Indexado em
  • Abra o Portão J
  • Genamics JournalSeek
  • CiteFactor
  • cosmos SE
  • Scimago
  • Diretório de Periódicos de Ulrich
  • Biblioteca de periódicos eletrônicos
  • RefSeek
  • Universidade de Hamdard
  • EBSCO AZ
  • Diretório de Indexação de Resumos para Periódicos
  • OCLC- WorldCat
  • Invocação Proquest
  • Scholarsteer
  • ESTRADA
  • Biblioteca Virtual de Biologia (vifabio)
  • publons
  • Fundação de Genebra para Educação e Pesquisa Médica
  • Google Scholar
Compartilhe esta página
Folheto de jornal
Flyer image

Abstrato

The Role of Lipids in Inflammation: Review of the Evolving Pathogenesis of Sickle Cell Disease

Anazoeze Jude Madu, Nada Abuknesha and Kebreab Ghebremeskel

The pathologic features of sickle cell disease had been known in the past to be as a result of red cell abnormality leading to vascular occlusion, haemolysis and consequent anaemia. Recent knowledge has revealed numerous pathogenetic pathways involving leukocytes, platelets and the vascular endothelium. Complex interactions between the inflammatory cytokines and the membrane lipids in sickle cell present several pathogenetic processes affecting disease severity. The mechanisms of membrane fluidity, aggregation, adhesion and inflammation are strongly associated with membrane lipid constitution. The omega -3 fatty acids via incorporation into the lipid membrane have been found to play a central role in suppressing inflammation in several disease processes. Variations in disease severity have been shown to correspond with levels of fatty acid desaturases involved in the synthesis of these fatty acids. The genes coding for these substances can also be manipulated to achieve a favorable outcome and may provide several possible therapeutic and prophylactic access points This review aims at exploring these delicate interactions and proffering possible targets to ameliorate disease features. The information and referenced publications quoted in this review were obtained from the PubMed Central database, using the search keywords; inflammation, sickle cell, fatty acids and cytokines