Title:
Ceramide and sphingosine-1-phosphate in cell death pathways: Relevance to the pathogenesis of Alzheimer’s disease

dc.contributor.authorSankha Shubhra Chakrabarti
dc.contributor.authorAritri Bir
dc.contributor.authorJit Poddar
dc.contributor.authorMaitrayee Sinha
dc.contributor.authorAnirban Ganguly
dc.contributor.authorSasanka Chakrabarti
dc.date.accessioned2026-02-07T08:15:44Z
dc.date.issued2016
dc.description.abstractThe metabolic turnover of sphingolipids produces several signaling molecules that profoundly affect the proliferation, differentiation and death of cells. In particular, an enormous body of information is available that defines the varied role of ceramide and sphingosine-1-phosphate in cell death and survival. This review specifically examines the role of ceramide and sphingosine-1- phosphate in triggering neuronal death in Alzheimer’s disease by analyzing the data from post-mortem studies and experimental research. There is compelling evidence that ceramide plays a key role in the neurodegeneration and amyloidogenesis occurring in the brain in Alzheimer’s disease. Further, it appears that ceramide and amyloid beta protein orchestrate an attack on mitochondria to set in the path-ways of cell death. However, the complexity of metabolic and signaling pathways of sphingolipid derivatives precludes an immediate identification of effective drug targets for the therapy of Alzheimer’s disease. © 2016 Bentham Science Publishers.
dc.identifier.doi10.2174/1567205013666160603004239
dc.identifier.issn15672050
dc.identifier.urihttps://doi.org/10.2174/1567205013666160603004239
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/28728
dc.publisherBentham Science Publishers B.V.
dc.subjectAlzheimer’s disease
dc.subjectAmyloid beta protein
dc.subjectApoptosis
dc.subjectCeramide
dc.subjectMitochondria
dc.subjectNecroptosis
dc.subjectSphingomyelin
dc.subjectSphingosine-1-phosphate
dc.titleCeramide and sphingosine-1-phosphate in cell death pathways: Relevance to the pathogenesis of Alzheimer’s disease
dc.typePublication
dspace.entity.typeReview

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