S-equol, a metabolite of dietary soy isoflavones, alleviates lipopolysaccharide-induced depressive-like behavior in mice by inhibiting neuroinflammation and enhancing synaptic plasticity

被引:4
|
作者
Lu, Cong [1 ]
Gao, Rongjing [1 ,2 ]
Zhang, Yingyu [1 ]
Jiang, Ning [3 ,4 ]
Chen, Ying [5 ]
Sun, Jing [1 ]
Wang, Qiong [1 ]
Fan, Bei [1 ]
Liu, Xinmin [3 ,4 ]
Wang, Fengzhong [1 ,2 ]
机构
[1] Chinese Acad Agr Sci CAAS, Inst Food Sci & Technol, Beijing 100193, Peoples R China
[2] Nanjing Agr Univ, Coll Food Sci & Technol, Nanjing 210095, Peoples R China
[3] Chinese Acad Med Sci CAMS, Inst Med Plant Dev, Beijing 100193, Peoples R China
[4] Peking Union Med Coll PUMC, Beijing 100193, Peoples R China
[5] China Acad Chinese Med Sci CACM, Inst Chinese Mat Med, Beijing 100700, Peoples R China
关键词
SOCIAL DEFEAT STRESS; MEMORY DEFICITS; EXPRESSION; BRAIN; INFLAMMATION; METAANALYSIS; ACTIVATION; CYTOKINES; WOMEN;
D O I
10.1039/d1fo00547b
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
Systemic injection with lipopolysaccharide can lead to depressive-like behavior in experimental animals by inducing neuroinflammation and is considered to be a classic model of depression. S-equol is a major metabolite of dietary soy isoflavones with antioxidant and anti-inflammatory effects, and it has many beneficial effects on human health, including alleviation of menopausal symptoms, osteoporosis, cancer, obesity, chronic kidney disease, and cognitive dysfunction. A recent study reported that S-equol inhibited lipopolysaccharide-stimulated neuroinflammation in astrocytes. However, there is no research on the antidepressant-like effects of S-equol. Therefore, the present study was conducted to evaluate the antidepressant-like effects of S-equol in a lipopolysaccharide-induced depression model in mice and explore its underlying mechanisms. Our results demonstrated that treatment with S-equol (10, 20 and 40 mg kg(-1)) for 19 days markedly reversed the behavior of acute LPS (1.0 mg kg(-1)) treated mice in sucrose preference, tail suspension and forced swimming tests, exerting antidepressant-like effects. In addition, S-equol administration significantly decreased the levels of pro-inflammatory cytokines (tumor necrosis factor, interleukin-6, interleukin-10, interleukin-1 beta), increased the levels of 5-hydroxytryptamine and norepinephrine, and normalized the release of tryptophan and kynurenine in the hippocampi of lipopolysaccharide-treated mice. Moreover, treatment with S-equol significantly up-regulated the expression of synaptic plasticity-related proteins (phospho synapsin, synapsin, postsynaptic density-95) and down-regulated the toll-like receptor 4/nuclear factor kappa B signaling pathway in the hippocampi of lipopolysaccharide-treated mice. These findings demonstrated that S-equol significantly alleviated the depressive-like behavior induced by acute systemic injection of LPS, and its antidepressant action was related to mediation of neuroinflammation via the TLR4/NF-kappa B signaling pathway, normalization of the monoamine neurotransmitter levels, reversal of tryptophan metabolism dysfunction, and enhancement of synaptic plasticity. The current study provides insight into the potential of S-equol in the prevention of depression.
引用
收藏
页码:5770 / 5778
页数:9
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