Reyes A A, Martin D, Settle S, Klahr S
Renal Division, Washington University School of Medicine, St. Louis, Missouri.
Kidney Int. 1992 Feb;41(2):403-13. doi: 10.1038/ki.1992.56.
There is a decrease in glomerular filtration rate (GFR) and effective renal plasma flow (ERPF) and an increase in mean arterial pressure (MAP) and renal vascular resistance (RVR) after release of bilateral ureteral obstruction (BUO) of 24 hours duration. The present studies examine the role of endothelium-derived relaxing factor (EDRF) in the renal hemodynamics of sham-operated rats (SOR) and rats in which BUO of 24 hours duration was unilaterally released. In both groups of rats, renal function and blood pressure were measured in the awake state under basal conditions and after administration of L-arginine (L-arg), the substrate for EDRF synthesis, followed by NwNAME, an L-arg antagonist, or after administration of NwNAME followed by L-arg. Administration of L-arg alone to SOR did not affect renal function, MAP or RVR. In SOR given L-arg and then NwNAME, there was significantly decreased GFR and ERPF and increased MAP and RVR. When NwNAME was given initially, similar changes were obtained, and these were reversed by the administration of L-arg. Rats given L-arginine immediately after unilateral release of BUO of 24 hours duration had significantly greater GFR and ERPF values and lower MAP and RVR than temporal controls. NwNAME given to BUO rats decreased renal function further and increased MAP and RVR. We found a dose-dependent increase in GFR and ERPF and a dose-dependent decrease in MAP and RVR in both SOR and rats with BUO given increasing amounts of L-arg. There was also a dose-dependent decrease in GFR and ERPF and an increase in MAP and RVR in SOR and rats with BUO given increasing amounts of NwNAME or NGNMA, the two different antagonists of L-arg. In another set of experiments, SOR and rats with BUO were given L-arg preoperatively (that is, 24 hr prior to study). Both groups of rats had significantly higher GFR and ERPF values and lower MAP and RVR than control rats. Sham-operated rats given NwNAME 24 hours prior to study had significantly lower GFR and ERPF and higher MAP and RVR than untreated rats. Rats with BUO given NwNAME prior to obstruction had no measurable renal function and had significantly higher values for MAP after release of obstruction. These studies confirm the role of L-arg administration, and presumably EDRF, in the regulation of MAP and renal function in sham-operated rats. The results of this study also suggest decreased availability of arginine for EDRF synthesis in rats with BUO.(ABSTRACT TRUNCATED AT 400 WORDS)
在双侧输尿管梗阻(BUO)持续24小时解除后,肾小球滤过率(GFR)和有效肾血浆流量(ERPF)降低,平均动脉压(MAP)和肾血管阻力(RVR)升高。本研究探讨内皮源性舒张因子(EDRF)在假手术大鼠(SOR)及单侧解除24小时持续时间的BUO的大鼠肾血流动力学中的作用。在两组大鼠中,于基础状态下及给予EDRF合成底物L-精氨酸(L-arg)后,再给予L-arg拮抗剂NwNAME,或先给予NwNAME再给予L-arg,在清醒状态下测量其肾功能和血压。单独给予SOR L-arg不影响肾功能、MAP或RVR。在给予L-arg然后NwNAME的SOR中,GFR和ERPF显著降低,MAP和RVR升高。当最初给予NwNAME时,获得类似变化,而给予L-arg可使其逆转。在单侧解除24小时持续时间的BUO后立即给予L-精氨酸的大鼠,其GFR和ERPF值显著高于同期对照,MAP和RVR较低。给予BUO大鼠NwNAME进一步降低肾功能并升高MAP和RVR。我们发现,给予SOR和BUO大鼠递增剂量的L-arg时,GFR和ERPF呈剂量依赖性增加,MAP和RVR呈剂量依赖性降低。给予SOR和BUO大鼠递增剂量的NwNAME或L-arg的两种不同拮抗剂NGNMA时,GFR和ERPF也呈剂量依赖性降低,MAP和RVR升高。在另一组实验中,术前(即研究前24小时)给予SOR和BUO大鼠L-arg。两组大鼠的GFR和ERPF值均显著高于对照大鼠,MAP和RVR较低。在研究前24小时给予NwNAME的假手术大鼠,其GFR和ERPF显著低于未处理大鼠,MAP较高。在梗阻前给予NwNAME的BUO大鼠无可测肾功能,梗阻解除后MAP值显著升高。这些研究证实了给予L-arg(推测还有EDRF)在调节假手术大鼠MAP和肾功能中的作用。本研究结果还提示,BUO大鼠中用于EDRF合成的精氨酸可用性降低。(摘要截断于400字)