Citral protects against LPS-induced endometritis by inhibiting ferroptosis through activating Nrf2 signaling pathway

被引:15
|
作者
Zhao, Weiliang [2 ]
Wang, Junrong [1 ]
Li, Yang [3 ]
Ye, Cong [1 ]
机构
[1] Jilin Univ, Dept Obstet & Gynecol, China Japan Union Hosp, Changchun 130033, Jilin, Peoples R China
[2] Jilin Univ, Dept Anesthesiol, China Japan Union Hosp, 126 Sendai St, Changchun 130033, Jilin, Peoples R China
[3] Jilin Univ, Dept Urol, China Japan Union Hosp, 126 Xiantai St, Changchun 130033, Peoples R China
关键词
LPS; Endometritis; Citral; Nrf2; Ferroptosis; LIPOPOLYSACCHARIDE-INDUCED ENDOMETRITIS; INFLAMMATION; WOMEN; ASSOCIATION; SUPPRESSION; MICE;
D O I
10.1007/s10787-023-01211-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IntroductionEndometritis is the inflammatory condition of the uterus. Citral, a component of lemongrass oil, is known to exhibit anti-inflammatory activity.AimThe effects of citral on LPS-induced endometritis were tested and the mechanisms were investigated.MethodsLPS-induced endometritis mice model was established and the effects of citral were detected using this model. Inflammatory cytokines were tested by ELISA. Ferroptosis was assessed by detecting GSH, ATP, MDA, and Fe2+ levels. Signaling pathway was tested by western blot analysis.ResultsCitral prevented LPS-induced endometritis through attenuating uterine pathological changes and inflammatory cytokine release. Meanwhile, citral prevents LPS-induced ferroptosis through attenuating MDA and Fe2+ levels, as well as increasing ATP and GSH levels. Furthermore, citral up-regulated Nrf2 and HO-1 expression and attenuated NF-kappa B activation. In addition, in Nrf2 knockdown mice, the inhibitory roles of citral on ferroptosis and endometritis were largely reversed.ConclusionTaken together, citral inhibited LPS-induced endometritis through preventing ferroptosis, which were regulated by Nrf2 signaling pathway.
引用
收藏
页码:1551 / 1558
页数:8
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