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一侧肾脏72%损伤对参与胍基化合物代谢的多个器官的影响:一项时间进程研究。

Influence of 72% injury in one kidney on several organs involved in guanidino compound metabolism: a time course study.

作者信息

Levillain O, Marescau B, Possemiers I, Al Banchaabouchi M, De Deyn P P

机构信息

Faculté de Médecine Lyon RTH Laennec, INSERM U 499, France.

出版信息

Pflugers Arch. 2001 Jul;442(4):558-69. doi: 10.1007/s004240100581.

Abstract

Arginine (Arg) produced from citrulline originates mostly from kidneys. Arg is involved in guanidino compound biosynthesis, which requires interorgan co-operation. In renal insufficiency, citrulline accumulates in the plasma in proportion to renal damage. Thus, disturbances in Arg and guanidino compound metabolism are expected in several tissues. An original use of the model of nephrectomy based on ligating branches of the renal artery allowed us to investigate Arg and guanidino compound metabolism simultaneously in injured (left) and healthy (right) kidneys. The left kidney of adult rats was subjected to 72% nephrectomy. Non-operated, sham-operated and nephrectomized rats were studied for a period of 21 days. Constant renal growth was observed only in the healthy kidneys. Guanidino compound levels were modified transiently during the first 48 h. The metabolism and/or tissue content of several guanidino compounds were disturbed throughout the experimental period. Arg synthesis was greatly reduced in the injured kidney, while it increased in the healthy kidney. The renal production of guanidinoacetic acid decreased in the injured kidney and its urinary excretion was reduced. The experimentally proven toxins alpha-keto-delta-guanidinovaleric acid and guanidinosuccinic acid (GSA) accumulated only in the injured kidney. The urinary excretion of GSA and methylguanidine increased in nephrectomized rats. When the injured kidney grew again, the level of some guanidino compounds tended to normalize. Nephrectomy affected the guanidino compound levels and metabolism in muscles and liver. In conclusion, the specific accumulation of toxic guanidino compounds in the injured kidney reflects disturbances in renal metabolism and function. The healthy kidney compensates for the injured kidney's loss of metabolic functions (e.g. Arg: production). This model is excellent for investigating renal metabolism when a disease destroys a limited area in one kidney, as is observed in patients.

摘要

由瓜氨酸产生的精氨酸主要源自肾脏。精氨酸参与胍基化合物的生物合成,这需要器官间的协作。在肾功能不全时,瓜氨酸会按肾损伤程度在血浆中蓄积。因此,预计多个组织中精氨酸和胍基化合物的代谢都会受到干扰。基于结扎肾动脉分支的肾切除模型的一项原创新应用,使我们能够同时研究受损(左)肾和健康(右)肾中的精氨酸和胍基化合物代谢。对成年大鼠的左肾进行了72%的肾切除。对未手术、假手术和肾切除的大鼠进行了为期21天的研究。仅在健康肾脏中观察到持续的肾脏生长。胍基化合物水平在最初48小时内有短暂变化。在整个实验期间,几种胍基化合物的代谢和/或组织含量受到干扰。受损肾脏中的精氨酸合成大幅减少,而健康肾脏中的精氨酸合成增加。受损肾脏中胍基乙酸的肾脏生成减少,其尿排泄也减少。实验证实的毒素α-酮-δ-胍基戊酸和胍基琥珀酸(GSA)仅在受损肾脏中蓄积。肾切除大鼠中GSA和甲基胍的尿排泄增加。当受损肾脏再次生长时,一些胍基化合物的水平趋于正常。肾切除影响了肌肉和肝脏中的胍基化合物水平和代谢。总之,有毒胍基化合物在受损肾脏中的特异性蓄积反映了肾脏代谢和功能的紊乱。健康肾脏可补偿受损肾脏代谢功能的丧失(如精氨酸:生成)。当疾病破坏一侧肾脏的有限区域时,如在患者中观察到的那样,该模型对于研究肾脏代谢非常出色。

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