Crespo M J, Dunbar D C
Department of Physiology, University of Puerto Rico-School of Medicine, PO Box 365067, San Juan, PR 00936-5067, USA.
Cell Mol Biol (Noisy-le-grand). 2003 Dec;49(8):1311-8.
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.
近期证据表明,肾素 - 血管紧张素系统(RAS)是参与糖尿病患者微血管和大血管疾病病因的系统之一。为了有助于阐明这种可能性,在糖尿病诱导后2周,评估了依那普利(25mg/kg/d)每日治疗对链脲佐菌素(STZ)诱导的糖尿病大鼠的影响。使用未治疗的糖尿病大鼠和年龄匹配的非糖尿病大鼠作为对照。血管研究包括测定主动脉环对去甲肾上腺素(NE)、血管紧张素II(Ang II)和乙酰胆碱(Ach)的反应。还评估了收缩压(SBP)、心输出量(CO)指数、血浆和血管中的血管紧张素转换酶(ACE)活性以及主动脉壁厚度。依那普利通过将最大舒张率从未治疗的糖尿病大鼠中的54.3±4.3%提高到89.8±6.2%(n = 9,p<0.05)以及将EC50值从未治疗的糖尿病动物中的32.6±9.9nmol/l降低到17.9±5.1nmol/l(n = 8,p<0.05),改善了Ach诱导的舒张。此外,依那普利使糖尿病大鼠中对NE的高反应正常化,而不改变EC50值。在依那普利治疗的糖尿病组中,观察到SBP显著降低(从158±4mmHg降至123±1mmHg,p<0.05),同时CO指数改善(从40±2ml/min×100g体重增加到50±1ml/min×100g体重)。治疗后糖尿病大鼠主动脉的中膜厚度也显著消退。糖尿病大鼠主动脉中的ACE活性比对照组增加了一倍(p<0.05),依那普利治疗后降低。这些结果表明血管RAS是糖尿病早期血管改变病因中的关键系统之一。因此,在糖尿病患者疾病的极早期治疗中,应考虑使用ACE抑制剂以及其他针对血管RAS的药理学方法。