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  lüll Leukotrienes and lipoxins: lipoxygenase-derived modulators of leukocyte  recruitment and vascular tone in glomerulonephritis Clarkson MR; McGinty A; Godson C; Brady HRNephrol Dial Transplant  1998[Dec]; 13 (12): 3043-51With the gradual elucidation of the cellular and molecular events that underpin  the inflammatory process, the pathogenetic complexities of glomerulonephritis are  slowly being unravelled. Lipoxygenase-derived eicosanoids play important  counter-regulatory roles within inflamed glomeruli. Leukotrienes, derived from  the 5-lipoxygenase pathway, are potent stimuli for leukocyte infiltration,  intrarenal vasoconstriction, and mesangial cell contraction in many forms of  experimental glomerulonephritis and probably in human disease. The recruitment of  12- and 15-lipoxygenase pathways, particularly during cell-cell interactions,  promotes the formation of lipoxins. The latter compounds antagonize many  leukotriene effects, attenuate neutrophil recruitment, and are potential 'braking  signals' within the inflammatory cascade that promote resolution of inflammation.  The generation and metabolism of leukotrienes and lipoxins is regulated  independently, and each family of eicosanoids mediates its biological activities  through distinct cell surface receptors and signal transduction pathways.  Leukotriene biosynthesis inhibitors and leukotriene receptor antagonists are  protective in several experimental models of glomerulonephritis. Initial studies  with lipoxins and synthetic lipoxin stable analogues suggest that it may be  possible to harness this and other putative anti-inflammatory system for  therapeutic gain [3,22,92].|Cell Movement/physiology[MESH]|Eicosanoids/*physiology[MESH]|Glomerulonephritis/*physiopathology[MESH]|Humans[MESH]|Leukocytes/*physiology[MESH]|Leukotrienes/*physiology[MESH]|Lipoxygenase/*physiology[MESH]|Vasomotor System/*physiopathology[MESH] |