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Background and Objective: In recent years many studies have reported that aspirin could have beneficial effect on learning and memory in different diseases of central nervous system. The objective of present study was to explore the effect of aspirin on learning and memory of Rats in pentylenetetrazole kindling model. Materials and Methods: In this experimental study Rats were divided randomly into six groups (n=8). Animals in three groups received aspirin (15 and 30 mg/kg, orally) and saline, one week before and during induction of kindling, respectivley. Kindling was induced in these groups by administration of pentylenetetrazole (PTZ: 40 mg/kg, ip). Two groups of animals received only aspirin 25 and 30 mg/kg orally. Other group received only saline throughout the study and served as health control group. After induction of kindling the learning and memory of Rats was tested in shuttle box. Study was divided to three stages of adaptation, acquisition and retention test. Initial Latency (IL) time before electrical shock and Step through latency (STL) time, 20 min or 24h after acquisition was evaluated as learning and memory index. Locomotor activity was also evaluated in open filed test. Results: PTZ kindling significantly decreased Initial Latency and Step through latency time, 20 min or also 24h after acquisition, and aspirin significantly increased these times in kindled animals (p<0.05). Aspirin also had no significant effect on locomotor activity of animals. Conclusion: This study showed that the administration of aspirin to kindled Rats improved learning and memory impairments induced by pentylenetetrazole kindling.

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Background and Objective: Antiepileptic drugs can partiality control or achieve the convulsion. There are controversial issues about the use and effect of ethanol to control epileptic convulsion seizers. This study was done to determine the effect of ethanol on microvascular alterations in the brain cortex of epileptic mice treated by valporic acid (VPA). Materials and Methods: In this experimental study, 36 BALB/c mice were allocated randomly into six groups including: 1-PTZ (Pentylenetetrazol), 2- Ethanol, 3- VPA+ PTZ, 4- ethanol + PTZ, 5-ethanol+ VPA+ PTZ and control groups. The animal brains were excluded and stained by Hematoxilin and eosin. Thirty-six optical microscopic field from each group were selected and microvascular count were determined. Immunohistochemical method was used for detection of injuries in the vascular brain tissue. Results: Mean number of brain microvascular cortex significantly increaed in PTZ+ethanol and PTZ+ethanol+VPA groups in compare to controls (P<0.05). Infiltration and thrombophlebitis were observed in vessels and cortical brain tissues in mice which received ethanol and PTZ. Proliferations in endothelial vascular cells were seen in PTZ and VPA+ethanol groups. Immunohistochemical method showed the endothelial cells of PTZ+ethanol groups were more stained in compare to the other experimental groups. Conclusion: Ethanol + PTZ cause cellular infiltration and damage to the cortical brain vessels although VPA reduces histological altheretions.