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Buspirone Ameliorates Colon Inflammation in Tnbs-Induced Rat Acute Colitis: The Involvement of Tlr4/Nf-Kb Pathway Publisher Pubmed



Rashidian A1, 2 ; Mohammadi S1, 2 ; Hamaneh AM1 ; Chaboki A1 ; Shayan M1, 2 ; Sheibani M3, 4 ; Abdollahi A5 ; Yousefimanesh H1, 2 ; Dehpour AR1, 2
Authors
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Authors Affiliations
  1. 1. Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Experimental Medicine Research Center, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Pharmacology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
  4. 4. Razi Drug Research Center, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Pathology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran

Source: Drug Research Published:2022


Abstract

Inflammatory bowel disease (IBD) is an inflammatory situation involving the whole digestive system. This illness includes ulcerative colitis and Crohn's disease. According to scientific research, the immune system plays an essential part in developing this disease. Recently, buspirone has been discovered to have anti-inflammatory properties. As a result, this research aims to see if buspirone provides anti-inflammatory effects in a rat model of TNBS-induced colitis. Control, TNBS, dexamethasone (2 mg/kg), and buspirone (5, 10, and 20 mg/kg) were randomly given to six groups of 36 male Wistar rats. Colitis was induced by intrarectal instillation of TNBS in all research groups except the control group, and rats were meliorated with dexamethasone and buspirone. Macroscopic and microscopic lesions appeared after colitis induction, while therapy with dexamethasone and buspirone significantly improved the lesions. TLR4 and pNF-κB expression were also enhanced during colitis induction. On the other hand, the administration of dexamethasone or buspirone resulted in a considerable reduction in their expression. Tissue TNF-α and MPO activity were enhanced after induction of colitis in terms of biochemical variables; however, administration of dexamethasone or buspirone reduced TNF-α and MPO activity. Eventually, in an animal model of severe colitis, buspirone displayed anti-inflammatory characteristics via lowering the TLR4/NF-κB signaling pathway's activity in an animal model of acute colitis. © 2022. Thieme. All rights reserved.
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