Grace Megan S, Dempsey Paddy C, Sethi Parneet, Mundra Piyushkumar A, Mellett Natalie A, Weir Jacquelyn M, Owen Neville, Dunstan David W, Meikle Peter J, Kingwell Bronwyn A
Baker Heart and Diabetes Institute, Melbourne, Victoria 3004, Australia.
Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Victoria 3800, Australia.
J Clin Endocrinol Metab. 2017 Jun 1;102(6):1991-1999. doi: 10.1210/jc.2016-3926.
Postprandial dysmetabolism in type 2 diabetes (T2D) is exacerbated by prolonged sitting and may trigger inflammation and oxidative stress. It is unknown what impact countermeasures to prolonged sitting have on the postprandial lipidome.
In this study, we investigated the effects of regular interruptions to sitting, compared with prolonged sitting, on the postprandial plasma lipidome.
Randomized crossover experimental trial.
Participants underwent three 7-hour conditions: uninterrupted sitting (SIT); light-intensity walking interruptions (LW); and simple resistance activity interruptions (SRA).
Baseline (fasting) and 7-hour (postprandial) plasma samples from 21 inactive overweight/obese adults with T2D were analyzed for 338 lipid species using mass spectrometry.
Using mixed model analysis (controlling for baseline outcome variable, gender, body mass index, and condition order), the percentage change in lipid species (baseline to 7 hours) was compared between conditions with Benjamini-Hochberg correction.
Thirty-seven lipids were different between conditions (P < 0.05). Compared with SIT, postprandial elevations in diacylglycerols, triacylglycerols, and phosphatidylethanolamines were attenuated in LW and SRA. Plasmalogens and lysoalkylphosphatidylcholines were reduced in SIT, compared with attenuated reductions or elevations in LW and SRA. Phosphatidylserines were elevated with LW, compared with reductions in SIT and SRA.
Compared with SIT, LW and SRA were associated with reductions in lipids associated with inflammation; increased concentrations of lipids associated with antioxidant capacity; and differential changes in species associated with platelet activation. Acutely interrupting prolonged sitting time may impart beneficial effects on the postprandial plasma lipidome of adults with T2D. Evidence on longer-term intervention is needed.
2型糖尿病(T2D)患者的餐后代谢紊乱会因长时间久坐而加剧,并可能引发炎症和氧化应激。长时间久坐的应对措施对餐后脂质组有何影响尚不清楚。
在本研究中,我们调查了与长时间久坐相比,定期打断久坐对餐后血浆脂质组的影响。
随机交叉试验。
参与者经历了三种7小时的情况:不间断久坐(SIT);轻度步行打断(LW);简单抗阻活动打断(SRA)。
对21名患有T2D的不活跃超重/肥胖成年人的基线(空腹)和7小时(餐后)血浆样本进行分析,使用质谱法检测338种脂质种类。
使用混合模型分析(控制基线结果变量、性别、体重指数和情况顺序),在进行Benjamini-Hochberg校正后,比较不同情况之间脂质种类(从基线到7小时)的百分比变化。
不同情况之间有37种脂质存在差异(P<0.05)。与SIT相比,LW和SRA中甘油二酯、甘油三酯和磷脂酰乙醇胺的餐后升高幅度有所减弱。与LW和SRA中减弱的降低或升高相比,SIT中的缩醛磷脂和溶血烷基磷脂酰胆碱减少。与SIT和SRA中的减少相比,LW使磷脂酰丝氨酸升高。
与SIT相比,LW和SRA与炎症相关脂质的减少、抗氧化能力相关脂质浓度的增加以及血小板活化相关种类的差异变化有关。急性打断长时间久坐可能对患有T2D的成年人的餐后血浆脂质组产生有益影响。需要关于长期干预的证据。