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1.
Food Chem Toxicol ; 46(6): 2239-43, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18407392

ABSTRACT

The illegal use of beta2-agonists as repartitioning agents to improve production performance and carcass composition can induce changes in various organs of exposed animals. The aim of the present study was to evaluate the effects induced by dietary beta-agonists on beta-AR, AnR and GR in male broiler target organs. Fifty-four male broiler chickens (Ross 508), 26 days old, were randomly divided into three homogeneous experimental groups and fed for 21 days with a standard diet containing placebo (group 1, control), 1ppm of clenbuterol (group 2) and 1ppm of cimaterol (group 3). Tissue samples of heart, lung, brain, testicle, spleen, thymus and Bursa of Fabricius were collected post-mortem then cytosol fractions were used for AnR (testicles) and GR (spleen, thymus and Bursa of Fabricius), and membrane fractions for beta-AR (all tissues but testicles) determination by binding assays. The dietary administration of beta-adrenergic agents as repartitioning agents induced a significant decrease in AnR concentration in the testicle, in GR levels in the lymphoid tissues and in beta-AR concentrations of different target organs of male chickens. Present data confirm those observed in female chickens and suggest that in poultry the regulation exerted by adrenergic stimulation on steroid receptor concentrations produces different effects than in mammals.


Subject(s)
Adrenergic beta-2 Receptor Agonists , Adrenergic beta-Agonists/toxicity , Chickens/physiology , Receptors, Adrenergic, beta/drug effects , Receptors, Steroid/drug effects , Adrenergic beta-1 Receptor Agonists , Adrenergic beta-1 Receptor Antagonists , Animals , Bursa of Fabricius/drug effects , Bursa of Fabricius/metabolism , Cell Membrane/drug effects , Cell Membrane/metabolism , Clenbuterol/toxicity , Cytosol/drug effects , Cytosol/metabolism , Diet , Ethanolamines/toxicity , Male , Nandrolone/analogs & derivatives , Nandrolone/toxicity , Propanolamines/toxicity , Receptors, Androgen/drug effects , Receptors, Glucocorticoid/drug effects , Spleen/drug effects , Spleen/metabolism , Thymus Gland/drug effects , Thymus Gland/metabolism
2.
J Vet Pharmacol Ther ; 29(2): 91-7, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16515662

ABSTRACT

In order to identify possible peripheral markers of illegal treatments with growth-promoting agents in veal calves, beta-adrenergic receptor (beta-AR) and glucocorticoid receptor (GR) concentrations were measured in lymphocytes of 12 male Friesian crossbred calves (six controls and six treated). The animals received a cocktail of anabolic and re-partitioning agents [17beta-oestradiol: 3 x 10 mg intramuscular (i.m.) doses at 17-day intervals; dexamethasone sodium phosphate: 4 mg/day for 6 days and 5 mg/day for six further days dissolved in milk; and clenbuterol: 20 microg/kg/day dissolved in milk for the last 40 days before slaughter]. Blood samples were collected by venipuncture at different time points and lymphocytes were isolated by density gradient centrifugation. Lymphocyte beta-AR and GR levels were measured by binding assays. Treatment with re-partitioning agents caused a significant down-regulation of lymphocyte beta-ARs 19 days after the beginning of clenbuterol administration and at day 55 (after dexamethasone withdrawal, just before slaughter). This phenomenon was partially reversed at day 50, after dexamethasone administration, at which time a significant decrease in GR concentrations also occurred. For both types of receptors, no significant changes in the dissociation constant values were observed at any time point. Lymphocytes express measurable concentrations of beta-ARs and GRs and the measurement of receptor levels highlights the fluctuation of receptor expression due to the dynamic interaction of the drugs used in combination. Lymphocyte receptor determination could therefore be included in a battery of biological assays to detect illegal treatments with anabolic agents in veal calves in the light of a multivariate approach.


