Determination of steady-state protein breakdown rate in vivo by the disappearance of protein-bound tracer-labeled amino acids: a method applicable in humans

被引:35
作者
Holm, Lars [1 ,2 ,3 ]
O'Rourke, Bruce [3 ]
Ebenstein, David [3 ]
Toth, Michael J. [4 ]
Bechshoeft, Rasmus [1 ,2 ]
Holstein-Rathlou, Niels-Henrik [5 ]
Kjaer, Michael [1 ,2 ]
Matthews, Dwight E. [3 ,4 ]
机构
[1] Univ Copenhagen, Bispebjerg Hosp, Dept Orthoped Surg M81, Inst Sports Med, Copenhagen, Denmark
[2] Univ Copenhagen, Ctr Hlth Aging, Fac Hlth & Med Sci, Copenhagen, Denmark
[3] Univ Vermont, Dept Chem, Burlington, VT 05405 USA
[4] Univ Vermont, Dept Med, Burlington, VT USA
[5] Univ Copenhagen, Dept Biomed Sci, Fac Hlth & Med Sci, Copenhagen, Denmark
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2013年 / 304卷 / 08期
关键词
protein kinetics; protein degradation; fractional breakdown rate; deuterated water; SKELETAL-MUSCLE; COLLAGEN-SYNTHESIS; ISOTOPIC METHOD; DEGRADATION; TURNOVER; LIVER; MYOFIBRILLAR; WATER; (H2O)-H-2; REUTILIZATION;
D O I
10.1152/ajpendo.00579.2012
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Holm L, O'Rourke B, Ebenstein D, Toth MJ, Bechshoeft R, Holstein-Rathlou N, Kjaer M, Matthews DE. Determination of steady-state protein breakdown rate in vivo by the disappearance of protein-bound tracer-labeled amino acids: a method applicable in humans. Am J Physiol Endocrinol Metab 304: E895-E907, 2013. First published February 19, 2013; doi:10.1152/ajpendo.00579.2012.-A method to determine the rate of protein breakdown in individual proteins was developed and tested in rats and confirmed in humans, using administration of deuterium oxide and incorporation of the deuterium into alanine that was subsequently incorporated into body proteins. Measurement of the fractional breakdown rate of proteins was determined from the rate of disappearance of deuterated alanine from the proteins. The rate of disappearance of deuterated alanine from the proteins was calculated using an exponential decay, giving the fractional breakdown rate (FBR) of the proteins. The applicability of this protein-specific FBR approach is suitable for human in vivo experimentation. The labeling period of deuterium oxide administration is dependent on the turnover rate of the protein of interest.
引用
收藏
页码:E895 / E907
页数:13
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