非西汀
医学
TLR4型
子痫前期
脂多糖
体内
药理学
肿瘤坏死因子α
内分泌学
内科学
蛋白尿
炎症
怀孕
化学
肾
生物化学
抗氧化剂
生物
生物技术
类黄酮
遗传学
作者
Ying Li,Yuanyuan Liu,Jinfeng Chen,Jian Hu
标识
DOI:10.1080/10641955.2021.2013874
摘要
This article is aimed to investigate the function and underlying action mechanism of Fisetin in LPS-induced PE rats.LPS-induced PE-like rat model was established to explore the effects of Fisetin on PE in vivo.Fisetin reduced hypertension, proteinuria, TNF-α, IL-6, IL-1β, MDA, and sFlt-1/PlGF ratio, but elevated the placental, fetal weight, GSH and SOD in PE rats. Moreover, Fisetin suppressed TLR4/NF-κB pathway, as well as promoting Nrf2/HO-1 pathway in placental tissues of PE rats.Fisetin exerted protective role and modulated the activation of TLR4/NF-κB and Nrf2/HO-1 pathways in PE-like rat models.
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