Abstract | BACKGROUND AND OBJECTIVE:
Inflammation is pivotal in atherosclerosis. C-reactive protein (CRP), in addition to being a cardiovascular risk marker, may also be proatherogenic. We have previously shown that in addition to the liver, human aortic endothelial cells (HAECs) synthesize and secrete CRP. Whereas CRP levels are increased in obesity, metabolic syndrome, and diabetes, levels of adiponectin are reduced in these conditions. We tested the hypothesis that adiponectin reduces CRP synthesis and secretion in HAECs under normoglycemic (5.5 mmol/ L glucose) and hyperglycemic conditions (15 mmol/ L glucose). METHODS AND RESULTS:
Adiponectin dose-dependently reduced CRP mRNA and protein from HAECs. Adiponectin treatment of HAECs significantly decreased IkappaB phosphorylation and NFkappaB binding activity. There was no effect of adiponectin on STAT or C/EBP transcriptional activity. Adiponectin also activated AMP kinase resulting in decreased NFkappaB activity and decreased CRP mRNA and protein. These effects of adiponectin were mimicked by AICAR, an activator of AMPK, and reversed by inhibition of AMPK. Thus, adiponectin reduces CRP synthesis and secretion from HAECs under hyperglycemia via upregulation of AMP kinase and downregulation of NFkappaB. Similar findings were observed in rat primary hepatocytes. CONCLUSIONS:
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Authors | Sridevi Devaraj, Natalie Torok, Mohan R Dasu, David Samols, Ishwarlal Jialal |
Journal | Arteriosclerosis, thrombosis, and vascular biology
(Arterioscler Thromb Vasc Biol)
Vol. 28
Issue 7
Pg. 1368-74
(Jul 2008)
ISSN: 1524-4636 [Electronic] United States |
PMID | 18451326
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Adiponectin
- CCAAT-Enhancer-Binding Protein-beta
- I-kappa B Proteins
- NF-kappa B
- RNA, Messenger
- STAT Transcription Factors
- C-Reactive Protein
- Mitogen-Activated Protein Kinases
- Adenylate Kinase
- Glucose
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Topics |
- Adenylate Kinase
(metabolism)
- Adiponectin
(metabolism)
- Animals
- C-Reactive Protein
(genetics, metabolism)
- CCAAT-Enhancer-Binding Protein-beta
(metabolism)
- Cells, Cultured
- Down-Regulation
- Endothelial Cells
(enzymology, metabolism)
- Enzyme Activation
- Glucose
(metabolism)
- Hepatocytes
(metabolism)
- Humans
- I-kappa B Proteins
(metabolism)
- Mitogen-Activated Protein Kinases
(metabolism)
- NF-kappa B
(metabolism)
- Phosphorylation
- RNA, Messenger
(metabolism)
- Rats
- STAT Transcription Factors
(metabolism)
- Transfection
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