Effects of oleanolic acid and ursolic acid on depression-like behaviors induced by maternal separation in mice

神经炎症 行为绝望测验 突触素 海马体 开阔地 高架加迷宫 前额叶皮质 内分泌学 熊果酸 心理学 内科学 神经可塑性 焦虑 医学 抗抑郁药 化学 神经科学 免疫组织化学 精神科 炎症 认知 色谱法
作者
Chang Hyeon Kong,Keontae Park,Do Yeon Kim,Jae Youn Kim,Woo Chang Kang,Mijin Jeon,Ji Won Min,Won Hyung Lee,Seo Yun Jung,Jong Hoon Ryu
出处
期刊:European Journal of Pharmacology [Elsevier BV]
卷期号:956: 175954-175954 被引量:8
标识
DOI:10.1016/j.ejphar.2023.175954
摘要

Oleanolic acid (OA) and ursolic acid (UA) are structural isomeric triterpenoids. Both triterpenoids have been reported to be able to improve depression. However, no studies have compared their effects in the same system. Whether OA or UA could ameliorate depression-like behaviors in maternal separation (MS)-induced depression-like model was investigated. MS model is a well-accepted mouse model that can reflect the phenotype and pathogenesis of depression. Depression is a mental illness caused by neuroinflammation or changes in neuroplasticity in certain brain regions, such as the prefrontal cortex and hippocampus. Depression-like behaviors were measured using splash test or forced swimming test. In addition, anxiety-like behaviors were also measured using the open field test or elevated plus-maze test. MS-treated female mice showed greater depression-like behaviors than male mice, and that OA improved several depression-like behaviors, whereas UA only relieved anxiety-like behavior of MS-treated mice. Microglial activation, expression levels of TNF-α, and mRNA levels of IDO1 were increased in the hippocampi of MS-treated female mice. However, OA and UA treatments attenuated such increases. In addition, expression levels of synaptophysin and PSD-95 were decreased in the hippocampi of MS-treated female mice. These decreased expression levels of synaptophysin were reversed by both OA and UA treatments, although decreased PSD-95 expression levels were only reversed by OA treatment. Our findings suggest that MS cause depression-like behaviors through female-specific neuroinflammation, changes of tryptophan metabolism, and alterations of synaptic plasticity. Our findings also suggest that OA could reverse MS-induced depression-like behaviors more effectively than UA.
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