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姜黄素通过抑制水通道蛋白4(AQP4)和p38丝裂原活化蛋白激酶(p38 MAPK)信号通路减轻慢性间歇性缺氧诱导的脑损伤。

Curcumin attenuates chronic intermittent hypoxia-induced brain injuries by inhibiting AQP4 and p38 MAPK pathway.

作者信息

Wang Bo, Li Wenyang, Jin Hongyu, Nie Xinshi, Shen Hui, Li Erran, Wang Wei

机构信息

Institute of Respiratory Diseases, The First Affiliated Hospital of China Medical University, Shenyang, 110001, People's Republic of China.

Institute of Respiratory Diseases, The First Affiliated Hospital of China Medical University, Shenyang, 110001, People's Republic of China.

出版信息

Respir Physiol Neurobiol. 2018 Sep;255:50-57. doi: 10.1016/j.resp.2018.05.006. Epub 2018 May 28.

Abstract

Chronic intermittent hypoxia (CIH) is one of the main features of obstructive sleep apnea (OSA), which is also commonly associated with neurocognitive impairments. The present study aimed to elucidate the beneficial effect of curcumin on CIH-induced brain injuries. Male balb/c mice (6 ∼ 8 weeks) were exposed to normoxia or a pattern of CIH (8 h/day, cycles of 180 s each, hypoxia: 5% O for 50 s, reoxygenation: 21% O for 50 s) for 10 weeks, along with daily curcumin treatment (50, 100, or 200 mg/kg, intragastrically) or its vehicle. The results showed that CIH induced significant brain edema, as well as neuronal apoptosis and astrogliosis in the cerebral cortex, brainstem, and cerebellum regions of brain. In addition, increased astrocytic AQP4 expression and activation of p38 MAPK pathway were observed after CIH exposure. Curcumin dose-dependently mitigated the brain edema and relevant cell alterations, showing a neuroprotective effect in CIH-induced brain injury. Together, these results suggest curcumin ameliorates the CIH-induced brain injuries, including brain edema, neuronal death and astrogliosis. The beneficial role of curcumin is mediated partially by regulating AQP4 and p38 MAPK pathway.

摘要

慢性间歇性缺氧(CIH)是阻塞性睡眠呼吸暂停(OSA)的主要特征之一,OSA通常也与神经认知障碍有关。本研究旨在阐明姜黄素对CIH诱导的脑损伤的有益作用。将雄性balb/c小鼠(6至8周)暴露于常氧环境或CIH模式(每天8小时,每个周期180秒,低氧:5%氧气持续50秒,复氧:21%氧气持续50秒)10周,同时每日进行姜黄素治疗(50、100或200毫克/千克,灌胃)或给予其溶媒。结果显示,CIH诱导了明显的脑水肿,以及大脑皮层、脑干和小脑区域的神经元凋亡和星形胶质细胞增生。此外,CIH暴露后观察到星形胶质细胞AQP4表达增加和p38丝裂原活化蛋白激酶(MAPK)途径激活。姜黄素剂量依赖性地减轻了脑水肿和相关细胞改变,在CIH诱导的脑损伤中显示出神经保护作用。总之,这些结果表明姜黄素可改善CIH诱导的脑损伤,包括脑水肿、神经元死亡和星形胶质细胞增生。姜黄素的有益作用部分是通过调节AQP4和p38 MAPK途径介导的。

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