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Early pre-diabetic state alters adaptation of myocardial glucose metabolism during ischemia in rats
- Source :
- Molecular and Cellular Biochemistry, Molecular and Cellular Biochemistry, Springer Verlag, 2005, 272 (1-2), pp.9-17. ⟨10.1007/s11010-005-4778-1⟩
- Publication Year :
- 2005
- Publisher :
- Springer Science and Business Media LLC, 2005.
-
Abstract
- International audience; Pre-diabetic subjects with high insulin secretory capacity have double risk of cardiovascular disease compared with subjects who do not develop insulin-resistance. It is well established that the ability of the myocardium to increase its glycolytic ATP production plays a crucial role in determining cell survival under conditions of ischemia. Up to now, whether the pre-diabetic state reduces the tolerance of the heart to ischemia by affecting its ability to increase its energy production through glycolysis remains unknown. The aim of the present study was to assess whether insulin resistance affects the ability of the myocardium to increase glycolysis under ischemic conditions. Male Wistar rats were fed for 8 weeks a fructose-enriched (33%) diet to induce a pre-diabetic state. Hearts were isolated and subjected to ex-vivo low-flow (2%) ischemia for 30 min. The fructose diet increased sarcolemmal GLUT4 localisation in myocardial cells under basal conditions compared with controls. This effect was not accompanied by increased glucose utilisation. Ischemia induced the translocation of GLUT4 to the plasma membrane in controls but did not significantly modify the distribution of these transporters in pre-diabetic hearts. Glycolytic flux under ischemic conditions was significantly lower in fructose-fed rat hearts compared with controls. The reduction of glycolytic flux during ischemia in fructose-fed rat hearts was not due to metabolic inhibition downstream hexokinase II since no cardiac accumulation of glucose-6-phosphate was detected. In conclusion, our results suggest that the pre-diabetic state reduces the tolerance of the myocardium to ischemia by decreasing glycolytic flux adaptation.
- Subjects :
- Male
pre-diabetic state
MESH: Glycogen
Clinical Biochemistry
Myocardial Ischemia
Muscle Proteins
MESH: Myocytes, Cardiac
030204 cardiovascular system & hematology
Sarcolemma
0302 clinical medicine
MESH: Diabetes Mellitus, Experimental
Myocytes, Cardiac
MESH: Animals
Glycolysis
Hexosephosphates
MESH: Sarcolemma
0303 health sciences
Glucose Transporter Type 4
MESH: Hexosephosphates
General Medicine
glycolysis
Adaptation, Physiological
3. Good health
MESH: Glucose
Protein Transport
MESH: Insulin Resistance
MESH: Monosaccharide Transport Proteins
MESH: Glycolysis
MESH: Myocardial Ischemia
glucose extraction
Glycogen
MESH: Protein Transport
medicine.medical_specialty
MESH: Myocardium
Monosaccharide Transport Proteins
MESH: Rats
Clinical chemistry
Ischemia
Fructose
ischemia
In Vitro Techniques
Carbohydrate metabolism
Biology
Diabetes Mellitus, Experimental
MESH: Prediabetic State
Prediabetic State
MESH: Muscle Proteins
03 medical and health sciences
Insulin resistance
[SDV.MHEP.CSC]Life Sciences [q-bio]/Human health and pathology/Cardiology and cardiovascular system
Internal medicine
medicine
Animals
Lactic Acid
Rats, Wistar
Molecular Biology
030304 developmental biology
Myocardium
MESH: Rats, Wistar
Cell Biology
medicine.disease
MESH: Adaptation, Physiological
MESH: Male
Rats
Glucose
Endocrinology
Basal (medicine)
biology.protein
GLUT4 translocation
MESH: Lactic Acid
MESH: Glucose Transporter Type 4
Insulin Resistance
MESH: Fructose
Flux (metabolism)
GLUT4
Subjects
Details
- ISSN :
- 15734919 and 03008177
- Volume :
- 272
- Database :
- OpenAIRE
- Journal :
- Molecular and Cellular Biochemistry
- Accession number :
- edsair.doi.dedup.....affe6d765b998293a7b3897451e8d85c
- Full Text :
- https://doi.org/10.1007/s11010-005-4778-1