Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2004-1-15
pubmed:abstractText
AMP-activated protein kinase (AMPK) is tightly regulated by the cellular AMP:ATP ratio and plays a central role in the regulation of energy homeostasis and metabolic stress. A pharmacological activator of AMPK, 5-amino-4-imidazole carboxamide riboside (AICAR) inhibited lipopolysaccharide (LPS)-induced expression of proinflammatory cytokines (tumor necrosis factor alpha, interleukin-1beta, and interleukin-6) and inducible nitric oxide synthase in primary rat astrocytes, microglia, and peritoneal macrophages. AICAR attenuates the LPS-induced activation of nuclear factor kappaB via downregulation of IkappaB kinase alpha/beta activity. It also inhibits nuclear translocation of CCAAT/enhancer-binding protein (C/EBP) transcription factor by inhibiting the expression of C/EBP-delta in brain glial cells. The dominant negative form of AMPKalpha2 (D157A) and its antisense documents a possible role of AMPK in the regulation of the cellular proinflammatory process. AICAR also inhibited the production of inflammatory mediators in serum and their expression in CNS of rats injected with a sublethal dose of LPS by intraperitoneal injection. These observations in cultured cells as well as in the animal model suggest that AICAR may be of therapeutic value in treating inflammatory diseases.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/AICA ribonucleotide, http://linkedlifedata.com/resource/pubmed/chemical/AMP-Activated Protein Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Aminoimidazole Carboxamide, http://linkedlifedata.com/resource/pubmed/chemical/Cytokines, http://linkedlifedata.com/resource/pubmed/chemical/Lipopolysaccharides, http://linkedlifedata.com/resource/pubmed/chemical/Multienzyme Complexes, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase Type II, http://linkedlifedata.com/resource/pubmed/chemical/Nos2 protein, rat, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Ribonucleotides, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1529-2401
pubmed:author
pubmed:issnType
Electronic
pubmed:day
14
pubmed:volume
24
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
479-87
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:14724246-AMP-Activated Protein Kinases, pubmed-meshheading:14724246-Active Transport, Cell Nucleus, pubmed-meshheading:14724246-Aminoimidazole Carboxamide, pubmed-meshheading:14724246-Animals, pubmed-meshheading:14724246-Brain, pubmed-meshheading:14724246-Cell Nucleus, pubmed-meshheading:14724246-Cells, Cultured, pubmed-meshheading:14724246-Cytokines, pubmed-meshheading:14724246-Inflammation, pubmed-meshheading:14724246-Lipopolysaccharides, pubmed-meshheading:14724246-Macrophages, Peritoneal, pubmed-meshheading:14724246-Multienzyme Complexes, pubmed-meshheading:14724246-Neuroglia, pubmed-meshheading:14724246-Nitric Oxide, pubmed-meshheading:14724246-Nitric Oxide Synthase, pubmed-meshheading:14724246-Nitric Oxide Synthase Type II, pubmed-meshheading:14724246-Protein-Serine-Threonine Kinases, pubmed-meshheading:14724246-Rats, pubmed-meshheading:14724246-Rats, Sprague-Dawley, pubmed-meshheading:14724246-Ribonucleotides, pubmed-meshheading:14724246-Transcription Factors
pubmed:year
2004
pubmed:articleTitle
5-aminoimidazole-4-carboxamide-1-beta-4-ribofuranoside inhibits proinflammatory response in glial cells: a possible role of AMP-activated protein kinase.
pubmed:affiliation
Department of Pediatrics and Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, South Carolina 29425, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.