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一氧化氮在L-精氨酸致大鼠残余肾代偿性增生中的作用
作者:刘必成1 John Haylor2 A. M. El Nahas2 
单位:1.南京铁道医学院附属医院,肾脏科,江苏南京,210009; 2.Sheffield Kidney Institute, University of Sheffield,UK
关键词:L-精氨酸 残余肾 代偿性增生 一氧化氮 大鼠 
分类号:R-33, R699.2, O611.62, R977.4
出版年·卷·期(页码):2000·19·第三期(152-155)
摘要:

目的:探讨一氧化氮(NO)在L-精氨酸(L-arg)所致肾大部切除(SNx)大鼠残余肾代偿性增生中的作用.方法:采用5/6肾大部切除大鼠为实验模型,实验组于手术后分别给予1%L-arg 或NO供体Molsidomine (MSD).实验分为假手术组(Sham)、SNx组、SNx加L-arg组和SNx加MSD组,观察指标为体重(BW)、残余肾重(KW)、肾重/体重(KW/BW)、尿蛋白定量、血压、Ccr、残余肾代偿性增生比率(CRG)、残余肾蛋白质、DNA含量、小管间质细胞PCNA免疫组化表达、尿NO代谢产物NO2-排泄量等.结果:L-arg组大鼠残余肾代偿性增生指标(KW、KW/BW、CRG、蛋白质、DNA及PCNA等)较其对照组明显增加(P小于0.05或0.001),MSD组上述指标与SNx组相比无显著统计学差异(P>0.05).L-arg及MSD组NO2-排泄量均较SNx组显著增加.结论:L-arg可刺激大鼠残余肾代偿性增生,这种作用可能与NO无关.

Objective  To investigate the role of nitric oxide (NO) in   L    arginine (  L    arg) potentiated compensatory renal growth in subtotal nephrectomy rats (SNx).Method  5/6 subtotal nephrectomy rats were used as the experimental model.The experimental rats were treated by 1%   L    arg and NO donor,molsidomine (MSD) after the operation.Four groups were designed in the experiment:Sham,SNx,SNx+  L    arg,SNx+MSD.The following parameters were observed:body weight (BW),remnant wet kidney weight (KW),KW/BW,urinary protein excretion,systolic blood pressure,Ccr,compensatory renal growth rate (CRG), protein and DNA content of the remnant kidney,tubulointerstitial immunostaining for PCNA, and excretion rate of NO  2  -.Results  SNx rats treated by   L    arg showed significantly increasing of KW (  P  <0.05), KW/BW (  P  <0.05), CRG(  P  <0.05),protein (    <0.05) and DNA content(  P  <0.001),tubulointerstitial immunostaining for PCNA (  P  <0.05),while the group treated by MSD showed no significant changes for the above parameters compared with those in SNx group (    P  >    0.05  ,respectively).However,both groups showed the significantly increased urinary excretion of NO  2  -.Conclusion  This pilot study suggested that compensatory renal growth potentiated by   L    arg might not be related with the activation of   L    arg/NO pathway.

参考文献:

[1] Brenner B M, Meyer T W, Hostetter T H. Dietary protein intake and the progressive nature of kidney disease, 1982
[2] 刘必成, Haylor J, Nahas A M. L-精氨酸对5/6肾大部切除大鼠残余肾代偿性增生的影响. 中华肾脏病杂志1998(4)
[3] Reyes A A, Karl I E, Klahr S. Role of arginine in health and in renal disease, 1994
[4] Blum M, Yachnin T, Wollman Y. Low nitric oxide production in patients with chronic renal failure. 1998. doi:10.1159/000045047
[5] Ketteler, Boder A, Noble A. Cytokines and L-arginine in renal injury and repair, 1994
[6] Mohaupt M, Schoecklmann H O, SchulzeLohoff E. Altered nitric oxide production and exogenous nitric oxide do not affect the proliferation of rat mesangial cells, 1994
[7] Barbul A. Arginine:biochemistry,physiology and therapeutic implications. 1986. doi:10.1177/0148607186010002227
[8] Waddington S N, Tam F W, Cook H T. Arginase activity is modulated by IL-4 and HOArg in nephritic glomeruli and mesangial cells, 1998  

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