Spallarossa P, Schiavo M, Rossettin P, Cordone S, Olivotti L, Cordera R, Brunelli C
Department of Internal Medicine, University of Genova, Italy.
Diabetes Care. 2001 Apr;24(4):738-42. doi: 10.2337/diacare.24.4.738.
Sulfonylureas block the activation of vascular potassium-dependent ATP channels and impair the vasodilating response to ischcmia in nondiabetic individuals, but it is not know whether this occurs in type 2 diabetic patients under chronic treatment with these drugs. Glimepiride, a new sulfonylurea, apparently has no cardiovascular interactions. The aim of our study was to compare the effect of the widely used compound glibenclamide, the pancreas-specific glimepiride, and diet treatment alone on brachial artery response to acute forearm ischemia.
Brachial artery examination was performed by a high-resolution ultrasound technique on 20 type 2 diabetic patients aged mean +/- SD) 67 +/- 2 years and on 18 nondiabetic patients matched for age, hypertension, and dislipidemia. Diabetic subjects underwent three separate evaluations at the end of each 8-week treatment period, during which they received glibenclamide, glimepiride, or diet alone according to crossover design. Scans were obtained before and after 4.5 min of forearm ischemia. Postischemic vasodilation and hyperemia were expressed as percent variations in vessel diameter and blood flow.
Postischemic vasodilation and hyperemia were, respectively, 5.42 +/- 0.90 and 331 +/- 38% during glibenclamide, 5.46 +/- 0.69 and 326 +/- 28% during glimepiride, and 5.17 +/- 0.64 and 357 +/- 35% during diet treatment (NS). These results were similar to those found in the nondiabetic patients (6.44 +/- 0.68 and 406 +/- 42%, NS).
In type 2 diabetic patients, the vasodilating response to forearm ischemia was the same whether patients were treated with diet treatment alone or with glibenclamide or glimepiride at blood glucose-lowering equipotent closes.
磺脲类药物可阻断非糖尿病个体血管中依赖钾离子的ATP通道的激活,并损害对缺血的血管舒张反应,但尚不清楚在接受这些药物长期治疗的2型糖尿病患者中是否也会出现这种情况。新型磺脲类药物格列美脲显然没有心血管相互作用。我们研究的目的是比较广泛使用的化合物格列本脲、胰腺特异性的格列美脲以及单纯饮食治疗对肱动脉对急性前臂缺血反应的影响。
采用高分辨率超声技术对20例2型糖尿病患者(平均年龄±标准差为67±2岁)和18例年龄、高血压和血脂异常相匹配的非糖尿病患者进行肱动脉检查。糖尿病受试者在每8周治疗期结束时进行三次单独评估,在此期间,他们根据交叉设计分别接受格列本脲、格列美脲或单纯饮食治疗。在4.5分钟前臂缺血前后进行扫描。缺血后血管舒张和充血以血管直径和血流量的百分比变化表示。
格列本脲治疗期间缺血后血管舒张和充血分别为5.42±0.90和331±38%,格列美脲治疗期间为5.46±0.69和326±28%,饮食治疗期间为5.17±0.64和 357±35%(无显著性差异)。这些结果与在非糖尿病患者中发现的结果相似(6.44±0.68和406±42%,无显著性差异)。
在2型糖尿病患者中,无论患者是接受单纯饮食治疗还是接受降糖等效剂量的格列本脲或格列美脲治疗,对前臂缺血的血管舒张反应都是相同的。