Effects of andrographolide on the activation of mitogen activated protein kinases and nuclear factor-κB in mouse peritoneal macrophage-derived foam cells / 中国结合医学杂志
Chin. j. integr. med
; Chin. j. integr. med;(12): 391-394, 2012.
Article
in En
| WPRIM
| ID: wpr-328508
Responsible library:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To observe the effect of andrographolide on the activation of mitogen-activated protein kinases (MAPKs) and expression of nuclear factor-κB (NF-κB) in macrophage foam cells.</p><p><b>METHODS</b>The mouse peritoneal macrophages were cultured in the media in the presence of oxidized low-density lipoprotein (ox-LDL), ox-LDL+andrographolide, or neither (control). The phosphorylation of MAPK molecules (p38MAPK, JNK, ERK1/2) and the expressions of NK-κB p65 were examined by Western blot.</p><p><b>RESULTS</b>As compared with cells in the control group, the expressions of phospho-p38 and NF-κB p65 were increased in the cells cultured with either ox-LDL or ox-LDL+andrographolide (P<0.01), but attenuated significantly in the presence of ox-LDL+ andrographolide when compared with ox-LDL (P<0.05). The phospho-JNK increased in the presence of either ox-LDL or ox-LDL+andrographolide when compared with control cells (P<0.01), but no significant difference existed between ox-LDL and ox-LDL+andrographolide (P>0.05). The expression of phospho-ERK1/2 was increased in the presence of ox-LDL compared with the control cells (P<0.01), but no significant differences existed between the cells cultured in the presence of ox-LDL+andrographolide and the control medium (P>0.05).</p><p><b>CONCLUSIONS</b>Andrographolide could inhibit the activation of ERK1/2, p38MAPK and NK-κB induced by ox-LDL in macrophage foam cells, which might be one of its mechanisms in preventing atherosclerosis.</p>
Full text:
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Index:
WPRIM
Main subject:
Pharmacology
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Vasculitis
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Cells, Cultured
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NF-kappa B
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Macrophages, Peritoneal
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MAP Kinase Signaling System
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Cell Biology
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Extracellular Signal-Regulated MAP Kinases
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JNK Mitogen-Activated Protein Kinases
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P38 Mitogen-Activated Protein Kinases
Limits:
Animals
Language:
En
Journal:
Chin. j. integr. med
Year:
2012
Type:
Article