期刊
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY
卷 154, 期 2, 页码 235-238出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.cbpb.2009.06.012
关键词
(H2O)-H-2; H-2 labeling; Fish growth; Fish protein synthesis
资金
- National Research Council of Norway through the Aquaculture Protein Centre, CoE, Norway
- National Institutes of Health [AG01025]
- Consejo Nacional para la Ciencia y la Tecnologia (CONACyT - Mexico)
- Secretaria de Educacion Publica (SEP - Mexico)
A comprehensive understanding of animal growth requires adequate knowledge of protein synthesis (PS), which in fish, has traditionally been determined by the flooding dose method. However, this procedure is limited to short-term assessments and may not accurately describe fish growth over extended periods of time. Since deuterium oxide ((H2O)-H-2) has been used to non-invasively quantify PS in mammals over short- and long-term periods, we aimed at determining if (H2O)-H-2 could also be used to measure PS in channel catfish. Fish were stocked in a 40-L aquarium with similar to 4% (H2O)-H-2 and sampled at 4,8 and 24 h (n = 6 at each time period) to determine H-2-labeling of body water (plasma), as well as protein-free and protein-bound H-2-labeled alanine. The labeling of body water reflected that of aquarium water and the labeling of protein-free alanine remained constant over 24 h and was similar to 3.8 times greater than that of body water. By measuring H-2-labeled alanine incorporation after 24 h of (H2O)-H-2 exposure we were able to calculate a rate of PS: 0.04 +/- 0.01% h(-1). These results demonstrate that PS in fish can be effectively measured using (H2O)-H-2 and, because this method yields integrative measures of PS, is relatively inexpensive and accounts for perturbations such as feeding, it is a novel and practical assessment option. Published by Elsevier Inc.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据