Effect of streptozotocin-induced diabetes on left ventricular function in adult rats: an in vivo Pinhole Gated SPECT study

<p>Abstract</p> <p>Background</p> <p>Recent studies have suggested that diabetes mellitus (DM) may cause left ventricular (LV) dysfunction directly resulting in increased susceptibility to heart failure. Using pinhole collimators and advances in data processing, gated S...

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Main Authors: Weytjens Caroline, Droogmans Steven, Cosyns Bernard, Lahoutte Tony, Van Camp Guy, Schoors Danny, Franken Philippe R
Format: Article
Language:English
Published: BMC 2007-10-01
Series:Cardiovascular Diabetology
Online Access:http://www.cardiab.com/content/6/1/30
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author Weytjens Caroline
Droogmans Steven
Cosyns Bernard
Lahoutte Tony
Van Camp Guy
Schoors Danny
Franken Philippe R
author_facet Weytjens Caroline
Droogmans Steven
Cosyns Bernard
Lahoutte Tony
Van Camp Guy
Schoors Danny
Franken Philippe R
author_sort Weytjens Caroline
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Recent studies have suggested that diabetes mellitus (DM) may cause left ventricular (LV) dysfunction directly resulting in increased susceptibility to heart failure. Using pinhole collimators and advances in data processing, gated SPECT was recently adapted to image the rat heart. The present study was aimed to assess this new imaging technique for quantifying LV function and remodeling from the Streptozotocin (STZ) rat model compared to controls.</p> <p>Methods</p> <p>Twenty one rats were randomly assigned to control or diabetic group. Six months after the induction of diabetes by STZ, Pinhole 99 m Tc-sestamibi gated SPECT was performed for determining rat LV volumes and function. Post-mortem histopathologic analysis was performed to evaluate the determinant of LV remodeling in this model.</p> <p>Results</p> <p>After six months, the normalized to body weight LV End-systolic volume was significantly different in diabetic rats compared to controls (0.46 ± 0.02 vs 0.33 ± 0.03 μL/g; p = 0.01). The normalized LV End-diastolic volume was also different in both groups (1.51 ± 0.03 vs 0.88 ± 0.05 μL/g; p = 0.001) and the normalized stroke volume was significantly higher in STZ-rats (1.05 ± 0.02 vs 0.54 ± 0.06 μL/g; p = 0.001). The muscular fibers were thinner at histology in the diabetic rats (0.44 ± 0.07 vs 0.32 ± 0.06 AU; p = 0.01).</p> <p>Conclusion</p> <p>Pinhole 99 m Tc-sestamibi gated SPECT can successfully be applied for the evaluation of cardiac function and remodeling in STZ-induced diabetic rats. In this model, LV volumes were significantly changed compared to a control population, leading to a LV dysfunction. These findings were consistent with the histopathological abnormalities. Finally, these data further suggest the presence of diabetes cardiomyopathy.</p>
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spelling doaj.art-a799791fa5e64fbfbab746dfadbdfbb42022-12-22T01:43:05ZengBMCCardiovascular Diabetology1475-28402007-10-01613010.1186/1475-2840-6-30Effect of streptozotocin-induced diabetes on left ventricular function in adult rats: an in vivo Pinhole Gated SPECT studyWeytjens CarolineDroogmans StevenCosyns BernardLahoutte TonyVan Camp GuySchoors DannyFranken Philippe R<p>Abstract</p> <p>Background</p> <p>Recent studies have suggested that diabetes mellitus (DM) may cause left ventricular (LV) dysfunction directly resulting in increased susceptibility to heart failure. Using pinhole collimators and advances in data processing, gated SPECT was recently adapted to image the rat heart. The present study was aimed to assess this new imaging technique for quantifying LV function and remodeling from the Streptozotocin (STZ) rat model compared to controls.</p> <p>Methods</p> <p>Twenty one rats were randomly assigned to control or diabetic group. Six months after the induction of diabetes by STZ, Pinhole 99 m Tc-sestamibi gated SPECT was performed for determining rat LV volumes and function. Post-mortem histopathologic analysis was performed to evaluate the determinant of LV remodeling in this model.</p> <p>Results</p> <p>After six months, the normalized to body weight LV End-systolic volume was significantly different in diabetic rats compared to controls (0.46 ± 0.02 vs 0.33 ± 0.03 μL/g; p = 0.01). The normalized LV End-diastolic volume was also different in both groups (1.51 ± 0.03 vs 0.88 ± 0.05 μL/g; p = 0.001) and the normalized stroke volume was significantly higher in STZ-rats (1.05 ± 0.02 vs 0.54 ± 0.06 μL/g; p = 0.001). The muscular fibers were thinner at histology in the diabetic rats (0.44 ± 0.07 vs 0.32 ± 0.06 AU; p = 0.01).</p> <p>Conclusion</p> <p>Pinhole 99 m Tc-sestamibi gated SPECT can successfully be applied for the evaluation of cardiac function and remodeling in STZ-induced diabetic rats. In this model, LV volumes were significantly changed compared to a control population, leading to a LV dysfunction. These findings were consistent with the histopathological abnormalities. Finally, these data further suggest the presence of diabetes cardiomyopathy.</p>http://www.cardiab.com/content/6/1/30
spellingShingle Weytjens Caroline
Droogmans Steven
Cosyns Bernard
Lahoutte Tony
Van Camp Guy
Schoors Danny
Franken Philippe R
Effect of streptozotocin-induced diabetes on left ventricular function in adult rats: an in vivo Pinhole Gated SPECT study
Cardiovascular Diabetology
title Effect of streptozotocin-induced diabetes on left ventricular function in adult rats: an in vivo Pinhole Gated SPECT study
title_full Effect of streptozotocin-induced diabetes on left ventricular function in adult rats: an in vivo Pinhole Gated SPECT study
title_fullStr Effect of streptozotocin-induced diabetes on left ventricular function in adult rats: an in vivo Pinhole Gated SPECT study
title_full_unstemmed Effect of streptozotocin-induced diabetes on left ventricular function in adult rats: an in vivo Pinhole Gated SPECT study
title_short Effect of streptozotocin-induced diabetes on left ventricular function in adult rats: an in vivo Pinhole Gated SPECT study
title_sort effect of streptozotocin induced diabetes on left ventricular function in adult rats an in vivo pinhole gated spect study
url http://www.cardiab.com/content/6/1/30
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