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Aminoaciduria resulting from cycloleucine administration in man.

作者信息

Brown R R

出版信息

Science. 1967 Jul 28;157(3787):432-4. doi: 10.1126/science.157.3787.432.

DOI:10.1126/science.157.3787.432
PMID:6028026
Abstract

Cycloleucine (1-aminocyclopentanecarboxylic acid) administration in cancer patients resulted in a reversible marked aminoaciduria consisting predominantly of cystine, ornithine, lysine, and arginine, with only minor elevations of other amino acids. Plasma levels of amino acids were essentially unchanged except for slight decreases in ornithine and lysine. This aminoaciduria is most likely due to a blockage by the drug of the renal tubular reabsorption of cystine, ornithine, lysine, and arginine, resulting in an aminoaciduria of the type seen in cystinuria.

摘要

相似文献

1
Aminoaciduria resulting from cycloleucine administration in man.
Science. 1967 Jul 28;157(3787):432-4. doi: 10.1126/science.157.3787.432.
2
[Modification of aminoaciduria in the rat after administration of cycloleucine: comparison with human cystinuria].给予环亮氨酸后大鼠氨基酸尿的改变:与人类胱氨酸尿症的比较
Clin Chim Acta. 1971 Jul;33(2):351-7. doi: 10.1016/0009-8981(71)90492-x.
3
The renal clearance of amino acids in cystinuria.胱氨酸尿症中氨基酸的肾脏清除率。
J Clin Invest. 1967 Jul;46(7):1162-71. doi: 10.1172/JCI105609.
4
Lysine infusion in cystinuria: theoretical renal thresholds for lysine.胱氨酸尿症中的赖氨酸输注:赖氨酸的理论肾阈值
Clin Sci. 1973 Feb;44(2):99-111. doi: 10.1042/cs0440099.
5
Diagnostic and genetic studies in 43 patients with classic cystinuria.对43例典型胱氨酸尿症患者的诊断和遗传学研究。
Clin Chem. 1991 Jan;37(1):68-73.
6
Urinary excretion of total cystine and the dibasic amino acids arginine, lysine and ornithine in relation to genetic findings in patients with cystinuria treated with sulfhydryl compounds.胱氨酸尿症患者使用巯基化合物治疗时,总胱氨酸以及二元氨基酸精氨酸、赖氨酸和鸟氨酸的尿排泄量与基因检测结果的关系。
Urol Res. 2003 Dec;31(6):417-25. doi: 10.1007/s00240-003-0366-6. Epub 2003 Oct 25.
7
Intravenous loading with arginine-hydrochloride and ornithine-aspartate in siblings of two families, presenting a familial neurological syndrome associated with cystinuria.在两个家族的兄弟姐妹中进行精氨酸盐酸盐和鸟氨酸天冬氨酸的静脉负荷试验,这些家族出现了与胱氨酸尿症相关的家族性神经综合征。
Biomedicine. 1976 Jun;24(3):191-9.
8
Defective metabolic clearance of plasma arginine and ornithine in lysinuric protein intolerance.赖氨酸尿性蛋白不耐受症中血浆精氨酸和鸟氨酸的代谢清除缺陷。
Metabolism. 1974 Aug;23(8):691-701. doi: 10.1016/0026-0495(74)90001-8.
9
Experimental cystinuria: the cycloleucine model. I. Amino acid interactions in renal and intestinal epithelia.实验性胱氨酸尿症:环亮氨酸模型。I. 肾和肠上皮中的氨基酸相互作用。
Can J Physiol Pharmacol. 1975 Dec;53(6):1027-36. doi: 10.1139/y75-143.
10
Ontogeny modifies manifestations of cystinuria genes: implications for counseling.个体发育改变胱氨酸尿症基因的表现:对遗传咨询的启示
J Pediatr. 1985 Mar;106(3):411-6. doi: 10.1016/s0022-3476(85)80666-1.

引用本文的文献

1
Mutual inhibition of L-cystine/L-cysteine and other neutral amino acids during tubular reabsorption. A microperfusion study in rat kidney.肾小管重吸收过程中L-胱氨酸/L-半胱氨酸与其他中性氨基酸的相互抑制作用。大鼠肾脏的微灌注研究。
Pflugers Arch. 1982 Nov 11;395(3):190-5. doi: 10.1007/BF00584808.
2
Evidence that cycloleucine affects the high-affinity systems of amino acid uptake in cultured human fibroblasts.环亮氨酸影响培养的人成纤维细胞中氨基酸摄取高亲和力系统的证据。
Biochem J. 1984 Nov 15;224(1):309-15. doi: 10.1042/bj2240309.
3
Transport of L-cystine in isolated perfused proximal straight tubules.
L-胱氨酸在离体灌注近端直小管中的转运。
Pflugers Arch. 1984 Jun;401(2):143-51. doi: 10.1007/BF00583874.
4
Immunopharmacologic activity of 1-aminocyclopentane-1-carboxylic acid.1-氨基环戊烷-1-羧酸的免疫药理活性
Experientia. 1968 Dec 15;24(12):1229-30. doi: 10.1007/BF02146638.
5
Cycloleucine (1-amino-cyclopentane carboxylic acid): tubular reabsorption and inhibitory effect on amino acid transport in the rat kidney. (Microperfusion experiments).环亮氨酸(1-氨基环戊烷羧酸):大鼠肾脏中的肾小管重吸收及对氨基酸转运的抑制作用。(微量灌注实验)
Pflugers Arch. 1975;353(3):241-53. doi: 10.1007/BF00584287.