Literature DB >> 3593670

Effects of a beta-agonist (clenbuterol) on growth, carcass composition, protein and energy metabolism of veal calves.

P E Williams, L Pagliani, G M Innes, K Pennie, C I Harris, P Garthwaite.   

Abstract

Twenty-two British Friesian bull calves were used in a comparative slaughter experiment to determine the effects of a beta-agonist (clenbuterol) on body composition and energy retention. Four calves were slaughtered at 18 d of age and constituted the initial slaughter group. Of the remaining calves, eight (group A, controls) were given milk replacer only, and ten calves (groups B and C, five calves per group) were given milk replacer plus clenbuterol (0.1 and 1.0 mg clenbuterol/kg milk replacer equivalent to approximately 2 and 20 micrograms/kg body-weight respectively over the 105 +/- 3 d of the experimental period). Calves were slaughtered over the weight range 146-177 kg. Clenbuterol had no significant effect on dry matter (DM) intake, daily live-weight gain or feed conversion ratio. DM digestibility of the milk replacer was not affected by treatment. Nitrogen balance was measured on three separate occasions starting when the calves weighed approximately 60, 110 and 130 kg. N retention was increased over the experimental period in clenbuterol-treated calves, although the effect only achieved significance in calves weighing approximately 110 kg live weight (P less than 0.05). Clenbuterol (20 micrograms/kg body-weight) increased estimated mean daily N retention in the carcass of the calves from 22 to 25 g whilst N retention in the non-carcass components decreased from to 8 g/d. Effects of clenbuterol on N retention occurred mainly in skeletal muscle. Fat in both carcass and non-carcass components was reduced by treatment with clenbuterol. The total energy content of live-weight gain was reduced from 1077 to 897 MJ in clenbuterol-treated calves and mean daily heat production was estimated to increase from 23.1 in controls to 25.9 MJ/d in calves in group C. In calves of mean live weight during balance of 120 and 136 kg, clenbuterol significantly increased daily urinary creatinine excretion and in 120 kg calves N tau-methylhistidine was significantly decreased (P less than 0.05). Based on estimates of muscle mass from urinary creatinine and protein degradation from N tau-methylhistidine excretion, the fractional breakdown rate of muscle protein in clenbuterol-treated calves was only 0.66 of that in the controls when the calves weighed 120 kg.

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Year:  1987        PMID: 3593670     DOI: 10.1079/bjn19870049

Source DB:  PubMed          Journal:  Br J Nutr        ISSN: 0007-1145            Impact factor:   3.718


  9 in total

1.  The effects of clenbuterol on satellite cell activation and the regeneration of skeletal muscle: an autoradiographic and morphometric study of whole muscle transplants in mice.

Authors:  P Roberts; J K McGeachie
Journal:  J Anat       Date:  1992-02       Impact factor: 2.610

2.  Long-term isoprenaline administration and its effect on the revascularisation and regeneration of skeletal muscle transplants in mice.

Authors:  P Roberts; J K McGeachie
Journal:  J Anat       Date:  1996-06       Impact factor: 2.610

3.  Effects of clenbuterol and ICI118551, a selective beta 2-antagonist, on the growth of skeletal muscle of suckling rats.

Authors:  R H Morton; E T Agbenyega; P A Hatton; A C Wareham
Journal:  Pflugers Arch       Date:  1995-12       Impact factor: 3.657

Review 4.  Multiple actions of beta-adrenergic agonists on skeletal muscle and adipose tissue.

Authors:  Y T Yang; M A McElligott
Journal:  Biochem J       Date:  1989-07-01       Impact factor: 3.857

Review 5.  Physiological parameter values for physiologically based pharmacokinetic models in food-producing animals. Part I: Cattle and swine.

Authors:  Zhoumeng Lin; Miao Li; Yu-Shin Wang; Lisa A Tell; Ronald E Baynes; Jennifer L Davis; Thomas W Vickroy; Jim E Riviere
Journal:  J Vet Pharmacol Ther       Date:  2020-04-08       Impact factor: 1.786

6.  Free intracellular and protein bound amino acids in tissues as affected by a mixed beta-adrenergic agonist.

Authors:  M Rguez-Mariscal; A S Del Barrio; J Larralde; J A Martínez
Journal:  Experientia       Date:  1993-04-15

7.  Effect of the beta-adrenoceptor agonist clenbuterol and phytohaemagglutinin on growth, protein synthesis and polyamine metabolism of tissues of the rat.

Authors:  S Bardocz; D S Brown; G Grant; A Pusztai; J C Stewart; R M Palmer
Journal:  Br J Pharmacol       Date:  1992-06       Impact factor: 8.739

8.  Epidemiologic study of an outbreak of clenbuterol poisoning in Catalonia, Spain.

Authors:  L Salleras; A Domínguez; E Mata; J L Taberner; I Moro; P Salvà
Journal:  Public Health Rep       Date:  1995 May-Jun       Impact factor: 2.792

9.  Postnatal β2 adrenergic treatment improves insulin sensitivity in lambs with IUGR but not persistent defects in pancreatic islets or skeletal muscle.

Authors:  Dustin T Yates; Leticia E Camacho; Amy C Kelly; Leah V Steyn; Melissa A Davis; Andrew T Antolic; Miranda J Anderson; Ravi Goyal; Ronald E Allen; Klearchos K Papas; William W Hay; Sean W Limesand
Journal:  J Physiol       Date:  2019-11-29       Impact factor: 5.182

  9 in total

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