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Pharmacokinetics of diminazene in plasma and lymph of goats
1996
Mamman, M. | McKeever, Declan J. | Aliu, Y.O. | Peregrine, A.S.
Diminazene aceturate is one of a limited number of drugs currently being used in animals to treat the tsetse fly-transmitted protozoal disease, African trypanosomiasis. Efficacy of the drug at the recommended single IM administered doses of 3.5 and 7.0 mg/kg of body weight is widely acknowledged. However, resistance to the drug at these dosages has been reported. Although the mechanisms of resistance to diminazene are poorly understood, field and experimental data indicate that it may develop naturally through administration of subcurative doses, or as a result of cross-resistance. Evidence from other experimental studies indicates that there are additional mechanisms by which trypanosomes may develop resistance to diminazene aceturate. For instance, some populations ot Trypanosoma brucei and T. vivax are refractory to treatment because of their ability to invade the CNS, a site that is believed to be poorly accessible to diminazene. Furthermore, in recent studies carried out in goats, it has been documented that the ability of T. Congolense IL 3274 to survive treatment with diminazene depends on the stage of infection when treatment is administered; populations of the parasite reappeared in animals that were treated on day 19 after tsetse fly challenge, whereas all goats were cured when treated on day 1 of infection. Because trypanosomes are confined to the skin on day 1 after infection, but thereafter invade the blood circulation, it is possible that the efficacy of the treatment on day 1 is attributable to exposure of the small number of parasites, relative to later stages of infection, to higher concentrations of drug than those attained in blood. The objective of the study reported here was to determine whether diminazene's pharmacokinetics differ between plasma and lymph draining the skin of goats and therefore account for the variation in therapeutic activity of the drug at different stages of a tsetse fly-transmitted infection. Peripheral lymph was used for this work because it appears to be identical in composition to tissue interstitial fluid, into which trypanosomes are inoculated by infected tsetse flies when feeding.
Afficher plus [+] Moins [-]Effect of volume variations on osteogenic capabilities of autogenous cancellous bone graft in dogs.
1996
DeVries W.J. | Runyon C.L. | Martinez S.A. | Ireland W.P.
Quantification of phenylbutazone in equine sera by use of high-performance liquid chromatography with a nonevaporative extraction technique.
1996
Peck K.E. | Ray A.C. | Manuel G. | Rao M.M. | Foos J.
Comparison of antinociceptive, cardiovascular, and respiratory effects, head ptosis, and position of pelvic limbs in mares after caudal epidural administration of xylazine and detomidine hydrochloride solution.
1996
Skarda R.T. | Muir W.W. III.
Characterization of polypeptides synthesized and secreted by oviductal epithelial cell explants obtained from young, fertile and aged, subfertile mares.
1996
Brinsko S.P. | Ignotz G.G. | Ball B.A. | Thomas P.G.A. | Currie W.B. | Ellington J.E.
Attempted transmission of Ehrlichia canis by Rhipicephalus sanguineus after passage in cell culture.
1996
Mathew J.S. | Ewing S.A. | Barker R.W. | Fox J.C. | Dawson J.E. | Warner C.K. | Murphy G.L. | Kocan K.M.
Spatial and temporal epidemiology of pseudorabies virus infection.
1996
Norman H.S. | Sischo W.M. | Pitcher P. | Nesselrodt A. | Day R.L.
High-speed exercise history and catastrophic racing fracture in Thoroughbreds.
1996
Estberg L. | Stover S.M. | Gardner I.A. | Drake C.M. | Johnson B. | Ardans A.
Pulmonary function measurements during repeated environmental challenge of horses with recurrent airway obstruction (heaves).
1996
Tesarowski D.B. | Viel L. | McDonell W.N.
Effect of 5-hydroxytryptamine type-2 receptor blockade on pulmonary function in calves with experimentally induced Pasteurella haemolytica pneumonia.
1996
Hare J.E. | Tesarowski D.B. | Dawe G.E. | Vlaminck K. | Shewen P.E. | Viel L.