Conjugated linoleic acids (CLA) as precursors of a distinct family of PUFA

被引:45
作者
Banni, S
Petroni, A
Blasevich, M
Carta, G
Cordeddu, L
Murru, E
Melis, MP
Mahon, A
Belury, MA
机构
[1] Univ Cagliari, Dipartimento Biol Sperimentale, I-09042 Cagliari, Italy
[2] Univ Milan, Dipartimento Sci Farmacol, Milan, Italy
[3] Ohio State Univ, Dept Human Nutr, Columbus, OH 43221 USA
关键词
D O I
10.1007/s11745-004-1341-0
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
One of the possibilities for distinct actions of c9,t11 - and the t10,c12-conjugated linoleic acid (CLA)isomers may be at the level of metabolism since the conjugated diene structure gives to CLA isomers and their metabolites a distinct pattern of incorporation into the lipid fraction and metabolism. In fact,CLA appears to undergo similar transformations as linoleic acid but with subtle isomer differences, which may account for their activity in lowering linoleic acid metabolites in those tissues rich in neutral lipids where CLA is preferentially incorporated. Furthermore, c9,t11 and t10,c12 isomers are metabolized at a different rate in the peroxisomes, where the shortened metabolite from t10,c12 is formed at a much higher proportion than the metabolite from c9,t11. This may account for the lower accumulation of t10,c12 isomer into cell lipids. CLA isomers may therefore be viewed as a "new" family of polyunsaturated fatty acids (PUFA) producing a distinct range of metabolites using the same enzymatic system as the other (i.e., n-3, n-6 and n-9) PUFA families. It is likely that perturbation of PUFA metabolism by CLA will have an impact on eicosanoid formation and metabolism, closely linked to the biological activities attributed to CLA.
引用
收藏
页码:1143 / 1146
页数:4
相关论文
共 28 条
[1]   LIQUID-CHROMATOGRAPHIC MASS-SPECTROMETRIC ANALYSIS OF CONJUGATED DIENE FATTY-ACIDS IN A PARTIALLY HYDROGENATED FAT [J].
BANNI, S ;
DAY, BW ;
EVANS, RW ;
CORONGIU, FP ;
LOMBARDI, B .
JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 1994, 71 (12) :1321-1325
[2]   Detection of conjugated C16 PUFAs in rat tissues as possible partial beta-oxidation products of naturally occurring conjugated linoleic acid and its metabolites [J].
Banni, S ;
Petroni, A ;
Blasevich, M ;
Carta, G ;
Angioni, E ;
Murru, E ;
Day, BW ;
Melis, MP ;
Spada, S ;
Ip, C .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2004, 1682 (1-3) :120-127
[3]   Characterization of conjugated diene fatty acids in milk, dairy products, and lamb tissues [J].
Banni, S ;
Carta, G ;
Contini, MS ;
Angioni, E ;
Deiana, M ;
Dessi, MA ;
Melis, MP ;
Corongiu, FP .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 1996, 7 (03) :150-155
[4]   Conjugated linoleic acid metabolism [J].
Banni, S .
CURRENT OPINION IN LIPIDOLOGY, 2002, 13 (03) :261-266
[5]  
Banni S, 2001, J LIPID RES, V42, P1056
[6]   Decrease in linoleic acid metabolites as a potential mechanism in cancer risk reduction by conjugated linoleic acid [J].
Banni, S ;
Angioni, E ;
Casu, V ;
Melis, MP ;
Carta, G ;
Corongiu, FP ;
Thompson, H ;
Ip, C .
CARCINOGENESIS, 1999, 20 (06) :1019-1024
[7]   DETECTION OF CONJUGATED DIENE ISOMERS OF LINOLEIC-ACID IN LIVER LIPIDS OF RATS FED A CHOLINE-DEVOID DIET INDICATES THAT THE DIET DOES NOT CAUSE LIPOPEROXIDATION [J].
BANNI, S ;
DAY, BW ;
EVANS, RW ;
CORONGIU, FP ;
LOMBARDI, B .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 1995, 6 (05) :281-289
[8]   The conjugated linoleic acid (CLA) isomer, t10c12-CLA, is inversely associated with changes in body weight and serum leptin in subjects with type 2 diabetes mellitus [J].
Belury, MA ;
Mahon, A ;
Banni, S .
JOURNAL OF NUTRITION, 2003, 133 (01) :257S-260S
[9]   Dietary conjugated linoleic acid in health: Physiological effects and mechanisms of action [J].
Belury, MA .
ANNUAL REVIEW OF NUTRITION, 2002, 22 :505-531
[10]   Dietary conjugated linoleic acid induces peroxisome-specific enzyme accumulation and ornithine decarboxylase activity in mouse liver [J].
Belury, MA ;
MoyaCamarena, SY ;
Liu, KL ;
Heuvel, JPV .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 1997, 8 (10) :579-584