Glyoxalase 1 Prevents Chronic Hyperglycemia Induced Heart-Explant Derived Cell Dysfunction.
Animals
Antioxidants
/ metabolism
Cell- and Tissue-Based Therapy
Chronic Disease
Diabetes Complications
Extracellular Vesicles
/ metabolism
Heart Failure
/ enzymology
Humans
Hyperglycemia
/ complications
Lactoylglutathione Lyase
/ genetics
Mice
Mice, Inbred C57BL
Mice, Transgenic
Myocardial Infarction
/ enzymology
Oxidative Stress
Reactive Oxygen Species
/ metabolism
cardiac stem cells
diabetes
extracellular vesicles
heart failure
hyperglycemia
myocardial infarction
oxidative stress
reactive dicarbonyls
Journal
Theranostics
ISSN: 1838-7640
Titre abrégé: Theranostics
Pays: Australia
ID NLM: 101552395
Informations de publication
Date de publication:
2019
2019
Historique:
received:
13
05
2019
accepted:
06
07
2019
entrez:
20
9
2019
pubmed:
20
9
2019
medline:
19
8
2020
Statut:
epublish
Résumé
Decades of work have shown that diabetes increases the risk of heart disease and worsens clinical outcomes after myocardial infarction. Because diabetes is an absolute contraindication to heart transplant, cell therapy is increasingly being explored as a means of improving heart function for these patients with very few other options. Given that hyperglycemia promotes the generation of toxic metabolites, the influence of the key detoxification enzyme glyoxalase 1 (Glo1) on chronic hyperglycemia induced heart explant-derived cell (EDC) dysfunction was investigated.
Identifiants
pubmed: 31534514
doi: 10.7150/thno.36639
pii: thnov09p5720
pmc: PMC6735395
doi:
Substances chimiques
Antioxidants
0
Reactive Oxygen Species
0
GLO1 protein, human
EC 4.4.1.5
Lactoylglutathione Lyase
EC 4.4.1.5
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
5720-5730Subventions
Organisme : CIHR
ID : FDN143278
Pays : Canada
Organisme : CIHR
ID : MC2-121291
Pays : Canada
Déclaration de conflit d'intérêts
Competing Interests: The authors have declared that no competing interest exists.
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