• 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

大鼠实验性范科尼综合征中的肽尿症

Peptiduria in experimental Fanconi syndrome in rats.

作者信息

Asatoor A M, Bending M R, Milne M D

出版信息

Clin Sci (Lond). 1979 Sep;57(3):277-9. doi: 10.1042/cs0570277.

DOI:10.1042/cs0570277
PMID:477261
Abstract
  1. The plasma concentrations and urinary output of proline and hydroxyproline contained in peptides were measured in normal rats and in rats with Fanconi syndrome produced by injection of sodium maleate. All animals received a prior injection of 10 mg of the dipeptide L-prolyl-L-hydroxy-proline to increase plasma and urinary peptide content. There was a significant increase of urinary output of the two imino acids contained in peptides and a fall in their plasma concentrations. 2. It is concluded that increased output of peptides derived from collagen degradation in the experimental Fanconi syndrome in rats is at least in part due to diminished tubular reabsorption of these compounds from the glomerular filtrate. The results are claimed to be relevant to the increased output of urinary peptides in the Fanconi syndrome in man.
摘要
  1. 对正常大鼠以及通过注射马来酸钠诱导产生范科尼综合征的大鼠,测量了肽中所含脯氨酸和羟脯氨酸的血浆浓度及尿量。所有动物事先均注射了10毫克二肽L-脯氨酰-L-羟脯氨酸,以增加血浆和尿液中的肽含量。肽中所含两种亚氨基酸的尿量显著增加,其血浆浓度下降。2. 得出的结论是,实验性大鼠范科尼综合征中源自胶原蛋白降解的肽输出增加,至少部分原因是这些化合物从肾小球滤液中的肾小管重吸收减少。据称这些结果与人类范科尼综合征中尿肽输出增加有关。

相似文献

1
Peptiduria in experimental Fanconi syndrome in rats.大鼠实验性范科尼综合征中的肽尿症
Clin Sci (Lond). 1979 Sep;57(3):277-9. doi: 10.1042/cs0570277.
2
Peptiduria in the Fanconi syndrome.
Ciba Found Symp. 1977(50):287-98. doi: 10.1002/9780470720318.ch16.
3
Peptide excretion in experimental Fanconi syndrome in the rat.大鼠实验性范科尼综合征中的肽排泄
Clin Sci Mol Med. 1978 Aug;55(2):205-12. doi: 10.1042/cs0550205.
4
Defective hydroxyproline metabolism in type II hyperprolinemia.II型高脯氨酸血症中羟脯氨酸代谢缺陷
Biochem Med. 1974 Aug;10(4):329-36. doi: 10.1016/0006-2944(74)90036-2.
5
Dinitrophenyl derivatization of imino acids, spectral characteristics and HPLC analysis: application in urinary peptide-derived hydroxyproline and proline assay.亚氨基酸的二硝基苯基衍生化、光谱特征及高效液相色谱分析:在尿肽衍生羟脯氨酸和脯氨酸测定中的应用
Ann Clin Biochem. 2007 Mar;44(Pt 2):164-72. doi: 10.1258/000456307780118226.
6
Detection of maleate-induced Fanconi syndrome by decreasing accumulation of 125I-3-iodo-alpha-methyl-L-tyrosine in the proximal tubule segment-1 region of renal cortex in mice: a trial of separate evaluation of reabsorption.通过减少小鼠肾皮质近端小管节段-1区域中125I-3-碘-α-甲基-L-酪氨酸的蓄积来检测马来酸盐诱导的范科尼综合征:重吸收单独评估试验
Ann Nucl Med. 2006 Apr;20(3):175-81. doi: 10.1007/BF03027427.
7
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.
8
High-performance liquid chromatographic analysis of free hydroxyproline and proline in blood plasma and of free and peptide-bound hydroxyproline in urine.血浆中游离羟脯氨酸和脯氨酸以及尿液中游离和肽结合羟脯氨酸的高效液相色谱分析。
J Chromatogr. 1985 May 3;339(2):285-92. doi: 10.1016/s0378-4347(00)84655-1.
9
The characteristic pattern of aminoaciduria in patients with aristolochic acid-induced Fanconi syndrome: could iminoaciduria be the hallmark of this syndrome?
Clin Nephrol. 2000 Sep;54(3):198-202.
10
Familial iminoglycinuria with normal intestinal absorption of glycine and imino acids in association with profound mental retardation, a possible "cerebral phenotype".伴有甘氨酸和亚氨基酸肠道吸收正常的家族性亚氨基甘氨酸尿症,与严重智力迟钝相关,一种可能的“脑表型”。
Helv Paediatr Acta. 1976 Aug;31(2):173-82.