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Metformin administration prevents memory impairment induced by hypobaric hypoxia in rats

机译:二甲双胍给药可防止大鼠缺氧诱导的记忆障碍

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Metformin, an antidiabetic biguanide, reduces hyperglycemia by improving glucose utilization and reducing gluconeogenesis. Recently, an increasing number of studies have shown that metformin also led to a significant clinical improvement in memory and cognition in different clinical settings. In the present study, we investigated whether metformin administration protects against memory impairment and neuron damage caused by acute exposure to hypobaric hypoxia and screened the possible molecular mechanisms with a focused gene array. We found that metformin treatment obviously attenuated spatial memory and recognition memory impairment resulting from acute hypobaric hypoxia exposure but had no effect on general locomotor and behavioral activity. Moreover, the results of Nissl and TUNEL staining showed that neuron damage and cell apoptosis caused by hypobaric hypoxia exposure was also inhibited by metformin pretreatment. At the molecular level, we found that metformin pretreatment not only prevented the changes of FOS, JUNB and BDNF at both mRNA and protein levels, but also increased the expression of the postsynaptic scaffold genes HOMER and PSD95 after exposure to hypobaric hypoxia. These data suggested that metformin pretreatment is a feasible strategy for preventing memory impairment under hypobaric hypoxia.
机译:二甲双胍,一个抗糖尿病双胍,通过改善葡萄糖利用率和还原葡糖生成来减少高血糖。最近,越来越多的研究表明,二甲双胍也导致了不同临床环境中的记忆和认知的显着临床改善。在本研究中,我们调查了二甲双胍给药是否可以防止因急性暴露于脓肿缺氧而导致的记忆障碍和神经元损伤,并用聚焦基因阵列筛选可能的分子机制。我们发现二甲双胍治疗明显减弱的空间记忆和识别记忆障碍,由急性缺氧缺氧暴露产生,但对一般运动和行为活动没有影响。此外,Nissl和Turnel染色的结果表明,由二甲双胍预处理抑制了由脓肿缺氧暴露引起的神经元损伤和细胞凋亡。在分子水平,我们发现二甲双胍预处理不仅可以防止FOS,JUNB和BDNF在mRNA和蛋白质水平的变化,而且还增加了暴露于低压缺氧后突触后支架基因HOMER和PSD95的表达。这些数据表明,二甲双胍预处理是一种可行的缺氧下记忆障碍的可行策略。

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