Abstract
IntroductionThe anticonvulsant effects of melatonin (MT) have been demonstrated in several different experimental seizure models. Thus, the present study aimed to determine the anticonvulsant efficacy of MT, the optimum time for its administration prior to the induction of a seizure, and its effective dose in a rat model of hyperthermic febrile seizures (FSs). MethodsThe present study included 72 male Sprague–Dawley rat pups divided into eight groups. The seizures were induced by keeping the rats in 45°C water and the experiments were performed in two steps. In the first step, the control group was given a vehicle injection and the study groups were given a MT injection (150mg/kg, intraperitoneal [i.p.]) at either 5, 10, or 15min prior to the induction of the seizure to determine the anticonvulsant effects of MT and its optimum time of administration. In the second step, a vehicle injection and three different doses of MT (80, 100, and 150mg/kg, i.p.) were administered 15min prior to the induction of the seizure to determine the dose at which anticonvulsant effects could be achieved. The anticonvulsant effects were assessed based on the latency of the FSs. ResultsIn the first-step experiments, the FS latency of the control group was 143.4±15.3s and the latencies of the groups given melatonin at either 5, 10, or 15min prior to the seizure were 174.2±28.9, 177.4±21.0, and 193.7±17.6s, respectively. Compared with the control group, the latencies for each of the study groups were significantly longer (p<0.001), with the longest latency observed in the group given melatonin 15min before the seizure. In the second-step experiments, the FS latencies of the groups that were given 80, 100, and 150mg/kg of MT 15min before the seizure were 238.7±4.0, 240.0±0.0, and 193.7±17.6s, respectively. These latencies were significantly longer than those of the control group (172.3±30.3s, p<0.001). ConclusionThe present study demonstrated that MT exerts anticonvulsant effects in a rat model of hyperthermic FSs and achieved its optimum efficacy at a dose of 80mg/kg when administered 15min prior to the induction of a seizure.
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