Effects of andrographolide on the activation of mitogen activated protein kinases and nuclear factor-κB in mouse peritoneal macrophage-derived foam cells
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Effects of andrographolide on the activation of mitogen activated protein kinases and nuclear factor-κB in mouse peritoneal macrophage-derived foam cells
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(英文版)2012年18卷第5期 页码:391-394
Affiliations:
1. Department of Emergency, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology,Wuhan,China
2. Department of Emergency, the Second Affiliated Hospital to Nanchang University,Nanchang,China
Li, Fx., Li, Ss. Effects of andrographolide on the activation of mitogen activated protein kinases and nuclear factor-κB in mouse peritoneal macrophage-derived foam cells., Chin. J. Integr. Med. 18, 391–394 (2012). https://doi.org/10.1007/s11655-011-0700-8
Fu-xing Li, Shu-sheng Li. Effects of andrographolide on the activation of mitogen activated protein kinases and nuclear factor-κB in mouse peritoneal macrophage-derived foam cells[J]. Chinese Journal of Integrative Medicine, 2012,18(5):391-394.
Li, Fx., Li, Ss. Effects of andrographolide on the activation of mitogen activated protein kinases and nuclear factor-κB in mouse peritoneal macrophage-derived foam cells., Chin. J. Integr. Med. 18, 391–394 (2012). https://doi.org/10.1007/s11655-011-0700-8DOI:
Fu-xing Li, Shu-sheng Li. Effects of andrographolide on the activation of mitogen activated protein kinases and nuclear factor-κB in mouse peritoneal macrophage-derived foam cells[J]. Chinese Journal of Integrative Medicine, 2012,18(5):391-394. DOI: 10.1007/s11655-011-0700-8.
Effects of andrographolide on the activation of mitogen activated protein kinases and nuclear factor-κB in mouse peritoneal macrophage-derived foam cells
摘要
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. 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. 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). 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.
Abstract
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. 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. 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). 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.
关键词
andrographolidemouse peritoneal macrophage foam cellsmitogen activated protein kinasesenuclear factor-κBatherosclerosis
Keywords
andrographolidemouse peritoneal macrophage foam cellsmitogen activated protein kinasesenuclear factor-κBatherosclerosis
references
Renu V, Frank D, Allen P, Andrew F, Stephen M. Lessons from sudden coronary death: a comprehensive morphological classification scheme for atherosclerotic lesions. Arterioscler Thromb Vasc Biol 2000;20:1262–1275.
Liu SM, Yang PY, Kang H, LU L, Zhang YF, Pan JW, et al. NDRG2 induced by oxidized LDL in macrophages antagonizes growth factor productions via selectively inhibiting ERK activation. Bio Chim Biophys Acta 2010;2:106–113.
Ross R. The pathgenesis of atherosclerosis: a perspective for the 1990s. Nature 1993;362:801–809.
Steinberg D. Low density lipoprotein oxidation and its pathobiological significance. J Biol Chem 1997;272:20963–20966.
Muslin AJ. MAPK signaling in cardiovascular health and disease: molecular mechanisms and therapeutic targets. Clin Sci (Lond) 2008;115:203–218.
de Winther MP, Kanters E, Kraal G, Hofker MH. Nuclear factor-κB signaling in atherogenesis. Arterioscler Thromb Vasc Biol 2005;25:904–914.
Li SS, Wang HW, Zhao HY, Guo ZL. Study of the effects and mechanisms of API on the prevention of reocclusion after thrombolysis. Chin J Emerg Med (Chin) 2002;11:152–154.
Zhang J, Li SS, Wang L. Effects of Andrographitis Paniculata extracts on the expression of CD40 in endothelial cells. J Huazhong Univ Sci Technol (Med Sci) 2007;27:138–141.
He JY, Liu QS. Separation of human serum lipoproteins and lipoprotein-deficit serum by one-step density gradient ultracentrifugation. Acade J Second Milit Med Univ (Chin) 2002;24:46.
Li R, Chen BD, Wu W, Bao L, Li J, Qi RM. Ginkgolide B suppresses intercellular adhesion molecule-1 expression via blocking nuclear factor-kappaB activation in human vascular endothelial cells stimulated by oxidized low-density lipoprotein. J Pharmacol Sci 2009;110:362–369.
Smith PK, Krohn RI, Hermanson GT, Mallia AK, Gartner FH, Provenzano MD, et al. Measurement of protein using bicinchiconic acid. Anal Biochem 1995;150:76–85.
He XF, Li XH, Li HH, He CY. Effect of total saponins of Panax Notoginseng on the formation of macrophage-derived foam cells in mice. China Pharm (Chin) 2007;18:2323–2325.
Pueyo ME, Gonzalez W, Nicoletti A, Savoie F, Arnal JF, Michel JB. Angiotension II stimulates endothelial vascular cell adhesion molecule-I via nuclear factorkappa B activation induced by intracellular oxidative stress. Arterioscler Thromb Vasc Biol 2000;3:645–651
Schmidt R, Bültmann A, Fischel S, Gillitzer A, Cullen P, Walch A, et al. Extracellular matrix metalloproteinase inducer (CD147) is a novel receptor on platelets, activates platelets, and augments nuclear factor κB-dependent inflammation in monocytes. Circ Res 2008;102:302–309.
Galis ZS, Sukhova GK, Lark MW, Libby P. Increased expression of matrix metalloproteinases and matrix degrading activity in vulnerable regions of human atherosclerosis plaques. J Clin Invest 1994;94:2493–2503.
Silverstein RL, Febbraio M. CD36 and atherosclerosis. Curr Opin lipidol 2000;1:483–491.
Zhao Ming, Liu YW, Wang XF, New LG, Han JH, Brunk UT. Activation of the p38 MAP kinase pathway is required for foam cell formation from macrophages exposed to oxidized LDL. APMIS 2002;110:458–468.
Liu XJ, Wang YF, Li GS. The pharmacological research progression of andrographolide and its derivant. J Chin Med Mater (Chin) 2003;26:135–138.
Andrographolide as an Anti-H1N1 drug and the mechanism related to retinoic acid-inducible gene-I-like receptors signaling pathway
Effects of Wenxiao Decoction (稳消方) on the expression of interleukin-6, intercellular adhesion molecular-1 and monocyte chemoattractant protein-1 in experimental atherosclerotic rabbits
Inhibitory effect of cryptotanshinone on angiogenesis and Wnt/β-catenin signaling pathway in human umbilical vein endothelial cells
Tanshinone II A inhibits dendritic cell-mediated adaptive immunity: Potential role in anti-atherosclerotic activity
Effects of Shenshao Decoction(参芍汤) on the inflammatory response in the aorta of a rat atherosclerotic model
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Institute of Basic Theories of Traditional Chinese Medicine, China Academy of Traditional Chinese Medicine
Department of Oncology, Clifford Hospital of Guangzhou University of Traditional Chinese Medicine
Department of Gynaecology and Obstetrics, Shenzhen Baoan Maternal and Child Health Hospital
Department of Obstetrics and Gynecology, First Affiliated Hospital of Jinan University
Shandong Provincial Corps Hospital of Chinese People’s Armed Police Forces