An increased need for dietary cysteine in support of glutathione synthesis may underlie the increased risk for mortality associated with low protein intake in the elderly

被引:59
作者
McCarty, Mark F. [1 ]
DiNicolantonio, James J. [2 ]
机构
[1] Catalyt Longev, Carlsbad, CA 92009 USA
[2] St Lukes Mid Amer Heart Inst, Prevent Cardiol Dept, Kansas City, MO USA
关键词
Aging; Cysteine; N-acetylcysteine; Glutathione; Leucine; Arginine; IGF-I; Oxidative stress; ALPHA-LIPOIC ACID; BETA-METHYLBUTYRATE HMB; ACETYL-L-CYSTEINE; ACUTE MYOCARDIAL-INFARCTION; L-ARGININE SUPPLEMENTATION; VASCULAR OXIDATIVE STRESS; AGE-RELATED LOSS; GROWTH-FACTOR-I; N-ACETYLCYSTEINE; LEUCINE SUPPLEMENTATION;
D O I
10.1007/s11357-015-9823-8
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
Restricted dietary intakes of protein or essential amino acids tend to slow aging and boost lifespan in rodents, presumably because they downregulate IGF-I/Akt/mTORC1 signaling that acts as a pacesetter for aging and promotes cancer induction. A recent analysis of the National Health and Nutrition Examination Survey (NHANES) III cohort has revealed that relatively low protein intakes in mid-life (under 10 % of calories) are indeed associated with decreased subsequent risk for mortality. However, in those over 65 at baseline, such low protein intakes were associated with increased risk for mortality. This finding accords well with other epidemiology correlating relatively high protein intakes with lower risk for loss of lean mass and bone density in the elderly. Increased efficiency of protein translation reflecting increased leucine intake and consequent greater mTORC1 activity may play a role in this effect; however, at present there is little solid evidence that leucine supplementation provides important long-term benefits to the elderly. Aside from its potential pro-anabolic impact, higher dietary protein intakes may protect the elderly in another way-by providing increased amino acid substrate for synthesis of key protective factors. There is growing evidence, in both rodents and humans, that glutathione synthesis declines with increasing age, likely reflecting diminished function of Nrf2-dependent inductive mechanisms that boost expression of glutamate cysteine ligase (GCL), rate-limiting for glutathione synthesis. Intracellular glutathione blunts the negative impact of reactive oxygen species (ROS) on cell health and functions both by acting as an oxidant scavenger and by opposing the pro-inflammatory influence of hydrogen peroxide on cell signaling. Fortunately, since GCL's K-m for cysteine is close to intracellular cysteine levels, increased intakes of cysteine-achieved from whole proteins or via supplementation with N-acetylcysteine (NAC)-can achieve a compensatory increase in glutathione synthesis, such that more youthful tissue levels of this compound can be restored. Supplementation with phase 2 inducers such as lipoic acid-can likewise increase glutathione levels by promoting increased GCL expression. In aging humans and/or rodents, NAC supplementation has exerted favorable effects on vascular health, muscle strength, bone density, cell-mediated immunity, markers of systemic inflammation, preservation of cognitive function, progression of neurodegeneration, and the clinical course of influenza-effects which could be expected to lessen mortality and stave off frailty. Hence, greater cysteine availability may explain much of the favorable impact of higher protein intakes on mortality and frailty risk in the elderly, and joint supplementation with NAC and lipoic acid could be notably protective in the elderly, particularly in those who follow plant-based diets relatively low in protein. It is less clear whether the lower arginine intake associated with low-protein diets has an adverse impact on vascular health.
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页数:12
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  • [1] Controlled trial of N-acetyleysteine for patients with probable Alzheimer's disease
    Adair, JC
    Knoefel, JE
    Morgan, N
    [J]. NEUROLOGY, 2001, 57 (08) : 1515 - 1517
  • [2] N-acetyl-L-cysteine improves survival and preserves motor performance in an animal model of familial amyotrophic lateral sclerosis
    Andreassen, OA
    Dedeoglu, A
    Klivenyi, P
    Beal, MF
    Bush, AI
    [J]. NEUROREPORT, 2000, 11 (11) : 2491 - 2493
  • [3] The key role of growth hormone-insulin-IGF-1 signaling in aging and cancer
    Anisimov, Vladimir N.
    Bartke, Andrzej
    [J]. CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2013, 87 (03) : 201 - 223
  • [4] Arthur JR, 2000, CELL MOL LIFE SCI, V57, P1825
  • [5] N-acetyl-cysteine in the treatment of Parkinson's disease. What are we waiting for?
    Arturo Martinez-Banaclocha, Marcos
    [J]. MEDICAL HYPOTHESES, 2012, 79 (01) : 8 - 12
  • [6] N-Acetylcysteine -: a safe antidote for cysteine/glutathione deficiency
    Atkuri, Kondala R.
    Mantovani, John J.
    Herzenberg, Leonard A.
    Herzenberg, Leonore A.
    [J]. CURRENT OPINION IN PHARMACOLOGY, 2007, 7 (04) : 355 - 359
  • [7] Survival in Older Men May Benefit From Being Slightly Overweight and Centrally Obese-A 5-Year Follow-up Study in 4,000 Older Adults Using DXA
    Auyeung, Tung Wai
    Lee, Jenny S. W.
    Leung, Jason
    Kwok, Timothy
    Leung, Ping Chung
    Woo, Jean
    [J]. JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2010, 65 (01): : 99 - 104
  • [8] Long-term effects of leucine supplementation on body composition
    Balage, Michele
    Dardevet, Dominique
    [J]. CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE, 2010, 13 (03) : 265 - 270
  • [9] N-Acetylcysteine elicited increase in complex I activity in synaptic mitochondria from aged mice:: implications for treatment of Parkinson's disease
    Banaclocha, MM
    [J]. BRAIN RESEARCH, 2000, 859 (01) : 173 - 175
  • [10] N-acetylcysteine potentiates the antihypertensive effect of ACE inhibitors in hypertensive patients
    Barrios, V
    Calderón, A
    Navarro-Cid, J
    Lahera, V
    Ruilope, LM
    [J]. BLOOD PRESSURE, 2002, 11 (04) : 235 - 239