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Evaluation of the Anti-Ulcerative Effects of Lacosamide in a Rat Model of Acetic Acid-Induced Colitis Publisher



Minaiyan M ; Mottaghi N
Authors

Source: Research in Pharmaceutical Sciences Published:2026


Abstract

Background and purpose: Colitis is a type of inflammatory bowel disease (IBD) with an unknown and complex etiology. Lacosamide is a known antiepileptic drug for which anti-inflammatory effects have been reported. This study investigates the ameliorative effects of lacosamide on acetic acid-induced colitis in rats. Experimental approach: Male Wistar rats were divided into different interventional groups, including normal and control colitis groups (normal saline, 5 mL/kg), two colitis groups (dexamethasone, 1 mg/kg) and mesalazine (100 mg/kg), four colitis groups received oral lacosamide (10, 20, or 40 mg/kg), or lacosamide enema (10 mg/kg). The treatments were conducted for five days following disease induction by acetic acid (3.5%, 2 mL). Colitis indices in tissue samples, as well as biochemical factors such as myeloperoxidase (MPO), malondialdehyde (MDA), and ferric reducing antioxidant power (FRAP), were assessed. Findings/Results: The trend of body weight drop was stopped by using lacosamide. Colon weight as well as ulcer index significantly decreased in the groups that received lacosamide (10-40 mg/kg via oral or rectal) compared to the control group. Histological findings showed that lacosamide (10 and 20 mg/kg via oral and enema) reduced inflammation markers and tissue damage while causing tissue regeneration. Levels of MDA and MPO significantly decreased while FRAP increased in lacosamide (10 and 20 mg/kg) groups, both oral and via enema. Conclusion and implications: Findings highlight the potential of lacosamide as an effective treatment in reducing inflammation and promoting ulcer healing. However, further studies are needed to elucidate the precise mechanisms of lacosamide's anti-inflammatory effects and to confirm these results in human disease. © 2025 Research in Pharmaceutical Sciences.