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Enhanced left ventricular systolic function early in type 2 diabetic mice: clinical implications
Jorge A Alvarez1, Maricela Reyes, Daniel Escobedo
1Department of Medicine, University of Texas Health Science Center in San Antonio, San Antonio, Texas, 78229-3900, USA.
Diabetes & Vascular Disease Research
|November 24, 2005
Summary
Type 2 diabetes in mice enhances early systolic function before structural changes occur. This improved cardiac performance may contribute to increased kidney filtration rates observed in early diabetes.
Area of Science:
- Cardiology
- Metabolic Diseases
- Physiology
Background:
- Diabetes mellitus is associated with cardiac dysfunction.
- Early diabetes may present with altered myocardial substrate availability.
- The impact of early diabetes on systolic function before structural changes is not well understood.
Purpose of the Study:
- To investigate if increased substrate availability in early type 2 diabetes enhances left ventricular systolic function.
- To determine if enhanced systolic function precedes myocardial structural changes in diabetes.
Main Methods:
- Utilized BKS.Cg-m +/+ Lepr db (db/db) mice (type 2 diabetes) and wild type controls.
- Determined in situ left ventricular pressure-volume relationships.
- Assessed parameters including power/EDV, positive dP/dt, preload recruitable stroke work, dP/dt--EDV relationship, and end-systolic elastance.
Main Results:
- db/db mice exhibited enhanced left ventricular systolic function compared to controls.
- Specific indicators of enhanced function included increased power/EDV, positive dP/dt, preload recruitable stroke work, dP/dt--EDV relationship, and end-systolic elastance.
- This enhancement occurred despite increased body weight but similar preload and afterload.
Conclusions:
- Early type 2 diabetes in db/db mice is associated with enhanced left ventricular systolic function.
- This enhanced systolic function may be a compensatory mechanism.
- Enhanced cardiac function could potentially explain increased renal glomerular filtration rates in early diabetes.