Department of Aging and Geriatrics, Institute on Aging, College of Medicine, University of Florida, Gainesville, FL 32611-0910, USA.
Rejuvenation Res. 2011 Jun;14(3):315-24. doi: 10.1089/rej.2010.1132. Epub 2011 Jun 1.
Obese older adults are particularly susceptible to sarcopenia and have a higher prevalence of disability than their peers of normal weight. Interventions to improve body composition in late life are crucial to maintaining independence. The main mechanisms underlying sarcopenia have not been determined conclusively, but chronic inflammation, apoptosis, and impaired mitochondrial function are believed to play important roles. It has yet to be determined whether impaired cellular quality control mechanisms contribute to this process. The objective of this study was to assess the effects of a 6-month weight loss program combined with moderate-intensity exercise on the cellular quality control mechanisms autophagy and ubiquitin-proteasome, as well as on inflammation, apoptosis, and mitochondrial function, in the skeletal muscle of older obese women. The intervention resulted in significant weight loss (8.0 ± 3.9 % vs. 0.4 ± 3.1% of baseline weight, p = 0.002) and improvements in walking speed (reduced time to walk 400 meters, - 20.4 ± 16% vs. - 2.5 ± 12%, p = 0.03). In the intervention group, we observed a three-fold increase in messenger RNA (mRNA) levels of the autophagy regulators LC3B, Atg7, and lysosome-associated membrane protein-2 (LAMP-2) compared to controls. Changes in mRNA levels of FoxO3A and its targets MuRF1, MAFBx, and BNIP3 were on average seven-fold higher in the intervention group compared to controls, but these differences were not statistically significant. Tumor necrosis factor-α (TNF-α) mRNA levels were elevated after the intervention, but we did not detect significant changes in the downstream apoptosis markers caspase 8 and 3. Mitochondrial biogenesis markers (PGC1α and TFAm) were increased by the intervention, but this was not accompanied by significant changes in mitochondrial complex content and activity. In conclusion, although exploratory in nature, this study is among the first to report the stimulation of cellular quality control mechanisms elicited by a weight loss and exercise program in older obese women.
肥胖的老年人尤其容易出现肌肉减少症,并且比体重正常的同龄人更容易残疾。改善晚年人体成分对于保持独立性至关重要。肌肉减少症的主要机制尚未得到明确确定,但慢性炎症、细胞凋亡和受损的线粒体功能被认为起着重要作用。目前尚不清楚细胞质量控制机制受损是否会导致这一过程。本研究的目的是评估为期 6 个月的减肥计划联合中等强度运动对老年肥胖女性骨骼肌中自噬和泛素蛋白酶体等细胞质量控制机制以及炎症、细胞凋亡和线粒体功能的影响。干预措施导致体重显著减轻(8.0±3.9%与基线体重的 0.4±3.1%相比,p=0.002)和步行速度提高(400 米行走时间减少,-20.4±16%与-2.5±12%相比,p=0.03)。在干预组中,我们观察到自噬调节剂 LC3B、Atg7 和溶酶体相关膜蛋白-2(LAMP-2)的信使 RNA(mRNA)水平增加了三倍。与对照组相比,FoxO3A 及其靶标 MuRF1、MAFBx 和 BNIP3 的 mRNA 水平平均增加了七倍,但这些差异没有统计学意义。肿瘤坏死因子-α(TNF-α)mRNA 水平在干预后升高,但我们没有检测到下游凋亡标志物 caspase 8 和 3 的显著变化。线粒体生物发生标志物(PGC1α 和 TFAm)在干预后增加,但线粒体复合物含量和活性没有显著变化。总之,尽管这是一项探索性研究,但本研究首次报道了减肥和运动计划对老年肥胖女性细胞质量控制机制的刺激作用。