Imai Junta
Department of Metabolism and Diabetes, Tohoku University Graduate School of Medicine.
Endocr J. 2018 Jul 28;65(7):677-684. doi: 10.1507/endocrj.EJ18-0241. Epub 2018 Jul 3.
In insulin-resistant states such as obesity, pancreatic β-cells proliferate to prevent blood glucose elevations. However, the mechanism(s) by which obesity induces compensatory β-cell responses is not fully understood. Recently, several studies have shown that signals from the liver, such as neuronal signals or humoral factors, regulate β-cell proliferation during obesity development. We previously reported a liver-brain-pancreas neuronal relay, consisting of afferent splanchnic nerves, the central nervous system and efferent vagal nerves, to promote this compensatory β-cell proliferation. Furthermore, we recently clarified the molecular mechanisms by which efferent vagal signals induce β-cell proliferation in this inter-organ neuronal network system. Herein, these liver-β-cell inter-organ networks are reviewed, focusing mainly on the neuronal network. The significance of the neuronal network system in the maintenance of glucose homeostasis is also discussed with reference to the relevant literature.
在肥胖等胰岛素抵抗状态下,胰腺β细胞会增殖以防止血糖升高。然而,肥胖诱导代偿性β细胞反应的机制尚未完全阐明。最近,多项研究表明,来自肝脏的信号,如神经信号或体液因子,在肥胖发展过程中调节β细胞增殖。我们之前报道了一种肝-脑-胰腺神经中继,由内脏传入神经、中枢神经系统和迷走神经传出神经组成,以促进这种代偿性β细胞增殖。此外,我们最近阐明了在这个器官间神经元网络系统中,迷走神经传出信号诱导β细胞增殖的分子机制。本文对这些肝脏-β细胞器官间网络进行综述,主要聚焦于神经元网络。还参考相关文献讨论了神经元网络系统在维持葡萄糖稳态中的意义。