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前庭核复合体中表达 VGLUT2 的神经元介导小鼠重力应激诱导的体温降低。

VGLUT2-expressing neurons in the vestibular nuclear complex mediate gravitational stress-induced hypothermia in mice.

机构信息

Department of Physiology, Gifu University Graduate School of Medicine, Gifu, Japan.

Department of Anatomy and Neuroscience, Shimane University School of Medicine, Izumo, Shimane, Japan.

出版信息

Commun Biol. 2020 May 8;3(1):227. doi: 10.1038/s42003-020-0950-0.

Abstract

The vestibular system, which is essential for maintaining balance, contributes to the sympathetic response. Although this response is involved in hypergravity load-induced hypothermia in mice, the underlying mechanism remains unknown. This study showed that hypergravity (2g) decreased plasma catecholamines, which resulted in hypoactivity of the interscapular brown adipose tissue (iBAT). Hypothermia induced by 2g load was significantly suppressed by administration of beta-adrenergic receptor agonists, suggesting the involvement of decrease in iBAT activity through sympathoinhibition. Bilateral chemogenetic activation of vesicular glutamate transporter 2 (VGLUT2)-expressing neurons in the vestibular nuclear complex (VNC) induced hypothermia. The VGLUT2-expressing neurons contributed to 2g load-induced hypothermia, since their deletion suppressed hypothermia. Although activation of vesicular gamma-aminobutyric acid transporter-expressing neurons in the VNC induced slight hypothermia instead of hyperthermia, their deletion did not affect 2g load-induced hypothermia. Thus, we concluded that 2g load-induced hypothermia resulted from sympathoinhibition via the activation of VGLUT2-expressing neurons in the VNC.

摘要

前庭系统对于维持平衡至关重要,它有助于交感神经反应。尽管这种反应涉及小鼠超重力负荷诱导的体温过低,但潜在的机制尚不清楚。本研究表明,超重力(2g)降低了血浆儿茶酚胺,导致肩胛间棕色脂肪组织(iBAT)活性降低。通过β-肾上腺素能受体激动剂给药,显著抑制了 2g 负荷诱导的体温过低,这表明通过交感神经抑制导致 iBAT 活性降低。在前庭核复合体(VNC)中表达囊泡谷氨酸转运体 2(VGLUT2)的神经元的双侧化学遗传激活诱导体温过低。VGLUT2 表达神经元有助于 2g 负荷诱导的体温过低,因为它们的缺失抑制了体温过低。尽管 VNC 中表达囊泡γ-氨基丁酸转运体的神经元的激活导致轻微的体温过低而不是体温过高,但它们的缺失并不影响 2g 负荷诱导的体温过低。因此,我们得出结论,2g 负荷诱导的体温过低是由于 VNC 中表达 VGLUT2 的神经元的激活引起的交感神经抑制所致。

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