Acute dietary carbohydrate manipulation and the subsequent inflammatory and hepcidin responses to exercise
Acute dietary carbohydrate manipulation and the subsequent inflammatory and hepcidin responses to exercise
复制标题
DOI:
10.1007/s00421-015-3252-3
复制
发表时间:
2015-12-01
影响因子:
3
通讯作者:
Peeling, Peter
中科院分区:
文献类型:
--
作者:
Badenhorst, Claire E.;Dawson, Brian;Peeling, Peter
Purpose To examine the effects of 24-h controlled carbohydrate intake on next day pre-and post-exercise inflammatory and hepcidin responses.Methods In a crossover design, 12 well-trained endurance athletes (Ht 181.08 +/- 7.68 cm; Wt 74.8 +/- 11.5 kg, VO2peak 68.9 +/- 7.2 ml kg(-1) min(-1)) completed two experimental (2-day) trials. On day 1, participants completed a glycogen depletion task, including a 16-km run (80 % vVO(2peak)) and 5 x 1 min efforts (130 % vVO(2peak)) separated by 2-min recovery. Subsequently, strict dietary control was enforced for 24 h, where low carbohydrate (LCHO 3 g kg(-1)) or high carbohydrate (HCHO 10 g kg(-1)) diets were provided. Twenty-four hours later, participants completed an 8 x 3 min interval running session at 85 % vVO(2peak) followed by 3-h monitored recovery. Venous blood samples were collected pre-, immediately post-and 3-h post-exercise, which were analyzed for interleukin-6, serum iron, ferritin and hepcidin.Results Interleukin-6 was elevated (p < 0.001) immediately post-exercise compared to baseline in both conditions, but was lower in HCHO (p = 0.015). Hepcidin levels were also lower at baseline (p = 0.049) in HCHO, and a large effect (d = 0.72) indicated a trend for lower levels at 3-h post-exercise compared to LCHO. Serum iron was increased post-exercise for both trials (p = 0.001), whereas serum ferritin remained unchanged.Conclusions Twenty-four hours of controlled low carbohydrate intake resulted in higher baseline hepcidin levels and post-exercise IL-6 responses than a high carbohydrate intake. Such hormone increases may be induced by gluconeogenic signaling of the liver, and may negatively impact an athlete's iron metabolism.