The Japanese Journal of Pharmacology · 1996 · 40 citations · 35 references
Life SciencesImmunologyPharmacologyCell AdhesionInflammationRenal PathophysiologyAdhesion MoleculesCell Adhesion ReceptorsInflammatory MediatorsInflammatory SignalingLeukocyte AdhesionRenal InflammationEndothelial Adhesion MoleculesEndothelial Cell AdhesionInflammatory Cytokine EffectsIntercellular Adhesion Molecule 1Leukocyte Adhesion MoleculesLeukocyte Adhesion SignalingNatural Product Pharmacology
It is known that adhesion molecules play a crucial role in the development of glomerulonephritis. Therefore, we investigated the effects of acteoside on the expression of intercellular adhesion molecule-1 (ICAM-1) in nephritic glomeruli, in vivo, and human umbilical vein endothelial cells (HUVECs) and rat mesangial cells, in vitro. Aceteoside treatment significantly decreased the up-regulation of ICAM-1 expression in nephritic glomeruli. Acteoside prevented the up-regulation of ICAM-1 expression mediated by inflammatory cytokines or phorbol 12-myristate 13-acetate on HUVECs and rat mesangial cells. Adhesion of neutrophils and macrophages to acteoside-treated HUVECs was suppressed to one half of that in untreated HUVECs. These data support the finding that acteoside inhibits the up-regulation of ICAM-1 in the nephritic glomeruli. Additionally, it is suggested that the antinephritic action of acteoside is due to the inhibition of intraglomerular accumulation of leukocytes through the prevention of the up-regulation of ICAM-1. This is the first paper demonstrating that the up-regulation of ICAM-1 in nephritic glomeruli is inhibited by a natural product, acteoside.
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Specific Acceptance of Cardiac Allograft After Treatment with Antibodies to ICAM-1 and LFA-1
Mitsuaki Isobe, Hideo Yagita∥, Ko Okumura et al. · Science · 1992 · 723 citations