Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2015 Jun 16:14:55.
doi: 10.1186/s12944-015-0053-y.

Sphingolipids in cardiovascular diseases and metabolic disorders

Affiliations
Review

Sphingolipids in cardiovascular diseases and metabolic disorders

Sonia Borodzicz et al. Lipids Health Dis. .

Abstract

Many investigations suggest the pivotal role of sphingolipids in the pathogenesis of lifestyle diseases such as myocardial infarction, hypertension, stroke, diabetes mellitus type 2 and obesity. Some studies suggest that sphingolipids are important factors in cellular signal transduction. They serve as biologically active components of cell membrane and are involved in many processes such as proliferation, maturation and apoptosis. Recently, ceramide and sphingosine-1-phosphate have become the target of many investigations. Ceramide is generated in three metabolic pathways and many factors induce its production as a cellular stress response. Ceramide has proapoptotic properties and acts as a precursor for many other sphingolipids. Sphingosine-1-phosphate is a ceramide derivative, acting antiapoptotically and mitogenically and it is importantly involved in cardioprotection. Further research on the involvement of sphingolipids in cellular pathophysiology may improve the prevention and therapy of lifestyle diseases.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Pathways of ceramide generation
Fig. 2
Fig. 2
Pathophysiological mechanisms of sphingolipids action

References

    1. Tirodkar TS, Voelkel-Johnson C. Sphingolipids in apoptosis. Exp Oncol. 2012;34:231–42. - PubMed
    1. Mao C, Obeid LM. Ceramidases: regulators of cellular responses mediated by ceramide, sphingosine, and sphingosine-1-phosphate. Biochim Biophys Acta. 2008;1781:424–34. doi: 10.1016/j.bbalip.2008.06.002. - DOI - PMC - PubMed
    1. Paugh SW, Paugh BS, Rahmani M, Kapitonov D, Almenara JA, Kordula T, et al. A selective sphingosine kinase 1 inhibitor integrates multiple molecular therapeutic targets in human leukemia. Blood. 2008;112:1382–91. doi: 10.1182/blood-2008-02-138958. - DOI - PMC - PubMed
    1. Gulbins E, Li PL. Physiological and pathophysiological aspects of ceramide. Am J Physiol Regul Integr Comp Physiol. 2006;290:R11–26. doi: 10.1152/ajpregu.00416.2005. - DOI - PubMed
    1. Car H, Żendzian-Piotrowska M, Fiedorowicz A, Prokopiuk S, Sadowska A, Kurek K. The role of ceramides in selected brain pathologies: ischemia/hypoxia, Alzheimer disease. Postepy Hig Med Dosw (Online) 2012;66:295–303. doi: 10.5604/17322693.999024. - DOI - PubMed