In Vivo Anti-Hyperglycemic Activity and Toxicity Evaluation of Two Bis-Coumarin Derivative As Potential Α-Glucosidase Inhibitors Publisher



Mohammadikhanaposhtani M¹ ; Bahrami T² ; Bandarian F³ ; Nasliesfahani E³ ; Roostaei D⁴ ; Zamani E² ; Aghajani F² ; Mahdavi M⁵ ; Ahangar N⁴ Show Affiliations
Source: Journal of Diabetes and Metabolic Disorders Published:2025

Abstract

Objectives: The in vivo assay is a key step in the development of a new compound as a drug. In the present work, bis-4-aminocoumarin derivative 3,3'-(p-tolylmethylene)bis(4-amino-2H-chromen-2-one) (PTBAC) and bis-4-hydroxycoumarin derivative 3,3'-((4-((1-(2-chlorobenzyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)methylene)bis(4-hydroxy-2H-chromen-2-one) (2CTMBHC) that showed high anti-α-glucosidase activity on the yeast form of this enzyme were selected for in vivo anti-hyperglycemic assay. Methods: The in vivo anti-hyperglycemic effect of PTBAC and 2CTMBHC was assessed using oral starch tolerance test in streptozotocin-induced diabetic albino mouse model, and the results were compared with acarbose as a representative inhibitor of intestinal α-glucosidase enzyme. Toxicity of the selected compounds was also evaluated in vivo. Results: The obtained results revealed that both selected compounds, PTBAC and 2CTMBHC, showed more anti-diabetic effects when compared with acarbose as a standard drug. In vivo anti-diabetic assays also demonstrated that bis-4-hydroxycoumarin derivative 2CTMBHC was more potent than bis-4-aminocoumarin derivative PTBAC. In vivo results were also confirmed by in vitro and in silico studies. Moreover, there was not any apparent signs of toxicity and mortality in in vivo toxicity assay. Conclusions: In summary, in vivo anti-hyperglycemic effects of two synthetic compounds PTBAC and 2CTMBHC was confirmed in this study. Given that these compounds exhibited no evidences of toxicity and mortality in mice, therefore, they are good candidates for further investigations. © The Author(s), under exclusive licence to Tehran University of Medical Sciences 2025.