Department of Physiology and Regenerative Medicine, Kindai University Faculty of Medicine, Osakasayama, Japan.
Life Science Research Institute, Kindai University, Osakasayama, Japan.
PLoS One. 2020 Feb 3;15(2):e0228685. doi: 10.1371/journal.pone.0228685. eCollection 2020.
The vestibular system controls balance, posture, blood pressure, and gaze. However, the roles of the vestibular system in energy and glucose metabolism remain unknown. We herein examined the roles of the vestibular system in obesity and impaired glucose metabolism using mice with vestibular lesions (VL) fed a high-sucrose/high-fat diet (HSHFD). VL was induced by surgery or arsenic. VL significantly suppressed body fat enhanced by HSHFD in mice. Glucose intolerance was improved by VL in mice fed HSHFD. VL blunted the levels of adipogenic factors and pro-inflammatory adipokines elevated by HSHFD in the epididymal white adipose tissue of mice. A β-blocker antagonized body fat and glucose intolerance enhanced by HSHFD in mice. The results of an RNA sequencing analysis showed that HSHFD induced alterations in genes, such as insulin-like growth factor-2 and glial fibrillary acidic protein, in the vestibular nuclei of mice through the vestibular system. In conclusion, we herein demonstrated that the dysregulation of the vestibular system influences an obese state and impaired glucose metabolism induced by HSHFD in mice. The vestibular system may contribute to the regulation of set points under excess energy conditions.
前庭系统控制平衡、姿势、血压和注视。然而,前庭系统在能量和葡萄糖代谢中的作用仍不清楚。我们使用前庭损伤(VL)的小鼠和高蔗糖/高脂肪饮食(HSHFD)来检查前庭系统在肥胖和葡萄糖代谢受损中的作用。VL 通过手术或砷诱导。VL 显著抑制了 HSHFD 增强的小鼠体脂肪。VL 改善了 HSHFD 喂养小鼠的葡萄糖不耐受。VL 减弱了 HSHFD 在小鼠附睾白色脂肪组织中升高的脂肪生成因子和促炎脂肪因子的水平。β-阻断剂拮抗了 HSHFD 增强的小鼠体脂肪和葡萄糖不耐受。RNA 测序分析的结果表明,HSHFD 通过前庭系统诱导了小鼠前庭核中胰岛素样生长因子-2 和神经胶质纤维酸性蛋白等基因的改变。总之,我们证明了前庭系统的失调会影响 HSHFD 诱导的肥胖状态和葡萄糖代谢受损的小鼠。前庭系统可能有助于在能量过剩条件下调节设定点。