Animal venoms are natural products that have served as a source of novel molecules that have inspired novel drugs for several diseases, including for metabolic diseases such as type-2 diabetes and obesity. From venoms, toxins such as exendin-4 () and crotamine () have demonstrated their potential as treatments for obesity. Moreover, other toxins such as Phospholipases A and Disintegrins have shown their potential to modulate insulin secretion in vitro. This suggests an unexplored diversity of venom peptides with a potential anti-obesogenic in Mexican rattlesnake venoms. For that reason, this study explored the in vitro effect of Crotalus venom peptide-rich fractions on models for insulin resistance, adipocyte lipid accumulation, antioxidant activity, and inflammation process through nitric oxide production inhibition. Our results demonstrated that the peptide-rich fractions of , and were capable of reverting insulin resistance, enhancing glucose consumption to normal control; , and diminished the lipid accumulation on adipocytes by 20%; , and had the most significant cellular antioxidant activity, having nearly 80% of ROS inhibition. and inhibited nitric oxide production by about 85%. We demonstrated the potential of these peptides from venoms to develop novel drugs to treat type-2 diabetes and obesity. Moreover, we described for the first time that venom peptide fractions have antioxidant and inflammatory properties in vitro models.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11471244PMC
http://dx.doi.org/10.1016/j.toxcx.2024.100209DOI Listing

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