Abstract

BackgroundThe effects of proanthocyanidins (PACs), isolated from blackcurrant (Ribes nigrum L.) leaves, on neutrophil accumulation during inflammatory processes were investigated in vivo and in vitro.MethodsIn vivo studies were performed using carrageenin-induced pleurisy in rats pre-treated with PACs. Exudate volume and PMNs accumulation were measured. Leukocyte cell adhesion molecules (LFA-1, Mac-1 and VLA-4) mobilization in circulating granulocytes were analysed by flow cytometry and endothelial cell adhesion molecules (ICAM-1 and VCAM-1) were detected by immunohistochemistry on lung sections.In vitro studies were conducted on endothelial LT2 cells, stimulated with TNF-α, to evaluate ICAM-1, IL-8 and VEGF mRNA expression upon PACs treatment.Data sets were examined by one-way analysis of variance (ANOVA) followed by a Scheffe post-hoc test.ResultsPretreatment of the animals with PACs (10, 30 and 60 mg/kg) inhibited dose-dependently carrageenin-induced pleurisy in rats by reducing pleural exudate formation and PMNs infliltration. Leukocyte cell adhesion molecules mobilization was not down-regulated on granulocytes by PACs. Immunohistochemistry on lung sections showed a decreased production of endothelial cell adhesion molecules.In vitro experiments demonstrated that PACs were able to significantly inhibit ICAM-1 but not IL-8 and VEGF165 mRNA expression. Moreover, VEGF121 mRNA expression was dose-dependently enhanced.ConclusionThis study provides evidence to support the anti-inflammatory activity of proanthocyanidins is related to an inhibition of leukocyte infiltration which can be explained at least in part by a down-regulation of endothelial adhesion molecules, ICAM-1 and VCAM-1 and that these compounds are capable of modulating TNF-α-induced VEGF transcription.

Highlights

  • Cell-cell and cell-extracellular matrix interactions play a central role in cell migration and leukocyte activation during the inflammatory process

  • In vitro experiments demonstrated that PACs were able to significantly inhibit ICAM-1 but not IL8 and VEGF165 mRNA expression

  • This study provides evidence to support the anti-inflammatory activity of proanthocyanidins is related to an inhibition of leukocyte infiltration which can be explained at least in part by a down-regulation of endothelial adhesion molecules, ICAM-1 and VCAM-1 and that these compounds are capable of modulating TNF-α-induced VEGF transcription

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Summary

Introduction

Cell-cell and cell-extracellular matrix interactions play a central role in cell migration and leukocyte activation during the inflammatory process. All the steps in the recruitment cascade are orchestrated by cell-adhesion molecules (CAMs) expressed on both leukocytes and endothelial cells, and different subsets of CAMs are responsible for the different steps in leukocyte extravasation [1]. This cascade includes the selectins, the integrins and members of the immunoglobulin superfamily. VCAM-1, a transmembrane endothelial protein, is the counter-receptor of VLA4 (Very Late Antigen-4, designated as α4β1 or CD49d/CD29) This latter beta-1 integrin mediates the adhesion of lymphocytes, monocytes, eosinophils and natural killer cells to activated endothelial cells [4]. The effects of proanthocyanidins (PACs), isolated from blackcurrant (Ribes nigrum L.) leaves, on neutrophil accumulation during inflammatory processes were investigated in vivo and in vitro

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