Gao Haiyan, Zhu Xianghua, Xi Yang, Li Qun, Shen Zhenzhong, Yang Yongjie
Department of Psychiatry, Xuzhou Oriental People's Hospital, Xuzhou, Jiangsu 221004, P.R. China.
Exp Ther Med. 2018 Feb;15(2):1574-1579. doi: 10.3892/etm.2017.5517. Epub 2017 Nov 16.
Atractylenolide I (AT-I), a major component of the rhizoma of Koidz., exerts a wide range of activities. The purpose of the present study was to investigate the anti-depressant-like effect of AT-I in a mouse model of chronic unpredictable mild stress (CUMS), and to explore the possible molecular mechanism involved. It was revealed that AT-I significantly ameliorated CUMS-induced depressive-like behaviors, as evidenced by increased sucrose preference as well as shortened immobility time in the forced swimming and the tail suspension test. In addition, AT-I reduced CUMS-induced decreases in the concentrations of serotonin and norepinephrine in the hippocampus. Furthermore, AT-I inhibited the activation of the nucleotide binding and oligomerization domain-like receptor family pyrin domain-containing 3 (NLRP3) inflammasome as well as the concentration of the pro-inflammatory cytokine interleukin (IL)-1β in the hippocampi of mice subjected to CUMS. In conclusion, the results of the present study suggested that AT-I exerts anti-depressant-like effects in a CUMS-induced model of depression in mice, the molecular mechanism of which is associated with the inhibition of NLRP3 inflammasome activation to decrease IL-1β production.
白术内酯 I(AT-I)是白术根茎的主要成分,具有多种活性。本研究旨在探讨 AT-I 在慢性不可预测轻度应激(CUMS)小鼠模型中的抗抑郁样作用,并探讨其可能的分子机制。结果显示,AT-I 显著改善了 CUMS 诱导的抑郁样行为,表现为蔗糖偏好增加以及在强迫游泳和悬尾试验中不动时间缩短。此外,AT-I 减少了 CUMS 诱导的海马中血清素和去甲肾上腺素浓度的降低。此外,AT-I 抑制了 CUMS 小鼠海马中核苷酸结合寡聚化结构域样受体家族含 pyrin 结构域 3(NLRP3)炎性小体的激活以及促炎细胞因子白细胞介素(IL)-1β的浓度。总之,本研究结果表明,AT-I 在 CUMS 诱导的小鼠抑郁模型中发挥抗抑郁样作用,其分子机制与抑制 NLRP3 炎性小体激活以减少 IL-1β产生有关。