HIF-1 reduces ischaemia-reperfusion injury in the heart by targeting the mitochondrial permeability transition pore

10.1093/cvr/cvu172

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Main Authors: Ong, S.-G, Lee, W.H, Theodorou, L, Kodo, K, Lim, S.Y, Shukla, D.H, Briston, T, Kiriakidis, S, Ashcroft, M, Davidson, S.M, Maxwell, P.H, Yellon, D.M, Hausenloy, D.J
Other Authors: DUKE-NUS MEDICAL SCHOOL
Format: Article
Published: 2020
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rat
Online Access:https://scholarbank.nus.edu.sg/handle/10635/183703
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spelling sg-nus-scholar.10635-1837032023-09-14T22:39:40Z HIF-1 reduces ischaemia-reperfusion injury in the heart by targeting the mitochondrial permeability transition pore Ong, S.-G Lee, W.H Theodorou, L Kodo, K Lim, S.Y Shukla, D.H Briston, T Kiriakidis, S Ashcroft, M Davidson, S.M Maxwell, P.H Yellon, D.M Hausenloy, D.J DUKE-NUS MEDICAL SCHOOL glycogen synthase kinase 360a hexokinase hexokinase ii hypoxia inducible factor 1 hypoxia inducible factor 1alpha mitochondrial permeability transition pore phosphoinositide dependent protein kinase 1 procollagen proline 2 oxoglutarate 4 dioxygenase protein serine threonine kinase inhibitor pyruvate dehydrogenase kinase unclassified drug von Hippel Lindau protein carrier protein hexokinase hexokinase 2, mouse Hif1a protein, mouse Hif1a protein, rat hypoxia inducible factor 1alpha mitochondrial permeability transition pore prolyl hydroxylase inhibitor protein serine threonine kinase pyruvate dehydrogenase (acetyl-transferring) kinase Vhlh protein, mouse von Hippel Lindau protein animal cell animal experiment animal model Article cell metabolism controlled study enzyme inhibition ex vivo study gene expression glycolysis heart infarction heart muscle cell heart protection immunoblotting in vitro study in vivo study ischemia male mitochondrial membrane potential mouse nonhuman oxidative stress oxygen consumption rat reperfusion injury animal cardiac muscle disease model dose response drug effects genetics heart mitochondrion knockout mouse metabolism Myocardial Infarction Myocardial Reperfusion Injury pathology protein stability signal transduction Sprague Dawley rat time factor Animals Disease Models, Animal Dose-Response Relationship, Drug Glycolysis Hexokinase Hypoxia-Inducible Factor 1, alpha Subunit Male Mice, Knockout Mitochondria, Heart Mitochondrial Membrane Transport Proteins Myocardial Infarction Myocardial Reperfusion Injury Myocardium Oxidative Stress Prolyl-Hydroxylase Inhibitors Protein Stability Protein-Serine-Threonine Kinases Rats, Sprague-Dawley Signal Transduction Time Factors Von Hippel-Lindau Tumor Suppressor Protein 10.1093/cvr/cvu172 Cardiovascular Research 104 1 24-36 2020-11-19T07:16:19Z 2020-11-19T07:16:19Z 2014 Article Ong, S.-G, Lee, W.H, Theodorou, L, Kodo, K, Lim, S.Y, Shukla, D.H, Briston, T, Kiriakidis, S, Ashcroft, M, Davidson, S.M, Maxwell, P.H, Yellon, D.M, Hausenloy, D.J (2014). HIF-1 reduces ischaemia-reperfusion injury in the heart by targeting the mitochondrial permeability transition pore. Cardiovascular Research 104 (1) : 24-36. ScholarBank@NUS Repository. https://doi.org/10.1093/cvr/cvu172 00086363 https://scholarbank.nus.edu.sg/handle/10635/183703 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Unpaywall 20201031
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic glycogen synthase kinase 360a
hexokinase
hexokinase ii
hypoxia inducible factor 1
hypoxia inducible factor 1alpha
mitochondrial permeability transition pore
phosphoinositide dependent protein kinase 1
procollagen proline 2 oxoglutarate 4 dioxygenase
protein serine threonine kinase inhibitor
pyruvate dehydrogenase kinase
unclassified drug
von Hippel Lindau protein
carrier protein
hexokinase
hexokinase 2, mouse
Hif1a protein, mouse
Hif1a protein, rat
hypoxia inducible factor 1alpha
mitochondrial permeability transition pore
prolyl hydroxylase inhibitor
protein serine threonine kinase
pyruvate dehydrogenase (acetyl-transferring) kinase
Vhlh protein, mouse
von Hippel Lindau protein
animal cell
animal experiment
animal model
Article
cell metabolism
controlled study
enzyme inhibition
ex vivo study
gene expression
glycolysis
heart infarction
heart muscle cell
