• 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

Whole body protein metabolism estimated by 15N tracer experiments and body composition of mice selected for different growth parameters.

作者信息

Schadereit R, Krawielitzki K

机构信息

Institut für die Biologie landwirtschaftlicher Nutztiere Dummerstorf-Rostock, Germany.

出版信息

Isotopes Environ Health Stud. 1998;34(1-2):127-34.

PMID:9854847
Abstract

Whole body protein synthesis was investigated in growing male mice which were long-time selected for high carcass protein amount (DU-6P, protein line) or for high body weight (DU-6, growth line) and in the unselected randomly bred control (DU-Ks). Six mice/line were housed singly in metabolic cages for the estimation of N balance, whole body protein synthesis (end-product method, single dose of 15N-labelled amino-acid mixture), and N distribution in the body. Another six mice/line were used for the determination of the body composition. All mice had free access to a commercial stock diet (crude protein 268 g, gross energy 19 MJ/kg dry matter) and to water. Body weight of both selection lines was about twice that of control mice at the same age. Selection for high body weight resulted in higher body fat content. Scaled to the corresponding body protein pools, the protein synthesis rates of selected mice were significantly higher than in controls, but were not significantly different between both selection lines in contrast to the protein deposition rates. The higher protein accretion in the protein line in comparison to the growth line seems to be due to a combination of a lower protein breakdown and an increased protein synthesis rate.

摘要

相似文献

1
Whole body protein metabolism estimated by 15N tracer experiments and body composition of mice selected for different growth parameters.
Isotopes Environ Health Stud. 1998;34(1-2):127-34.
2
Whole body protein metabolism estimated by (15)n tracer experiments and body composition of mice selected for different growth parameters.通过(15)N示踪实验估算的全身蛋白质代谢以及根据不同生长参数选择的小鼠的身体组成。
Isotopes Environ Health Stud. 1997 Jul;33(1-2):127-34. doi: 10.1080/10256019708036340.
3
Dietary control of protein turnover.蛋白质周转的饮食控制。
Diabete Metab. 1987 Nov-Dec;13(6):630-42.
4
Intrinsic properties of muscle satellite cells are changed in response to long-term selection of mice for different growth traits.为了获得不同的生长性状而对小鼠进行长期选育后,肌肉卫星细胞的内在特性会发生改变。
Cell Tissue Res. 2002 Dec;310(3):339-48. doi: 10.1007/s00441-002-0637-5. Epub 2002 Oct 29.
5
15N-labelled yeast protein--a valid tracer for calculating whole-body protein parameters in infants: a comparison between [15N]-yeast protein and [15N]-glycine.
Hum Nutr Clin Nutr. 1983 Sep;37(5):317-27.
6
[The determination of the rate of protein synthesis of the whole body of growing broilers].[生长肉鸡全身蛋白质合成速率的测定]
Arch Tierernahr. 1988 Jul-Aug;38(7-8):565-72.
7
Voluntary exercise and its effects on body composition depend on genetic selection history.自愿运动及其对身体成分的影响取决于基因选择历史。
Obesity (Silver Spring). 2009 Jul;17(7):1402-9. doi: 10.1038/oby.2009.51. Epub 2009 Mar 12.
8
NTP technical report on the toxicity and metabolism studies of chloral hydrate (CAS No. 302-17-0). Administered by gavage to F344/N rats and B6C3F1 mice.国家毒理学计划关于水合氯醛(化学物质登记号:302-17-0)毒性和代谢研究的技术报告。通过灌胃法给予F344/N大鼠和B6C3F1小鼠。
Toxic Rep Ser. 1999 Aug(59):1-66, A1-E7.
9
Whole-body protein turnover of a carnivore, Felis silvestris catus.食肉动物家猫的全身蛋白质周转率。
Br J Nutr. 2003 Jan;89(1):29-37. doi: 10.1079/BJN2002735.
10
Effect of selection for growth on normal and reduced protein diets on weight gain, feed intake, feed efficiency and body composition in mice.选择生长对正常和低蛋白饮食的小鼠体重增加、采食量、饲料效率及身体组成的影响。
J Anim Breed Genet. 2006 Dec;123(6):362-8. doi: 10.1111/j.1439-0388.2006.00616.x.