Please use this identifier to cite or link to this item: https://doi.org/10.1155/2012/845698
Title: The diabetic heart: Too sweet for its own good?
Authors: Whittington, H.J
Babu, G.G
Mocanu, M.M
Yellon, D.M
Hausenloy, D.J 
Keywords: alloxan
caspase 3
creatine kinase
G protein coupled receptor
glucokinase
glycogen synthase kinase 3beta
Janus kinase 2
nitric oxide synthase
phosphatidylinositol 3 kinase
protein bcl 2
protein kinase B
protein kinase C
reactive oxygen metabolite
streptozocin
vasculotropin
age
apoptosis
calcium cell level
cell survival
diabetic cardiomyopathy
disease predisposition
dyslipidemia
ex vivo study
experimental model
experimental study
glucose tolerance
glucose transport
heart left ventricle function
heart muscle cell
heart protection
heart ventricle fibrillation
hyperglycemia
hypertension
in vitro study
in vivo study
insulin dependent diabetes mellitus
ischemic heart disease
ischemic preconditioning
mitochondrial permeability
non insulin dependent diabetes mellitus
nonhuman
obesity
pancreas islet beta cell
pH
priority journal
protein expression
protein phosphorylation
reperfusion injury
review
sensitivity analysis
upregulation
Issue Date: 2012
Citation: Whittington, H.J, Babu, G.G, Mocanu, M.M, Yellon, D.M, Hausenloy, D.J (2012). The diabetic heart: Too sweet for its own good?. Cardiology Research and Practice 1 (1) : 845698. ScholarBank@NUS Repository. https://doi.org/10.1155/2012/845698
Rights: Attribution 4.0 International
Abstract: Diabetes mellitus is a major risk factor for ischemic heart disease (IHD). Patients with diabetes and IHD experience worse clinical outcomes, suggesting that the diabetic heart may be more susceptible to ischemia-reperfusion injury (IRI). In contrast, the animal data suggests that the diabetic heart may be either more, equally, or even less susceptible to IRI. The conflicting animal data may be due to the choice of diabetic and/or IRI animal model. Ischemic conditioning, a phenomenon in which the heart is protected against IRI by one or more brief nonlethal periods of ischemia and reperfusion, may provide a novel cardioprotective strategy for the diabetic heart. Whether the diabetic heart is amenable to ischemic conditioning remains to be determined using relevant animal models of IRI and/or diabetes. In this paper, we review the limitations of the current experimental models used to investigate IRI and cardioprotection in the diabetic heart. © 2012 Hannah J. Whittington et al.
Source Title: Cardiology Research and Practice
URI: https://scholarbank.nus.edu.sg/handle/10635/183236
ISSN: 20900597
DOI: 10.1155/2012/845698
Rights: Attribution 4.0 International
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