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星形胶质细胞调节剂阿润地酸对严重缺氧时脑和呼吸功能的影响。

Effects of arundic acid, an astrocytic modulator, on the cerebral and respiratory functions in severe hypoxia.

作者信息

Fukushi Isato, Takeda Kotaro, Yokota Shigefumi, Hasebe Yohei, Sato Yutaka, Pokorski Mieczyslaw, Horiuchi Jouji, Okada Yasumasa

机构信息

Department of Biomedical Engineering, Graduate School of Science and Engineering, Toyo University, 2100 Kujirai, Kawagoe, Saitama 350-8585, Japan; Clinical Research Center, Murayama Medical Center, 2-37-1 Gakuen, Musashimurayama, Tokyo 208-0011, Japan.

Clinical Research Center, Murayama Medical Center, 2-37-1 Gakuen, Musashimurayama, Tokyo 208-0011, Japan; Fujita Memorial Nanakuri Institute, Fujita Health University, 423 Oodori-cho, Tsu, Mie 514-1296, Japan.

出版信息

Respir Physiol Neurobiol. 2016 Jun;226:24-9. doi: 10.1016/j.resp.2015.11.011. Epub 2015 Nov 22.

Abstract

Mild hypoxia increases ventilation, but severe hypoxia depresses it. The mechanism of hypoxic ventilatory depression, in particular, the functional role of the cerebrum, is not fully understood. Recent progress in glial physiology has provided evidence that astrocytes play active roles in information processing in various brain functions. We investigated the hypothesis that astrocytic activation is necessary to maintain the cerebral function and ventilation in hypoxia, by examining the responses of EEG and ventilation to severe hypoxia before and after administration of a modulator of astrocytic function, arundic acid, in unanesthetized mice. Ventilatory parameters were measured by whole body plethysmography. When hypoxic ventilatory depression occurred, gamma frequency band of EEG was suppressed. Arundic acid further suppressed ventilation, and the EEG power was suppressed in a dose-dependent manner. Arundic acid also suppressed hypoxia-induced c-Fos expression in the hypothalamus. We conclude that severe hypoxia suppresses the cerebral function which could reduce the stimulus to the brainstem resulting in ventilatory depression. Astrocytic activation in hypoxia may counteract both cerebral and ventilatory suppression.

摘要

轻度缺氧会增加通气量,但重度缺氧会抑制通气。尤其是缺氧性通气抑制的机制,特别是大脑的功能作用,尚未完全明确。神经胶质生理学的最新进展提供了证据,表明星形胶质细胞在各种脑功能的信息处理中发挥着积极作用。我们研究了这样一个假说:通过在未麻醉小鼠中,在给予星形胶质细胞功能调节剂阿仑酸前后,检测脑电图(EEG)和通气对重度缺氧的反应,来验证星形胶质细胞激活对于在缺氧状态下维持脑功能和通气是必要的。通气参数通过全身体积描记法进行测量。当出现缺氧性通气抑制时,脑电图的γ频段受到抑制。阿仑酸进一步抑制通气,并且脑电图功率以剂量依赖的方式受到抑制。阿仑酸还抑制了下丘脑缺氧诱导的c-Fos表达。我们得出结论,重度缺氧会抑制脑功能,这可能会减少对脑干的刺激,从而导致通气抑制。缺氧时星形胶质细胞的激活可能会抵消脑和通气的抑制作用。

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