Literature DB >> 7124943

N tau-methylhistidine release: contributions of rat skeletal muscle, GI tract, and skin.

S J Wassner, J B Li.   

Abstract

The relative contributions of skeletal muscle, gastrointestinal tract, and skin to urinary N tau-methylhistidine (MH) excretion were estimated during in vitro studies using the rat hemicorpus preparation. After 0.5 h of perfusion, MH release into the perfusate was linear for 3 h and averaged 29.8 nmol . h-1 . 100 g hemicorpus-1. In vivo, 24-h urinary MH excretion averaged 37.3 nmol . h-1 . 100 g body wt-1. The ratio of soft tissue to skin weight is equal (3.2:1) in the whole rat and in the hemicorpus. The gastrointestinal tract released 16.0 nmol . h-1 . 100 g body wt-1 or approximately 41% of the total urinary MH excretion. Preparations perfused with or without skin showed modest differences in the rate of MH release that were not statistically significant. Skeletal muscle contains 89.8% of total body MH content, whereas gastrointestinal tract and skin contain 3.8 and 6.4%, respectively. Gastrointestinal tract actomyosin turns over rapidly with a fractional catabolic rate of 24%/day versus 1.4%/day for skeletal muscle actomyosin.

Entities:  

Mesh:

Substances:

Year:  1982        PMID: 7124943     DOI: 10.1152/ajpendo.1982.243.4.E293

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  16 in total

Review 1.  Protein intake and athletic performance.

Authors:  P W Lemon; D N Proctor
Journal:  Sports Med       Date:  1991-11       Impact factor: 11.136

Review 2.  Regulation of protein turnover in skeletal and cardiac muscle.

Authors:  P H Sugden; S J Fuller
Journal:  Biochem J       Date:  1991-01-01       Impact factor: 3.857

3.  Protein synthesis during the developmental growth of the small and large intestine of the rat.

Authors:  D F Goldspink; S E Lewis; F J Kelly
Journal:  Biochem J       Date:  1984-01-15       Impact factor: 3.857

4.  Interactive effects of insulin and corticosterone on myofibrillar protein turnover in rats as determined by N tau-methylhistidine excretion.

Authors:  F M Tomas; A J Murray; L M Jones
Journal:  Biochem J       Date:  1984-06-01       Impact factor: 3.857

5.  The influence of intestinal flora on wound healing in mice.

Authors:  M Okada
Journal:  Surg Today       Date:  1994       Impact factor: 2.549

6.  Increased protein degradation after eccentric exercise.

Authors:  G J Kasperek; R D Snider
Journal:  Eur J Appl Physiol Occup Physiol       Date:  1985

7.  3-Methylhistidine turnover in the whole body, and the contribution of skeletal muscle and intestine to urinary 3-methylhistidine excretion in the adult rat.

Authors:  D J Millward; P C Bates
Journal:  Biochem J       Date:  1983-08-15       Impact factor: 3.857

8.  Acute alterations in sodium flux in vitro lead to decreased myofibrillar protein breakdown in rat skeletal muscle.

Authors:  M N Goodman
Journal:  Biochem J       Date:  1987-10-01       Impact factor: 3.857

9.  Contrasting response of protein degradation to starvation and insulin as measured by release of N tau-methylhistidine or phenylalanine from the perfused rat heart.

Authors:  D M Smith; P H Sugden
Journal:  Biochem J       Date:  1986-07-15       Impact factor: 3.857

10.  Effects of rapid or slow body mass reduction on body composition in adult rats.

Authors:  Shinji Tai; Yasukimi Tsurumi; Yukari Yokota; Mitsuhiko Masuhara; Koji Okamura
Journal:  J Clin Biochem Nutr       Date:  2009-08-28       Impact factor: 3.114

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.