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. Author manuscript; available in PMC: 2010 Jul 27.
Published in final edited form as: Neuropsychobiology. 2008 Oct 3;58(2):81–90. doi: 10.1159/000159776

Table 4.

Comparison of pharmacokinetic parameters following intravenous bolus administration of naltrexone in Wistar, LAD-1 and HAD-1 rats by analysis of variance

a Comparison of pharmacokinetic parameters

Parameters LAD-1 rat HAD-1 rat Wistar rat ANOVA result, p
C0, ng/ml 5,828±2,105.5 9,303±2,105.5 5,632±1,935.2 0.320a
Half-life, min 63.5±23.4 70.9±33.7 58.9±11 0.724a
AUC, min × ng/ml 35,547±9,290.6 49,368±14,085.1 26,099±4,493.5 0.013b
AUC_D, min × kg × ng/ml/mg 16,157.8±4,223 22,440.1±6,402.3 11,863.2±2,042.5 0.013b
Cl, ml/min/kg 65±14.8 48±14.1 86±13.9 0.007b
Vss, ml/kg 3,043.5±871.9 2,439.6±1,271.2 2,651.8±644.2 0.594a
AUMC, min × min × ng/ml 1,829,172.426±
1,000,206.778
1,536,266.505±
607,546.849
656,693.955±
216,576.746
0.079c
MRT, min 49±16.5 51.8±26.8 31.1±6.6 0.098c

C0 = Extrapolated concentration at zero time; AUC = area under the blood level-time curve; AUC_D = dose-normalized AUC; Cl = clearance; Vss = volume of distribution at steady state; AUMC = area under the first moment curve; MRT = mean residence time.

a

Not significant;

b

highly significant;

c

not significant – borderline.