M. Mamman et al., COMPARATIVE PHARMACOKINETICS OF DIMINAZENE IN NONINFECTED BORAN (BOS-INDICUS) CATTLE AND BORAN CATTLE INFECTED WITH TRYPANOSOMA-CONGOLENSE, Antimicrobial agents and chemotherapy, 37(5), 1993, pp. 1050-1055
The pharmacokinetics of diminazene in five female Boran (Bos indicus)
cattle before and then during acute and chronic phases of experimental
infections with Trypanosoma congolense were investigated. A 7.0% (wt/
vol) solution of diminazene aceturate (Berenil) was used in all three
phases of the study and administered as a single intramuscular dose of
3.5 mg of diminazene base per kg of body weight. There were no signif
icant differences between the values of pharmacokinetic parameters for
the noninfected cattle and the values for cattle with a chronic T. co
ngolense infection. However, the maximum concentration of the drug in
plasma during the acute phase of infection (8.25 +/- 1.72 mug/ml) was
significantly (P < 0.01) greater than that during chronic infection (5
.04 +/- 0.26 mug/ml) and that in the noninfected state (4.76 +/- 0.76
mug/ml). Similarly, the time to maximum concentration of the drug in p
lasma when diminazene was administered during the acute phase of infec
tion (18.00 +/- 6.71 min) was significantly (P < 0.02) shorter than th
at for noninfected cattle (36.00 +/- 8.22 min) and that during chronic
infection (33.75 +/- 7.50 min). The volume of distribution at steady
state during acute infection (1.01 +/- 0.31 liter/kg) was significantl
y (P < 0.01) smaller than that in the noninfected state (1.37 +/-0.17
liter/kg) and that in chronic infection (1.51 +/- 0.24 liter/kg). Eigh
t hours after the drug had been administered, the concentration-time d
ata profiles for each of the three study phases were very similar. Mea
n concentrations of diminazene in plasma 48 h after administration of
the drug were 0.43 +/- 0.07 mug/ml in noninfected cattle, 0.43 +/- 0.1
1 mug/ml during the acute phase of trypanosome infection, and 0.44 +/-
0.09 mug/ml during the chronic phase of the infection. Results of the
present study indicate that the area under the concentration-time cur
ve for diminazene in trypanosome-infected cattle did not differ signif
icantly from that for noninfected cattle. It, therefore, appears that
the total amount of diminazene attained and maintained in the plasma o
f cattle is not significantly altered during infection with T. congole
nse.