Resveratrol as a nontoxic excipient stabilizes insulin in a bioactive hexameric form

• Published in: Journal of computer-aided molecular design Vol. 34; no. 8; pp. 915 - 927
• Main Authors: Pathak, Bani Kumar, Das, Debajyoti, Bhakta, Sayan, Chakrabarti, Partha, Sengupta, Jayati
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 01.08.2020; Springer Nature B.V
• Subjects: Animal Anatomy; Atomic force microscopy; Biocompatibility; Biological activity; Chemistry; Chemistry and Materials Science; Computer Applications in Chemistry; Crystal structure; Fibrillation; Formulations; Histology; Insulin; Microscopy; Morphology; Phenols; Physical Chemistry; Three dimensional models; Toxicity; Nontoxic preservative; Bioactivity; Anti-fibrillation activity; Insulin aggregation; Oligomer structure
• ISSN: 0920-654X; 1573-4951
• DOI: 10.1007/s10822-020-00311-3

Insulin aggregation is the leading cause of considerable reduction in the amount of active drug molecules in liquid formulations manufactured for diabetes management. Phenolic compounds, such as phenol and m-cresol, are routinely used to stabilize insulin in a hexameric form during its commercial preparation. However, long term usage of commercial insulin results in various adverse secondary responses, for which toxicity of the phenolic excipients is primarily responsible. In this study we aimed to find out a nontoxic insulin stabilizer. To that end, we have selected resveratrol, a natural polyphenol, as a prospective nontoxic insulin stabilizer because of its structural similarity with commercially used phenolic compounds. Atomic force microscopy visualization of resveratrol-treated human insulin revealed that resveratrol has a unique ability to arrest hINS in a soluble oligomeric form having discrete spherical morphology. Most importantly, resveratrol-treated insulin is nontoxic for HepG2 cells and it effectively maintains low blood glucose in a mouse model. Cryo-electron microscopy revealed 3D morphology of resveratrol-stabilized insulin that strikingly resembles crystal structures of insulin hexamer formulated with m-cresol. Significantly, we found that, in a condition inductive to amyloid fibrillation at physiological pH, resveratrol is capable of stabilizing insulin more efficiently than m-cresol. Thus, this study describes resveratrol as an effective nontoxic natural molecule that can be used for stabilizing insulin in a bioactive oligomeric form during its commercial formulation. Graphic Abstract