Cited by 266Cardiovascular Function and Risk FactorsCardiac Fibrosis and RemodelingDiabetes, Cardiovascular Risks, and Lipoproteins

Echocardiographic assessment of cardiac function in diabetic db/db and transgenic db/db-hGLUT4 mice

Semeniuk, Lisa M., Kryski, Albert J., Severson, David L.·2002·American Journal of Physiology-Heart and Circulatory Physiology

Abstract

Control db/+ and diabetic db/ db mice at 6 and 12 wk of age were subjected to echocardiography to determine whether contractile function was reduced in vivo and restored in transgenic db/ db-human glucose transporter 4 (hGLUT4) mice (12 wk old) in which cardiac metabolism has been normalized. Systolic function was unchanged in 6-wk-old db/ db mice, but fractional shortening and velocity of circumferential fiber shortening were reduced in 12-wk-old db/ db mice (43.8 ± 2.1% and 8.3 ± 0.5 circs/s, respectively) relative to db/+ control mice (59.5 ± 2.3% and 11.8 ± 0.4 circs/s, respectively). Doppler flow measurements were unchanged in 6-wk-old db/ db mice. The ratio of E and A transmitral flows was reduced from 3.56 ± 0.29 in db/+ mice to 2.40 ± 0.20 in 12-wk-old db/ dbmice, indicating diastolic dysfunction. Thus a diabetic cardiomyopathy with systolic and diastolic dysfunction was evident in 12-wk-old diabetic db/ db mice. Cardiac function was normalized in transgenic db/ db-hGLUT4 mice, indicating that altered cardiac metabolism can produce contractile dysfunction in diabetic db/ db hearts.

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Crossref · 10.1152/ajpheart.00088.2002

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  • In animal models of obesity, most in vivo studies reveal mildly impaired systolic function that is absent in younger animals (<12 wk of age) but becomes evident between 12 and 20 wk of age.

    “Generally, most studies reveal evidence of mildly impaired systolic function in vivo that is absent in younger animals (<12 wk of age) but become evident between 12 and 20 wk of age (34, 53, 313, 357, 361, 388).”

    From Cardiac remodeling in obesity (2008) · cites this paper as [313]

  • Fewer studies reveal changes in diastolic function in animal models of obesity.

    “Fewer studies reveal changes in diastolic function (53, 313).”

    From Cardiac remodeling in obesity (2008) · cites this paper as [313]

  • In db/db mice, systolic and diastolic dysfunction by echocardiography is absent at 6 wk of age but present at 12 wk of age.

    “Similar findings have been reported in db/db mice with evidence of systolic and diastolic function by echocardiography that was absent in 6-wk-old (shortly after onset of hyperglycemia) but present in 12-wk-old mice (313).”

    From Cardiac remodeling in obesity (2008) · cites this paper as [313]

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References 43 · Cited by 266

Authors
Semeniuk, L. M., Kryski, A. J., & Severson, D. L.
Affiliations
  • Department of Pharmacology and Therapeutics and
  • University of Calgary (CA)
Venue
American Journal of Physiology-Heart and Circulatory Physiology
Published
2002-09-01
Volume
283
Issue
3
Pages
H976-H982
ISSN
  • 0363-6135 (ISSN-L)
  • 1522-1539
OpenAlex
W2155799150
Cited by
266
References
43
Citations by year
2026: 5 · 2025: 10 · 2024: 4 · 2023: 4 · 2022: 10 · 2021: 13 · 2020: 9 · 2019: 11 · 2018: 7 · 2017: 10 · 2016: 8 · 2015: 19 · 2014: 16 · 2013: 14 · 2012: 16
FWCI
6.14
Type
journal article
Language
en
Open access
closed
Locations
  • American Journal of Physiology-Heart and Circulatory Physiology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Function and Risk Factors
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Fibrosis and Remodeling
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
Keywords
diabetic cardiomyopathy, db/db mice, glucose transporter 4, cardiac contractile dysfunction, systolic dysfunction, diastolic dysfunction, myocardial metabolism, echocardiography, fractional shortening
MeSH terms
Animals, Diabetes Mellitus, Type 2, Diastole, Echocardiography, Male, Mice, Inbred C57BL, Mice, Transgenic, Monosaccharide Transport Proteins, Muscle Proteins, Cardiomyopathies, Systole, Reproducibility of Results, Observer Variation, Glucose Transporter Type 4, Mice

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