LIPIDS AND OXIDIZED LIPIDS IN HUMAN ATHEROMA AND NORMAL AORTA

被引:138
作者
CARPENTER, KLH
TAYLOR, SE
BALLANTINE, JA
FUSSELL, B
HALLIWELL, B
MITCHINSON, MJ
机构
[1] UNIV COLL SWANSEA,DEPT CHEM,CTR MASS SPECTROMETRY SERV,SERC,SWANSEA SA2 8PP,W GLAM,WALES
[2] UNIV LONDON KINGS COLL,PHARMACOL GRP,LONDON WC2R 2LS,ENGLAND
关键词
ATHEROSCLEROSIS; ATHEROMA; NORMAL AORTA; LIPID; OXYSTEROL; HYDROXYOCTADECADIENOIC ACID; (HUMAN);
D O I
10.1016/0005-2760(93)90151-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
Lipids and oxidised lipids were analysed by GC and GC-MS in samples of human atheroma (necrotic gruel from the interior of advanced atherosclerotic plaques in the aorta) and human normal aorta (lesion-free intima plus inner media) from necropsy subjects. Cholest-5-en-3beta,26-diol and cholest-5-en-3beta,7beta-diol were detected in all the atheroma samples examined but not in significant amounts in normal aorta. In atheroma, cholest-5-en-3beta,26-diol was approximately proportional to cholesterol. Several isomeric hydroxyoctadecadienoic acids were detected in atheroma, and, in smaller amounts, in normal aorta. Many of the components of atheroma showed a high degree of cross-correlation on linear regression analysis, whilst cross-correlations were somewhat weaker for normal aorta. Atheroma showed a vast accumulation of lipid, especially cholesterol, in comparison to normal aorta. The atheroma samples contained a larger proportion of linoleate relative to oleate than the normal aorta. Levels of fatty acids relative to cholesterol were lower for atheroma than for normal aorta. The chemical composition of atheroma appeared unrelated to the age of the subject, whereas age-related increases in linoleate, oleate and cholesterol content were seen in the samples of normal aorta.
引用
收藏
页码:121 / 130
页数:10
相关论文
共 30 条
[1]  
ANDERSSON S, 1989, J BIOL CHEM, V264, P8222
[2]   CONNECTIVE-TISSUE RESPONSES TO OXYSTEROLS [J].
BARANOWSKI, A ;
ADAMS, CWM ;
HIGH, OBB ;
BOWYER, DB .
ATHEROSCLEROSIS, 1982, 41 (2-3) :255-266
[3]   LONG CHAIN FATTY ALCOHOLS IN NORMAL AND NEOPLASTIC TISSUES [J].
BLANK, ML ;
SNYDER, F .
LIPIDS, 1970, 5 (03) :337-+
[4]  
Brooks C.J.W., 1983, BIOCHEM SOC T, V11, P700
[5]   SQUALENE 26-HYDROXYCHOLESTEROL AND 7-KETOCHOLESTEROL IN HUMAN ATHEROMATOUS PLAQUES [J].
BROOKS, CJW ;
HARLAND, WA ;
STEEL, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1966, 125 (03) :620-&
[6]   LIPIDS OF HUMAN ATHEROMA .4. CHARACTERISATION OF A NEW GROUP OF POLAR STEROL ESTERS FROM HUMAN ATHEROSCLEROTIC PLAQUES [J].
BROOKS, CJW ;
STEEL, G ;
GILBERT, JD ;
HARLAND, WA .
ATHEROSCLEROSIS, 1971, 13 (02) :223-&
[7]   OXIDATION OF CHOLESTERYL LINOLEATE BY HUMAN MONOCYTE-MACROPHAGES INVITRO [J].
CARPENTER, KLH ;
BALLANTINE, JA ;
FUSSELL, B ;
ENRIGHT, JH ;
MITCHINSON, MJ .
ATHEROSCLEROSIS, 1990, 83 (2-3) :217-229
[8]   CHOLESTANOL AND 26-HYDROXYCHOLESTEROL IN NORMAL AND ATHEROSCLEROTIC HUMAN AORTA [J].
FUMAGALLI, R ;
GALLI, G ;
URNA, G .
LIFE SCIENCES PT-2 BIOCHEMISTRY GENERAL AND MOLECULAR BIOLOGY, 1971, 10 (01) :25-+
[9]   ISOLATION AND IDENTIFICATION OF CHOLESTEROL ALPHA-OXIDE AND OTHER MINOR STEROLS IN HUMAN SERUM [J].
GRAY, MF ;
LAWRIE, TDV ;
BROOKS, CJW .
LIPIDS, 1971, 6 (11) :836-&
[10]   LIPIDS OF HUMAN ATHEROMA .5. OCCURRENCE OF A NEW GROUP OF POLAR STEROL ESTERS IN VARIOUS STAGES OF HUMAN ATHEROSCLEROSIS [J].
HARLAND, WA ;
GILBERT, JD ;
STEEL, G ;
BROOKS, CJW .
ATHEROSCLEROSIS, 1971, 13 (02) :239-&