Comparison of Clenbuterol and Salbutamol Accumulation in the Liver of Two Different Mouse Strains

被引:9
作者
Vulic, Ana [1 ]
Pleadin, Jelka [1 ]
Durgo, Ksenija [2 ]
Scortichini, Giampiero [3 ]
Stojkovic, Ranko [4 ]
机构
[1] Croatian Vet Inst, Analyt Chem Lab, Zagreb 10000, Croatia
[2] Fac Food Technol & Biotechnol, Zagreb 10000, Croatia
[3] Ist Zooprofilatt Sperimentale Abruzzo & Molise G, I-64100 Teramo, Italy
[4] Rudjer Boskovic Inst, Div Mol Med, Zagreb 10000, Croatia
关键词
BETA-AGONISTS; RESIDUES; TISSUE; CONSUMPTION; WITHDRAWAL; VEAL;
D O I
10.1093/jat/bku022
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In the European Union, beta(2)-adrenergic agonists like clenbuterol and salbutamol are banned from use as growth promoters. Although clenbuterol and salbutamol both accumulate in the liver, differences in the accumulation rate can be seen among animal species due to different beta(2)-adrenoreceptor distributions. The aim of this study was to compare the accumulation of the two in the liver tissue of two different mouse strains. The study included 200 8-week-old BALB/c and C57/BL/6 mice. One group of BALB/c (40) and one group of C57/BL/6 (40) mice were treated with 2.5 mg/kg body mass clenbuterol per os for 28 days. The remaining two animal groups were treated with salbutamol in the same manner. The animals were then randomly sacrificed on day 1, 15 and 30 post treatments. Despite of the same treatment dose, the results revealed clenbuterol to persist in the liver tissue longer than salbutamol. On post treatment day 30, the concentration of clenbuterol residue in C57/BL/6 and BALB/c mice liver tissue were 0.23 +/- 0.02 and 0.21 +/- 0.03 ng/g, respectively, while residues of salbutamol were not detected. When comparing the accumulation of both compounds between the two mouse strains, it becomes apparent that no significant difference (P > 0.05) in the accumulation rate can be found.
引用
收藏
页码:265 / 271
页数:7
相关论文
共 17 条
[1]  
[Anonymous], 2002, Off J Eur Commun, VL221, P1
[2]  
Brambilla G, 1997, JAMA-J AM MED ASSOC, V278, P635, DOI 10.1001/jama.278.8.635
[3]   Clinical and pharmacological profile in a clenbuterol epidemic poisoning of contaminated beef meat in Italy [J].
Brambilla, G ;
Cenci, T ;
Franconi, F ;
Galarini, R ;
Macrì, A ;
Rondoni, F ;
Strozzi, M ;
Loizzo, A .
TOXICOLOGY LETTERS, 2000, 114 (1-3) :47-53
[4]  
Commission of the European Communities, 1996, OFFICIAL J EUROPEA L, V125, P1
[5]   OBSERVATIONS ON THE EFFECTS OF LONG-TERM WITHDRAWAL ON CARCASS COMPOSITION AND RESIDUE CONCENTRATIONS IN CLENBUTEROL-MEDICATED CATTLE [J].
ELLIOTT, CT ;
CROOKS, SRH ;
MCEVOY, JGD ;
MCCAUGHEY, WJ ;
HEWITT, SA ;
PATTERSON, D ;
KILPATRICK, D .
VETERINARY RESEARCH COMMUNICATIONS, 1993, 17 (06) :459-468
[6]  
Gojmerac T, 2002, FOOD TECHNOL BIOTECH, V40, P343
[7]   Xenobiotic clenbuterol in food producing male pigs: Various tissue residue accumulation on days after withdrawal [J].
Gojmerac, Tihomira ;
Pleadin, Jelka ;
Bratos, Igor ;
Vulic, Ana ;
Vahcic, Nada .
MEAT SCIENCE, 2008, 80 (03) :879-884
[8]   Measurement of β-agonist residues in retinal tissue of food producing animals [J].
Gowik, P ;
Jülicher, B ;
Ladwig, M ;
Behrendt, D .
ANALYST, 2000, 125 (06) :1103-1107
[9]   TISSUE DISTRIBUTION AND RESIDUES OF CLENBUTEROL, SALBUTAMOL, AND TERBUTALINE IN TISSUES OF TREATED BROILER-CHICKENS [J].
MALUCELLI, A ;
ELLENDORFF, F ;
MEYER, HHD .
JOURNAL OF ANIMAL SCIENCE, 1994, 72 (06) :1555-1560
[10]   FOOD POISONING RELATED TO CONSUMPTION OF ILLICIT BETA-AGONIST IN LIVER [J].
MARTINEZNAVARRO, JF .
LANCET, 1990, 336 (8726) :1311-1311