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Glyoxalase-1 overexpression reduces endothelial dysfunction and attenuates early renal impairment in a rat model of diabetes
by
De Mey, Jo G. R.
, Flyvbjerg, Allan
, Sieber, Jonas
, Stehouwer, Coen D. A.
, Miyata, Toshio
, Janssen, Ben J. A.
, Peutz-Kootstra, Carine J.
, Mundel, Peter H.
, Brownlee, Michael
, Schalkwijk, Casper G.
, Brouwers, Olaf
, Niessen, Petra M. G.
, Østergaard, Jakob A.
in
Animals
/ Biological and medical sciences
/ Diabetes
/ Diabetes Mellitus - metabolism
/ Diabetes. Impaired glucose tolerance
/ Endocrine pancreas. Apud cells (diseases)
/ Endocrinopathies
/ Endothelium
/ Enzymes
/ Etiopathogenesis. Screening. Investigations. Target tissue resistance
/ Glucose
/ Human Physiology
/ Hyperglycemia
/ Hypotheses
/ Immunohistochemistry
/ Inflammation
/ Internal Medicine
/ Kidneys
/ Lactoylglutathione Lyase - genetics
/ Lactoylglutathione Lyase - metabolism
/ Male
/ Medical sciences
/ Medicine
/ Medicine & Public Health
/ Metabolic Diseases
/ Nephrology. Urinary tract diseases
/ Nephropathies. Renovascular diseases. Renal failure
/ Oxidative stress
/ Proteins
/ Pyruvaldehyde - metabolism
/ Rats
/ Rats, Transgenic
/ Renal failure
/ Veins & arteries
2014
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Glyoxalase-1 overexpression reduces endothelial dysfunction and attenuates early renal impairment in a rat model of diabetes
by
De Mey, Jo G. R.
, Flyvbjerg, Allan
, Sieber, Jonas
, Stehouwer, Coen D. A.
, Miyata, Toshio
, Janssen, Ben J. A.
, Peutz-Kootstra, Carine J.
, Mundel, Peter H.
, Brownlee, Michael
, Schalkwijk, Casper G.
, Brouwers, Olaf
, Niessen, Petra M. G.
, Østergaard, Jakob A.
in
Animals
/ Biological and medical sciences
/ Diabetes
/ Diabetes Mellitus - metabolism
/ Diabetes. Impaired glucose tolerance
/ Endocrine pancreas. Apud cells (diseases)
/ Endocrinopathies
/ Endothelium
/ Enzymes
/ Etiopathogenesis. Screening. Investigations. Target tissue resistance
/ Glucose
/ Human Physiology
/ Hyperglycemia
/ Hypotheses
/ Immunohistochemistry
/ Inflammation
/ Internal Medicine
/ Kidneys
/ Lactoylglutathione Lyase - genetics
/ Lactoylglutathione Lyase - metabolism
/ Male
/ Medical sciences
/ Medicine
/ Medicine & Public Health
/ Metabolic Diseases
/ Nephrology. Urinary tract diseases
/ Nephropathies. Renovascular diseases. Renal failure
/ Oxidative stress
/ Proteins
/ Pyruvaldehyde - metabolism
/ Rats
/ Rats, Transgenic
/ Renal failure
/ Veins & arteries
2014
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Glyoxalase-1 overexpression reduces endothelial dysfunction and attenuates early renal impairment in a rat model of diabetes
by
De Mey, Jo G. R.
, Flyvbjerg, Allan
, Sieber, Jonas
, Stehouwer, Coen D. A.
, Miyata, Toshio
, Janssen, Ben J. A.
, Peutz-Kootstra, Carine J.
, Mundel, Peter H.
, Brownlee, Michael
, Schalkwijk, Casper G.
, Brouwers, Olaf
, Niessen, Petra M. G.
, Østergaard, Jakob A.
in
Animals
/ Biological and medical sciences
/ Diabetes
/ Diabetes Mellitus - metabolism
/ Diabetes. Impaired glucose tolerance
/ Endocrine pancreas. Apud cells (diseases)
/ Endocrinopathies
/ Endothelium
/ Enzymes
/ Etiopathogenesis. Screening. Investigations. Target tissue resistance
/ Glucose
/ Human Physiology
/ Hyperglycemia
/ Hypotheses
/ Immunohistochemistry
/ Inflammation
/ Internal Medicine
/ Kidneys
/ Lactoylglutathione Lyase - genetics
/ Lactoylglutathione Lyase - metabolism
/ Male
/ Medical sciences
/ Medicine
/ Medicine & Public Health
/ Metabolic Diseases
/ Nephrology. Urinary tract diseases
/ Nephropathies. Renovascular diseases. Renal failure
/ Oxidative stress
/ Proteins
/ Pyruvaldehyde - metabolism
/ Rats
/ Rats, Transgenic
/ Renal failure
/ Veins & arteries
2014
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Glyoxalase-1 overexpression reduces endothelial dysfunction and attenuates early renal impairment in a rat model of diabetes
Journal Article
Glyoxalase-1 overexpression reduces endothelial dysfunction and attenuates early renal impairment in a rat model of diabetes
2014
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Overview
Aims/hypothesis
In diabetes, advanced glycation end-products (AGEs) and the AGE precursor methylglyoxal (MGO) are associated with endothelial dysfunction and the development of microvascular complications. In this study we used a rat model of diabetes, in which rats transgenically overexpressed the MGO-detoxifying enzyme glyoxalase-I (GLO-I), to determine the impact of intracellular glycation on vascular function and the development of early renal changes in diabetes.
Methods
Wild-type and
Glo1
-overexpressing rats were rendered diabetic for a period of 24 weeks by intravenous injection of streptozotocin. Mesenteric arteries were isolated to study ex vivo vascular reactivity with a wire myograph and kidneys were processed for histological examination. Glycation was determined by mass spectrometry and immunohistochemistry. Markers for inflammation, endothelium dysfunction and renal dysfunction were measured with ELISA-based techniques.
Results
Diabetes-induced formation of AGEs in mesenteric arteries and endothelial dysfunction were reduced by
Glo1
overexpression. Despite the absence of advanced nephrotic lesions, early markers of renal dysfunction (i.e. increased glomerular volume, decreased podocyte number and diabetes-induced elevation of urinary markers albumin, osteopontin, kidney-inflammation-molecule-1 and nephrin) were attenuated by
Glo1
overexpression. In line with this, downregulation of
Glo1
in cultured endothelial cells resulted in increased expression of inflammation and endothelium dysfunction markers. In fully differentiated cultured podocytes incubation with MGO resulted in apoptosis.
Conclusions/interpretation
This study shows that effective regulation of the GLO-I enzyme is important in the prevention of vascular intracellular glycation, endothelial dysfunction and early renal impairment in experimental diabetes. Modulating the GLO-I pathway therefore may provide a novel approach to prevent vascular complications in diabetes.
Publisher
Springer Berlin Heidelberg,Springer,Springer Nature B.V
Subject
/ Biological and medical sciences
/ Diabetes
/ Diabetes Mellitus - metabolism
/ Diabetes. Impaired glucose tolerance
/ Endocrine pancreas. Apud cells (diseases)
/ Enzymes
/ Etiopathogenesis. Screening. Investigations. Target tissue resistance
/ Glucose
/ Kidneys
/ Lactoylglutathione Lyase - genetics
/ Lactoylglutathione Lyase - metabolism
/ Male
/ Medicine
/ Nephrology. Urinary tract diseases
/ Nephropathies. Renovascular diseases. Renal failure
/ Proteins
/ Rats
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