Literature DB >> 6615483

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

D J Millward, P C Bates.   

Abstract

The tissue origin of 3-methylhistidine (N tau-methylhistidine) was investigated in adult female rats. The decay of labelling of urinary 3-methylhistidine was compared with the labelling of protein-bound 3-methylhistidine in skeletal muscle and intestine after the injection of [methyl-14C]methionine. The decay curve for urinary 3-methylhistidine was much steeper than that in muscle or intestine, falling to values lower than those in either tissue after 30 days. The lack of decay of labelling in muscle during the first 30 days is shown to result from the persistence of label in the precursor S-adenosylmethionine. The relative labelling of urinary, skeletal-muscle and intestinal 3-methylhistidine cannot be explained in terms of skeletal muscle accounting for a major proportion of urinary 3-methylhistidine. Measurements were also made of the steady-state synthesis rate of protein-bound 3-methylhistidine in intestinal smooth muscle in vivo in adult female rats. This involved measurement of the overall rate of protein synthesis and measurement of the relative rates of synthesis of 3-methylhistidine and of mixed protein. The synthesis rate of 3-methylhistidine was 29.1%/day, compared with the overall rate of 77.1%/day for mixed, non-mucosal intestinal protein. Measurement of the amount of 3-methylhistidine in skeletal muscle (0.632 +/- 0.024 mumol/g) and in the whole body (0.332 +/- 0.013 mumol/g) indicate that, although the muscle pool is 86% of the total, because of its slow turnover rate of 1.1-1.6%/day, it only accounts for 38-52% of the observed excretion. Measurements of the mass of the intestine (9.95 g/250 g body wt.) and protein-bound 3-methylhistidine content (0.160 mumol/g of tissue) indicate a pool size of 1.59 mumol/250 micrograms rat. Thus 463 nmol of the urinary excretion/day would originate from the intestine, 22% of the total. The tissue source of the remaining urinary excretion is not identified, but other non-muscle sources constituting about 10% of the whole-body pool could account for this with turnover rates of only 6%/day, a much lower value than the turnover rate in the intestine.

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Year:  1983        PMID: 6615483      PMCID: PMC1152287          DOI: 10.1042/bj2140607

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  12 in total

1.  Fractional flux rates of Nt-methylhistidine in skin and gastrointestine: the contribution of these tissues to urinary excretion of Nt-methylhistidine in the rat.

Authors:  N Nishizawa; T Noguchi; S Hareyama; R Funabiki
Journal:  Br J Nutr       Date:  1977-07       Impact factor: 3.718

2.  Relationship between rates of methylation and synthesis of heart protein.

Authors:  C A Watkins; H E Morgan
Journal:  J Biol Chem       Date:  1979-02-10       Impact factor: 5.157

3.  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

4.  Efflux of 3-methylhistidine from the leg in cancer patients who experience weight loss.

Authors:  K Lundholm; K Bennegård; E Edén; G Svaninger; P W Emery; M J Rennie
Journal:  Cancer Res       Date:  1982-11       Impact factor: 12.701

5.  Nutrition and protein turnover.

Authors:  P J Garlick; G A Clugston; M A McNurlan; V R Preedy; E B Fern
Journal:  Biochem Soc Trans       Date:  1982-08       Impact factor: 5.407

6.  Fractional catabolic rates of myosin and actin estimated by urinary excretion of Ntau-methylhistidine: the effect of dietary protein level on catabolic rates under conditions of restricted food intake.

Authors:  N Nishizawa; M Shimbo; S Hareyama; R Funabiki
Journal:  Br J Nutr       Date:  1977-05       Impact factor: 3.718

7.  Myofibrillar protein turnover and urinary N-tau-methylhistidine output. Response to dietary supply of protein and energy.

Authors:  L N Haverberg; L Deckelbaum; C Bilmazes; H N Munro; V R Young
Journal:  Biochem J       Date:  1975-12       Impact factor: 3.857

8.  The kinetics of myofibrillar protein breakdown in perfused rat skeletal muscle.

Authors:  L C Ward; P J Buttery
Journal:  Biochim Biophys Acta       Date:  1979-10-18

9.  A rapid and convenient technique for measuring the rate of protein synthesis in tissues by injection of [3H]phenylalanine.

Authors:  P J Garlick; M A McNurlan; V R Preedy
Journal:  Biochem J       Date:  1980-11-15       Impact factor: 3.857

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

Authors:  S J Wassner; J B Li
Journal:  Am J Physiol       Date:  1982-10
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  14 in total

1.  Castration differentially alters basal and leucine-stimulated tissue protein synthesis in skeletal muscle and adipose tissue.

Authors:  Qianning Jiao; Anne M Pruznak; Danuta Huber; Thomas C Vary; Charles H Lang
Journal:  Am J Physiol Endocrinol Metab       Date:  2009-09-15       Impact factor: 4.310

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.  The effect of chronic ethanol ingestion on synthesis and degradation of soluble, contractile and stromal protein fractions of skeletal muscles from immature and mature rats.

Authors:  V R Preedy; T J Peters
Journal:  Biochem J       Date:  1989-04-01       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.  Insulin-like growth factor-I (IGF-I) and especially IGF-I variants are anabolic in dexamethasone-treated rats.

Authors:  F M Tomas; S E Knowles; P C Owens; C S Chandler; G L Francis; L C Read; F J Ballard
Journal:  Biochem J       Date:  1992-02-15       Impact factor: 3.857

6.  Time course of the effect of catabolic doses of corticosterone on protein turnover in rat skeletal muscle and liver.

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

Review 7.  Mobilisation of structural proteins during exercise.

Authors:  A Viru
Journal:  Sports Med       Date:  1987 Mar-Apr       Impact factor: 11.136

8.  Whole-body protein breakdown and 3-methylhistidine excretion during brief fasting, starvation, and intravenous repletion in man.

Authors:  S F Lowry; G D Horowitz; M Jeevanandam; A Legaspi; M F Brennan
Journal:  Ann Surg       Date:  1985-07       Impact factor: 12.969

Review 9.  Malignant disease: nutritional implications of disease and treatment.

Authors:  S Holmes; J W Dickerson
Journal:  Cancer Metastasis Rev       Date:  1987       Impact factor: 9.264

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

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