Badr K F, Lakkis F G
Department of Medicine, Emory University, Atlanta, Georgia.
Ann N Y Acad Sci. 1994 Nov 15;744:216-28. doi: 10.1111/j.1749-6632.1994.tb52739.x.
Figure 4 is a schematic summary of current evidence implicating products of the 15-lipoxygenase pathway of arachidonic acid metabolism, principally 15-S-HETE and LXA4, as endogenous antagonists for the proinflammatory actions of leukotrienes. Here, we have presented evidence for the pathophysiologic relevance of leukotrienes in glomerular immune injury and the emerging data on the multifaceted counterinflammatory actions of 15-lipoxygenase products as they relate specifically to the renal glomerulus. Clearly, these concepts are of a broader nature and would be expected to pertain to inflammatory reactions in general, be they in the glomerulus, the renal interstitium, or in extrarenal sites. The extent to which these early observations can be exploited to design strategies for the control of self-destructive inflammatory reactions in the kidney and elsewhere will be determined by future studies. Imaginative design of molecular tools for the manipulation of these enzyme systems in vivo, however, represents a potentially fruitful area of research towards the attainment of a highly worthwhile goal: the cure of glomerulonephritis.
图4是当前证据的示意图总结,这些证据表明花生四烯酸代谢的15-脂氧合酶途径的产物,主要是15-S-羟二十碳四烯酸(15-S-HETE)和脂氧素A4(LXA4),作为白三烯促炎作用的内源性拮抗剂。在此,我们提供了白三烯在肾小球免疫损伤中的病理生理相关性的证据,以及15-脂氧合酶产物多方面抗炎作用的新数据,这些作用与肾小球密切相关。显然,这些概念具有更广泛的性质,预计将普遍适用于炎症反应,无论其发生在肾小球、肾间质还是肾外部位。这些早期观察结果在多大程度上可用于设计控制肾脏及其他部位自我毁灭性炎症反应的策略,将由未来的研究确定。然而,巧妙设计用于体内操纵这些酶系统的分子工具,代表了实现一个非常有价值目标(治愈肾小球肾炎)的潜在富有成果的研究领域。