Changes in conjugated linoleic acid composition within samples obtained from a single source

被引:11
作者
Adlof, RO [1 ]
Copes, LC [1 ]
Walter, EL [1 ]
机构
[1] ARS, Natl Ctr Agr Utilizat Res, USDA, Peoria, IL 61604 USA
关键词
conjugated; linoleic; CLA; composition; isomers; HPLC; GC;
D O I
10.1007/s11745-001-0723-7
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
Conjugated linoleic acid (CLA; 9c,11t-18:2) and CLA isomers have been reported, in animals, to exhibit a variety of health-related benefits. Silver ion high-performance liquid chromatography (Ag-HPLC) was found to provide better resolution of the isomers than gas chromatography. Most commercially available samples of CLA, prepared by base-catalyzed isomerization of linoleic acid (9c,12c-18:2), are composed of mixtures of four major isomers. While these isomers have been characterized, we found significant changes in CLA isomer ratios within samples obtained from the same producer/commercial supplier over a period of 1.5 yr. In the first sample, the four cis/trans isomers (8t,10c-18:2, 9c,11t-18:2, 10t,12c-18:2 and 11c,13t-18:2) were present in a ratio of approximately 1:2:2:1, while in the second sample they were present in almost equal proportions. If indeed certain daily levels of CLA intake are required to produce suggested health benefits in humans, changes in concentrations of specific CLA isomers could significantly impact these effects. Care must be taken to analyze the CLA used in human and animal studies.
引用
收藏
页码:315 / 317
页数:3
相关论文
共 19 条
[11]   Conjugated linoleic acid and disease prevention: A review of current knowledge [J].
MacDonald, HB .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 2000, 19 (02) :111S-118S
[12]   Diazomethane as a highly selective fatty acid methylating reagent for use in gas chromatographic analysis [J].
Mueller, HW .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 1996, 679 (1-2) :208-209
[13]   Inhibition of hepatic stearoyl-CoA desaturase activity by trans-10,cis-12 conjugated linoleic acid and its derivatives [J].
Park, Y ;
Storkson, JM ;
Ntambi, JM ;
Cook, ME ;
Sih, CJ ;
Pariza, MW .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2000, 1486 (2-3) :285-292
[14]   Evidence that the trans-10,cis-12 isomer of conjugated linoleic acid induces body composition changes in mice [J].
Park, Y ;
Storkson, JM ;
Albright, KJ ;
Liu, W ;
Pariza, MW .
LIPIDS, 1999, 34 (03) :235-241
[15]   Invited commentary - Atherosclerosis and conjugated linoleic acid [J].
Rudel, LL .
BRITISH JOURNAL OF NUTRITION, 1999, 81 (03) :177-179
[16]   Conjugated linoleic acid - The good news about animal fat [J].
Steinhart, C .
JOURNAL OF CHEMICAL EDUCATION, 1996, 73 (12) :A302-A303
[17]   Dietary effect of conjugated linoleic acid on lipid levels in white adipose tissue of Sprague-Dawley rats [J].
Yamasaki, M ;
Mansho, K ;
Mishima, H ;
Kasai, M ;
Sugano, M ;
Tachibana, H ;
Yamada, K .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1999, 63 (06) :1104-1106
[18]  
Yurawecz MP, 1999, FETT-LIPID, V101, P277, DOI 10.1002/(SICI)1521-4133(199908)101:8<277::AID-LIPI277>3.0.CO
[19]  
2-C