PUBLICATION

Honokiol ameliorates radiation-induced brain injury via the activation of SIRT3

Authors
Liao, G., Zhao, Z., Yang, H., Li, X.
ID
ZDB-PUB-201022-3
Date
2020
Source
The Journal of international medical research   48: 300060520963993 (Journal)
Registered Authors
Keywords
Honokiol, cyclooxygenase-2, ionizing irradiation, radiation-induced brain injury, reactive oxygen species, sirtuin 3
MeSH Terms
  • Animals
  • Biphenyl Compounds
  • Brain/metabolism
  • Brain Injuries*
  • Lignans
  • Oxidative Stress
  • Reactive Oxygen Species
  • Sirtuin 3*/genetics
  • Sirtuin 3*/metabolism
  • Zebrafish/metabolism
PubMed
33081556 Full text @ J Int Med Res
Abstract
Sirtuin 3 (SIRT3) plays a vital role in regulating oxidative stress in tissue injury. The aim of this study was to evaluate the radioprotective effects of honokiol (HKL) in a zebrafish model of radiation-induced brain injury and in HT22 cells.
The levels of reactive oxygen species (ROS), tumor necrosis factor-alpha (TNF-α), and interleukin-1 beta (IL-1β) were evaluated in the zebrafish brain and HT22 cells. The expression levels of SIRT3 and cyclooxygenase-2 (COX-2) were measured using western blot assays and real-time polymerase chain reaction (RT-PCR).
HKL treatment attenuated the levels of ROS, TNF-α, and IL-1β in both the in vivo and in vitro models of irradiation injury. Furthermore, HKL treatment increased the expression of SIRT3 and decreased the expression of COX-2. The radioprotective effects of HKL were achieved via SIRT3 activation.
HKL attenuated oxidative stress and pro-inflammatory responses in a SIRT3-dependent manner in radiation-induced brain injury.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping