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. 2019 Mar 15;36(4):859–869. doi: 10.1007/s12640-019-00021-1

Table 2.

Effect of PTE on serum and total brain concentration of CZP, CBZ and OXC

Treatment (mg/kg) Serum concentration Total brain concentration
A
  CZP (0.04) 16.40 ± 2.12 (ng/ml) 4.45 ± 0.61 (ng/g tissue)
  CZP (0.04) + PTE (100) 14.28 ± 1.20 (ng/ml) 4.40 ± 0.32 (ng/g tissue)
Student’s t test: p = 0.1977 Student’s t test: p = 0.4705
B
  CBZ (5.9) 2.06 ± 0.10 (μg/ml) 3.72 ± 0.45 (μg/g tissue)
  CBZ (5.9) + PTE (100) 2.41 ± 0.06 (μg/ml)** 5.45 ± 0.36 (μg/g tissue)**
Student’s t test: p = 0.0043 Student’s t test: p = 0.0039
C
  OXC (9.02) 2.97 ± 0.19 (μg/ml) 3.46 ± 0.27 (μg/g tissue)
  OXC (9.02) + PTE (100) 4.23 ± 0.46 (μg/ml)* 5.47 ± 0.58 (μg/g tissue)**
Student’s t test: p = 0.0104 Student’s t test: p = 0.0027

PTE, CZP, CBZ, and OXC were administered ip 30 min before the samples collection. Each experimental group consisted of 10 mice. Results are presented as the mean ± SEM. Serum and brain concentrations of the studied antiepileptic drugs were analyzed using the Student t test. *p < 0.05, **p < 0.01 vs. control (treated with antiepileptic drug alone) group. CBZ carbamazepine, CZP clonazepam, OXC oxcarbazepine, PTE pterostilbene