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艾地苯醌口服给药可诱导大脑中的神经生长因子,并改善基底前脑损伤大鼠的学习和记忆能力。

Oral administration of idebenone induces nerve growth factor in the brain and improves learning and memory in basal forebrain-lesioned rats.

作者信息

Nitta A, Murakami Y, Furukawa Y, Kawatsura W, Hayashi K, Yamada K, Hasegawa T, Nabeshima T

机构信息

Department of Neuropsychopharmacology and Hospital Pharmacy, Nagoya University School of Medicine, Japan.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1994 Apr;349(4):401-7. doi: 10.1007/BF00170887.

Abstract

Nerve growth factor plays an important role in the survival and maintenance of cholinergic neurons in the central neuronal system. In senile dementia of the Alzheimer type, learning and memory are impaired by the loss of neurons in the magnocellular cholinergic neuronal system. It is therefore, of interest to investigate the role of nerve growth factor in this degenerative disorder. Since nerve growth factor does not cross the blood-brain barrier and is easily metabolized by peptidases when administered peripherally, it can be used for medical treatment only when directly injected into the brain. We demonstrate here that the oral administration of idebenone, a potent in vitro nerve growth factors synthesis stimulator, induced an increase in nerve growth factor protein and mRNA, and in choline acetyltransferase activity, in basal forebrain lesioned rats, but not in intact rats. Idebenone also ameliorated the behavioral deficits in habituation, water maze, and passive avoidance tasks in these animals. These results suggest that idebenone stimulated nerve growth factor synthesis in vivo and ameliorates the behavioral deficits which were accompanied with the recovery of the reduced choline acetyltransferase activity in the basal forebrain-lesioned rats.

摘要

神经生长因子在中枢神经系统胆碱能神经元的存活和维持中起着重要作用。在阿尔茨海默型老年痴呆症中,大细胞胆碱能神经元系统中的神经元丧失会损害学习和记忆。因此,研究神经生长因子在这种退行性疾病中的作用很有意义。由于神经生长因子不能穿过血脑屏障,并且在外周给药时容易被肽酶代谢,所以只有直接注入大脑时才能用于医学治疗。我们在此证明,口服艾地苯醌(一种体外有效的神经生长因子合成刺激剂)可诱导基底前脑损伤大鼠的神经生长因子蛋白和mRNA以及胆碱乙酰转移酶活性增加,但对完整大鼠无此作用。艾地苯醌还改善了这些动物在习惯化、水迷宫和被动回避任务中的行为缺陷。这些结果表明,艾地苯醌在体内刺激了神经生长因子的合成,并改善了行为缺陷,这些行为缺陷伴随着基底前脑损伤大鼠中降低的胆碱乙酰转移酶活性的恢复。

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