HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Myocardial glucose uptake evaluated by positron emission tomography and fluorodeoxyglucose during hyperglycemic clamp in IDDM patients. Role of free fatty acid and insulin levels.

Abstract
Myocardial and whole-body glucose metabolism was assessed in 19 insulin-dependent diabetes mellitus (IDDM) patients. A hyperglycemic clamp was performed 1) in the absence of insulin at free fatty acid (FFA) levels of 1.0 mmol/l (test 1); 2) in the absence of insulin at low FFA levels (0.1 mmol/l) by means of a lipid-lowering drug, acipimox (test 2); 3) during insulin infusion to achieve systemic levels of 400 pmol/l and FFA levels of 0.1 mmol/l (test 3); and 4) at the insulin levels of test 3 but increasing FFA to 1.0 mmol/l by means of heparin and intralipid infusion (test 4). Myocardial glucose uptake was measured by positron emission tomography (PET) and 2-[18F]fluoro-2-deoxy-D-glucose. Whole-body glucose uptake was measured in the four conditions by the glucose infusion rate during the PET scanning period. Myocardial glucose uptakes were 40.3 +/- 18.0, 395.5 +/- 139.6, 852.2 +/- 99.1, and 1,388.4 +/- 199.1 mumol.kg tissue-1.min-1 (mean +/- SD) and whole-body glucose uptakes were 10.1 +/- 2.3, 10.1 +/- 3.4, 42.8 +/- 5.8, and 30.5 +/- 5.6 mumol.kg body wt-1.min-1 during tests 1, 2, 3, and 4, respectively. Thus, in IDDM patients without coronary artery disease under the condition of hyperglycemia, an increase of myocardial glucose uptake was obtained either by lowering of FFA levels during hypoinsulinemia or by an increase in FFA levels during hyperinsulinemia. In both conditions no significant changes of whole-body glucose uptake were demonstrated.
AuthorsL D Monti, G Lucignani, C Landoni, R M Moresco, P Piatti, I Stefani, G Pozza, F Fazio
JournalDiabetes (Diabetes) Vol. 44 Issue 5 Pg. 537-42 (May 1995) ISSN: 0012-1797 [Print] United States
PMID7729612 (Publication Type: Clinical Trial, Journal Article)
Chemical References
  • Fat Emulsions, Intravenous
  • Fatty Acids, Nonesterified
  • Hypolipidemic Agents
  • Insulin
  • Pyrazines
  • Fluorodeoxyglucose F18
  • Somatostatin
  • Deoxyglucose
  • Glucose
  • acipimox
Topics
  • Adult
  • Biological Transport, Active
  • Deoxyglucose (analogs & derivatives, pharmacokinetics)
  • Diabetes Mellitus, Type 1 (blood, drug therapy, metabolism)
  • Fat Emulsions, Intravenous (administration & dosage)
  • Fatty Acids, Nonesterified (blood)
  • Fluorodeoxyglucose F18
  • Glucose (metabolism)
  • Glucose Clamp Technique
  • Humans
  • Hypolipidemic Agents (administration & dosage)
  • Insulin (administration & dosage, blood)
  • Male
  • Myocardium (metabolism)
  • Pyrazines (administration & dosage)
  • Somatostatin (administration & dosage)
  • Tomography, Emission-Computed

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: