Activation of Cellular Antioxidant Defense System by Naturally Occurring Dibenzopyrone Derivatives Confers Neuroprotection against Oxidative Insults.
Yanan HouJie LiJun-Chen WuQuan-Xiang WuJian-Guo FangPublished in: ACS chemical neuroscience (2021)
Seven dibenzopyrone phenolic derivatives, i.e., alternariol (1), alternariol 5-O-methyl ether (2), altenusin B (3), dehydroaltenusin (4), altenuene (5), altenusin (6), and alterlactone (7), were isolated from endophytic fungi Alternaria alternata extract, and these compounds' structures were elucidated based on various spectroscopic data. Compound 3, a diphenic acid derivative, was determined as a new compound. In this study, compounds 3, 4, 6, and 7 displayed remarkable neuroprotective effects against oxidative injuries by acting as potent activators of nuclear factor-erythroid derived 2-like 2 (Nrf2) in PC12 cells. A mechanistic study indicated that these compounds induced the nuclear accumulation of Nrf2, promoted the expression of Nrf2-governed cytoprotective genes, and increased the cellular antioxidant capacity. More importantly, genetic silence of Nrf2 expression deprived the observed cytoprotection, highlighting the important role of Nrf2 in the protection of these compounds.
Keyphrases
- oxidative stress
- nuclear factor
- poor prognosis
- diabetic rats
- genome wide
- electronic health record
- high resolution
- binding protein
- gene expression
- molecular docking
- mass spectrometry
- inflammatory response
- high glucose
- transcription factor
- blood brain barrier
- molecular dynamics simulations
- subarachnoid hemorrhage
- ionic liquid
- deep learning
- bioinformatics analysis