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   <subfield code="a">Pycnogenol inhibits tumor necrosis factor-α-induced nuclear factor kappa B activation and adhesion molecule expression in human vascular endothelial cells</subfield>
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   <subfield code="c">[Q. Peng, Z. Wei, B. H. S. Lau*]</subfield>
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   <subfield code="a">Abstract.: The transcriptional regulatory protein nuclear factor kappa B (NF-κB) participates in the control of gene expression of many modulators of inflammatory and immune responses, including vascular cell adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1). The heightened expression of these adhesion molecules has been reported to play a critical role in atherosclerosis, inflammation, ischemic vascular disorders, diabetes, and cancer metastasis. In the present study, we investigated the effect of pycnogenol, an antioxidant phytochemical, on the activation of NF-κB and the induction of VCAM-1 and ICAM-1 in tumor necrosis factor (TNF)-α-treated human umbilical vein endothelial cells (HUVECs). Gel-shift analysis of HUVEC demonstrated that pretreatment with pycnogenol exhibited a concentration-dependent suppression of TNF-α-induced activation of NF-κB. Induction of VCAM-1 and ICAM-1 surface expression by TNF-α was dose-dependently reduced by pycnogenol. TNF-α significantly increased the release of superoxide anion and hydrogen peroxide from HUVECs. Pycnogenol dose-dependently inhibited their release. The ability of pycnogenol to inhibit NF-κB activation and VCAM-1 and ICAM-1 expression suggests that this phytochemical may play an important role in halting or preventing the atherogenic process.</subfield>
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   <subfield code="a">Birkhäuser Verlag Basel,, 2000</subfield>
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   <subfield code="a">Key words. Pycnogenol</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">nuclear factor kappa B</subfield>
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   <subfield code="a">adhesion molecule</subfield>
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   <subfield code="a">antioxidant</subfield>
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   <subfield code="a">Peng</subfield>
   <subfield code="D">Q.</subfield>
   <subfield code="u">Department of Microbiology and Molecular Genetics, School of Medicine, Loma Linda University, Loma Linda (California 92350, USA), Fax +1 909 558 4035, e-mail: bLau@som.llu.edu, US</subfield>
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   <subfield code="u">Department of Microbiology and Molecular Genetics, School of Medicine, Loma Linda University, Loma Linda (California 92350, USA), Fax +1 909 558 4035, e-mail: bLau@som.llu.edu, US</subfield>
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   <subfield code="a">Lau*</subfield>
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   <subfield code="u">Department of Microbiology and Molecular Genetics, School of Medicine, Loma Linda University, Loma Linda (California 92350, USA), Fax +1 909 558 4035, e-mail: bLau@som.llu.edu, US</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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