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. 2010 Mar 3;159(7):1511–1522. doi: 10.1111/j.1476-5381.2009.00634.x

Table 1.

Effects of kindling and PB treatment on distribution of PB in plasma, cerebral cortex and hippocampus

PTZ-PB
PB-CT
14 day treatment 40 day treatment 14 day treatment 40 day treatment
Plasma, µg·mL−1 72.19 ± 6.98 77.04 ± 5.16 64.84 ± 11.04 66.50 ± 16.52
Cortex, µg·g−1 tissue 23.44 ± 3.58 20.53 ± 3.19 23.45 ± 4.89 16.74 ± 5.00*
Cortex/plasma, mL·g−1 0.32 ± 0.06 0.27 ± 0.04* 0.36 ± 0.04 0.25 ± 0.04**
Hippocampus, µg·g−1 tissue 52.26 ± 9.57 35.93 ± 5.56** 32.06 ± 5.59 26.21 ± 5.12*
Hippocampus/plasma, mL·g−1 0.72 ± 0.11 0.47 ± 0.08** 0.50 ± 0.06 0.39 ± 0.10*

The treated kindled rats (PTZ-PB rats) and age-matched treated rats (PB-CT rats) were orally given PB (45 mg·kg−1·day−1, i.g.) for consecutive 14 or 40 days. At 1 h after PB administration (i.g.), PB concentrations in plasma, cerebral cortex, and hippocampus were measured. Each value is presented as mean ± SD (n= 8).

*

P < 0.05,

**

P < 0.01 versus the 14th day using Student's t-test.

PB, phenobarbital; PTZ, pentylenetetrazole.