Laboratório de Pesquisa do Exercício, Escola de Educação Física, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Eur J Nutr. 2013 Apr;52(3):975-83. doi: 10.1007/s00394-012-0404-7. Epub 2012 Jul 6.
Vascular disease is the principal cause of death and disability in patients with diabetes, and endothelial dysfunction seems to be the major cause in its pathogenesis. Since L-arginine levels are diminished in conditions such as type 1 and type 2 diabetes, in this work we aimed to verify the effects of L-arginine supplementation (7 g/day) over the endothelial function and oxidative stress markers in young male adults with uncomplicated type 1 diabetes. We also investigated the influences of L-arginine administration on vascular/oxidative stress responses to an acute bout of exercise.
Ten young adult male subjects with uncomplicated type 1 diabetes and twenty matched controls volunteered for this study. We analysed the influence of L-arginine supplementation (7 g/day during 1 week) over lower limb blood flow (using a venous occlusion plethysmography technique), oxidative stress marker (TBARS, Carbonyls), anti-oxidant parameters (uric acid and TRAP) and total tNOx in rest conditions and after a single bout of submaximal exercise (VO₂ at 10 % below the second ventilatory threshold). Data described as mean ± standard error (SE). Alpha level was P < 0.05.
Glycaemic control parameters were altered in type 1 diabetic subjects, such as HbA1c (5.5 ± 0.03 vs. 8.3 ± 0.4 %) and fasted glycaemia (94.8 ± 1.4 vs. 183 ± 19 mg/dL). Oxidative stress/damage markers (carbonyls and TBARS) were increased in the diabetic group, while uric acid was decreased. Rest lower limb blood flow was lower in type 1 diabetic subjects than in healthy controls (3.53 ± 0.35 vs. 2.66 ± 0.3 ml 100 ml⁻¹ min⁻¹). L-Arginine supplementation completely recovered basal blood flow to normal levels in type 1 diabetics' subjects (2.66 ± 0.3 to 4.74 ± 0.86 ml 100 ml⁻¹ min⁻¹) but did not interfere in any parameter of redox state or exercise.
Our findings highlight the importance of L-arginine for the improvement of vascular function in subjects with diabetes, indicating that L-arginine supplementation could be an essential tool for the treatment for the disease complications, at least in non-complicated diabetes. However, based on our data, it is not possible to draw conclusions regarding the mechanisms by which L-arginine therapy is inducing improvements on cardiovascular function, but this important issue requires further investigations.
血管疾病是糖尿病患者死亡和残疾的主要原因,而内皮功能障碍似乎是其发病机制的主要原因。由于 1 型和 2 型糖尿病等情况下 L-精氨酸水平降低,因此在这项工作中,我们旨在验证 L-精氨酸补充(每天 7 克)对无并发症 1 型糖尿病年轻男性成年人内皮功能和氧化应激标志物的影响。我们还研究了 L-精氨酸给药对急性运动时血管/氧化应激反应的影响。
10 名无并发症 1 型糖尿病的年轻成年男性受试者和 20 名匹配的对照自愿参加了这项研究。我们分析了 L-精氨酸补充(7 克/天,持续 1 周)对下肢血流(使用静脉闭塞体积描记术技术)、氧化应激标志物(TBARS、羰基)、抗氧化参数(尿酸和 TRAP)和总 tNOx 的影响,以及在休息条件下和单次亚最大运动(第二通气阈值以下 10%的 VO₂)后。数据表示为平均值±标准误差(SE)。α水平为 P<0.05。
1 型糖尿病患者的血糖控制参数发生改变,例如 HbA1c(5.5±0.03 与 8.3±0.4%)和空腹血糖(94.8±1.4 与 183±19 mg/dL)。氧化应激/损伤标志物(羰基和 TBARS)在糖尿病组中增加,而尿酸减少。1 型糖尿病患者的下肢基础血流低于健康对照组(3.53±0.35 与 2.66±0.3 ml/100 ml⁻¹ min⁻¹)。L-精氨酸补充完全将 1 型糖尿病患者的基础血流恢复到正常水平(2.66±0.3 至 4.74±0.86 ml/100 ml⁻¹ min⁻¹),但对氧化还原状态或运动的任何参数均无影响。
我们的发现强调了 L-精氨酸对改善糖尿病患者血管功能的重要性,表明 L-精氨酸补充可能是治疗疾病并发症的重要工具,至少在非复杂性糖尿病中是这样。然而,根据我们的数据,尚无法得出关于 L-精氨酸治疗如何改善心血管功能的机制的结论,但这一重要问题需要进一步研究。