PHARMACODYNAMICS AND PHARMACOKINETICS OF CARPROFEN, A NONSTEROIDAL ANTIINFLAMMATORY DRUG, IN HEALTHY COWS AND COWS WITH ESCHERICHIA-COLI ENDOTOXIN-INDUCED MASTITIS

被引:67
作者
LOHUIS, JACM
VANWERVEN, T
BRAND, A
VANMIERT, ASJPAM
ROHDE, E
LUDWIG, B
HEIZMANN, P
REHM, WF
机构
[1] STATE UNIV UTRECHT,COLL VET MED,DIV PHARMACOL PHARM & TOXICOL,DEPT BASIC SCI,3584 CL UTRECHT,NETHERLANDS
[2] F HOFFMANN LA ROCHE & CO LTD,PHARMACEUT RES DEPT,CH-4002 BASEL,SWITZERLAND
关键词
D O I
10.1111/j.1365-2885.1991.tb00830.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The pharmacodynamics of carprofen and its pharmacokinetics in plasma and milk of healthy cows and cows with endotoxin-induced mastitis were studied after a single intravenous dose of 0.7 mg/kg body weight. Carprofen was administered to five clinically healthy cows and to the same cows 3 weeks later, 2 h after intramammary infusion of endotoxin. Mastitis developed in all endotoxin-infused quarters. The pharmacokinetic characteristics of carprofen in healthy cows were a small volume of distribution (0.09 l/kg), a relatively low systemic clearance (2.4 ml/h kg), and a long elimination half-life (30.7 h). In the mastitic cows, systemic clearance (1.4 ml/h kg) was significantly lower (P < 0.01), and elimination half-life (43.0 h) was significantly longer (P < 0.01) than in the normal animals. Concentrations of carprofen in milk from healthy quarters were below the limit of detection for the assay (0.022-mu-g/ml). In milk from mastitic quarters, concentrations of carprofen increased up to 0.164-mu-g/ml during the first 12 h after induction of mastitis, but were less than 0.022-mu-g/ml at 24 to 48 h. Compared with the untreated mastitic controls, carprofen treatment significantly reduced the heart rate (P < 0.01), rectal temperature (P < 0.001), quarter swelling (P < 0.01) and other parameters measured. Local and systemic adverse reactions to carprofen were not observed.
引用
收藏
页码:219 / 229
页数:11
相关论文
共 25 条
[11]   THE IMPORTANCE OF STEREOCHEMISTRY IN THE CLINICAL PHARMACOKINETICS OF THE 2-ARYLPROPIONIC ACID NON-STEROIDAL ANTI-INFLAMMATORY DRUGS [J].
HUTT, AJ ;
CALDWELL, J .
CLINICAL PHARMACOKINETICS, 1984, 9 (04) :371-373
[12]  
LEES P, 1988, VET REC, V120, P522
[13]   FLUNIXIN MEGLUMINE AND FLURBIPROFEN IN COWS WITH EXPERIMENTAL ESCHERICHIA-COLI MASTITIS [J].
LOHUIS, JACM ;
VANLEEUWEN, W ;
VERHEIJDEN, JHM ;
BRAND, A ;
VANMIERT, ASJPAM .
VETERINARY RECORD, 1989, 124 (12) :305-308
[14]  
LUDWIG B, 1989, SCHWEIZ ARCH TIERH, V131, P99
[15]   PLASMA-CONCENTRATION, MAMMARY EXCRETION AND SIDE-EFFECTS OF PHENYLBUTAZONE AFTER REPEATED ORAL-ADMINISTRATION IN HEALTHY COWS [J].
MARTIN, K ;
ANDERSSON, L ;
STRIDSBERG, M ;
WIESE, B ;
APPELGREN, LE .
JOURNAL OF VETERINARY PHARMACOLOGY AND THERAPEUTICS, 1984, 7 (02) :131-138
[16]   EXTENDED LEAST-SQUARES NONLINEAR-REGRESSION - A POSSIBLE SOLUTION TO THE CHOICE OF WEIGHTS PROBLEM IN ANALYSIS OF INDIVIDUAL PHARMACOKINETIC DATA [J].
PECK, CC ;
BEAL, SL ;
SHEINER, LB ;
NICHOLS, AI .
JOURNAL OF PHARMACOKINETICS AND BIOPHARMACEUTICS, 1984, 12 (05) :545-558
[17]  
RANDALL LO, 1976, ARCH INT PHARMACOD T, V220, P94
[18]  
SHEINER LB, 1985, J PHARMACOKINETICS B, V13, P18
[19]  
STRUB KM, 1982, EUR J RHEUMATOL INFL, V5, P478
[20]  
TEELMANN K, 1983, KLEINTIERPRAXIS, V28, P177