Propane-2-sulfonic acid octadec-9-enyl-amide alleviates scopolamine-induced spatial learning and memory deficits in mice

被引:2
作者
Li, Ying [1 ]
Lu, Huahui [2 ]
Xie, Shangjin [3 ]
Cong, Ying [4 ]
Wang, Ying [1 ]
Zhu, Maoshu [2 ]
Zhou, Juan [5 ]
机构
[1] Xiamen Med Coll, Dept Pharm, Xiamen 361023, Peoples R China
[2] Fifth Hosp Xiamen, Xiamen 361101, Fujian, Peoples R China
[3] Xiamen Univ Hosp, Xiamen 361105, Peoples R China
[4] Weihai Cent Hosp, Pharm Dept, Weihai 264400, Peoples R China
[5] Xiamen Univ, Dept Obstet & Gynecol, Affiliated Hosp 1, Xiamen 361101, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Propane-2-sulfonic acid octadec-9-enyl-amide; Scopolamine; Acetylcholine; Synaptic plasticity; HIPPOCAMPAL NEUROGENESIS; DUAL AGONIST; ALPHA; RATS; NEUROPLASTICITY;
D O I
10.1016/j.bbrc.2020.03.110
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Our previous reports demonstrated that the novel peroxisome proliferator-activated receptors alpha and gamma (PPAR alpha/gamma) dual agonist propane-2-sulfonic acid octadec-9-enyl-amide (N15) alleviates cognitive ability in the chronic phase of ischemic stroke. However, the potential effects of N15 on Alzheimer's disease (AD) animal models have not been elucidated. In the present study, we investigated the effects of N15 on scopolamine-induced cognitive dysfunction and cholinergic system ability. N15 (50, 100 or 200 mg/kg) was administered to mice via oral gavage for 21 days, and spatial cognitive dysfunction was induced via an intraperitoneal injection of scopolamine (4 mg/kg) for 6 days. We found that N15 pretreatment markedly ameliorated scopolamine-induced spatial cognitive impairment and enhanced cholinergic system reactivity in the hippocampus. N15 pretreatment also significantly increased the expression levels of growth-associated protein-43, synaptophysin, brain-derived neurotrophic factor and neurotrophin-3 in the hippocampus. Our data demonstrate that N15 has an anti-amnesic effect, which may be mediated by enhancing cholinergic activity and synaptic plasticity. These findings support N15 as a potent neuropharmacological drug against AD. (C) 2020 Published by Elsevier Inc.
引用
收藏
页码:283 / 288
页数:6
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