Literature DB >> 1174569

Ntau-methylhistidine content of mixed proteins in various rat tissues.

L N Haverberg, P T Omstedt, H N Munro, V R Young.   

Abstract

In order to use Ntau-methylhistidine (3-methylhistidine) excretion in the urine as a measure of muscle protein breakdown, it is necessary to demonstrate that other tissues are not important sources of this protein constituent. Accordingly, the concentration of Ntau-methylhistidine in blood serum and in the mixed proteins of heart, brain, lung, kidney, diaphragm, spleen, testis, stomach, liver and hind leg skeletal muscle was measured in male rats of approx. 400 g body weight. The free Ntau-methylhistidine concentration of rat serum was less than 2 nmol per ml. In contrast, measurable amounts of Ntau-methylhistidine were found in the mixed proteins of all tissues and organs examined. The highest concentration was found in skeletal muscle (658 nmol/g tissue). Assuming muscle mass to be 45% of body weight, it has been estimated that the muscle contains more than ten times the total amount of this amino acid present in all of the other organs analyzed, which together account for about 20% of total body weight. These findings indicate that skeletal muscle is likely to be the major source of urinary Ntau-methylhistidine and the latter is, in consequence, a reflection of myofibrillar protein breakdown in skeletal muscle.

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Year:  1975        PMID: 1174569     DOI: 10.1016/0005-2795(75)90315-3

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  23 in total

Review 1.  Dysregulation of skeletal muscle protein metabolism by alcohol.

Authors:  Jennifer L Steiner; Charles H Lang
Journal:  Am J Physiol Endocrinol Metab       Date:  2015-03-10       Impact factor: 4.310

2.  Genetic studies on the muscle protein turnover rate of coturnix quail.

Authors:  Y Maeda; K Hayashi; T Hashiguchi; S Okamoto
Journal:  Biochem Genet       Date:  1986-04       Impact factor: 1.890

3.  Myofibrillar protein degradation after eccentric exercise.

Authors:  A C Snyder; D R Lamb; C P Salm; M D Judge; E D Aberle; E W Mills
Journal:  Experientia       Date:  1984-01-15

4.  Diurnal response in endogenous amino acid oxidation of meal-fed rats.

Authors:  R W Wannemacher; R E Dinterman
Journal:  Biochem J       Date:  1980-09-15       Impact factor: 3.857

5.  Reappraisal of the quantitative importance of non-skeletal-muscle source of N tau-methylhistidine in urine.

Authors:  C I Harris
Journal:  Biochem J       Date:  1981-03-15       Impact factor: 3.857

6.  Quantitative importance of non-skeletal-muscle sources of N tau-methylhistidine in urine.

Authors:  D J Millward; P C Bates; G K Grimble; J G Brown; M Nathan; M J Rennie
Journal:  Biochem J       Date:  1980-07-15       Impact factor: 3.857

7.  Increased myofibrillar protein catabolism in Duchenne muscular dystrophy measured by 3-methylhistidine excretion in the urine.

Authors:  R O McKeran; D Halliday; P Purkiss
Journal:  J Neurol Neurosurg Psychiatry       Date:  1977-10       Impact factor: 10.154

8.  Protein metabolism after unilateral femoral fracture in the rat, and comparison with sham operation.

Authors:  K N Frayn; R A Little; C J Threlfall
Journal:  Br J Exp Pathol       Date:  1980-10

9.  [Effect of orally-administered triglycerides on muscle proteolysis in the rat].

Authors:  T Kaufmann; H Reinauer
Journal:  Z Ernahrungswiss       Date:  1983-09

10.  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

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