Table 2.
Antiepileptic effect of CPM on PTZ induced seizure in mice.
| Treatment | Seizure latency (s) | Death latency (s) | Seizure rate (%) | Death rate (%) |
|---|---|---|---|---|
| Model | 83.56 ± 22.51 | 197.28 ± 30.18 | 100 | 100 |
| Positive | 1800 ± 0∗∗ | 1800 ± 0∗∗ | 0∗∗ | 0∗∗ |
| 100 mg/kg | 85.10 ± 19.26 | 208.54 ± 31.57 | 100 | 100 |
| 200 mg/kg | 124.25 ± 20.67∗ | 383.10 ± 49.38∗∗ | 100 | 70∗ |
| 400 mg/kg | 209.90 ± 26.29∗∗ | 452.62 ± 65.12∗∗ | 100 | 40∗∗ |
PTZ: pentylenetetrazole; CPM: Cicadae Periostracum. Diazepam was used as a positive control. Mice were divided into five groups (n = 20): model group (mice were treated with normal saline, 20 mL/kg, p.o.), positive group (mice were treated with diazepam, 4 mg/kg, i.p.), and three tested CPM groups (mice were treated with CPM at the doses of 100, 200, and 400 mg/kg, p.o.). The chi-squared test was used to analyze significance of anticonvulsant effects against PTZ-induced seizures among groups (inhibition (%) and mortality (%)). All other data were presented as mean ± SD (n = 20), and statistical analyses were performed using the two-tailed Student's t test, ∗p < 0.05 and ∗∗p < 0.01 vs. model.