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. 2011 Nov 9;31(45):16423–16434. doi: 10.1523/JNEUROSCI.2506-11.2011

Table 5.

Kindling parameters and effect of valproate in good and poor valproate responders

Parameter Poor responders Good responders p
Kindling development
    Initial ADT (μA) 190.6 ± 28.6 (110–590) 159.1 ± 23.3 (90–330) 0.2384
    Kindling rate (number of stimulations until stage V) 7.4 ± 0.5 (5–12) 7.7 ± 0.9 (5–12) 0.8011
    Cumulative afterdischarge duration until stage V (sec) 151.9 ± 12.2 (52–250) 210.1 ± 28.3 (110–385) 0.1747
Effect of VPA on ADTs in kindled rats
    Control ADT (μA) in fully kindled rats 83.3 ± 8.3 (39–145) 55.8 ± 6.7 (29–110)* 0.0246
    VPA ADT (% of individual control ADT) 123.3 ± 16.2 (25–233) 394.8 ± 34.5 (245–640)*** <0.0001
    VPA plasma level (μg/ml) 383.7 ± 10.0 (320–461) 380.5 ± 14.9 (303–441) 0.7860

For comparison of kindling development and the effect of VPA on ADTs, the group of 27 kindled rats was divided into poor responders (individual ADT increase after 200 mg/kg VPA, i.p., below mean group increase of ADT of 234%; n = 16) and good responders (individual ADT increase >234%; n = 11). Good and poor responders did not differ in kindling development (Mann–Whitney U test). Good and poor responders significantly differed in the predrug (control) ADT determined after injection of saline and in the effect of VPA on ADTs (Student's t test; marked by asterisks). The average VPA concentration was about the same in good and poor responders (Mann–Whitney U test). Data are means ± SEM (range).