Ameliorative effect of vanillic acid against scopolamine-induced learning and memory impairment in rat via attenuation of oxidative stress and dysfunctional synaptic plasticity

被引:5
作者
Choi, Ga-Young [1 ]
Lee, In-Seo [2 ]
Moon, Eunyoung [1 ]
Choi, Hyosung [1 ]
Park, Ji-Ho [2 ]
Kweon, Hee-Seok [1 ]
机构
[1] Korea Basic Sci Inst, Ctr Res Equipment, Cheongju 28119, South Korea
[2] Kyung Hee Univ, Grad Sch East West Med Sci, Dept Gerontol, AgeTech Serv Convergence Major, Yongin 17104, South Korea
基金
新加坡国家研究基金会;
关键词
vanillic acid; scopolamine; oxidant stress; memory impairment; acetylcholinesterase; synaptic plasticity; LONG-TERM POTENTIATION; COGNITIVE IMPAIRMENT; ACETYLCHOLINESTERASE; MODEL; NEUROINFLAMMATION; INDUCTION; DEFICITS; BRAIN; AREA;
D O I
10.1016/j.biopha.2024.117000
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Alzheimer's disease (AD) is characterized by cognitive impairment, loss of learning and memory, and abnormal behaviors. Scopolamine (SCOP) is a non-selective antagonist of muscarinic acetylcholine receptors that exhibits the behavioral and molecular hallmarks of AD. Vanillic acid (VA), a phenolic compound, is obtained from the roots of a traditional plant called Angelica sinensis, and has several pharmacologic effects, including antimicrobial, anti-inflammatory, anti-angiogenic, anti-metastatic, and antioxidant properties. Nevertheless, VA's neuroprotective potential associated with the memory has not been thoroughly investigated. Therefore, this study investigated whether VA treatment has an ameliorative effect on the learning and memory impairment induced by SCOP in rats. Behavioral experiments were utilized to assess the learning and memory performance associated with the hippocampus. Using western blotting analysis and assay kits, the neuronal damage, oxidative stress, and acetylcholinesterase activity responses of hippocampus were evaluated. Additionally, the measurement of longterm potentiation was used to determine the function of synaptic plasticity in organotypic hippocampal slice cultures. In addition, the synaptic vesicles' density and the length and width of the postsynaptic density were evaluated using electron microscopy. Consequently, the behavioral, biochemical, electrophysiological, and ultrastructural analyses revealed that VA treatment prevents learning and memory impairments caused by SCOP in rats. The study's findings suggest that VA has a neuroprotective effect on SCOP-induced learning and memory impairment linked to the hippocampal cholinergic system, oxidative damage, and synaptic plasticity. Therefore, VA may be a prospective therapeutic agent for treating AD.
引用
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页数:14
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