Laboratory of Pathophysiology, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, 812-8582, Japan.
Division of Integrative Physiology, Department of Physiology, Jichi Medical University School of Medicine, 3311-1 Yakushiji, Shimotsuke, Tochigi, 329-0498, Japan.
Neurochem Res. 2017 Sep;42(9):2658-2665. doi: 10.1007/s11064-017-2281-1. Epub 2017 May 2.
Molecular hydrogen (H), as a new medical gas, has protective effects in neurological disorders including Parkinson's disease (PD). In our previous report, the neuroprotective effect of drinking water with saturated H (H water) in PD mice might be due to stomach-brain interaction via release of gastric hormone, ghrelin. In the present study, we assessed the effect of H-induced ghrelin more precisely. To confirm the contribution of ghrelin in H water-drinking PD model mice, ghrelin-knock out (KO) mice were used. Despite the speculation, the effect of H water was still observed in ghrelin-KO PD model mice. To further check the involvement of ghrelin, possible contribution of ghrelin-induced vagal afferent effect was tested by performing subdiaphragmatic vagotomy before treating with H water and administration of MPTP (1-methyl- 4-phenyl-1,2,3,6-tetrahydropyridine). The protective effect of H water was still observed in the vagotomized mice in substantia nigra, suggesting that stimulation of vagal afferent nerves is not involved in H-induced neuroprotection. Other neuroprotective substitutes in ghrelin-KO mice were speculated because H-induced neuroprotection was not cancelled by ghrelin receptor antagonist, D-Lys GHRP-6, in ghrelin-KO PD model mice, unlike in wild-type PD model mice. Our results indicate that ghrelin may not be the only factor for H-induced neuroprotection and other factors can substitute the role of ghrelin when ghrelin is absent, raising intriguing options of research for H-responsive factors.
氢气(H)作为一种新型医学气体,在包括帕金森病(PD)在内的神经紊乱中有保护作用。在我们之前的报告中,PD 小鼠饮用饱和 H(H 水)的神经保护作用可能是通过释放胃激素——ghrelin 实现的胃-脑相互作用。在本研究中,我们更精确地评估了 H 诱导的 ghrelin 的作用。为了确认 ghrelin 在 H 水饮用 PD 模型小鼠中的作用,使用了 ghrelin 敲除(KO)小鼠。尽管有这种猜测,但在 ghrelin-KO PD 模型小鼠中仍然观察到了 H 水的作用。为了进一步检查 ghrelin 的参与情况,通过在给予 H 水和 MPTP(1-甲基-4-苯基-1,2,3,6-四氢吡啶)之前进行膈下迷走神经切断术,测试了 ghrelin 诱导的迷走传入效应的可能贡献。在迷走神经切断的小鼠中仍然观察到 H 水在黑质中的保护作用,这表明刺激迷走传入神经不参与 H 诱导的神经保护。在 ghrelin-KO PD 模型小鼠中,ghrelin 受体拮抗剂 D-Lys GHRP-6 并没有取消 H 水的神经保护作用,这表明 ghrelin-KO 小鼠中存在其他神经保护替代物,而在野生型 PD 模型小鼠中则不是这样。我们的结果表明,ghrelin 可能不是 H 诱导神经保护的唯一因素,当 ghrelin 缺失时,其他因素可以替代 ghrelin 的作用,这为 H 反应性因素的研究提供了有趣的选择。