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1.
Journal of Southern Medical University ; (12): 2419-2422, 2010.
Article in Chinese | WPRIM | ID: wpr-323646

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effects of AICAR on the activity of transcription factor FOXO1 and expression of ubiquitin ligase MuRF1 in rat cardiomyocytes, and explore the possible role of AMP-activated protein kinase (AMPK) in proteolysis pathways.</p><p><b>METHODS</b>In vitro cultured neonatal rat cardiac myocytes were treated with AICAR, and Western blotting was used to detect the phosphorylation of FOXO1 and expression of MuRF1 in the cells.</p><p><b>RESULTS</b>AICAR activated AMPK in rat cardiac myocytes. Activated AMPK significantly inhibited the phosphorylation of FOXO1 and increased MuRF1 protein expression.</p><p><b>CONCLUSION</b>AMPK may regulate proteolysis by activating FOXO1 transcription factor and up-regulating MuRF1 expression.</p>


Subject(s)
Animals , Rats , AMP-Activated Protein Kinases , Metabolism , Aminoimidazole Carboxamide , Pharmacology , Cells, Cultured , Forkhead Transcription Factors , Metabolism , Muscle Proteins , Metabolism , Myocytes, Cardiac , Metabolism , Nerve Tissue Proteins , Metabolism , Rats, Sprague-Dawley , Ribonucleotides , Pharmacology , Tripartite Motif Proteins , Ubiquitin-Protein Ligases , Metabolism
2.
Chinese Journal of Cardiology ; (12): 605-609, 2009.
Article in Chinese | WPRIM | ID: wpr-236445

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the association between hemoglobin scavenger receptor (CD163) expression levels on monocytic surfaces and coronary atherosclerotic severity in patients with coronary heart disease (CHD) as well as the roles of CD163 in inflammation and lipidperoxidation.</p><p><b>METHODS</b>Eighty-four patients were diagnosed as CHD according to the results of coronary angiography and ACC/AHA diagnostic criteria. The patients were divided into 3 groups: acute myocardial infarction (AMI) group (n = 30), unstable angina (UA) group (n = 30), stable angina (SA) group (n = 24). Another 20 patients with normal coronary artery served as control. Expression levels of CD163 on monocytes were detected by means of flow cytometry, and the results were shown as mean fluorescence intensity (mfi). All patients underwent coronary angiography and the results were further evaluated by Jenkins score. Serum CRP and LDL-C were also measured.</p><p><b>RESULTS</b>The expression levels of CD163 on monocytes in peripheral blood were significantly higher in CHD patients compared to controls (P < 0.01) in the order of AMI group [(84.4 +/- 6.9) mfi] > UA group [(64.1 +/- 5.5) mfi, P < 0.01 vs. AMI] > SA group [(46.7 +/- 6.5) mfi, P < 0.01 vs. AMI and UA] > control group [(22.0 +/- 6.1) mfi, P < 0.01 vs. AMI, UA and SA]. The expression levels of CD163 on monocytes in patients with CHD were positively correlated with Jenkins score (r = 0.9107, P < 0.01), CRP (r = 0.766, P < 0.01) and LDL-C (r = 0.749, P < 0.01).</p><p><b>CONCLUSIONS</b>Expression levels of CD163 was significantly increased in patients with CHD and positively correlated with coronary heart disease severity and serum CRP and LDL-C.</p>


Subject(s)
Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Antigens, CD , Metabolism , Antigens, Differentiation, Myelomonocytic , Metabolism , C-Reactive Protein , Cholesterol, LDL , Blood , Coronary Disease , Metabolism , Pathology , Inflammation , Lipid Peroxidation , Receptors, Cell Surface , Metabolism , Severity of Illness Index
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