Angiotensin II increases ROS production in cardiac fibroblasts by inducing p22phox over-expression / 南方医科大学学报
Journal of Southern Medical University
; (12): 202-204, 2009.
Article
in Zh
| WPRIM
| ID: wpr-339031
Responsible library:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the changes in the reactive oxygen species (ROS) in rat cardiac fibroblasts exposed to angiotensin II (Ang II) treatment and explore the possible pathways that mediate ROS production.</p><p><b>METHODS</b>In vitro cultured fetal rat cardiac fibroblasts treated with apocynin (APO, 100 micromol/L), Ang II (10(-7) mol/L), or APO+Ang II (10(-7) mol/L Ang II was added 1 h after 100 micromol/L APO), and the ROS levels and p22phox expression in the cells were detected using fluorescent microscope and immunohistochemistry, respectively.</p><p><b>RESULTS</b>Compared with the normal control cells, Ang II treatment of the cardiac fibroblasts resulted in significantly increased ROS production, the effect of which was inhibited by the application of APO. p22phox expression was hardly detected by immunohistochemistry in the control cells, but over-expressed in AngII-treated cells. APO substantially decreased the over-expression of p22phox induced by Ang II.</p><p><b>CONCLUSION</b>Ang II increases ROS production in fetal rat cardiac fibroblasts probably by inducing p22phox over-expression.</p>
Full text:
1
Index:
WPRIM
Main subject:
Pharmacology
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Angiotensin II
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Cells, Cultured
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Reactive Oxygen Species
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Rats, Sprague-Dawley
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NADPH Oxidases
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Cell Biology
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Fibroblasts
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Animals, Newborn
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Metabolism
Limits:
Animals
Language:
Zh
Journal:
Journal of Southern Medical University
Year:
2009
Type:
Article