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Delaying brain mitochondrial decay and aging with mitochondrial antioxidants and metabolites.
Ann N Y Acad Sci. 2002 Apr; 959:133-66.AN

Abstract

Mitochondria decay with age due to the oxidation of lipids, proteins, RNA, and DNA. Some of this decay can be reversed in aged animals by feeding them the mitochondrial metabolites acetylcarnitine and lipoic acid. In this review, we summarize our recent studies on the effects of these mitochondrial metabolites and mitochondrial antioxidants (alpha-phenyl-N-t-butyl nitrone and N-t-butyl hydroxylamine) on the age-associated mitochondrial decay of the brain of old rats, neuronal cells, and human diploid fibroblast cells. In feeding studies in old rats, these mitochondrial metabolites and antioxidants improve the age-associated decline of ambulatory activity and memory, partially restore mitochondrial structure and function, inhibit the age-associated increase of oxidative damage to lipids, proteins, and nucleic acids, elevate the levels of antioxidants, and restore the activity and substrate binding affinity of a key mitochondrial enzyme, carnitine acetyltransferase. These mitochondrial metabolites and antioxidants protect neuronal cells from neurotoxin- and oxidant-induced toxicity and oxidative damage; delay the normal senescence of human diploid fibroblast cells, and inhibit oxidant-induced acceleration of senescence. These results suggest a plausible mechanism: with age, increased oxidative damage to proteins and lipid membranes, particularly in mitochondria, causes a deformation of structure of enzymes, with a consequent decrease of enzyme activity as well as substrate binding affinity for their substrates; an increased level of substrate restores the velocity of the reaction and restores mitochondrial function, thus delaying mitochondrial decay and aging. This loss of activity due to coenzyme or substrate binding appears to be true for a number of other enzymes as well, including mitochondrial complex III and IV.

Authors+Show Affiliations

Division of Biochemistry and Molecular Biology, University of California, Berkeley, California 94720, USA.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
Review

Language

eng

PubMed ID

11976193

Citation

Liu, Jiankang, et al. "Delaying Brain Mitochondrial Decay and Aging With Mitochondrial Antioxidants and Metabolites." Annals of the New York Academy of Sciences, vol. 959, 2002, pp. 133-66.
Liu J, Atamna H, Kuratsune H, et al. Delaying brain mitochondrial decay and aging with mitochondrial antioxidants and metabolites. Ann N Y Acad Sci. 2002;959:133-66.
Liu, J., Atamna, H., Kuratsune, H., & Ames, B. N. (2002). Delaying brain mitochondrial decay and aging with mitochondrial antioxidants and metabolites. Annals of the New York Academy of Sciences, 959, 133-66.
Liu J, et al. Delaying Brain Mitochondrial Decay and Aging With Mitochondrial Antioxidants and Metabolites. Ann N Y Acad Sci. 2002;959:133-66. PubMed PMID: 11976193.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Delaying brain mitochondrial decay and aging with mitochondrial antioxidants and metabolites. AU - Liu,Jiankang, AU - Atamna,Hani, AU - Kuratsune,Hirohiko, AU - Ames,Bruce N, PY - 2002/4/27/pubmed PY - 2002/6/5/medline PY - 2002/4/27/entrez SP - 133 EP - 66 JF - Annals of the New York Academy of Sciences JO - Ann N Y Acad Sci VL - 959 N2 - Mitochondria decay with age due to the oxidation of lipids, proteins, RNA, and DNA. Some of this decay can be reversed in aged animals by feeding them the mitochondrial metabolites acetylcarnitine and lipoic acid. In this review, we summarize our recent studies on the effects of these mitochondrial metabolites and mitochondrial antioxidants (alpha-phenyl-N-t-butyl nitrone and N-t-butyl hydroxylamine) on the age-associated mitochondrial decay of the brain of old rats, neuronal cells, and human diploid fibroblast cells. In feeding studies in old rats, these mitochondrial metabolites and antioxidants improve the age-associated decline of ambulatory activity and memory, partially restore mitochondrial structure and function, inhibit the age-associated increase of oxidative damage to lipids, proteins, and nucleic acids, elevate the levels of antioxidants, and restore the activity and substrate binding affinity of a key mitochondrial enzyme, carnitine acetyltransferase. These mitochondrial metabolites and antioxidants protect neuronal cells from neurotoxin- and oxidant-induced toxicity and oxidative damage; delay the normal senescence of human diploid fibroblast cells, and inhibit oxidant-induced acceleration of senescence. These results suggest a plausible mechanism: with age, increased oxidative damage to proteins and lipid membranes, particularly in mitochondria, causes a deformation of structure of enzymes, with a consequent decrease of enzyme activity as well as substrate binding affinity for their substrates; an increased level of substrate restores the velocity of the reaction and restores mitochondrial function, thus delaying mitochondrial decay and aging. This loss of activity due to coenzyme or substrate binding appears to be true for a number of other enzymes as well, including mitochondrial complex III and IV. SN - 0077-8923 UR - https://www.unboundmedicine.com/medline/citation/11976193/Delaying_brain_mitochondrial_decay_and_aging_with_mitochondrial_antioxidants_and_metabolites_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0077-8923&date=2002&volume=959&spage=133 DB - PRIME DP - Unbound Medicine ER -