Abnormal cardiac function in the streptozotocin-diabetic rat. Changes in active and passive properties of the left ventricle
- PMID: 2200804
- PMCID: PMC296750
- DOI: 10.1172/JCI114734
Abnormal cardiac function in the streptozotocin-diabetic rat. Changes in active and passive properties of the left ventricle
Abstract
To provide an integrated assessment of changes in systolic and diastolic function in diabetic rats, we measured conscious hemodynamics and performed ex vivo analysis of left ventricular passive-elastic properties. Rats given streptozotocin (STZ) 65 mg/kg i.v. (n = 14) were compared with untreated age-matched controls (n = 15) and rats treated with insulin after administration of STZ (n = 11). After 7 d, diabetic rats exhibited decreases in heart rate and peak developed left ventricular (LV) pressure during aortic occlusion. After 26 d of diabetes there were significant decreases in resting LV systolic pressure, developed pressure, and maximal +dP/dt, whereas LV end-diastolic pressure increased and the time constant of LV relaxation was prolonged. The passive LV pressure-volume relationship was progressively shifted away from the pressure axis, and the overall chamber stiffness constant was decreased. However, "operating chamber stiffness" calculated at end-diastolic pressure was increased at 7 d, and unchanged at 26 d. LV cavity/wall volume and end-diastolic volume were increased after 26 d of diabetes. Myocardial stiffness was unchanged at both time intervals. All of the above abnormalities were reversed by the administration of insulin. We conclude that the hemodynamic and passive-elastic changes that occur in diabetic rats represent an early dilated cardiomyopathy which is reversible with insulin.
Similar articles
-
Acute effects of methoxamine on left ventricular-arterial coupling in streptozotocin-diabetic rats: a pressure-volume analysis.Can J Physiol Pharmacol. 2000 May;78(5):415-22. Can J Physiol Pharmacol. 2000. PMID: 10841437
-
Abnormal cardiac function in the streptozotocin-induced non-insulin-dependent diabetic rat: noninvasive assessment with doppler echocardiography and contribution of the nitric oxide pathway.J Am Coll Cardiol. 1999 Dec;34(7):2111-9. doi: 10.1016/s0735-1097(99)00436-2. J Am Coll Cardiol. 1999. PMID: 10588232
-
[Relation between systolic and diastolic elastic muscle properties and the morphology of the hypertrophic pressure-loaded left ventricle].Z Kardiol. 1987 Nov;76(11):706-12. Z Kardiol. 1987. PMID: 3424906 German.
-
Habitual exercise attenuates myocardial stiffness in diabetes mellitus in rats.Am J Physiol. 1996 Nov;271(5 Pt 2):H2126-33. doi: 10.1152/ajpheart.1996.271.5.H2126. Am J Physiol. 1996. PMID: 8945933
-
Rat strain-related differences in myocardial adrenergic tone and the impact on cardiac fibrosis, adrenergic responsiveness and myocardial structure and function.Pharmacol Res. 2007 Apr;55(4):287-94. doi: 10.1016/j.phrs.2006.12.005. Epub 2006 Dec 28. Pharmacol Res. 2007. PMID: 17257851
Cited by
-
Alteration in haemodynamics and pathological changes in the cardiovascular system during the development of Type 2 diabetes mellitus in OLETF rats.Diabetologia. 2003 Aug;46(8):1161-9. doi: 10.1007/s00125-003-1156-y. Epub 2003 Jul 11. Diabetologia. 2003. PMID: 12856125
-
Early alterations in myocardia and vessels of the diabetic rat heart: an FTIR microspectroscopic study.Biochem J. 2006 Aug 1;397(3):427-36. doi: 10.1042/BJ20060171. Biochem J. 2006. PMID: 16719841 Free PMC article.
-
Caffeic acid phenethyl amide ameliorates ischemia/reperfusion injury and cardiac dysfunction in streptozotocin-induced diabetic rats.Cardiovasc Diabetol. 2014 Jun 12;13:98. doi: 10.1186/1475-2840-13-98. Cardiovasc Diabetol. 2014. PMID: 24923878 Free PMC article.
-
Chronic Rho-kinase inhibition improves left ventricular contractile dysfunction in early type-1 diabetes by increasing myosin cross-bridge extension.Cardiovasc Diabetol. 2015 Jul 22;14:92. doi: 10.1186/s12933-015-0256-6. Cardiovasc Diabetol. 2015. PMID: 26194354 Free PMC article.
-
Hyperglycemia and heart dysfunction: an oxidant mechanism contributing to heart failure in diabetes.J Endocrinol Invest. 2002 May;25(5):485-8. doi: 10.1007/BF03344043. J Endocrinol Invest. 2002. PMID: 12035949 Review. No abstract available.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources