• Awanish Mishra and Rajesh Kumar Goel.
• Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala, Punjab, India; Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Rae Bareli, Uttar Pradesh, India.
• Neuroscience. 2016 Dec 17; 339: 319-328.

AbstractOur previous studies have suggested a strong involvement of serotonergic innervations in epileptogenesis and associated memory impairment. Several studies have suggested that the modulation of 5-HT3 receptors could serve as a promising tool for the management of epilepsy and memory deficit. The present study was envisaged to confirm this hypothesis. In this study, kindling was induced in male Swiss Albino mice using a subconvulsive dose of pentylenetetrazole (PTZ) (35mg/kg at 48±2h). Once the animals were kindled, they were treated with a vehicle, ondansetron (0.1, 0.5, 1mg/kg/day; i.p.), m-chlorophenylbiguanide (m-CPBG) (1mg/kg/day; i.p.), and ondansetron+m-CPBG for 20days. On days 5, 10, 15, and 20, they were administered a PTZ challenging dose (35mg/kg) to assess the seizure severity score; thereafter, memory was evaluated. After behavioral assessment on day 20, the animals were sacrificed and their brains were isolated to estimate cortical and hippocampal neurotransmitter levels (glutamate and gamma aminobutyric acid (GABA) by the high-performance liquid chromatography with the fluorescence detection method, and the nitrite level and acetylcholinesterase (AChE) activity by the microplate reader method). Ondansetron treatment significantly reduced the seizure severity and improved the acquisition performance in a dose-dependent manner. Neurochemical analysis suggested that ondansetron treatment significantly reduced the nitrite level and AChE activity in the cortex as well as in the hippocampus. The outcome of this study suggests the reduction in AChE activity and the nitrite level could be considered as protective mechanisms of ondansetron for amelioration of PTZ kindling and associated memory deficit.Copyright © 2016 IBRO. Published by Elsevier Ltd. All rights reserved.

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