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Journal of Nutrition Vol. 117 No. 9 September 1987, pp. 1550-1555
Copyright © 1987 by American Society for Nutrition
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Utilization of the L- and DL-Isomers of {alpha}-Keto-ß-methylvaleric Acid by Rats and Comparative Efficacy of the Keto Analogs of Branched-Chain Amino Acids Provided as Ornithine, Lysine and Histidine Salts1

Martha A. Funk2, Karen R. Lowry and David H. Baker3

Department of Animal Sciences and Division of Nutritional Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801

Three experiments were conducted to quantitatively evaluate the growth-promoting capacity of {alpha}-keto analogs of the branched-chain amino acids (BCAA). Basal chemically defined diets were formulated to be singly deficient in the BCAA under study; analogs therefore were evaluated as sources of supplemental amino acid activity. Analogs of isoleucine tested included {alpha}-keto-ß-L-methylvalerate (L-KMV) as the Na salt (L-KMV-Na) and {alpha}-keto-ß-DL-methylvalerate (DL-KMV) as the Na (DL-KMV-Na), ornithine (DL-KMV-Orn)and lysine (DL-KMV-Lys) salts. Sloperatio efficacy values were L-KMV-Na, 65%; DL-KMV-Na, 44%; DL-KMV-Orn, 41%; DL-KMV-Lys, 43%. Alloisoleucine accumulated in the plasma of rats fed all sources of KMV, but its concentration was three times greater when DL-KMV was fed than when L-KMV was fed. The analog of valine tested was {alpha}-ketolsovalerate as the omithine (KIV-Orn), lysine (KIC-Lys) and histidine (KIC-His) salts with resulting efficacies of 50, 38 and 49%, respectively. Slope-ratio efficacies of KIC-Orn and KIC-His were statistically similar and efficacy of KIC-Lys was inferior to both KIC-Orn and KIC-His.


KEY WORDS: • leucine • isoleucine • valine • keto analogs • ketomethylvaleric acid

1 Appreciation is expressed to Ross Laboratories, Columbus, OH, for financial support of the work reported herein.

2 National Institutes of Health graduate student trainee in Nutritional Sciences (AM07497).

3 Author to whom reprint requests should be addressed.

Manuscript received 23 March 1987. Revision accepted 26 May 1987.







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