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Review
. 2008 Feb;196(2):497-504.
doi: 10.1016/j.atherosclerosis.2007.09.018. Epub 2007 Oct 25.

Ceramide: a common pathway for atherosclerosis?

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Review

Ceramide: a common pathway for atherosclerosis?

Jean Bismuth et al. Atherosclerosis. 2008 Feb.

Abstract

Plasma sphingomyelin concentration is correlated with the development of atherosclerosis. It has been found to exist in significantly higher concentrations in aortic plaque. This appears to have clinical relevance as well as it has been shown to be an independent predictor of coronary artery disease. Ceramide, the backbone of sphingolipids, is the key component which affects atherosclerotic changes through its important second-messenger role. This paper sheds light on some of the current literature supporting the significance of ceramide with respect to its interactions with lipids, inflammatory cytokines, homocysteine and matrix metalloproteinases. Furthermore, the potential therapeutic implications of modulating ceramide concentrations are also discussed.

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Figures

Fig. 1
Fig. 1
Sphingolipid biosynthetic pathway and potential inhibitors. Multiple compounds are outlined, but the most convincing data is that for myriocin and is therefore the only one discussed in the text. * First rate-limiting step in the sphinglipid biosynthetic pathway. Myriocin is isolated from Isari Sinclairii (fungal species) and is a potent and specific inhibitor of serine palmitoyltransferase, the enzyme which is the catalyst in this step.

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References

    1. Jiang XC, Paultre F, Pearson TA, et al. Plasma sphingomyelin level as a risk factor for coronary artery disease. Arterioscler Thromb Vasc Biol. 2000;20:2614–8. - PubMed
    1. Schissel SL, Tweedie-Hardman J, Rapp JH, et al. Rabbit aorta and human atherosclerotic lesions hydrolyze the sphingomyelin of retained low-density lipoprotein. Proposed role for arterial-wall sphingomyelinase in subendothelial retention and aggregation of atherogenic lipoproteins. J Clin Invest. 1996;98:1455–64. - PMC - PubMed
    1. Li Z, Basterr MJ, Hailemariam TK, et al. The effect of dietary sphingolipids on plasma sphingomyelin metabolism and atherosclerosis. Biochim Biophys Acta. 2005;1735:130–4. - PubMed
    1. Tabas I, Li Y, Brocia RW, et al. Lipoprotein lipase and sphingomyelinase synergistically enhance the association of atherogenic lipoproteins with smooth muscle cells and extracellular matrix. A possible mechanism for low density lipoprotein and lipoprotein(a) retention and macrophage foam cell formation. J Biol Chem. 1993;268:20419–32. - PubMed
    1. Schissel SL, Jiang X, Tweedie-Hardman J, Jeong T, et al. Secretory sphingomyelinase, a product of the acid sphingomyelinase gene, can hydrolyze atherogenic lipoproteins at neutral pH. Implications for atherosclerotic lesion development. J Biol Chem. 1998;273:2738–46. - PubMed

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