...
首页> 外文期刊>Kidney international. >Renal synthesis of arginine in chronic renal failure: In vivo and in vitro studies in rats with 5//6 nephrectomy
【24h】

Renal synthesis of arginine in chronic renal failure: In vivo and in vitro studies in rats with 5//6 nephrectomy

机译:慢性肾衰竭中精氨酸的肾脏合成:5 // 6肾切除术大鼠体内和体外研究

获取原文
           

摘要

Renal synthesis of arginine in chronic renal failure: In vivo and in vitro studies in rats with 5/6 nephrectomy. Synthesis of arginine (Arg) from citrulline (Cit) by the kidney is a major source of Arg for the body. The high level of plasma Cit in chronic renal failure is often thought to result from the impairment of the renal conversion of Cit to Arg. To verify this assumption, we performed two studies in Sprague-Dawley rats with 5/6 nephrectomy (CRF rats) and in sham-operated rats (CONT rats). In study I synthesis of Arg by isolated proximal convoluted tubules (PCT; the nephron segment exhibiting the highest Arg synthesis) was measured in vitro with two concentrations of Cit (200 or 50 M) corresponding to those observed in plasma of rats with or without renal failure. In study II the net renal uptake of Cit and release of Arg were determined in vivo by measuring PAH clearance and arterial and renal venous Arg, and Cit concentrations in anesthetized rats. The in vitro results showed that Arg synthesis increased only in proportion to the hypertrophy of remnant PCT (+50%), and was highly and similarly dependent on Cit concentration in PCT of remnant and normal kidneys (Arg production with 200 M Cit was 3 times higher than with 50 M Cit for both CONT and CRF). The in vivo results showed that renal Cit uptake and Arg release were not altered in CRF: -286 28 versus -326 16 nmol Cit min-1 (NS), and + 390 47 versus + 399 22 nmol Arg min-1 (NS) in CONT and CRF rats, respectively. This maintenance of a normal Arg synthesis in CRF in the face of a significant reduction in renal plasma flow (-30%) and glomerular filtration rate (-60%), probably results from the cumulative effects of hypertrophy of remnant PCTs, hyperfiltration in remnant nephrons and high plasma Cit concentration increasing the amount of Cit filtered. Thus, the high plasma level of Cit in CRF, being a consequence of the progressive decline in functioning nephrons able to synthetize Arg, also represents a peripheral adaptatation that enables a reduced mass of functional tissue to maintain a constant renal Arg synthesis.
机译:慢性肾衰竭中精氨酸的肾脏合成:5/6肾切除大鼠的体内和体外研究。肾脏从瓜氨酸(Cit)合成精氨酸(Arg)是人体精氨酸的主要来源。慢性肾衰竭中血浆Cit的高水平通常被认为是由于Cit向Arg的肾脏转化受损所致。为了验证这一假设,我们在进行5/6肾切除术的Sprague-Dawley大鼠(CRF大鼠)和假手术大鼠(CONT大鼠)中进行了两项研究。在研究I中,在体外用分离的近曲小管(PCT;显示最高Arg合成的肾单位)合成Arg的两种浓度的Cit(200或50 M),分别对应于有或没有肾的大鼠血浆中观察到的浓度失败。在研究II中,通过测量麻醉大鼠的PAH清除率以及动脉和肾静脉Arg和Cit浓度来确定体内Cit的肾脏净吸收和Arg的释放。体外结果表明,Arg合成仅与残余PCT的肥大成比例增加(+50 %),并且高度相似地依赖于残余肾脏和正常肾脏PCT中的Cit浓度(200 M Cit的Arg产量为3比CONT和CRF的50 M Cit高两倍)。体内结果显示,CRF中的肾Cit摄取和Arg释放没有改变:-286 28 vs -326 16 nmol Cit min-1(NS)和+ 390 47 vs + 399 22 nmol Arg min-1(NS)分别在CONT和CRF大鼠中。面对肾血浆流量(-30 %)和肾小球滤过率(-60 %)显着降低,CRF中正常Arg合成的这种维持可能是由于残留PCTs肥大,超滤的累积效应残留肾单位和血浆Cit浓度高会增加过滤的Cit量。因此,由于能够合成Arg的功能性肾单位的逐渐减少的结果,CRF中Cit的血浆水平高,也代表了外周适应,其使得功能组织的质量降低以维持恒定的肾脏Arg合成。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号