• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

马来酸诱导的范科尼综合征中肾小管渗漏的证据。

Evidence for renal tubular leakage in maleic acid-induced Fanconi syndrome.

作者信息

Maesaka J K, McCaffery M

出版信息

Am J Physiol. 1980 Nov;239(5):F507-13. doi: 10.1152/ajprenal.1980.239.5.F507.

DOI:10.1152/ajprenal.1980.239.5.F507
PMID:7435624
Abstract

Micropuncture and microinjection studies were performed in Sprague-Dawley rats 20 h after subcutaneous injection of buffered maleic acid (MA) or buffer alone in experimental and control rats, respectively. Collections were made from earliest and latest accessible portions of proximal tubule (PT). Lissamine green injections and microperfusion of PT demonstrated leakage of lissamine green from late PT sites in MA-treated rats, whereas inulin leakage occurred at a more distal site. Whole kidney GFR was 58% lower in MA-treated rats despite comparable single nephron GFR in PT of both groups. Microinjections of PT with [methoxy-3H]inulin resulted in injected inulin recovery from the contralateral kidney in MA-treated rats of 24.0 +/- 2.0 compared with 4.7 +/- 0.89% in controls, suggesting that tubular leakage of inulin accounted for the lower whole kidney GFR. Net sodium and phosphate transport in early PT was similar in both groups but was decreased in late PT segments in MA-treated rats. Sodium and phosphate excretion in final urine were, however, comparable in both groups. The significantly lower plasma phosphate concentration might account for the blunted phosphaturia in MA-treated rats. These studies demonstrate a segmental effect of MA on 1) tubular leakage to lissamine green from late PT and inulin beyond the late PT, and 2) decreased net sodium and phosphate transport in the PT.

摘要

分别在实验大鼠和对照大鼠皮下注射缓冲马来酸(MA)或仅注射缓冲液20小时后,对斯普拉格 - 道利大鼠进行微穿刺和微量注射研究。从近端小管(PT)最早和最晚可及的部分进行收集。 Lissamine green注射和PT的微灌注显示,在MA处理的大鼠中,Lissamine green从PT晚期部位渗漏,而菊粉渗漏发生在更远端的部位。尽管两组PT中的单个肾单位GFR相当,但MA处理的大鼠的全肾GFR降低了58%。用[甲氧基 - 3H]菊粉对PT进行微量注射后,MA处理的大鼠对侧肾脏中注射菊粉的回收率为24.0 +/- 2.0,而对照组为4.7 +/- 0.89%,这表明菊粉的肾小管渗漏是全肾GFR降低的原因。两组早期PT中的钠和磷酸盐净转运相似,但MA处理的大鼠晚期PT段中的钠和磷酸盐净转运减少。然而,两组最终尿液中的钠和磷酸盐排泄相当。 MA处理的大鼠中血浆磷酸盐浓度明显较低可能是磷尿症减弱的原因。这些研究证明了MA对1)从PT晚期到Lissamine green以及PT晚期以外的菊粉的肾小管渗漏,以及2)PT中钠和磷酸盐净转运减少的节段性影响。

相似文献

1
Evidence for renal tubular leakage in maleic acid-induced Fanconi syndrome.马来酸诱导的范科尼综合征中肾小管渗漏的证据。
Am J Physiol. 1980 Nov;239(5):F507-13. doi: 10.1152/ajprenal.1980.239.5.F507.
2
Urinary loss of glucose, phosphate, and protein by diffusion into proximal straight tubules injured by D-serine and maleic acid.葡萄糖、磷酸盐和蛋白质通过扩散进入受D-丝氨酸和马来酸损伤的近端直小管而从尿液中流失。
Lab Invest. 1985 Jun;52(6):605-10.
3
Membrane permeability as a cause of transport defects in experimental Fanconi syndrome. A new hypothesis.膜通透性作为实验性范科尼综合征转运缺陷的一个原因。一个新假说。
J Clin Invest. 1976 May;57(5):1181-9. doi: 10.1172/JCI108386.
4
Tracer microinjection study of renal tubular phosphate reabsorption in the rat.大鼠肾小管磷重吸收的示踪剂微量注射研究。
J Clin Invest. 1972 Sep;51(9):2271-6. doi: 10.1172/JCI107036.
5
Renal handling of lysozyme in experimental Fanconi syndrome.实验性范科尼综合征中溶菌酶的肾脏处理
J Lab Clin Med. 1978 Jul;92(1):135-40.
6
Maleic acid-induced reabsorptive dysfunction in the proximal and distal nephron.马来酸诱导的近端和远端肾单位重吸收功能障碍。
Am J Physiol. 1983 Sep;245(3):F339-44. doi: 10.1152/ajprenal.1983.245.3.F339.
7
A micropuncture study of renal phosphate transport in rats with chronic renal failure and secondary hyperparathyroidism.对患有慢性肾衰竭和继发性甲状旁腺功能亢进的大鼠进行肾脏磷酸盐转运的微穿刺研究。
J Clin Invest. 1978 Apr;61(4):884-94. doi: 10.1172/JCI109014.
8
Tubular transport and urinary excretion of phosphate after renal denervation in the anesthetized rat.麻醉大鼠肾去神经支配后磷酸盐的肾小管转运及尿排泄
Am J Physiol. 1981 Jun;240(6):F481-6. doi: 10.1152/ajprenal.1981.240.6.F481.
9
Insights into the biochemical mechanism of maleic acid-induced Fanconi syndrome.对马来酸诱导范科尼综合征生化机制的见解。
Kidney Int. 1995 Nov;48(5):1542-8. doi: 10.1038/ki.1995.444.
10
Effect of maleic acid on sodium-linked tubular transport in experimental Fanconi syndrome.马来酸对实验性范科尼综合征中钠相关肾小管转运的影响。
Nephron. 1973;10(5):306-19. doi: 10.1159/000180202.

引用本文的文献

1
Exogenous adenosine triphosphate (ATP) preserves proximal tubule microfilament structure and function in vivo in a maleic acid model of ATP depletion.外源性三磷酸腺苷(ATP)在马来酸诱导的ATP耗竭雄性大鼠模型中可在体内维持近端肾小管微丝结构和功能。
J Clin Invest. 1993 Oct;92(4):1940-9. doi: 10.1172/JCI116787.
2
Phagocytosis of E. coli by renal tubular epithelia.肾小管上皮细胞对大肠杆菌的吞噬作用。
Yale J Biol Med. 1984 Nov-Dec;57(6):817-24.
3
Pathophysiology of human proximal tubular transport defects.人类近端肾小管转运缺陷的病理生理学
Klin Wochenschr. 1982 Oct 1;60(19):1201-11. doi: 10.1007/BF01716723.
4
Idiopathic Fanconi syndrome with progressive renal failure: a case report and discussion.伴有进行性肾衰竭的特发性范科尼综合征:一例病例报告及讨论
Yale J Biol Med. 1990 Jan-Feb;63(1):15-28.