Yamaguchi Keiji, Futatsuki Takahiro, Ushikai Jumpei, Kuroki Chiharu, Minami Toshiaki, Kakihana Yasuyuki, Kuwaki Tomoyuki
Department of Physiology, Kagoshima University Graduate School of Medical and Dental Sciences, Sakuragaoka 8-35-1, Kagoshima 890-8544, Japan; Department of Emergency and Intensive Care Medicine, Kagoshima University Graduate School of Medical and Dental Sciences, Sakuragaoka 8-35-1, Kagoshima 890-8544, Japan; Department of Anesthesiology, Osaka Medical College, 2-7 Daigakumachi, Takatsuki 569-8686, Japan.
Department of Physiology, Kagoshima University Graduate School of Medical and Dental Sciences, Sakuragaoka 8-35-1, Kagoshima 890-8544, Japan; Department of Emergency and Intensive Care Medicine, Kagoshima University Graduate School of Medical and Dental Sciences, Sakuragaoka 8-35-1, Kagoshima 890-8544, Japan.
Respir Physiol Neurobiol. 2015 Jan 15;206:11-4. doi: 10.1016/j.resp.2014.11.003. Epub 2014 Nov 11.
Hypothalamic orexin-containing neurons are activated by CO2 and contribute to hypercapnic ventilatory activation. However, their role in oxygen-related regulation of breathing is not well defined. In this study, we examined whether an experimental model mimicking apnea-induced repetitive hypoxemia (intermittent hypoxia [IH]) activates orexin-containing neurons. Mice were exposed to IH (5×5min at 10% O2), intermittent hyperoxia (IO; 5×5min at 50% O2), sustained hypoxia (SH; 25min at 10% O2), or sham stimulation. Their brains were examined using double immunohistochemical staining for orexin and c-Fos. The results indicated that IH (25.8±3.0%), but not SH (9.0±1.5%) activated orexin-containing neurons when compared to IO (5.5±0.6%) and sham stimulation (5.9±1.4%). These results correlate with those of our previous work showing that IH-induced respiratory long-term facilitation is dependent on orexin-containing neurons. Taken together, orexin contributes to repetitive hypoxia-induced respiratory activation and the hypoxic activation of orexin-containing neurons is pattern dependent.
下丘脑含食欲素神经元被二氧化碳激活,并参与高碳酸血症通气激活。然而,它们在与氧气相关的呼吸调节中的作用尚未明确界定。在本研究中,我们研究了一种模拟呼吸暂停诱导的重复性低氧血症(间歇性低氧[IH])的实验模型是否会激活含食欲素神经元。将小鼠暴露于间歇性低氧(10%氧气下5×5分钟)、间歇性高氧(50%氧气下5×5分钟)、持续性低氧(10%氧气下25分钟)或假刺激。使用食欲素和c-Fos的双重免疫组织化学染色检查它们的大脑。结果表明,与间歇性高氧(5.5±0.6%)和假刺激(5.9±1.4%)相比,间歇性低氧(25.8±3.0%)而非持续性低氧(9.0±1.5%)激活了含食欲素神经元。这些结果与我们之前的研究结果相关,即间歇性低氧诱导的呼吸长期易化依赖于含食欲素神经元。综上所述,食欲素参与重复性低氧诱导的呼吸激活,且含食欲素神经元的低氧激活具有模式依赖性。