Oral L-Arginine Modulates Blood Lactate and Interleukin-6 After Exercise in HIV-Infected Men

被引:2
作者
Alves, G. N. [1 ]
Tavares, A. M. V. [2 ]
Vieira, P. J. C. [2 ]
Sprinz, E. [3 ]
Ribeiro, J. P. [1 ]
机构
[1] Hosp Clin Porto Alegre, Div Cardiol, BR-90035007 Porto Alegre, RS, Brazil
[2] Hosp Clin Porto Alegre, Exercise Pathophysiol Res Lab, BR-90035007 Porto Alegre, RS, Brazil
[3] Hosp Clin Porto Alegre, Div Internal Med, BR-90035007 Porto Alegre, RS, Brazil
关键词
nitric oxide; cytokines; inflammation; lactate; exercise; NITRIC-OXIDE SYNTHASE; INDUCED INCREASE; SKELETAL-MUSCLE; SUPPLEMENTATION; PERFORMANCE; PATHOGENESIS; METABOLISM; EXPRESSION; CAPACITY;
D O I
10.1055/s-0032-1331740
中图分类号
G8 [体育];
学科分类号
04 ; 0403 ;
摘要
The acute administration of L-arginine (L-arg), a nitric oxide (NO) precursor, reduces lactate (LAC) concentration after exercise in healthy individuals. Lower concentration of L-arg may enhance the action of some inflammatory cytokines in HIV-1 infected patients. We tested the hypothesis that acute L-arg administration may reduce post-exercise blood LAC and inflammatory cytokines levels in HIV-infected patients. 10 HIV-infected men performed 2 maximal incremental cardiopulmonary exercise tests, separated by one week. 30 min before each test, patients received oral placebo or 20 g of L-arg, in random order. Blood LAC, tumor necrosis factor alpha (TNF-alpha), interleukin-6 (IL-6), and interleukin-10 (IL-10) were measured before and up to 60 min after exercise. L-arg administration had no significant effect on exercise performance. Compared to placebo, L-arg administration reduced maximal post-exercise blood LAC from 8.7 +/- 0.6 to 6.9 +/- 0.4 mmol.L-1 (p<0.05). L-arg administration had no significant effect on TNF-alpha or IL-10 concentrations, but increased post-exercise IL-6 (placebo=19 +/- 3pg.mL(-1); L-arg=63 +/- 8 pg.mL(-1); p<0.05). In HIV-1 infected men, acute administration of L-arg reduces post-exercise blood LAC and increases IL-6 levels, suggesting the activation of the L-arg-NO pathway, with possible anti-inflammatory consequences.
引用
收藏
页码:339 / 343
页数:5
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