• Anti-aging nutrient
L-carnosine, not to be confused with
The body manufactures carnosine from common dietary proteins, and for this reason there is no daily requirement of this substance.
Among advocates of carnosine, there is a controversy regarding whether the proper dose is 50–150 mg per day or nearer to 1,000 mg daily. However, until carnosine has actually been shown to have any medical benefits, this argument cannot be settled.
Carnosine is widely marketed as an anti-aging nutrient. However, while there are a large number of studies that hint carnosine might help slow various aspects of aging, the quality of these studies is as yet far too low to provide any reliable evidence for benefit. 1-20
There is some actual evidence that carnosine may be helpful for children with
Free radicals are thought to play a role in many illnesses, and on this basis many antioxidant substances have been studied for potential health-promoting properties. The best evaluated are
Other weak evidence hints that oral carnosine might be helpful for
It has been hypothesized that taking supplements of the amino acid alanine can raise carnosine levels in muscle, and, in turn, enhance
The use of carnosine has not been associated with any significant side effects. However, the body deploys a range of enzymes, called carnosinases, to break down carnosine. There may be a reason for the presence of these enzymes, and overcoming them by providing large amounts of supplemental carnosine could conceivably cause harm in some as-yet unrecognized way. Maximum safe doses in young children, pregnant or nursing women, or people with severe liver or kidney disease have not been established.
11. Kantha SS, Wada S, Tanaka H, et al. Carnosine sustains the retention of cell morphology in continuous fibroblast culture subjected to nutritional insult. Biochem Biophys Res Commun . 1996;223:278–82.
17. Schmidt AM, Yan SD, Wautier JL, et al. Activation of receptor for advanced glycation end products: a mechanism for chronic vascular dysfunction in diabetic vasculopathy and atherosclerosis. Circ Res . 1999;84:489–97.
27. Babizhayev MA. Rejuvenation of visual functions in older adult drivers and drivers with cataract during a short-term administration of N-acetylcarnosine lubricant eye drops. Rejuvenation Res . 2004;7:186–98.
31. Stvolinskii SL, Fedorova TN, Yuneva MO, et al. Protective effect of carnosine on Cu,Zn-superoxide dismutase during impaired oxidative metabolism in the brain in vivo. Bull Exp Biol Med . 2003;135:130–2.
33. MV, Aksenov MY, Markesbery WR, et al. Aging in a dish: age-dependent changes of neuronal survival, protein oxidation, and creatine kinase BB expression in long-term hippocampal cell culture. J Neurosci Res . 1999;58:308–17.
36. Butterfield DA. Alzheimer's beta-amyloid peptide and free radical oxidative stress. In: Gilbert DL, Colton CA, eds. Reactive Oxygen Species in Biological Systems: An Interdisciplinary Approach . New York: Plenum; 1999:609–638.
37. Carney JM, Starke-Reed PE, Oliver CN, et al. Reversal of age-related increase in brain protein oxidation, decrease in enzyme activity, and loss in temporal and spatial memory by chronic administration of the spin-trapping compound N-tert-butyl-alpha phenylnitrone. Proc Natl Acad Sci USA . 1991;88:3633–6.
40. Forster MJ, Dubey A, Dawson KM, et al. Age-related losses of cognitive function and motor skills in mice are associated with oxidative protein damage in the brain. Proc Natl Acad Sci USA . 1996;93:4765–9.
42. Huang X, Cuajungco MP, Atwood CS, et al. Cu(II) potentiation of Azheimer Ab neurotoxicity. Correlation with cell-free hydrogen peroxide production and metal reduction. J Biol Chem . 1999;274:37111–6.
43. Mark RJ, Lovell MA, Markesbery WR, et al. A role for 4-hydroxynonenal, an aldehydic product of lipid peroxidation, in disruption of ion homeostasis and neuronal death induced by amyloid beta-peptide. J Neurochem . 1997;68:255–64.
44. Munch G, Mayer S, Michaelis J, et al. Influence of advanced glycation end-products and AGE-inhibitors on nucleation-dependent polymerization of beta-amyloid peptide. Biochim Biophys Acta . 1997;1360:17–29.
45. Munch G, Schinzel R, Loske C, et al. Alzheimer's disease—synergistic effects of glucose deficit, oxidative stress and advanced glycation endproducts. Journal of Neural Transmission . 1998;105:439–61.
46. Smith MA, Sayre LM, Anderson VE, et al. Cytochemical demonstration of oxidative damage in Alzheimer disease by immunochemical enhancement of the carbonyl reaction with 2,4-dinitrophenylhydrazine. J HistochemCytochem . 1998;46:731–5.
54. Kendrick IP, Harris RC, Kim HJ, et al. The effects of 10 weeks of resistance training combined with beta-alanine supplementation on whole body strength, force production, muscular endurance and body composition. Amino Acids. 2008 Jan 4.
Last reviewed April 2009 by EBSCO CAM Review Board
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