Zhao Ming, Huang Xin, Cheng Xiang, Lin Xiao, Zhao Tong, Wu Liying, Yu Xiaodan, Wu Kuiwu, Fan Ming, Zhu Lingling
Department of Cognitive Science, Beijing Institute of Basic Medical Sciences, Beijing, P.R.China.
Co-innovation Center of Neuroregeneration, Nantong University, Nantong, JS, China.
PLoS One. 2017 Mar 29;12(3):e0174477. doi: 10.1371/journal.pone.0174477. eCollection 2017.
Exposure to hypobaric hypoxia causes neuron cell damage, resulting in impaired cognitive function. Effective interventions to antagonize hypobaric hypoxia-induced memory impairment are in urgent need. Ketogenic diet (KD) has been successfully used to treat drug-resistant epilepsy and improves cognitive behaviors in epilepsy patients and other pathophysiological animal models. In the present study, we aimed to explore the potential beneficial effects of a KD on memory impairment caused by hypobaric hypoxia and the underlying possible mechanisms. We showed that the KD recipe used was ketogenic and increased plasma levels of ketone bodies, especially β-hydroxybutyrate. The results of the behavior tests showed that the KD did not affect general locomotor activity but obviously promoted spatial learning. Moreover, the KD significantly improved the spatial memory impairment caused by hypobaric hypoxia (simulated altitude of 6000 m, 24 h). In addition, the improving-effect of KD was mimicked by intraperitoneal injection of BHB. The western blot and immunohistochemistry results showed that KD treatment not only increased the acetylated levels of histone H3 and histone H4 compared to that of the control group but also antagonized the decrease in the acetylated histone H3 and H4 when exposed to hypobaric hypoxia. Furthermore, KD-hypoxia treatment also promoted PKA/CREB activation and BDNF protein expression compared to the effects of hypoxia alone. These results demonstrated that KD is a promising strategy to improve spatial memory impairment caused by hypobaric hypoxia, in which increased modification of histone acetylation plays an important role.
暴露于低压低氧环境会导致神经元细胞损伤,进而造成认知功能受损。迫切需要有效的干预措施来对抗低压低氧诱导的记忆损伤。生酮饮食(KD)已成功用于治疗耐药性癫痫,并改善癫痫患者及其他病理生理动物模型中的认知行为。在本研究中,我们旨在探讨生酮饮食对低压低氧所致记忆损伤的潜在有益作用及其潜在的可能机制。我们发现所使用的生酮饮食配方具有生酮作用,并提高了血浆酮体水平,尤其是β-羟基丁酸水平。行为测试结果表明,生酮饮食不影响一般运动活动,但明显促进空间学习。此外,生酮饮食显著改善了低压低氧(模拟海拔6000米,24小时)所致的空间记忆损伤。此外,腹腔注射β-羟基丁酸可模拟生酮饮食的改善效果。蛋白质印迹和免疫组织化学结果表明,与生酮饮食对照组相比,生酮饮食治疗不仅增加了组蛋白H3和组蛋白H4的乙酰化水平,而且对抗了暴露于低压低氧时组蛋白H3和H4乙酰化水平的降低。此外,与生酮饮食联合低氧处理相比,单独低氧处理还促进了蛋白激酶A/环磷腺苷效应元件结合蛋白(PKA/CREB)的激活和脑源性神经营养因子(BDNF)蛋白的表达。这些结果表明,生酮饮食是改善低压低氧所致空间记忆损伤的一种有前景的策略,其中组蛋白乙酰化修饰增加起着重要作用。