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Abstract Title:

Isorhamnetin alleviates lipopolysaccharide-induced acute lung injury by inhibiting mTOR signaling pathway.

Abstract Source:

Immunopharmacol Immunotoxicol. 2022 Jun ;44(3):387-399. Epub 2022 Mar 21. PMID: 35306954

Abstract Author(s):

Bo Yang, Ling Ma, Yuli Wei, Yunyao Cui, Xiaohe Li, Yiying Wei, Shanshan Zhang, Liang Zhang, Honggang Zhou, Guangshun Wang, Xiaoping Li

Article Affiliation:

Bo Yang

Abstract:

Acute Lung Injury (ALI) is an acute hypoxic respiratory insufficiency caused by various traumatic factors, manifested as progressive hypoxemia and respiratory distress, and lung imaging shows a heterogeneous osmotic outbreak. Isorhamnetin (ISO) is a flavonoid compound isolated and purified from medicinal plants, such asL. and Ginkgo, and has multiple pharmacological functions, such as anti-tumor, anti-myocardial hypoxia, and cardiovascular protection. Our previous study has shown that ISO could attenuate lipopolysaccharide (LPS)-induced acute lung injury in mice, but its mechanism is not clear.In this study, we used LPS-induced mouse and cell models to research the mechanism of ISO alleviating acute lung injury.The results showed that ISO could attenuate the injury of type II alveolar epithelial cells by inhibiting the TLR4/NF-κB pathway. Further studies showed that ISO could inhibit the activation of mTOR signalandand promote autophagy in alveolar epithelial cells to reduce lung injury caused by LPS. In addition, ISO could inhibit LPS-induced epithelial cell apoptosis.Overall, ISO could suppress injury and apoptosis of epithelial cells and activate autophagy to protect epithelial cellsinhibiting mTOR signal and attenuating LPS-induced acute lung injury in mice.

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