heart protection
immunoblotting
in vitro study
in vivo study
ischemia
male
mitochondrial membrane potential
mouse
nonhuman
oxidative stress
oxygen consumption
rat
reperfusion injury
animal
cardiac muscle
disease model
dose response
drug effects
genetics
heart mitochondrion
knockout mouse
metabolism
Myocardial Infarction
Myocardial Reperfusion Injury
pathology
protein stability
signal transduction
Sprague Dawley rat
time factor
Animals
Disease Models, Animal
Dose-Response Relationship, Drug
Glycolysis
Hexokinase
Hypoxia-Inducible Factor 1, alpha Subunit
Male
Mice, Knockout
Mitochondria, Heart
Mitochondrial Membrane Transport Proteins
Myocardial Infarction
Myocardial Reperfusion Injury
Myocardium
Oxidative Stress
Prolyl-Hydroxylase Inhibitors
Protein Stability
Protein-Serine-Threonine Kinases
Rats, Sprague-Dawley
Signal Transduction
Time Factors
Von Hippel-Lindau Tumor Suppressor Protein
spellingShingle glycogen synthase kinase 360a
hexokinase
hexokinase ii
hypoxia inducible factor 1
hypoxia inducible factor 1alpha
mitochondrial permeability transition pore
phosphoinositide dependent protein kinase 1
procollagen proline 2 oxoglutarate 4 dioxygenase
protein serine threonine kinase inhibitor
pyruvate dehydrogenase kinase
unclassified drug
von Hippel Lindau protein
carrier protein
hexokinase
hexokinase 2, mouse
Hif1a protein, mouse
Hif1a protein, rat
hypoxia inducible factor 1alpha
mitochondrial permeability transition pore
prolyl hydroxylase inhibitor
protein serine threonine kinase
pyruvate dehydrogenase (acetyl-transferring) kinase
Vhlh protein, mouse
von Hippel Lindau protein
animal cell
animal experiment
animal model
Article
cell metabolism
controlled study
enzyme inhibition
ex vivo study
gene expression
glycolysis
heart infarction
heart muscle cell
heart protection
immunoblotting
in vitro study
in vivo study
ischemia
male
mitochondrial membrane potential
mouse
nonhuman
oxidative stress
oxygen consumption
rat
reperfusion injury
animal
cardiac muscle
disease model
dose response
drug effects
genetics
heart mitochondrion
knockout mouse
metabolism
Myocardial Infarction
Myocardial Reperfusion Injury
pathology
protein stability
signal transduction
Sprague Dawley rat
time factor
Animals
Disease Models, Animal
Dose-Response Relationship, Drug
Glycolysis
Hexokinase
Hypoxia-Inducible Factor 1, alpha Subunit
Male
Mice, Knockout
Mitochondria, Heart
Mitochondrial Membrane Transport Proteins
Myocardial Infarction
Myocardial Reperfusion Injury
Myocardium
Oxidative Stress
Prolyl-Hydroxylase Inhibitors
Protein Stability
Protein-Serine-Threonine Kinases
Rats, Sprague-Dawley
Signal Transduction
Time Factors
Von Hippel-Lindau Tumor Suppressor Protein
Ong, S.-G
Lee, W.H
Theodorou, L
Kodo, K
Lim, S.Y
Shukla, D.H
Briston, T
Kiriakidis, S
Ashcroft, M
Davidson, S.M
Maxwell, P.H
Yellon, D.M
Hausenloy, D.J
HIF-1 reduces ischaemia-reperfusion injury in the heart by targeting the mitochondrial permeability transition pore
description 10.1093/cvr/cvu172
author2 DUKE-NUS MEDICAL SCHOOL
author_facet DUKE-NUS MEDICAL SCHOOL
Ong, S.-G
Lee, W.H
Theodorou, L
Kodo, K
Lim, S.Y
Shukla, D.H
Briston, T
Kiriakidis, S
Ashcroft, M
Davidson, S.M
Maxwell, P.H
Yellon, D.M
Hausenloy, D.J
format Article
author Ong, S.-G
Lee, W.H
Theodorou, L
Kodo, K
Lim, S.Y
Shukla, D.H
Briston, T
Kiriakidis, S
Ashcroft, M
Davidson, S.M
Maxwell, P.H
Yellon, D.M
Hausenloy, D.J
author_sort Ong, S.-G
title HIF-1 reduces ischaemia-reperfusion injury in the heart by targeting the mitochondrial permeability transition pore
title_short HIF-1 reduces ischaemia-reperfusion injury in the heart by targeting the mitochondrial permeability transition pore
title_full HIF-1 reduces ischaemia-reperfusion injury in the heart by targeting the mitochondrial permeability transition pore
title_fullStr HIF-1 reduces ischaemia-reperfusion injury in the heart by targeting the mitochondrial permeability transition pore
title_full_unstemmed HIF-1 reduces ischaemia-reperfusion injury in the heart by targeting the mitochondrial permeability transition pore
title_sort hif-1 reduces ischaemia-reperfusion injury in the heart by targeting the mitochondrial permeability transition pore
publishDate 2020
url https://scholarbank.nus.edu.sg/handle/10635/183703
_version_ 1779153127204716544