참고문헌
- Kuldo JM, Ogawara KI, Werner N, Asgeirsdottir SA, Kamps JA, Kok RJ, Molema G. Molecular pathways of endothelial cell activation for (targeted) pharmacological intervention of chronic inflammatory diseases. Curr Vasc Pharmacol. 2005;3:11-39. https://doi.org/10.2174/1570161052773898
- Libby P. Inflammatory mechanisms: the molecular basis of inflammation and disease. Nutr Rev. 2007;65:S140-S146. https://doi.org/10.1301/nr.2007.dec.S140-S146
- Poston RN, Haskard DO, Coucher JR, Gall NP, Johnson-Tidey RR. Expression of intercellular adhesion molecule-1 in atherosclerotic plaques. Am J Pathol. 1992;140:665-673.
- Mahmoudi M, Curzen N, Gallagher PJ. Atherogenesis: the role of inflammation and infection. Histopathology. 2007;50:535-546. https://doi.org/10.1111/j.1365-2559.2006.02503.x
- Schirmer SH, Fledderus JO, van der Laan AM, van der Pouw-Kraan TC, Moerland PD, Volger OL, Baggen JM, Böhm M, Piek JJ, Horrevoets AJ, van Royen N. Suppression of inflammatory signaling in monocytes from patients with coronary artery disease. J Mol Cell Cardiol. 2009;46:177-185. https://doi.org/10.1016/j.yjmcc.2008.10.029
- Damnjanovic G, Jelic M, Dindic B, Ilic S. Serum concentration of soluble adhesive molecules in patients with different forms of coronary artery disease. Vojnosanit Pregl. 2009;66:265-270. https://doi.org/10.2298/VSP0904265D
- Rubio-Guerra AF, Vargas-Robles H, Serrano AM, Lozano- Nuevo JJ, Escalante-Acosta BA. Correlation between the levels of circulating adhesion molecules and atherosclerosis in type-2 diabetic normotensive patients: circulating adhesion molecules and atherosclerosis. Cell Adh Migr. 2009;3:369-372. https://doi.org/10.4161/cam.3.4.9463
- Chai H, Wang Q, Huang L, Xie T, Fu Y. Ginsenoside Rb1 inhibits tumor necrosis factor-alpha-induced vascular cell adhesion molecule-1 expression in human endothelial cells. Biol Pharm Bull. 2008;31:2050-2056. https://doi.org/10.1248/bpb.31.2050
- Wang N, Wan JB, Chan SW, Deng YH, Yu N, Zhang QW, Wang YT, Lee SM. Comparative study on saponin fractions from Panax notoginseng inhibiting inflammation-induced endothelial adhesion molecule expression and monocyte adhesion. Chin Med. 2011;6:37. https://doi.org/10.1186/1749-8546-6-37
- Lee YJ, Jin YR, Lim WC, Park WK, Cho JY, Jang S, Lee SK. Ginsenoside-Rb1 acts as a weak phytoestrogen in MCF-7 human breast cancer cells. Arch Pharm Res. 2003;26:58-63. https://doi.org/10.1007/BF03179933
- Korivi M, Hou CW, Huang CY, Lee SD, Hsu MF, Yu SH, Chen CY, Liu YY, Kuo CH. Ginsenoside-Rg1 protects the liver against exhaustive exercise-induced oxidative stress in rats. Evid Based Complement Alternat Med. 2012;2012:932165.
- Zhang G, Liu A, Zhou Y, San X, Jin T, Jin Y. Panax ginseng ginsenoside-Rg2 protects memory impairment via anti-apoptosis in a rat model with vascular dementia. J Ethnopharmacol. 2008;115:441-448. https://doi.org/10.1016/j.jep.2007.10.026
- Wan JB, Lee SM, Wang JD, Wang N, He CW, Wang YT, Kang JX. Panax notoginseng reduces atherosclerotic lesions in ApoEdeficient mice and inhibits TNF-alpha-induced endothelial adhesion molecule expression and monocyte adhesion. J Agric Food Chem. 2009;57:6692-6697. https://doi.org/10.1021/jf900529w
- Dou L, Lu Y, Shen T, Huang X, Man Y, Wang S, Li J. Panax notogingseng saponins suppress RAGE/MAPK signaling and NF-kappaB activation in apolipoprotein-E-deficient atherosclerosis- prone mice. Cell Physiol Biochem. 2012;29:875-882. https://doi.org/10.1159/000315061
- Rockel C, Hartung T. Systematic review of membrane components of gram-positive bacteria responsible as pyrogens for inducing human monocyte/macrophage cytokine release. Front Pharmacol. 2012;3:56.
- Hien TT, Kim ND, Kim HS, Kang KW. Ginsenoside Rg3 inhibits tumor necrosis factor-alpha-induced expression of cell adhesion molecules in human endothelial cells. Pharmazie. 2010;65:699-701.
