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在人类休息和长时间中等强度运动期间,抑制脂肪分解会增加白细胞介素-6。

Suppressing lipolysis increases interleukin-6 at rest and during prolonged moderate-intensity exercise in humans.

作者信息

Holmes Anna G, Watt Matthew J, Febbraio Mark A

机构信息

Skeletal Muscle Research Laboratory, School of Medical Sciences, RMIT University, P.O. Box 71, Bundoora 3083, Victoria, Australia.

出版信息

J Appl Physiol (1985). 2004 Aug;97(2):689-96. doi: 10.1152/japplphysiol.00195.2004. Epub 2004 Apr 9.

Abstract

IL-6 induces lipolysis when administered to humans. Consequently, it has been hypothesized that IL-6 is released from skeletal muscle during exercise to act in a "hormonelike" manner and increase lipolysis from adipose tissue to supply the muscle with substrate. In the present study, we hypothesized that suppressing lipolysis, and subsequent free fatty acid (FFA) availability, would result in a compensatory elevation in IL-6 at rest and during exercise. First, we had five healthy men ingest nicotinic acid (NA) at 30-min intervals for 120 min at rest [10 mg/kg body mass (initial dose), 5 mg/kg body mass (subsequent doses)]. Plasma was collected and analyzed for FFA and IL-6. After 120 min, plasma FFA concentration was attenuated (0 min: 0.26 +/- 0.05 mmol/l; 120 min: 0.09 +/- 0.02 mmol/l; P < 0.01), whereas plasma IL-6 was concomitantly increased approximately eightfold (0 min: 0.75 +/- 0.18 pg/ml; 120 min: 6.05 +/- 0.89 pg/ml; P < 0.001). To assess the effect of lipolytic suppression on the exercise-induced IL-6 response, seven active, but not specifically trained, men performed two experimental exercise trials with (NA) or without [control (Con)] NA ingestion 60 min before (10 mg/kg body mass) and throughout (5 mg/kg body mass every 30 min) exercise. Blood samples were obtained before ingestion, 60 min after ingestion, and throughout 180 min of cycling exercise at 62 +/- 5% of maximal oxygen consumption. IL-6 gene expression, in muscle and adipose tissue sampled at 0, 90, and 180 min, was determined by using semiquantitative real-time PCR. IL-6 mRNA increased in Con (rest vs. 180 min; P < 0.01) approximately 13-fold in muscle and approximately 42-fold in fat with exercise. NA increased (rest vs. 180 min; P < 0.01) IL-6 mRNA 34-fold in muscle, but the treatment effect was not statistically significant (Con vs. NA, P = 0.1), and 235-fold in fat (Con vs. NA, P < 0.01). Consistent with the study at rest, NA completely suppressed plasma FFA (180 min: Con, 1.42 +/- 0.07 mmol/l; NA, 0.10 +/- 0.01 mmol/l; P < 0.001) and increased plasma IL-6 (180 min: Con, 9.81 +/- 0.98 pg/ml; NA, 19.23 +/- 2.50 pg/ml; P < 0.05) during exercise. In conclusion, these data demonstrate that circulating IL-6 is markedly elevated at rest and during prolonged moderate-intensity exercise when lipolysis is suppressed.

摘要

白细胞介素-6(IL-6)作用于人体时会诱导脂肪分解。因此,有人提出假说,认为运动期间IL-6从骨骼肌释放出来,以“类激素”方式发挥作用,增加脂肪组织的脂肪分解,为肌肉提供底物。在本研究中,我们提出假说,认为抑制脂肪分解及随后的游离脂肪酸(FFA)供应,会导致静息和运动期间IL-6代偿性升高。首先,我们让5名健康男性在静息状态下每隔30分钟摄入一次烟酸(NA),共摄入120分钟[10毫克/千克体重(初始剂量),5毫克/千克体重(后续剂量)]。采集血浆并分析FFA和IL-6。120分钟后,血浆FFA浓度降低(0分钟:0.26±0.05毫摩尔/升;120分钟:0.09±0.02毫摩尔/升;P<0.01),而血浆IL-6相应增加约8倍(0分钟:0.75±0.18皮克/毫升;120分钟:6.05±0.89皮克/毫升;P<0.001)。为评估脂肪分解抑制对运动诱导的IL-6反应的影响,7名活跃但未经过专门训练的男性进行了两项实验性运动试验,一组在运动前60分钟(10毫克/千克体重)及运动全程(每30分钟5毫克/千克体重)摄入NA,另一组不摄入NA[对照组(Con)]。在摄入前、摄入后60分钟以及在最大耗氧量的62±5%进行180分钟骑行运动的全程采集血样。在0、90和180分钟采集的肌肉和脂肪组织中,通过半定量实时PCR测定IL-6基因表达。运动时,Con组(静息与180分钟相比;P<0.01)肌肉中IL-6 mRNA增加约13倍,脂肪中增加约42倍。NA使肌肉中IL-6 mRNA增加34倍(静息与180分钟相比;P<0.01),但处理效果无统计学意义(Con组与NA组相比,P = 0.1),脂肪中增加235倍(Con组与NA组相比,P<0.01)。与静息状态下的研究一致,NA在运动期间完全抑制了血浆FFA(180分钟:Con组,1.42±0.07毫摩尔/升;NA组,0.10±0.01毫摩尔/升;P<0.001),并使血浆IL-6升高(180分钟:Con组,9.81±0.98皮克/毫升;NA组,19.23±2.50皮克/毫升;P<0.05)。总之,这些数据表明,当脂肪分解受到抑制时,静息和长时间中等强度运动期间循环IL-6会显著升高。

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