Literature DB >> 6644183

Lipids of human atherosclerotic plaques and xanthomas: clues to the mechanism of plaque progression.

J H Rapp, W E Connor, D S Lin, T Inahara, J M Porter.   

Abstract

While the content of fatty streaks and fibrous plaques has been extensively studied in autopsied specimens, little is known about the lipid composition of advanced human atherosclerotic plaques requiring surgical removal. We have analyzed free cholesterol, cholesteryl ester, and the cholesteryl ester fatty acid content in 19 carotid and 7 femoral obliterative plaques obtained at endarterectomy. These were compared with values from each subject's plasma and from xanthomas removed from eight patients. The total cholesterol content was 75.1 mg/g dry weight for carotid plaques, 56.0 mg/g for femoral plaques, and 106.8 mg/g for xanthomas. The free cholesterol content was 56.6% and 50.4% of the total cholesterol for carotid and femoral plaques, respectively, while the free cholesterol of xanthomas was only 25.5%. The fatty acids of cholesteryl esters were analyzed in an attempt to identify the site of their esterification, i.e., within plasma or within plaque. This can be determined using the ratio of linoleic acid (18:2) to oleic acid (18:1) in the cholesteryl ester. The ratios were 0.36 for xanthoma, 1.62 for carotid plaque, 1.73 for femoral plaque, and 2.51 in plasma. These data emphasize two chemical changes occurring with evolution of the atherosclerotic process: 1) The cholesteryl ester fatty acid composition of the plaque becomes increasingly similar to that of plasma, and 2) there is a continuing increase in the percentage of free cholesterol. These alterations reflect a decreased metabolic efficiency within atherosclerotic lesions and may initiate events that enhance plaque progression.

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Year:  1983        PMID: 6644183

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  21 in total

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3.  Enhanced vascular permeability facilitates entry of plasma HDL and promotes macrophage-reverse cholesterol transport from skin in mice.

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Journal:  J Lipid Res       Date:  2014-12-03       Impact factor: 5.922

4.  Intermittent hypoxia induces murine macrophage foam cell formation by IKK-β-dependent NF-κB pathway activation.

Authors:  Toshihiro Imamura; Orit Poulsen; Gabriel G Haddad
Journal:  J Appl Physiol (1985)       Date:  2016-07-28

5.  Melittin stimulates fatty acid release through non-phospholipase-mediated mechanisms and interacts with the dopamine transporter and other membrane-spanning proteins.

Authors:  Dove J Keith; Amy J Eshleman; Aaron Janowsky
Journal:  Eur J Pharmacol       Date:  2010-10-20       Impact factor: 4.432

6.  Lipoxygenase contributes to the oxidation of lipids in human atherosclerotic plaques.

Authors:  V A Folcik; R A Nivar-Aristy; L P Krajewski; M K Cathcart
Journal:  J Clin Invest       Date:  1995-07       Impact factor: 14.808

7.  Cholesterol in human atherosclerotic plaque is a marker for underlying disease state and plaque vulnerability.

Authors:  Zhu Chen; Marina Ichetovkin; Marc Kurtz; Emanuel Zycband; Douglas Kawka; John Woods; Xuanmin He; Andrew S Plump; Eric Hailman
Journal:  Lipids Health Dis       Date:  2010-06-11       Impact factor: 3.876

8.  IL-22 is induced by S100/calgranulin and impairs cholesterol efflux in macrophages by downregulating ABCG1.

Authors:  Bijoy Chellan; Ling Yan; Timothy J Sontag; Catherine A Reardon; Marion A Hofmann Bowman
Journal:  J Lipid Res       Date:  2013-12-23       Impact factor: 5.922

9.  Immunohistochemical distribution of lipoprotein epitopes in xanthomata from patients with familial hypercholesterolemia.

Authors:  N Sugiyama; S Marcovina; A M Gown; H Seftel; B Joffe; A Chait
Journal:  Am J Pathol       Date:  1992-07       Impact factor: 4.307

10.  Hypertension in rats does not potentiate hypercholesterolemia and aortic cholesterol deposition induced by a hypercholesterolemic diet.

Authors:  H Mori; K Ishiguro; H Okuyama
Journal:  Lipids       Date:  1993-02       Impact factor: 1.880

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