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   <subfield code="a">Vascular anti-inflammatory effects of curcumin on HMGB1-mediated responses in vitro</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Dong-Chan Kim, Wonhwa Lee, Jong-Sup Bae]</subfield>
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   <subfield code="a">Aim and objective: High mobility group box 1 (HMGB1) protein up-regulates proinflammatory cytokines in several inflammatory diseases. Curcumin is a polyphenol responsible for the yellow color of the curry spice turmeric. It possesses diverse pharmacological properties such as anti-inflammatory, anti-oxidant, anti-proliferative and anti-angiogenic activities. However, the effects of curcumin on HMGB1-mediated proinflammatory responses have not been studied. Methods: The anti-inflammatory activities of curcumin were determined by measuring solute flux, leukocyte adhesion and migration and activation of proinflammatory proteins in HMGB1-activated human umbilical vein endothelial cells. Results: Curcumin inhibited the release of HMGB1 by lipopolysaccharide (LPS)- and HMGB1-mediated barrier disruption, neutrophil adhesion and migration, and expression of cell adhesion molecules. Further studies revealed that curcumin down-regulated the cell surface receptor of HMGB1 in human endothelial cells. Conclusion: These findings suggest that curcumin exerts anti-inflammatory effects in HMGB1-mediated proinflammatory responses, endorsing its usefulness as therapy for vascular inflammatory diseases.</subfield>
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   <subfield code="a">Springer Basel AG, 2011</subfield>
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   <subfield code="a">Curcumin</subfield>
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   <subfield code="a">HMGB1</subfield>
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   <subfield code="a">Endothelium</subfield>
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   <subfield code="a">Inflammation</subfield>
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   <subfield code="a">HMGB1 : High mobility group box 1</subfield>
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   <subfield code="a">HUVECs : Human umbilical vein endothelial cells</subfield>
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   <subfield code="a">CAM : Cell adhesion molecule</subfield>
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   <subfield code="a">ICAM : Intracellular cell adhesion molecule</subfield>
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   <subfield code="a">TEM : Transendothelial migration</subfield>
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   <subfield code="a">LPS : Lipopolysaccharide</subfield>
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   <subfield code="a">ECM : Extracellular cell adhesion molecule</subfield>
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   <subfield code="a">Kim</subfield>
   <subfield code="D">Dong-Chan</subfield>
   <subfield code="u">Laboratory of Microvascular Circulation Research, NEUORNEX Inc., 711-823, Daegu, Republic of Korea</subfield>
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   <subfield code="a">Lee</subfield>
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   <subfield code="u">Department of Biochemistry and Cell Biology, School of Medicine, Daegu, Republic of Korea</subfield>
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   <subfield code="u">College of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University, 1370 Sankyuk-dong, Buk-gu, 702-701, Daegu, Republic of Korea</subfield>
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   <subfield code="t">Inflammation Research</subfield>
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   <subfield code="g">60/12(2011-12-01), 1161-1168</subfield>
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