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. 2015 Aug 1;8(8):9360–9367.

Table 3.

Pharmacokinetic parameters of metroprolol and and omeprazole in control-group and MS-275-group rats (mean ± SD, n = 10)

Parameters AUC(0-t) AUC(0-∞) t1/2 CL V Cmax

ng/mL h* ng/mL h* h L/h/kg L/kg ng/mL
Metroprolol (CYP2D6) Low 1459.0 ± 398.5 1493.7 ± 397.8 1.9 ± 0.7 7.2 ± 2.2 20.0 ± 9.1 403.9 ± 121.7
Medium 1016.4 ± 223.9 1025.2 ± 222.9 1.8 ± 0.9 10.2 ± 2.1 27.3 ± 19.0 374.1 ± 63.7**
High 746.4 ± 277.1** 751.2 ± 275.9** 1.3 ± 0.2 14.4 ± 3.4** 27.9 ± 8.7 309.9 ± 71.6**
Control 1151.8 ± 201.8 1158.3 ± 196.6 1.3 ± 0.3 8.8 ± 1.4 16.4 ± 6.4 563.1 ± 156.6
Omeprazole (CYP2C19) Low 361.2 ± 172.8** 370.7 ± 172.0** 1.8 ± 0.5 32.3 ± 13.7** 93.3 ± 62.6** 324.2 ± 190.3**
Medium 327.8 ± 95.8** 341.8 ± 87.0** 1.9 ± 1.0 30.9 ± 7.4** 88.6 ± 66.1 294.6 ± 129.9**
High 367.7 ± 158.8** 455.1 ± 112.5** 10.1 ± 17.8 28.5 ± 20.0 160.4 ± 122.7** 179.9 ± 68.8**
Control 905.9 ± 279.7 923.0 ± 295.3 1.4 ± 0.9 12.2 ± 4.9 23.2 ± 11.7 795.3 ± 229.5

Compared MS-275 group with the control group,

*

P<0.05;

**

P<0.01.