demonstrate that GABAergic neural circuitry in the ventromedial hypothalamus (VMH) mediates chronic stress-induced bone loss. We show that GABAergic inputs in the dorsomedial VMH arise from a specific group of somatostatin neurons in the posterior region of the bed nucleus of the stria terminalis, which is indispensable for stress-induced bone loss and is able to trigger bone loss in the absence of stressors. In addition, the sympathetic system and glutamatergic neurons in the nucleus tractus solitarius were employed to regulate stress-induced bone loss. Our study has therefore identified the central neural mechanism by which chronic stress-induced mood disorders, such as anxiety, influence bone metabolism.
骨代谢的稳态由中枢神经系统调节,而焦虑等情绪障碍与骨代谢异常有关,但我们对调节骨代谢的中枢神经回路的了解有限。在这里,我们证明了在模拟空间站的隔离环境中,船员的慢性应激导致骨密度降低和焦虑增加。然后,我们使用小鼠模型证明了腹内侧下丘脑(VMH)中的 GABA 能神经回路介导了慢性应激引起的骨丢失。我们表明,背内侧 VMH 中的 GABA 能传入来自终纹床核后区的特定生长抑素神经元群,这对于应激引起的骨丢失是必不可少的,并且能够在没有应激源的情况下引发骨丢失。此外,孤束核中的交感神经系统和谷氨酸能神经元被用来调节应激引起的骨丢失。因此,我们的研究确定了中枢神经机制,即慢性应激引起的情绪障碍(如焦虑)如何影响骨代谢。