Nutritional role of the leucine metabolite beta-hydroxy beta-methylbutyrate (HMB)

被引:201
作者
Nissen, SL [1 ]
Abumrad, NN [1 ]
机构
[1] CORNELL UNIV MED COLL, N SHORE UNIV HOSP, MANHASSET, NY 11030 USA
关键词
muscle; immune; cholesterol; health;
D O I
10.1016/S0955-2863(97)00048-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This review develops the hypothesis that a metabolite of leucine termed beta-hydroxy beta-methylbutyrate (HMB) plays a key role in animal metabolism and that in certain circumstances insufficient amounts of HMB are either consumed in the diet or produced endogenously to supply tissue needs. The origin and metabolism of HMB is reviewed including the role of HMB in cholesterol biosynthesis. HMB feeding studies in animals are reviewed, which indicate that dietary supplementation of HMB can improve immune function and health and can increase the fat content of milk in lactating animals. Seven human studies are reviewed where HMB was fed. The results of both animal and human studies indicate that dietary supplementation of HMB is safe, as evidenced by lack of physical adverse effects and a lack of effect on blood hematology and chemistry. The only consistent change in blood chemistry was a decrease in LDL cholesterol, which changed 7% (P <.01). In humans undergoing resistance training, HMB supplementation increased lean mass gains from 50 to 200%, with similar percentage increases in strength when compared with unsupplemented subjects. The effects of HMB on muscle size and function seems to result from a diminution of exercise-related muscle damage and muscle protein breakdown. A general hypothesis is proposed that HMB is metabolized to HMG-CoA in tissues such as muscle, mammary tissue, and certain immune cells and is used for de novo cholesterol synthesis. In times of stimulated grown and/or differentiation, HMG-CoA may be rate-limiting for cholesterol synthesis, which could limit cell growth or function. It is proposed that feeding HMB can provide a saturating source of cytosolic HMG-CoA for cholesterol synthesis and in turn allow for maximal cell growth and function. (C) Elsevier Science Inc. 1997.
引用
收藏
页码:300 / 311
页数:12
相关论文
共 78 条
[1]   THE DISPOSAL OF AN INTRAVENOUSLY ADMINISTERED AMINO-ACID LOAD ACROSS THE HUMAN FOREARM [J].
ABUMRAD, NN ;
RABIN, D ;
WISE, KL ;
LACY, WW .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1982, 31 (05) :463-470
[2]   THE SIGNIFICANCE OF CERTAIN CARBOXYLIC ACIDS AS INTERMEDIATES IN THE BIOSYNTHESIS OF CHOLESTEROL [J].
ADAMSON, LF ;
GREENBERG, DM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1957, 23 (03) :472-479
[3]  
ATTMAN PO, 1984, ANN NUTR METAB, V28, P29, DOI 10.1159/000176779
[4]  
BACHHAWAT BK, 1955, J BIOL CHEM, V216, P727
[5]   IN-VITRO AND IN-VIVO INHIBITION OF HEPATIC CHOLESTEROL-SYNTHESIS BY 3-HYDROXY-3-METHYLGLUTARIC ACID [J].
BEG, ZH ;
LUPIEN, PJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1972, 260 (03) :439-&
[6]  
BERNLOHR RW, 1972, J BIOL CHEM, V247, P4893
[7]  
BLOCH K, 1954, J BIOL CHEM, V211, P687
[8]  
BLOMSTRAND E, 1991, J APPL PHYSIOL, V68, P83
[9]  
BRUZZONE P, 1991, SURGERY, V109, P768
[10]   ALPHA-KETOISOCAPROATE IS SUPERIOR TO LEUCINE IN SPARING GLUCOSE-UTILIZATION IN HUMANS [J].
BUCKSPAN, R ;
HOXWORTH, B ;
CERSOSIMO, E ;
DEVLIN, J ;
HORTON, E ;
ABUMRAD, N .
AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 251 (06) :E648-E653