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Updated: Feb 9, 2026

Modeling and Evaluation of Murine Diabetic Cardiomyopathy Model
Published on: November 29, 2024
Enalapril improves vascular and cardiac function in streptozotocin-diabetic rats
1Department of Physiology, University of Puerto Rico-School of Medicine, PO Box 365067, San Juan, PR 00936-5067, USA. mcrespo@rcm.upr.edu
Abstract:
Recent evidence points to the renin-angiotensin system (RAS) as one of the systems involved in the etiology of micro- and macrovascular disease in diabetic patients. To help elucidate this possibility, the effect of daily treatment with enalapril (25 mg/kg/d) was evaluated in streptozotocin (STZ)-diabetic rats at 2 weeks following the induction of diabetes. Untreated diabetic rats and non-diabetic rats that were age-matched were used for comparison. Vascular studies included the determination of aortic ring responses to norepinephrine (NE), angiotensin II (Ang II) and acetylcholine (Ach). Systolic blood pressure (SBP), cardiac output (CO) indices, plasmatic and vascular angiotensin-converting enzyme (ACE) activity and thickness of the aortic wall were also assessed. Enalapril improved Ach-induced relaxation by increasing the maximal relaxation from 54.3 +/- 4.3% in untreated diabetic rats to 89.8 +/- 6.2% (n=9, p<0.05) and by decreasing the EC50 value from 32.6 +/- 9.9 nmol/l in untreated diabetic animals to 17.9 +/- 5.1 nmol/l (n=8, p<0.05). In addition, enalapril normalized the high responses to NE found in diabetic rats without inducing changes in the EC50 value. A significant reduction in SBP (from 158 +/- 4 mm Hg to 123 +/- 1 mm Hg, p<0.05), combined with an improved CO index (from 40 +/- 2 ml/min x 100 g BW to 50 +/- 1 ml/min x 100 g BW), was observed in the enalapril-treated diabetic group. A significant regression of the media thickness was also observed in the aorta of diabetic rats after treatment. ACE activity in the aorta of diabetic rats, that was doubled compared to controls (p<0.05), decreased after enalapril treatment. These results point to the vascular RAS as one of the key systems in the etiology of vascular alterations at early stages of diabetes. Therefore, ACE inhibitors, as well as other pharmacological approaches targeting the vascular RAS, should be considered in the treatment of diabetic patients from the very early stages of the condition.
Insights
Enalapril treatment improved vascular function and reduced blood pressure in diabetic rats, suggesting the renin-angiotensin system plays a key role in diabetic vascular disease.
Area of Science:
- Cardiovascular Pharmacology
- Endocrinology
- Diabetic Complications
Background:
- The renin-angiotensin system (RAS) is implicated in micro- and macrovascular complications of diabetes.
- Diabetic vascular disease involves alterations in vascular responses and structure.
Purpose of the Study:
- To investigate the effects of enalapril on vascular function and related parameters in streptozotocin-induced diabetic rats.
- To elucidate the role of the vascular RAS in early-stage diabetic vascular alterations.
Main Methods:
- Daily enalapril treatment (25 mg/kg/d) in STZ-diabetic rats for 2 weeks.
- Assessment of aortic ring responses to norepinephrine, angiotensin II, and acetylcholine.
- Measurement of systolic blood pressure, cardiac output, plasma and vascular ACE activity, and aortic wall thickness.
Main Results:
- Enalapril improved acetylcholine-induced relaxation and normalized norepinephrine responses in diabetic rat aortas.
- Treatment significantly reduced systolic blood pressure and improved cardiac output index.
- Aortic media thickness regressed, and vascular ACE activity decreased following enalapril administration.
Conclusions:
- The vascular RAS is a critical factor in the early development of vascular alterations in diabetes.
- Angiotensin-converting enzyme (ACE) inhibitors like enalapril show promise for treating early-stage diabetic vascular disease.
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