Hamilton Marc T, Hamilton Deborah G, Zderic Theodore W
Department of Biomedical Sciences, University of Missouri-Columbia, Columbia, MO 65211, USA.
Diabetes. 2007 Nov;56(11):2655-67. doi: 10.2337/db07-0882. Epub 2007 Sep 7.
It is not uncommon for people to spend one-half of their waking day sitting, with relatively idle muscles. The other half of the day includes the often large volume of nonexercise physical activity. Given the increasing pace of technological change in domestic, community, and workplace environments, modern humans may still not have reached the historical pinnacle of physical inactivity, even in cohorts where people already do not perform exercise. Our purpose here is to examine the role of sedentary behaviors, especially sitting, on mortality, cardiovascular disease, type 2 diabetes, metabolic syndrome risk factors, and obesity. Recent observational epidemiological studies strongly suggest that daily sitting time or low nonexercise activity levels may have a significant direct relationship with each of these medical concerns. There is now a need for studies to differentiate between the potentially unique molecular, physiologic, and clinical effects of too much sitting (inactivity physiology) separate from the responses caused by structured exercise (exercise physiology). In theory, this may be in part because nonexercise activity thermogenesis is generally a much greater component of total energy expenditure than exercise or because any type of brief, yet frequent, muscular contraction throughout the day may be necessary to short-circuit unhealthy molecular signals causing metabolic diseases. One of the first series of controlled laboratory studies providing translational evidence for a molecular reason to maintain high levels of daily low-intensity and intermittent activity came from examinations of the cellular regulation of skeletal muscle lipoprotein lipase (LPL) (a protein important for controlling plasma triglyceride catabolism, HDL cholesterol, and other metabolic risk factors). Experimentally reducing normal spontaneous standing and ambulatory time had a much greater effect on LPL regulation than adding vigorous exercise training on top of the normal level of nonexercise activity. Those studies also found that inactivity initiated unique cellular processes that were qualitatively different from the exercise responses. In summary, there is an emergence of inactivity physiology studies. These are beginning to raise a new concern with potentially major clinical and public health significance: the average nonexercising person may become even more metabolically unfit in the coming years if they sit too much, thereby limiting the normally high volume of intermittent nonexercise physical activity in everyday life. Thus, if the inactivity physiology paradigm is proven to be true, the dire concern for the future may rest with growing numbers of people unaware of the potential insidious dangers of sitting too much and who are not taking advantage of the benefits of maintaining nonexercise activity throughout much of the day.
人们在醒着的时间里,有一半时间是坐着的,肌肉相对处于闲置状态,这种情况并不罕见。一天中的另一半时间则包含了通常大量的非运动性身体活动。鉴于家庭、社区和工作场所环境中技术变革的步伐不断加快,即使在那些已经不进行运动的人群中,现代人类可能仍未达到身体活动最少的历史巅峰状态。我们在此的目的是研究久坐行为,尤其是坐着,对死亡率、心血管疾病、2型糖尿病、代谢综合征风险因素和肥胖的影响。近期的观察性流行病学研究强烈表明,每日久坐时间或低水平的非运动活动量可能与上述每一项医学问题都存在显著的直接关联。现在需要开展研究,以区分久坐(不活动生理学)可能具有的独特分子、生理和临床效应与有组织的运动(运动生理学)所引发的反应。理论上,这可能部分是因为非运动活动产热在总能量消耗中通常占比远大于运动,或者是因为一天中任何形式的短暂但频繁的肌肉收缩对于阻断导致代谢疾病的不健康分子信号可能是必要的。首批一系列对照实验室研究之一,为维持高水平日常低强度和间歇性活动提供了分子层面依据,这些研究源于对骨骼肌脂蛋白脂肪酶(LPL,一种对控制血浆甘油三酯分解代谢、高密度脂蛋白胆固醇及其他代谢风险因素至关重要的蛋白质)细胞调控的研究。通过实验减少正常的自发站立和行走时间,对LPL调控的影响远大于在正常非运动活动水平之上增加剧烈运动训练。那些研究还发现,不活动引发了与运动反应在性质上不同的独特细胞过程。总之,不活动生理学研究正在兴起。这些研究开始引发一个具有潜在重大临床和公共卫生意义的新担忧:如果普通不运动的人久坐时间过长,在未来几年他们的代谢可能会变得更不健康,从而限制了日常生活中通常大量的间歇性非运动身体活动。因此,如果不活动生理学范式被证明是正确的,那么未来令人担忧的可能是越来越多的人没有意识到久坐的潜在隐患,也没有利用在一天中大部分时间保持非运动活动的益处。