Yu Tianzheng, Khraibi Ali A
Department of Physiological Sciences, Eastern Virginia Medical School, 700 W. Olney Road, Norfolk, VA 23507, USA.
Life Sci. 2008 Aug 29;83(9-10):364-8. doi: 10.1016/j.lfs.2008.06.025. Epub 2008 Jul 9.
The renin-angiotensin system (RAS) plays an important role in the regulation of blood pressure, fluid and electrolyte homeostasis. The RAS is activated and renal interstitial hydrostatic pressure (RIHP) is decreased in diabetic rats. The objective of this study was to evaluate the roles of proximal tubule reabsorption and RAS in the decreased RIHP and blunted natriuretic and diuretic responses to acute saline volume expansion (VE) in diabetic rats. Enalapril was utilized to inhibit angiotensin II (AII) formation. Diabetes mellitus (DM) was induced by a single intraperitoneal (i.p.) injection of streptozotocin (STZ, 65 mg/kg). RIHP was measured by a polyethylene (PE) matrix that was chronically implanted in the left kidney. Fractional excretion of phosphate (FE(Pi)) and fractional excretion of lithium (FE(Li)) were used as indexes for proximal tubule reabsorption. VE significantly increased both FE(Li) and FE(Pi) in all groups of rats studied. However, the increase in FE(Li) (DeltaFE(Li)=17.26+/-3.83%) and FE(Pi) (DeltaFE(Pi)=7.38+/-2.37%) in diabetic rats (DC, n=12) were significantly lower as compared with those in nondiabetic control rats (NC, n=8; DeltaFE(Li)=32.15+/-4.71% and DeltaFE(Pi)=20.62+/-3.27%). The blunted increases in FE(Li) and FE(Pi) were associated with an attenuated increase in RIHP (DeltaRIHP) in DC (1.8+/-0.4 mm Hg) compared with NC rats (4.3+/-0.3 mm Hg). Enalapril treatment (25 mg/kg/day in drinking water) had no effect on nondiabetic rats (NE, n=8) as compared with untreated NC rats, but significantly improved RIHP response (DeltaRIHP) to VE in diabetic rats (DE, n=9; 2.8+/-0.5 mm Hg). Both DeltaFE(Li) and DeltaFE(Pi) were restored by enalapril treatment in diabetic rats and no significant differences were found in DeltaFE(Li) and DeltaFE(Pi) between DE (DeltaFE(Li)=26.81+/-4.94% and DeltaFE(Pi)=10.45+/-4.67%) and NC groups of rats in response to VE. These data suggest that the activated RAS and the decrease in RIHP may play an important role in the increased proximal tubule reabsorption, and the attenuated natriuretic and diuretic responses to acute volume expansion in diabetic rats.
肾素-血管紧张素系统(RAS)在血压调节、体液和电解质平衡中发挥着重要作用。糖尿病大鼠的RAS被激活,肾间质静水压(RIHP)降低。本研究的目的是评估近端肾小管重吸收和RAS在糖尿病大鼠RIHP降低以及对急性生理盐水扩容(VE)的利钠和利尿反应减弱中的作用。使用依那普利抑制血管紧张素II(AII)的形成。通过单次腹腔注射链脲佐菌素(STZ,65mg/kg)诱导糖尿病(DM)。通过长期植入左肾的聚乙烯(PE)基质测量RIHP。磷酸盐排泄分数(FE(Pi))和锂排泄分数(FE(Li))用作近端肾小管重吸收的指标。在所有研究的大鼠组中,VE均显著增加了FE(Li)和FE(Pi)。然而,与非糖尿病对照大鼠(NC,n = 8;DeltaFE(Li)=32.15±4.71%和DeltaFE(Pi)=20.62±3.27%)相比,糖尿病大鼠(DC,n = 12)的FE(Li)(DeltaFE(Li)=17.26±3.83%)和FE(Pi)(DeltaFE(Pi)=7.38±2.37%)的增加显著更低。与NC大鼠(4.3±0.3mmHg)相比,DC中FE(Li)和FE(Pi)增加减弱与RIHP(DeltaRIHP)增加减弱相关(1.8±0.4mmHg)。与未治疗的NC大鼠相比,依那普利治疗(饮用水中25mg/kg/天)对非糖尿病大鼠(NE,n = 8)无影响,但显著改善了糖尿病大鼠(DE,n = 9;2.8±0.5mmHg)对VE的RIHP反应(DeltaRIHP)。依那普利治疗使糖尿病大鼠的DeltaFE(Li)和DeltaFE(Pi)均恢复正常,并且在对VE的反应中,DE组(DeltaFE(Li)=26.81±4.94%和DeltaFE(Pi)=10.45±4.67%)与NC组大鼠的DeltaFE(Li)和DeltaFE(Pi)之间未发现显著差异。这些数据表明,激活的RAS和RIHP降低可能在糖尿病大鼠近端肾小管重吸收增加以及对急性容量扩张的利钠和利尿反应减弱中起重要作用。