Meclofenamic Acid for Inhibition of Human Vascular Smooth Muscle Cell Proliferation and Migration: An In Vitro Study
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作者:
Wolfgang Schober
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机构:Department of Diagnostic Radiology,
Wolfgang Schober
Rainer Kehlbach
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机构:Department of Diagnostic Radiology,
Rainer Kehlbach
Regina Gebert
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机构:Department of Diagnostic Radiology,
Regina Gebert
Jakub Wiskirchen
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机构:Department of Diagnostic Radiology,
Jakub Wiskirchen
Enno Rodegerdts
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机构:Department of Diagnostic Radiology,
Enno Rodegerdts
Claus D. Claussen
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机构:Department of Diagnostic Radiology,
Claus D. Claussen
Stephan H. Duda
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机构:Department of Diagnostic Radiology,
Stephan H. Duda
机构:
[1] Department of Diagnostic Radiology,
[2] Eberhard-Karls-Universitat,undefined
[3] Hoppe-Seyler-Strasse 3,undefined
[4] D-72076
Tubingen,undefined
[5] Germany,undefined
来源:
CardioVascular and Interventional Radiology
|
2002年
/
25卷
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摘要:
Purpose: The aim of the study was to examine
the effects of meclofenamic acid on proliferation, clonogenic activity,
migratory ability, cell cycle distribution and p44/42 MAPK (mitogen
activated protein kinase) expression in serum-stimulated human aortic
smooth muscle cells (haSMCs).
Methods: haSMCs were
treated with meclofenamic acid in three different concentrations (10
mM, 100 mM, 200 mM) for 4 days. Then meclofenamic acid-free
culture medium was supplemented until day 20. Growth kinetics were
assessed. Cell cycle analysis was performed by flow cytometry.
Clonogenic activity was evaluated with colony formation assays.
Migratory ability was investigated by stimulation with platelet-derived
growth factor (PDGF-BB) in 24-well plates with 8 mm pores membrane
inserts. p44/42 MAPK was detected by Western blot technique.
Results: Meclofenamic acid inihibited the proliferation,
clonogenic activity and migratory ability of haSMCs in a dose-dependent
manner. Cell cycle analysis revealed a G2/M-phase block. The p44/42
MAPK was significantly reduced.
Conclusion: Meclofenamic
acid inhibits the proliferation and migration of haSMCs. If a
sufficient dose of meclofenamic acid can be applied systemically or by
local drug delivery it could be a valuable substance to prevent
restenosis after angioplasty.