Division of Hypothalamic Research, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Division of Hypothalamic Research, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA; Division of Endocrinology & Metabolism, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA; Department of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX, USA; Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Mol Metab. 2018 Mar;9:114-130. doi: 10.1016/j.molmet.2018.01.006. Epub 2018 Jan 31.
Exercise training has several well-established health benefits, including many related to body weight, appetite control, and blood glucose homeostasis. However, the molecular mechanisms and, in particular, the hormonal systems that mediate and integrate these beneficial effects are poorly understood. In the current study, we aimed to investigate the role of the hormone ghrelin and its receptor, the growth hormone secretagogue receptor (GHSR; ghrelin receptor), in mediating the effects of exercise on food intake and blood glucose following exercise as well as in regulating exercise endurance capacity.
We used two mouse models of treadmill running to characterize the changes in plasma ghrelin with exercise. We also assessed the role of the ghrelin system to influence food intake and blood glucose after exercise, exercise endurance, and parameters potentially linked to responses to exercise. Mice lacking GHSRs (GHSR-null mice) and wild-type littermates were studied.
An acute bout of exercise transiently elevated plasma acyl-ghrelin. Without the action of this increased ghrelin on GHSRs (as in GHSR-null mice), high intensity interval exercise markedly reduced food intake compared to control mice. The effect of exercise to acutely raise blood glucose remained unmodified in GHSR-null mice. Exercise-induced increases in plasma ghrelin positively correlated with endurance capacity, and time to exhaustion was reduced in GHSR-null mice as compared to wild-type littermates. In an effort to mechanistically explain their reduced exercise endurance, exercised GHSR-null mice exhibited an abrogated sympathoadrenal response, lower overall insulin-like growth factor-1 levels, and altered glycogen utilization.
Exercise transiently increases plasma ghrelin. GHSR-null mice exhibit decreased food intake following high intensity interval exercise and decreased endurance when submitted to an exercise endurance protocol. These data suggest that an intact ghrelin system limits the capacity of exercise to restrict food intake following exercise, although it enhances exercise endurance.
运动训练有许多已确立的健康益处,包括与体重、食欲控制和血糖稳态相关的益处。然而,介导和整合这些有益作用的分子机制,特别是激素系统,还知之甚少。在本研究中,我们旨在研究激素 ghrelin 及其受体生长激素促分泌素受体(GHSR;ghrelin 受体)在介导运动对运动后食物摄入和血糖的影响以及调节运动耐力方面的作用。
我们使用两种跑步机跑步的小鼠模型来研究运动过程中血浆 ghrelin 的变化。我们还评估了 ghrelin 系统在运动后影响食物摄入和血糖、运动耐力以及与运动反应相关的潜在参数中的作用。研究了缺乏 GHSRs(GHSR 缺失小鼠)和野生型同窝小鼠。
急性运动短暂升高了酰基 ghrelin 的血浆水平。如果没有这种增加的 ghrelin 对 GHSRs 的作用(如在 GHSR 缺失小鼠中),高强度间歇运动与对照小鼠相比明显减少了食物摄入。GHSR 缺失小鼠的运动引起的血糖急性升高效应未改变。运动引起的血浆 ghrelin 增加与耐力能力呈正相关,与野生型同窝小鼠相比,GHSR 缺失小鼠的疲劳时间缩短。为了从机制上解释它们减少的运动耐力,运动后的 GHSR 缺失小鼠表现出交感肾上腺反应减弱、整体胰岛素样生长因子-1 水平降低以及糖原利用改变。
运动短暂地增加了血浆 ghrelin。GHSR 缺失小鼠在进行高强度间歇运动后食物摄入减少,并且在进行运动耐力方案时耐力降低。这些数据表明,完整的 ghrelin 系统限制了运动在运动后限制食物摄入的能力,尽管它增强了运动耐力。