• 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

Protein load in argininosuccinic aciduria: thoughts on its biochemical implications.

作者信息

Böhles H, Harms D, Heid H, Sitzmann F C, Fekl W

出版信息

Z Ernahrungswiss. 1978 Jun;17(2):65-71. doi: 10.1007/BF02021112.

DOI:10.1007/BF02021112
PMID:556398
Abstract

A patient with argininosuccinc aciduria was charged with 50 grams of protein, which was followed by considerable hyperammonemia. There was no response in further urea formation; but there was a considerable production of orotic acid, a precursor of pyrimidines. This makes orotic acid to an important diagnostic tool for the diagnosis of impaired urea formation. The patient's plasma amino acid pattern led to the suggestion that orotic acid synthesis is initiated by increased de novo formation of carbamyl phosphate in the cytosol and not by deviation of already existing intramitochondrial carbamyl phosphate.

摘要

相似文献

1
Protein load in argininosuccinic aciduria: thoughts on its biochemical implications.
Z Ernahrungswiss. 1978 Jun;17(2):65-71. doi: 10.1007/BF02021112.
2
Argininosuccinic aciduria: metabolic studies and effects of treatment with keto-analogues of essential amino acids.精氨琥珀酸尿症:代谢研究及必需氨基酸酮类似物治疗的效果
Eur J Pediatr. 1978 Jul 19;128(4):225-33. doi: 10.1007/BF00445607.
3
Argininosuccinic aciduria. A developmental and biochemical case study.精氨琥珀酸尿症。一项发育与生化的病例研究。
J Neurol Sci. 1983 Aug;60(2):217-33. doi: 10.1016/0022-510x(83)90064-3.
4
Argininosuccinic aciduria: long-term treatment with arginine.精氨琥珀酸尿症:精氨酸长期治疗
J Inherit Metab Dis. 1987;10(2):152-61. doi: 10.1007/BF01800042.
5
Argininosuccinic aciduria in adult: a clinical, electrophysiological and biochemical study.成人精氨酸琥珀酸尿症:一项临床、电生理及生化研究。
Adv Exp Med Biol. 1982;153:83-93. doi: 10.1007/978-1-4757-6903-6_11.
6
First case of argininosuccinic aciduria in Japan: clinical observations and treatment.日本首例精氨琥珀酸尿症:临床观察与治疗
Adv Exp Med Biol. 1982;153:95-100. doi: 10.1007/978-1-4757-6903-6_12.
7
Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis.精氨酸,对于尿素合成先天性代谢缺陷患者而言是一种必需氨基酸。
J Clin Invest. 1984 Dec;74(6):2144-8. doi: 10.1172/JCI111640.
8
Effect of dietary protein and physical exercise on patients with arginino-succinic aciduria.饮食蛋白质和体育锻炼对精氨琥珀酸尿症患者的影响。
Nutr Metab. 1977;21 Suppl 1:75-7. doi: 10.1159/000176116.
9
Diagnosis of argininosuccinic aciduria after valproic acid-induced hyperammonemia.
Neurology. 1987 May;37(5):886-7. doi: 10.1212/wnl.37.5.886.
10
Neonatal argininosuccinic aciduria-survival after early diagnosis and dietary management.新生儿精氨琥珀酸尿症——早期诊断与饮食管理后的生存情况
J Pediatr. 1980 Mar;96(3 Pt 1):429-31. doi: 10.1016/s0022-3476(80)80688-3.

引用本文的文献

1
Argininosuccinic aciduria: metabolic studies and effects of treatment with keto-analogues of essential amino acids.精氨琥珀酸尿症:代谢研究及必需氨基酸酮类似物治疗的效果
Eur J Pediatr. 1978 Jul 19;128(4):225-33. doi: 10.1007/BF00445607.

本文引用的文献

1
A COLORIMETRIC DETERMINATION OF OROTIC ACID.乳清酸的比色测定法
J Vitaminol (Kyoto). 1963 Sep 10;9:217-26. doi: 10.5925/jnsv1954.9.217.
2
A FAMILY AFFECTED BY ARGININO-SUCCINIC ACIDURIA.一个受精氨酸琥珀酸尿症影响的家庭。
Helv Paediatr Acta. 1963 Nov;18:339-48.
3
Metabolic abnormalities detected in a survey of mentally backward individuals in Northern Ireland.在北爱尔兰对智力落后个体的一项调查中检测到的代谢异常。
Arch Dis Child. 1962 Oct;37(195):505-13. doi: 10.1136/adc.37.195.505.
4
Argininosuccinic aciduria: identification and reactions of the abnormal metabolite in a newly described form of mental disease, with some preliminary metabolic studies.精氨基琥珀酸尿症:一种新描述的精神疾病中异常代谢产物的鉴定与反应,以及一些初步的代谢研究
Biochem J. 1960 Oct;77(1):135-44. doi: 10.1042/bj0770135.
5
A disease, probably hereditary characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism.一种可能为遗传性的疾病,其特征为严重智力缺陷和氨基酸代谢持续明显异常。
Lancet. 1958 Jan 25;1(7013):182-7. doi: 10.1016/s0140-6736(58)90666-4.
6
Metabolism of compounds labeled with 15 N by an infant with congenital hyperammonemia.
Pediatr Res. 1972 Apr;6(4):252-60. doi: 10.1203/00006450-197204000-00007.
7
Effect of low, normal and high dietary protein intake on urinary amino acid excretion and plasma aminogram in children.低、正常和高膳食蛋白质摄入量对儿童尿氨基酸排泄和血浆氨基酸谱的影响。
Nutr Metab. 1974;16(4):223-37. doi: 10.1159/000175493.
8
Metabolic and genetic studies of a family with ornithine transcarbamylase deficiency.一个患有鸟氨酸转氨甲酰酶缺乏症的家族的代谢和遗传学研究。
Pediatr Res. 1974 Jan;8(1):5-12. doi: 10.1203/00006450-197401000-00002.
9
Two carbamyl phosphate synthetases of mammals: specific roles in control of pyrimidine and urea biosynthesis.哺乳动物的两种氨甲酰磷酸合成酶:在嘧啶和尿素生物合成控制中的特定作用。
Adv Enzyme Regul. 1972;10:249-71. doi: 10.1016/0065-2571(72)90017-9.
10
[The significance of the hydrogen ion concentration and the addition of ADP in the determination of ammonia with glutamate dehydrogenase. An improved enzymic determination of ammonia, I (author's transl)].[氢离子浓度及添加二磷酸腺苷在谷氨酸脱氢酶法测定氨中的意义。氨的一种改良酶法测定,I(作者译)]
Z Klin Chem Klin Biochem. 1973 Oct;11(10):421-5.