Department of Obstetrics and Gynecology, Shengli Oilfield Central Hospital, Dongying City, Shandong Province, China.
Hypertens Pregnancy. 2022 Feb;41(1):23-30. doi: 10.1080/10641955.2021.2013874. Epub 2021 Dec 22.
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.
本文旨在研究非瑟酮在脂多糖诱导的 PE 大鼠中的作用及其潜在作用机制。
建立 LPS 诱导的 PE 样大鼠模型,以探讨非瑟酮对 PE 的体内作用。
非瑟酮降低了高血压、蛋白尿、TNF-α、IL-6、IL-1β、MDA 和 sFlt-1/PlGF 比值,但增加了 PE 大鼠的胎盘和胎儿体重、GSH 和 SOD。此外,非瑟酮抑制了 TLR4/NF-κB 通路,并促进了 PE 大鼠胎盘组织中的 Nrf2/HO-1 通路。
非瑟酮在 PE 样大鼠模型中发挥了保护作用,并调节了 TLR4/NF-κB 和 Nrf2/HO-1 通路的激活。