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. 2000 Jul;44(7):1964–1969. doi: 10.1128/aac.44.7.1964-1969.2000

TABLE 1.

Effects of ACV and HDP-P-ACV on serum WHV DNA levels in WHV infection

Treatmenta 109 WHV genomes/ml of serum ± SD at:
% Changeb ± SD at:
P vs placeboc
Time zero 4 Wks Nadir 4 Wks Nadir At 4 wks Maximum
Expt 1
 Placebo 234 ± 221 212 ± 165 166 ± 90 +14 ± 65 +2.3 ± 84
 ACV (20 mg/kg b.i.d.) 167 ± 96 127 ± 69 88 ± 40 −15 ± 33 −39 ± 22 NS NS
 HDP-P-ACV (10 mg/kg b.i.d.) 86 ± 77 3.7 ± 4.7 3.7 ± 4.7 −95 ± 9 −95 ± 8.5 <0.05 <0.05
 HDP-P-ACV (20 mg/kg b.i.d.) 282 ± 165 89 ± 120 42 ± 39 −66 ± 38 −84 ± 12 <0.05 <0.05
Expt 2
 Placebo 17.0 ± 11.7 29.3 ± 19.1 29.4 ± 18.8 +61 ± 43 +72 ± 28
 HDP-P-ACV (5 mg/kg b.i.d.) 34.0 ± 14.5 11.3 ± 12.8 5.36 ± 4.78 −72 ± 21 −86 ± 8.2 <0.001 <0.001
 HDP-P-ACV (30 mg/kg q.d.) 47.3 ± 42.0 22.0 ± 22.6 16.5 ± 20.1 −58 ± 13 −72 ± 13 <0.001 <0.001
a

The number of animals in each group was four in every instance. 

b

By using each WHV-infected animal as its own control, the percent change from time zero was calculated for each animal at 4 weeks and also for the nadir observed during weeks 1 through 6. 

c

The means ± standard deviations of the percent change at 4 weeks and the maximal percent change (weeks 1 through 6) were calculated and tested for statistical significance versus values for the placebo by using the Student-Newman-Keuls multiple comparisons test (Instat2; Graphpad Software, San Diego, Calif.). NS, not significant.