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首页> 外文期刊>Rejuvenation research >An exploratory analysis of the effects of a weight loss plus exercise program on cellular quality control mechanisms in older overweight women.
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An exploratory analysis of the effects of a weight loss plus exercise program on cellular quality control mechanisms in older overweight women.

机译:探索性减肥加运动计划对老年超重女性细胞质量控制机制的影响的分析。

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摘要

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-alpha (TNF-alpha) 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 (PGC1alpha 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.
机译:肥胖的老年人特别容易遭受肌肉减少症的影响,并且比正常体重的同龄人的残疾患病率更高。改善晚年身体组成的干预措施对于维持独立性至关重要。肌肉减少症的潜在主要机制尚未定论,但慢性炎症,细胞凋亡和线粒体功能受损被认为起重要作用。尚未确定受损的细胞质量控制机制是否有助于该过程。这项研究的目的是评估为期6个月的减肥计划与中等强度的锻炼相结合,对自噬和泛素-蛋白酶体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。肥胖的老年妇女的骨骼肌。干预导致体重显着减少(8.0 +/- 3.9%与基线重量的0.4 +/- 3.1%,p = 0.002),步行速度得到改善(步行400米的时间减少了-20.4 +/- 16%与-2.5 +/- 12%,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)水平与对照相比增加了三倍。与对照组相比,干预组FoxO3A及其靶MuRF1,MAFBx和BNIP3的mRNA水平变化平均要高七倍,但这些差异在统计学上并不显着。干预后肿瘤坏死因子-α(TNF-α)mRNA水平升高,但我们未发现下游凋亡标志物caspase 8和3发生显着变化。线粒体生物发生标志物(PGC1alpha和TFAm)通过干预而增加,但这并没有伴随着线粒体复合物含量和活性的显着变化。总之,尽管本质上是探索性的,但该研究还是第一个报告了由肥胖女性的减肥和锻炼计划引起的细胞质量控制机制刺激的研究。

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