Docosahexaenoic acid protects against lipopolysaccharide-induced fetal growth restriction via inducing the ubiquitination and degradation of NF-κB p65 in placental trophoblasts

• Published in: The Journal of nutritional biochemistry 2023-08, Vol.118, p.109359-109359, Article 109359
• Main Authors: Bo, Qingli, Xie, Yali, Lin, Qiulin, Fu, Lin, Hu, Chunqiu, Zhang, Zhiqiang, Meng, Qingchong, Xu, Feixiang, Wang, Guoxiu, Miao, Ziyang, Wang, Hua, Xu, Dexiang
• Format: Article
• Language: English
• Subjects: Animals; Docosahexaenoic Acids - metabolism; Docosahexaenoic Acids - pharmacology; Female; Fetal Growth Retardation - chemically induced; FGR; Humans; Inflammation; Inflammation - metabolism; Lipopolysaccharides - metabolism; Mice; NF-kappa B - metabolism; Placenta; Placenta - metabolism; PPAR gamma - genetics; PPAR gamma - metabolism; PPARγ; Pregnancy; Trophoblasts - metabolism; Ubiquitination
• ISSN: 0955-2863; 1873-4847
• DOI: 10.1016/j.jnutbio.2023.109359

Lipopolysaccharide (LPS) could induce adverse birth outcomes by evoking inflammation. We investigated the effect and mechanism of docosahexaenoic acid (DHA) on LPS-induced placental inflammation and fetal growth restriction (FGR). In vivo, pregnant CD-1 mice were divided into four groups: Ctrl, DHA, LPS and DHA+LPS group. We found that DHA pretreatment reduced the incidence of FGR induced by LPS and activated the expression of peroxisome proliferators-activated receptor gamma (PPARγ) in placental tissue. Moreover, the LPS-induced increase of mRNA levels of Tnf-α, Il-6, Il-1β, Mip-2 and Kc in placental tissue was significantly attenuated by DHA pretreatment. A similar effect of DHA was observed in serum of pregnant mice and amniotic fluid. In contrast, the levels of the IL-10 were significantly increased after DHA pretreatment. In vitro, we clarified that DHA antagonized the activation of the NF-κB signaling pathway induced by LPS, which was dependent on PPARγ. Subsequently, CHX (translation inhibitor) was used to indicated that PPARγ significantly increased the degradation rate of p65, an effect that was inhibited by MG132 (proteasome inhibitor) treatment. Finally, it was confirmed that the activation of PPARγ could significantly promote the ubiquitination and degradation of p65. Our results suggested that DHA alleviated LPS-induced inflammatory responses and FGR by activating PPARγ expression, leading to p65 ubiquitination and degradation. [Display omitted]