Measurement of kinetic parameters of skeletal muscle protein synthesis in rats by deuterated water.
- Author:
Ying TIAN
1
;
Qian-Qian DAI
2
;
Chan-Fang MENG
2
;
Yi SUN
2
;
Jing PENG
2
;
Yu CHEN
2
Author Information
1. Department of Nutrition, School of Tourism and Culinary Science, Yangzhou University, Yangzhou 225127, China. tianyingjob@126.com.
2. Department of Nutrition, School of Tourism and Culinary Science, Yangzhou University, Yangzhou 225127, China.
- Publication Type:Journal Article
- MeSH:
Alanine;
Amino Acids;
blood;
Animals;
Deuterium;
Gas Chromatography-Mass Spectrometry;
Kinetics;
Male;
Muscle Proteins;
biosynthesis;
Muscle, Skeletal;
metabolism;
Protein Biosynthesis;
Rats;
Rats, Sprague-Dawley;
Water
- From:
Acta Physiologica Sinica
2017;69(3):311-315
- CountryChina
- Language:Chinese
-
Abstract:
The aim of the present study was to measure the kinetic parameters of skeletal muscle protein synthesis in rats by deuterated water (HO). Twenty Sprague-Dawley (SD) rats were labeled byHO through intraperitoneal injection and drinking. At the each end of the 1st, 3rd, 5th, 6th and 10th week after the firstHO labeling, four rats were sacrificed by cardiac puncture for blood plasma and quadriceps femoris sampling. Skeletal muscle protein and free amino acids in plasma were purified, hydrolyzed by hydrochloric acid and derived. The deuterium enrichments ofH-labeled alanyl in skeletal muscle protein and plasma protein-boundH-labeled alanine were determined by gas chromatography-mass spectrometry (GC-MS). The fractional synthesis rate of skeletal muscle protein and synthetic dynamic equation were calculated. The fractional synthetic rate of skeletal muscle protein was 12.8%/week, and synthetic dynamic equation was f= 0.158 × (1 - e). The results suggest that the kinetic parameters of skeletal muscle protein synthesis can be measured byHO labeling, and the method can be applied in long-term labeling experiment.
