Lefkowith J B, Nagamatsu T, Pippin J, Schreiner G F
Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110.
Am J Physiol. 1991 Aug;261(2 Pt 2):F213-20. doi: 10.1152/ajprenal.1991.261.2.F213.
Nephrotoxic nephritis (NTN) is characterized by an influx of leukocytes into the glomerulus, with accompanying glomerular dysfunction and a marked increase in glomerular eicosanoid production. We examined the relationship between the glomerular inflammatory cell infiltrate and the concomitant metabolic/functional changes in this model of renal disease using a combination of in vivo immunologic strategies to both decrease [X-irradiation and cobra venom factor (CVF)] and increase (preimmunization with rabbit immunoglobulin G or accelerated NTN) the inflammatory cell infiltrate. With the use of these manipulations, a close correlation between glomerular leukocytes and the proteinuria of NTN was observed. The ablative strategies (X-irradiation and CVF) also attenuated the increase in leukotriene B4 (LTB4) generation seen with NTN and virtually completely prevented the increase in thromboxane B2 (TxB2) production (basal and angiotensin II elicited). Accelerated NTN, in contrast, increased and prolonged the rise in glomerular LTB4 production and exacerbated the increase in TxB2 production. Glomerular prostaglandin E2 production was not altered by the induction of nephritis nor any of the aforementioned immunologic manipulations. Regression analysis established that glomerular TxB2 production correlated significantly with the leukocyte influx at both 3 and 24 h. Glomerular LTB4 production correlated only with the presence of leukocytes at 3 h. Both glomerular TxB2 and LTB4 production were closely correlated with the renal dysfunction as assessed by proteinuria. These data suggest that leukocytes play a direct critical role in both the functional and metabolic alterations that occur in the setting of NTN. They further imply that leukocytes are crucial to the observed increase in glomerular eicosanoid production.(ABSTRACT TRUNCATED AT 250 WORDS)
肾毒性肾炎(NTN)的特征是白细胞流入肾小球,伴有肾小球功能障碍以及肾小球类花生酸生成显著增加。我们使用体内免疫策略组合,既减少(X射线照射和眼镜蛇毒因子(CVF))又增加(用兔免疫球蛋白G预免疫或加速NTN)炎症细胞浸润,来研究这种肾脏疾病模型中肾小球炎性细胞浸润与伴随的代谢/功能变化之间的关系。通过这些操作,观察到肾小球白细胞与NTN蛋白尿之间存在密切相关性。消融策略(X射线照射和CVF)还减弱了NTN时白三烯B4(LTB4)生成的增加,并几乎完全阻止了血栓素B2(TxB2)生成的增加(基础水平和血管紧张素II诱导的)。相比之下,加速NTN增加并延长了肾小球LTB4生成的升高,并加剧了TxB2生成的增加。肾小球前列腺素E2生成不受肾炎诱导或上述任何免疫操作的影响。回归分析表明,肾小球TxB2生成在3小时和24小时时均与白细胞流入显著相关。肾小球LTB4生成仅在3小时时与白细胞的存在相关。肾小球TxB2和LTB4生成均与通过蛋白尿评估的肾功能障碍密切相关。这些数据表明,白细胞在NTN情况下发生的功能和代谢改变中起直接关键作用。它们进一步暗示,白细胞对于观察到的肾小球类花生酸生成增加至关重要。(摘要截断于250字)