Supplementing Glycine and N-Acetylcysteine (GlyNAC) in Older Adults Improves Glutathione Deficiency, Oxidative Stress, Mitochondrial Dysfunction, Inflammation, Physical Function, and Aging Hallmarks: A Randomized Clinical Trial

被引:68
|
作者
Kumar, Premranjan [1 ]
Liu, Chun [1 ]
Suliburk, James [2 ]
Hsu, Jean W. [3 ]
Muthupillai, Raja [4 ]
Jahoor, Farook [3 ]
Minard, Charles G. [5 ]
Taffet, George E. [6 ]
Sekhar, Rajagopal, V [1 ,7 ]
机构
[1] USDA ARS, Dept Med, Sect Endocrinol Diabet & Metab, Translat Metab Unit, Washington, DC 20250 USA
[2] USDA ARS, Dept Surg, Washington, DC 20250 USA
[3] USDA ARS, Childrens Nutr Res Ctr, Washington, DC 20250 USA
[4] Baylor St Lukes Med Ctr, Houston, TX USA
[5] Baylor Coll Med, Inst Clin & Translat Res, Houston, TX 77030 USA
[6] Baylor Coll Med, Sect Geriatr, Dept Med, Houston, TX 77030 USA
[7] Baylor Coll Med, Houston, TX 77030 USA
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2023年 / 78卷 / 01期
基金
美国国家卫生研究院;
关键词
Clinical trials; GlyNAC; Metabolism; Oxidative stress; Successful aging; INSULIN-RESISTANCE; SKELETAL-MUSCLE; NITRIC-OXIDE; CYSTEINE; CELLS; PATHOGENESIS; METABOLISM; STRENGTH; DECLINE;
D O I
10.1093/gerona/glac135
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background Elevated oxidative stress (OxS), mitochondrial dysfunction, and hallmarks of aging are identified as key contributors to aging, but improving/reversing these defects in older adults (OA) is challenging. In prior studies, we identified that deficiency of the intracellular antioxidant glutathione (GSH) could play a role and reported that supplementing GlyNAC (combination of glycine and N-acetylcysteine [NAC]) in aged mice improved GSH deficiency, OxS, mitochondrial fatty-acid oxidation (MFO), and insulin resistance (IR). To test whether GlyNAC supplementation in OA could improve GSH deficiency, OxS, mitochondrial dysfunction, IR, physical function, and aging hallmarks, we conducted a placebo-controlled randomized clinical trial. Methods Twenty-four OA and 12 young adults (YA) were studied. OA was randomized to receive either GlyNAC (N = 12) or isonitrogenous alanine placebo (N = 12) for 16-weeks; YA (N = 12) received GlyNAC for 2-weeks. Participants were studied before, after 2-weeks, and after 16-weeks of supplementation to assess GSH concentrations, OxS, MFO, molecular regulators of energy metabolism, inflammation, endothelial function, IR, aging hallmarks, gait speed, muscle strength, 6-minute walk test, body composition, and blood pressure. Results Compared to YA, OA had GSH deficiency, OxS, mitochondrial dysfunction (with defective molecular regulation), inflammation, endothelial dysfunction, IR, multiple aging hallmarks, impaired physical function, increased waist circumference, and systolic blood pressure. GlyNAC (and not placebo) supplementation in OA improved/corrected these defects. Conclusion GlyNAC supplementation in OA for 16-weeks was safe and well-tolerated. By combining the benefits of glycine, NAC and GSH, GlyNAC is an effective nutritional supplement that improves and reverses multiple age-associated abnormalities to promote health in aging humans.
引用
收藏
页码:75 / 89
页数:15
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