A total of 98 animals were used in this experiment (P 12 (n = 32), 18 (n = 40), and 25 (n = 34)). At the dose of 100 mg/kg used in our study, PTZ elicits two types of convulsive seizures, which differ by developmental profile, seizure generator, and by pharmacological sensitivity. Appearance of minimal (mS, mostly clonic convulsions involving head and forelimb muscles with preserved righting reflexes) seizures is age-dependent. They are regularly elicited by PTZ in P15 and older animals but not in younger rats [25]. In contrast, generalized tonic-clonic seizures (GTCS), starting with short running phase and accompanied by a loss of righting reflexes, can be induced already in P1 rats [26].
After PTZ injection, animals were individually placed in Plexiglass cages and their behavior was monitored for 30 min by an experienced observer. Incidence and latency of both seizure types (mS and GTCS) and other behavioral phenomena (e.g., isolated myoclonic jerks) and abnormalities were also recorded. To assess the severity of epileptic phenomena, animals were assigned a score for the most severe behavioral characteristics as follows [27]:
-no changes
-abnormal behavior (e.g., automatisms, increased orienting reaction)
-isolated myoclonic jerks
-atypical or prolonged minimal seizures
-clonic seizures (mS) involving head and forelimb muscles with preserved righting reflexes (older term minimal metrazol seizures)
-generalized seizures without the tonic phase (GCS)
-complete generalized tonic-clonic seizures (GTCS)
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