EVIDENCE FOR CHANGES IN THE ALZHEIMERS-DISEASE BRAIN CORTICAL MEMBRANE-STRUCTURE MEDIATED BY CHOLESTEROL

被引:165
作者
MASON, RP
SHOEMAKER, WJ
SHAJENKO, L
CHAMBERS, TE
HERBETTE, LG
机构
[1] UNIV CONNECTICUT, CTR HLTH, DEPT RADIOL, FARMINGTON, CT 06030 USA
[2] UNIV CONNECTICUT, CTR HLTH, DEPT PSYCHIAT, FARMINGTON, CT 06030 USA
[3] UNIV CONNECTICUT, CTR HLTH, DEPT MED, FARMINGTON, CT 06030 USA
[4] UNIV CONNECTICUT, CTR HLTH, DEPT BIOCHEM, FARMINGTON, CT 06030 USA
[5] UNIV CONNECTICUT, CTR HLTH, TRAVELERS CTR AGING, FARMINGTON, CT 06030 USA
[6] UNIV CONNECTICUT, CTR HLTH, NEUROBIOL LAB, FARMINGTON, CT 06030 USA
关键词
X-RAY DIFFRACTION; ALZHEIMERS DISEASE; NEURAL MEMBRANE STRUCTURE AND COMPOSITION;
D O I
10.1016/0197-4580(92)90116-F
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Small angle X-ray diffraction analysis of Alzheimer's disease (AD) lipid membranes extracted from cortical gray matter showed significant, reproducible structure changes relative to age-matched control samples. Specifically, there was an average 4 angstrom reduction in the lipid bilayer width and significant changes in the membrane electron density profiles of AD cortical samples. There were no significant structure differences in the membrane bilayers isolated from an unaffected region (cerebellum) of the AD brain. Lipid and protein analysis of 6 AD and 6 age-matched controls showed that the phospholipid:protein mass ratio was unchanged but that the unesterified cholesterol:phospholipid (C: PL) mole ratio decreased by 30% in the AD temporal gyrus relative to age-matched controls. By contrast, the C:PL mole ratio in the cerebellum did not change significantly. X-ray diffraction analysis of a cholesterol enriched AD sample demonstrated a virtual restoration of the normal membrane bilayer width and electron density profile, suggesting that the cholesterol deficit played a major role in the AD lipid membrane structure perturbation. Alterations in the composition and structure of the membrane bilayer may play an important role in the pathophysiology of AD by altering the activity and catabolism of membrane-bound proteins, including the beta-amyloid precursor protein.
引用
收藏
页码:413 / 419
页数:7
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