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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Dietary prenylated flavonoid xanthohumol alleviates oxidative damage and accelerates diabetic wound healing via Nrf2 activation

Thumbnail
Συγγραφέας
Lu X., Liu M., Dong H., Miao J., Stagos D., Liu M.
Ημερομηνία
2022
Γλώσσα
en
DOI
10.1016/j.fct.2022.112813
Λέξη-κλειδί
glutathione
glutathione disulfide
hydrogen peroxide
hydroxymethylglutaryl coenzyme A reductase kinase
kelch like ECH associated protein 1
malonaldehyde
reactive oxygen metabolite
superoxide dismutase
transcription factor Nrf2
xanthohumol
flavonoid
kelch like ECH associated protein 1
propiophenone derivative
transcription factor Nrf2
xanthohumol
animal experiment
animal model
animal tissue
apoptosis
Article
cell damage
controlled study
cytotoxicity
diabetic wound
enzyme activation
HaCat cell line
histopathology
human
human cell
immunofluorescence
immunoprecipitation
in vitro study
MTT assay
nonhuman
nucleocytoplasmic transport
oxidation
polyacrylamide gel electrophoresis
protein degradation
protein expression
protein synthesis
Western blotting
wound healing
animal
chemistry
diabetic complication
drug effect
genetics
male
metabolism
oxidative stress
pathophysiology
prenylation
rat
skin ulcer
Sprague Dawley rat
wound healing
Animals
Diabetes Complications
Flavonoids
Humans
Kelch-Like ECH-Associated Protein 1
Male
NF-E2-Related Factor 2
Oxidative Stress
Prenylation
Propiophenones
Rats
Rats, Sprague-Dawley
Skin Ulcer
Wound Healing
Elsevier Ltd
Εμφάνιση Μεταδεδομένων
Επιτομή
Diabetic skin ulcer is one of the most common complications in patients suffering diabetes mellitus. Xanthohumol (XN), a hop-derived prenylated dietary flavonoid, has multiple health beneficial bioactivities. In the present study, we reported XN alleviates oxidative damage and accelerates diabetic wound healing via Nrf2 activation. In vitro, XN attenuated hydrogen peroxide (H2O2)-induced cytotoxicity, ROS production, cell apoptosis, as well as high glucose-induced cell damage. Mechanistic studies further demonstrated that XN could stabilize nuclear factor erythroid 2-related factor 2 (Nrf2) and promote its nuclear translocation, which was associated with AMPKα activation and covalent modification of Keap1 by XN. In vivo, XN increased Nrf2 expression and accelerated diabetic wound healing. Our study revealed a novel function of XN in diabetic wound healing as well as the underlying molecular mechanisms, suggesting XN is a promising lead compound and a potential food and/or drug candidate for the treatment of diabetic skin ulcers. © 2022 Elsevier Ltd
URI
http://hdl.handle.net/11615/76024
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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