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人参皂苷Rg1通过调节大鼠的NF-κB/NLRP3信号通路减轻慢性不可预测性轻度应激诱导的抑郁样效应。

Ginsenoside Rg1 attenuates chronic unpredictable mild stress-induced depressive-like effect via regulating NF-κB/NLRP3 pathway in rats.

作者信息

Zhang Yong-Qiang, Wang Xu-Bo, Xue Ran-Ran, Gao Xin-Xue, Li Wu

机构信息

Department of Psychiatry, Jining City Psychiatric Hospital, Jining, Shandong, China.

出版信息

Neuroreport. 2019 Sep 4;30(13):893-900. doi: 10.1097/WNR.0000000000001302.

DOI:10.1097/WNR.0000000000001302
PMID:31373969
Abstract

Ginsenoside (GS Rg1), which has neuroprotection and anti-inflammation activities, is the main active ingredient of Radix Ginseng. However, its antidepressant-like effect in rats remains unclear. Our study was conducted to investigate whether GS Rg1 confers an antidepressant effect in rats exposed to a chronic unpredictable mild stress model of depression and to explore its possible mechanisms. Our results revealed that GS Rg1 treatments for 3 weeks alleviated the depression-related behaviors of chronic unpredictable mild stress-exposed rats, as indicated by increasing sucrose preference, improving locomotor activity and shortening immobile time in both the forced swimming tests and tail suspension tests. And these ameliorative effects of GS Rg1 treatment were involved with regulating chronic unpredictable mild stress-induced pro-inflammatory cytokine interleukin beta (IL-1β) related neuro-inflammation. In addition, we further found that GS Rg1 reversed chronic unpredictable mild stress-induced IL-1β elevation, possibly by inhibiting nuclear factor kappa B pathway activation and regulating nucleotide binding and oligomerization domain-like receptor family pyrin domain-containing 3 inflammasome expression. In short, our results suggested that GS Rg1 exerted a potential antidepressant-like effect in chronic unpredictable mild stress rat model of depression, which may provide an insight into the potential of GS Rg1 in therapeutic implications for depression.

摘要

人参皂苷(GS Rg1)具有神经保护和抗炎活性,是人参的主要活性成分。然而,其在大鼠中的抗抑郁样作用尚不清楚。我们进行这项研究是为了调查GS Rg1是否对暴露于慢性不可预测轻度应激抑郁模型的大鼠具有抗抑郁作用,并探讨其可能的机制。我们的结果显示,连续3周给予GS Rg1治疗可减轻慢性不可预测轻度应激大鼠的抑郁相关行为,这表现为在强迫游泳试验和悬尾试验中蔗糖偏好增加、运动活动改善以及不动时间缩短。GS Rg1治疗的这些改善作用与调节慢性不可预测轻度应激诱导的促炎细胞因子白细胞介素β(IL-1β)相关的神经炎症有关。此外,我们进一步发现GS Rg1可能通过抑制核因子κB通路激活和调节含核苷酸结合寡聚化结构域样受体家族吡咯结构域3炎性小体表达来逆转慢性不可预测轻度应激诱导的IL-1β升高。简而言之,我们的结果表明GS Rg1在慢性不可预测轻度应激抑郁大鼠模型中发挥了潜在的抗抑郁样作用,这可能为GS Rg1在抑郁症治疗中的潜在应用提供了见解。

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