4.7 Article

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

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EUROPEAN JOURNAL OF PHARMACOLOGY
卷 956, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.ejphar.2023.175954

关键词

Depression; Maternal separation; Neuroinflammation; Kynurenine pathway; Indoleamine 2 3-dioxygenase; Synaptic plasticity

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This study investigates the effects of oleanolic acid (OA) and ursolic acid (UA) on depression-like behaviors in maternal separation (MS)-induced depression-like model. It is found that OA is more effective than UA in reversing depression-like behaviors caused by maternal separation.
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 depressionlike 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-& alpha;, 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 MSinduced depression-like behaviors more effectively than UA.

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