Subject(s)
Adrenergic beta-Agonists/pharmacology , Anabolic Agents/pharmacology , Clenbuterol/pharmacology , Estradiol/pharmacology , Lymphocytes/drug effects , Receptors, Adrenergic, beta/drug effects , Receptors, Glucocorticoid/drug effects , Anabolic Agents/blood , Animals , Anti-Inflammatory Agents/pharmacology , Cattle , Clenbuterol/blood , Dexamethasone/pharmacology , Drug Interactions , Lymphocytes/metabolism , Male , Receptors, Adrenergic, beta/metabolism , Receptors, Glucocorticoid/metabolism
4.
Vet J ; 168(3): 297-303, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15501147

ABSTRACT

The effect of transportation on blood cortisol and catecholamine levels, lymphocyte glucocorticoid receptor (GR) and beta-adrenergic receptor (beta-AR) concentrations was investigated in calves. Blood samples were collected from 24 six-month-old calves before departure (T(0)), on arrival (T(1)), and at 24 h (T(2)) and one week (T(3)) after arrival. Animals were loaded and transported about 950 km, from the Midy-Pyrenes region (Cahors, France) to the Piedmont region (Italy), over a total of 14 h. Serum cortisol levels and plasma catecholamines (adrenaline, noradrenaline) were determined by radioimmunoassay. Lymphocyte GRs and beta-ARs were measured through binding assays. A significant (P < 0.05) increase in cortisol and catecholamine concentrations was observed immediately after transport. The increase in hormone levels at time T(1) was negatively correlated with lymphocyte GR and beta-AR concentrations. At times T(2) and T(3), blood cortisol and catecholamine levels and lymphocyte GRs and beta-ARs returned to normal. The results demonstrate the activation of the hypothalamic-pituitary-adrenal axis and the catecholaminergic system in long-term transported calves. However, these systems returned to normal within 24 h after the end of transport.


Subject(s)
Catecholamines/blood , Cattle/blood , Glucocorticoids/metabolism , Hydrocortisone/blood , Lymphocytes/blood , Transportation , Animals , Cattle/immunology , Male , Radioimmunoassay/veterinary , Receptors, Adrenergic, beta/metabolism , Receptors, Glucocorticoid/metabolism , Time Factors
5.
J Anim Physiol Anim Nutr (Berl) ; 88(3-4): 94-100, 2004 Apr.
Article in English | MEDLINE | ID: mdl-15059232

ABSTRACT

Illegal dietary supplementation with beta(2)-agonists has been shown to increase protein deposition and decrease fat accretion in domestic animals. In poultry the metabolic and endocrine responses to beta(2)-agonists are not fully elucidated. In this trial the effects of dietary clenbuterol (1 p.p.m.) and cimaterol (1 p.p.m.) on muscle composition and endocrine response of male broiler chickens were studied. Dietary clenbuterol induced a slight, but in general not significant, improvement of zootechnical performances and carcass yields. Chemical composition of muscle was not influenced by dietary treatments, even if a slight improvement of protein content was observed in treated groups. No effects on fatty acid composition of meat were detected. Both clenbuterol and cimaterol treatments caused a downregulation in testicular androgen receptors and in pulmonary, cardiac and central nervous system beta-adrenergic receptors.


Subject(s)
Adrenergic beta-Agonists/administration & dosage , Body Composition/drug effects , Chickens/metabolism , Clenbuterol/administration & dosage , Ethanolamines/administration & dosage , Muscle, Skeletal/drug effects , Receptors, Androgen/drug effects , Adrenergic beta-Agonists/pharmacology , Animal Feed , Animals , Chickens/anatomy & histology , Chickens/growth & development , Clenbuterol/pharmacology , Dietary Supplements , Down-Regulation/drug effects , Ethanolamines/pharmacology , Male , Muscle, Skeletal/metabolism , Random Allocation , Receptors, Adrenergic, beta/drug effects , Receptors, Adrenergic, beta/metabolism , Receptors, Androgen/metabolism , Weight Gain
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