Abstract
The development of renal dysfunction in experimental glomerulonephritis (GN) is mediated in part by enhanced leukotriene (LT) formation. In our studies the pathophysiological role of LTs was investigated through pharmacological inhibition of LT biosynthesis in a rat model of nephrotoxic serum nephritis. MK-0591, an indirect inhibitor of 5-lipoxygenase activity, was co-administered to rats injected with nephrotoxic rabbit serum, followed by assessment of renal function, morphology and microsomal LTC 4 synthase activity on day 7. A significant improvement in glomerular function was noted ( p < 0.05), together with a 50% reduction in proteinuria ( p < 0.01) in animals receiving MK-0591 (60 mg kg −1 day −1). In addition, the fall in renal LTC 4 synthase activity which occurred in nephritic rats (to 74% of control values, p < 0.01) was prevented in drug-treated animals. Based on these results, it appears that inhibition of LT biosynthesis protects against both renal impairment and alterations in LTC 4 synthase activity during the development of experimental GN, and may provide a useful therapeutic adjunct in the treatment of this disease.
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