C-13 MAS NMR studies of crystalline cholesterol and lipid mixtures modeling atherosclerotic plaques

被引:45
作者
Guo, W [1 ]
Hamilton, JA [1 ]
机构
[1] BOSTON UNIV, SCH MED, DEPT BIOPHYS, CTR ADV BIOMED RES W302, BOSTON, MA 02118 USA
关键词
D O I
10.1016/S0006-3495(96)79482-1
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Cholesterol and cholesteryl esters are the predominant lipids of atherosclerotic plaques. To provide fundamental data for the quantitative study of plaque lipids in situ, crystalline cholesterol (CHOL) and CHOL/cholesteryl ester (CE) mixtures with other lipids were studied by solid-state nuclear magnetic resonance with magic-angle-sample spinning, Highly distinctive spectra for three different crystalline structures of CHOL were obtained. When CHOL crystals were mixed with isotropic CE oil, solubilized CHOL (similar to 13 mol % CHOL) was detected by characteristic resonances such as C5, C6, and C3; the excess crystalline CHOL (either anhydrous or monohydrate) remained in its original crystalline structure, without being affected by the coexisting CE. By use of C-13-enriched CHOL the solubility of CHOL in the CE liquid-crystalline phase (similar to 8 mol %) was measured. When phosphatidylcholine was hydrated in presence of CHOL and CE, magic-angle-sampling nuclear magnetic resonance revealed liquid-crystalline CHOL/phosphatidylcholine multilayers with approximately an equal molar ratio of CHOL/phosphatidylcholine. Excess CHOL existed in the monohydrate crystalline form, and CE in separate oil or crystalline phases, depending on the temperature, The magic-angle-sampling nuclear magnetic resonance protocol for identifying different lipid phases was applied to intact (ex vivo) atherosclerotic plaques of cholesterol-fed rabbits. Liquid, liquid-crystalline, and solid phases of CE were characterized.
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页码:2857 / 2868
页数:12
相关论文
共 32 条
[11]   MOLECULAR-ORGANIZATION AND MOTIONS OF CHOLESTERYL ESTERS IN CRYSTALLINE AND LIQUID-CRYSTALLINE PHASES - A C-13 AND H-1 MAGIC-ANGLE-SPINNING NMR-STUDY [J].
GUO, W ;
HAMILTON, JA .
BIOCHEMISTRY, 1993, 32 (35) :9038-9052
[12]  
HAMILTON JA, 1978, J BIOL CHEM, V253, P5193
[13]  
HAMILTON JA, 1979, J BIOL CHEM, V254, P5435
[14]  
HAMILTON JA, 1983, J BIOL CHEM, V258, P2821
[15]  
HAMILTON JA, 1977, J BIOL CHEM, V252, P8071
[16]  
HAMILTON JA, 1996, BIOPHYS J, V70
[17]   PHASE-TRANSITION AND CRYSTAL-STRUCTURE OF THE 37-DEGREES-C FORM OF CHOLESTEROL [J].
HSU, LY ;
NORDMAN, CE .
SCIENCE, 1983, 220 (4597) :604-606
[18]   INFRARED MICROIMAGING OF ATHEROSCLEROTIC ARTERIES [J].
KODALI, DR ;
SMALL, DM ;
POWELL, J ;
KRISHNAN, K .
APPLIED SPECTROSCOPY, 1991, 45 (08) :1310-1317
[19]   A C-13 NUCLEAR MAGNETIC-RESONANCE STUDY OF AORTIC LESIONS AND CHOLESTERYL ESTER RICH LIPOPROTEINS FROM ATHEROSCLEROTIC RABBITS [J].
KROON, PA ;
QUINN, DM ;
CORDES, EH .
BIOCHEMISTRY, 1982, 21 (11) :2745-2753
[20]  
LOOMIS CR, 1979, J LIPID RES, V20, P525