Nagao T, Nagamatsu T, Suzuki Y
Department of Pharmacology, Faculty of Pharmacy, Meijo University, Nagoya, Japan.
Eur J Pharmacol. 1996 Nov 28;316(1):73-80. doi: 10.1016/s0014-2999(96)00662-0.
The antinephritic effect of DP-1904 [6-(1-imidazolylmethyl)-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid hydrochloride], a thromboxane A2 synthase inhibitor, was evaluated using an experimental model of membranous nephropathy, viz. accelerated passive Heymann nephritis in which the glomerular injury is mediated by immune complexes. DP-1904 markedly inhibited the develop-ent of glomerular alteration as well as the elevation of proteinuria and plasma creatinine. When the treatment was started from the 22nd day, at which time proteinuria is fully developed, DP-1904 showed beneficial effects on proteinuria and glomerular histopathological changes. DP-1904 apparently decreased the deposition of both rabbit immunoglobulin G and rat immunoglobulin G on glomerular basement membrane in nephritic rats. A single administration of DP-1904 restored the decreased renal tissue blood flow, inhibited glomerular thromboxane B2 production and increased glomerular prostaglandin E2 and 6-keto prostaglandin F1 alpha production in nephritic rats. These results suggest that DP-1904 may be an effective agent for the treatment of idiopathic membranous nephropathy and that the beneficial effect of this drug may be due to the elimination of glomerular immune deposits and to an increase in renal tissue blood flow related to amelioration of the abnormal metabolism of arachidonic acid.
血栓素A2合酶抑制剂DP - 1904(6 -(1 -咪唑基甲基)- 5,6,7,8 -四氢萘- 2 -羧酸盐酸盐)的抗肾炎作用,通过膜性肾病的实验模型进行评估,即加速被动型海曼肾炎,其中肾小球损伤由免疫复合物介导。DP - 1904显著抑制了肾小球病变的发展以及蛋白尿和血浆肌酐的升高。当从第22天开始治疗时,此时蛋白尿已充分发展,DP - 1904对蛋白尿和肾小球组织病理学变化显示出有益作用。DP - 1904明显减少了肾炎大鼠肾小球基底膜上兔免疫球蛋白G和大鼠免疫球蛋白G的沉积。单次给予DP - 1904可恢复肾炎大鼠肾组织血流的减少,抑制肾小球血栓素B2的产生,并增加肾小球前列腺素E2和6 -酮前列腺素F1α的产生。这些结果表明,DP - 1904可能是治疗特发性膜性肾病的有效药物,并且该药物的有益作用可能归因于肾小球免疫沉积物的清除以及与花生四烯酸异常代谢改善相关的肾组织血流增加。