- Monaco C, Paleolog E. Nuclear factor kappaB: a potential therapeutic target in atherosclerosis and thrombosis. Cardiovasc Res. 2004;61:671-682. https://doi.org/10.1016/j.cardiores.2003.11.038
- Kim SW, Kim CE, Kim MH. Flavonoids inhibit high glucoseinduced up-regulation of ICAM-1 via the p38 MAPK pathway in human vein endothelial cells. Biochem Biophys Res Commun. 2011;415:602-607. https://doi.org/10.1016/j.bbrc.2011.10.115
- Zhang XL, Wen L, Chen YJ, Zhu Y. Vascular endothelial growth factor up-regulates the expression of intracellular adhesion molecule-1 in retinal endothelial cells via reactive oxygen species, but not nitric oxide. Chin Med J (Engl). 2009;122:338-343.
- Ho AW, Wong CK, Lam CW. Tumor necrosis factor-alpha up-regulates the expression of CCL2 and adhesion molecules of human proximal tubular epithelial cells through MAPK signaling pathways. Immunobiology. 2008;213:533-544. https://doi.org/10.1016/j.imbio.2008.01.003
- Tang G, Minemoto Y, Dibling B, Purcell NH, Li Z, Karin M, Lin A. Inhibition of JNK activation through NF-kappaB target genes. Nature. 2001;414:313-317. https://doi.org/10.1038/35104568
- Lee ES, Choi JS, Kim MS, You HJ, Ji GE, Kang YH. Ginsenoside metabolite compound K differentially antagonizing tumor necrosis factor-α-induced monocyte-endothelial trafficking. Chem Biol Interact. 2011;194:13-22. https://doi.org/10.1016/j.cbi.2011.08.008
피인용 문헌
- Ropivacaine attenuates endotoxin plus hyperinflation-mediated acute lung injury via inhibition of early-onset Src-dependent signaling vol.14, pp.1, 2014, https://doi.org/10.1186/1471-2253-14-57
- Luteolin Protects HUVECs from TNF-α-induced Oxidative Stress and Inflammation via its Effects on the Nox4/ROS-NF-κB and MAPK Pathways vol.21, pp.8, 2013, https://doi.org/10.5551/jat.23697
- LPS Induces Occludin Dysregulation in Cerebral Microvascular Endothelial Cells via MAPK Signaling and Augmenting MMP-2 Levels vol.2015, pp.None, 2013, https://doi.org/10.1155/2015/120641
- Naringin inhibits lipopolysaccharide-induced damage in human umbilical vein endothelial cells via attenuation of inflammation, apoptosis and MAPK pathways vol.68, pp.4, 2013, https://doi.org/10.1007/s10616-015-9908-3
- Linagliptin inhibits lipopolysaccharide-stimulated interleukin-6 production, intranuclear p65 expression, and p38 mitogen-activated protein kinase phosphorylation in human umbilical vein endothelial c vol.2, pp.1, 2013, https://doi.org/10.1186/s41100-016-0030-6
- 2-Chloroethanol Induced Upregulation of Matrix Metalloproteinase-2 in Primary Cultured Rat Astrocytes Via MAPK Signal Pathways vol.10, pp.None, 2016, https://doi.org/10.3389/fnins.2016.00593
- Inhibitory effects of Kaempferia parviflora extract on monocyte adhesion and cellular reactive oxygen species production in human umbilical vein endothelial cells vol.56, pp.3, 2013, https://doi.org/10.1007/s00394-015-1141-5
- Engineering of mesoporous silica nanoparticles for release of ginsenoside CK and Rh2 to enhance their anticancer and anti-inflammatory efficacy: in vitro studies vol.19, pp.7, 2013, https://doi.org/10.1007/s11051-017-3949-9
- Transcriptome Profiling Analysis Reveals the Potential Mechanisms of Three Bioactive Ingredients of Fufang E’jiao Jiang During Chemotherapy-Induced Myelosuppression in Mice vol.9, pp.None, 2018, https://doi.org/10.3389/fphar.2018.00616
- Identification of certain Panax species to be potential substitutes for Panax notoginseng in hemostatic treatments vol.134, pp.None, 2013, https://doi.org/10.1016/j.phrs.2018.05.005
- Inhibitory Effect of Scopoletin Isolated from Sorbus commixta on TNF-α-Induced Inflammation in Human Vascular Endothelial EA.hy926 Cells through NF-κB Signaling Pathway Suppression vol.30, pp.4, 2013, https://doi.org/10.5352/jls.2020.30.4.343
- Nutraceuticals for prevention of atherosclerosis: Targeting monocyte infiltration to the vascular endothelium vol.44, pp.6, 2013, https://doi.org/10.1111/jfbc.13200
- Small-Molecule Induction Promotes Corneal Endothelial Cell Differentiation From Human iPS Cells vol.9, pp.None, 2013, https://doi.org/10.3389/fbioe.2021.788987
- The promising therapeutic potentials of ginsenosides mediated through p38 MAPK signaling inhibition vol.7, pp.11, 2013, https://doi.org/10.1016/j.heliyon.2021.e08354