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Carnitine function and requirements during the life cycle
Abstract
l ‐Carnitine has been described as a “conditionally essential” nutrient for humans. Segments of the human population suggested as having a requirement for carnitine include infants (premature and full‐term), patients on long‐term parenteral nutrition, and perhaps children. The evidence to support these claims includes 1 ) low circulating carnitine concentrations; 2 ) abnormal (or at least different) circulating metabolite concentrations (free fatty acids, triglycerides, ketone bodies), and 3 ) very limited and inconsistent growth data. A number of subjective observations and anecdotal case reports have been offered in support of a requirement for carnitine. Exogenous carnitine is required to maintain “normal” (in the epidemiologic sense) plasma or serum carnitine concentrations in humans of all ages. But “functional carnitine deficiency,” defined by abnormal clinical presentation correctable by carnitine administration, has not been demonstrated in an otherwise normal (nonpathologic) population. On the other hand, nutritional or pharmacological intervention with carnitine or its esters may be beneficial for very premature infants, infants and children with various clinical conditions associated with low circulating carnitine concentrations, and in some chronic diseases associated with the aging process.— Rebouche, C. J. Carnitine function and requirements during the life cycle. FASEB J. 6: 3379‐3386; 1992.
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Cited by
Flanagan, J. L., Simmons, P. A., Vehige, J., Willcox, M. D., & Garrett, Q. (2010) · Nutrition & Metabolism · doi:10.1186/1743-7075-7-30 · Cited by 611
“The pathway in mammals is unique using protein-bound lysine that is enzymatically methylated to form trimethyllysine as a post-translational modification of protein synthesis [6].”
BackgroundCarnitine metabolism to trimethylamine by an unusual Rieske-type oxygenase from human microbiota
Zhu, Y., Jameson, E., Crosatti, M., Schäfer, H., Rajakumar, K., Bugg, T. D. H., & Chen, Y. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1316569111 · Cited by 372
CARNITINE METABOLISM AND ITS REGULATION IN MICROORGANISMS AND MAMMALS
Rebouche, C. J., & Seim, H. (1998) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.18.1.39 · Cited by 362
Self-citationCarnitine, mitochondrial function and therapy
Zammit, V. A., Ramsay, R. R., Bonomini, M., & Arduini, A. (2009) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2009.04.024 · Cited by 149
Carnitine transport: Pathophysiology and metabolism of known molecular defects
Tein, I. (2003) · Journal of Inherited Metabolic Disease · doi:10.1023/a:1024481016187 · Cited by 140
Role of Carnitine in Non-alcoholic Fatty Liver Disease and Other Related Diseases: An Update
Li, N., & Zhao, H. (2021) · Frontiers in Medicine · doi:10.3389/fmed.2021.689042 · Cited by 79
Renal adaptation to dietary carnitine in humans
Rebouche, C., Lombard, K., & Chenard, C. (1993) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/58.5.660 · Cited by 68
Self-citationHuang, W., Shaikh, S. N., Ganapathy, M. E., Hopfer, U., Leibach, F. H., Carter, A. L., & Ganapathy, V. (1999) · Biochemical Pharmacology · doi:10.1016/s0006-2952(99)00219-1 · Cited by 22
Metadata
- Authors
- Rebouche, C. J.
- Venue
- The FASEB Journal
- Publisher
- Wiley
- Published
- 1992-12
- Volume
- 6
- Issue
- 15
- Pages
- 3379-3386
- ISSN
- 0892-6638 (ISSN-L)
- 1530-6860
- OpenAlex
- W1483354304
- Cited by
- 336
- References
- 0
- FWCI
- 3.65
- Type
- journal article
- Language
- en
- Open access
- closed
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