| Literature DB >> 32069075 |
Xue-Liang Zhou1, Xia Wu1, Rong-Rong Zhu2, Hua Xu1, Yun-Yun Li1, Qi-Rong Xu1, Sheng Liu1, Song-Qing Lai1, Xinping Xu1, Li Wan1, Qi-Cai Wu1, Ji-Chun Liu1.
Abstract
Both the Notch1 and Keap1-Nrf2 signaling pathways have cardioprotective effects, but the role of Notch1-Nrf2 crosstalk in myocardial ischemia-reperfusion injury is unclear. In this study, we established hypoxia-reoxygenation in neonate rat myocardial cells and employed γ-secretase inhibitor and curcumin to inhibit and activate the Notch1 and Keap1-Nrf2 signaling pathways, respectively. We found that the combined action of the Notch1 and Keap1-Nrf2 signaling pathways significantly increased cardiomyocyte viability, inhibited cardiomyocyte apoptosis, reduced the formation of reactive oxygen species, and increased antioxidant activities. In conclusion, these findings suggest that Notch1-Nrf2 crosstalk exerts myocardial protection by reducing the formation of reactive oxygen species.Entities:
Keywords: DRO; Keap1; Notch1 signaling; Nrf2; ROS; myocardial protection; protection du myocarde; signalisation Notch1
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Year: 2020 PMID: 32069075 DOI: 10.1139/bcb-2018-0398
Source DB: PubMed Journal: Biochem Cell Biol ISSN: 0829-8211 Impact factor: 3.626