1. Alizarin and Purpurin from Rubia tinctorum L. Suppress Insulin Fibrillation and Reduce the Amyloid-Induced Cytotoxicity
- Author
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Wen Wang, Wei Qi, Xin Peng, Jiaxing Zhang, Rongxin Su, and Zhimin He
- Subjects
Rubia tinctorum ,Amyloid ,Physiology ,Cognitive Neuroscience ,medicine.medical_treatment ,Phenylalanine ,Alizarin ,Biochemistry ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Anthraquinones ,medicine ,Cytotoxicity ,030304 developmental biology ,0303 health sciences ,biology ,Amyloidosis ,Insulin ,Cell Biology ,General Medicine ,medicine.disease ,biology.organism_classification ,chemistry ,030217 neurology & neurosurgery - Abstract
Alizarin (1,2-dihydroxyanthraquinone) and purpurin (1,2,4-trihydroxyanthraquinone), natural anthraquinone compounds from Rubia tinctorum L., are reported to have diverse biological effects including antibacterial, antitumor, antioxidation, and so on, but the inhibition activity against amyloid aggregation has been rarely reported. In this study, we used insulin as a model protein to explore the anti-amyloid effects of the two compounds. The results showed that alizarin and purpurin inhibited the formation of insulin fibrils in a dose-dependent manner and reduced insulin-induced cytotoxicity. Meanwhile, purpurin had a more significant inhibitory effect on insulin amyloid fibrils compared with alizarin. In addition, computer simulations indicated that the two compounds interacted mainly with the hydrophobic residues of insulin chain B and interfered with the binding of phenylalanine residues. The research indicated that natural anthraquinone compounds had potential effects in preventing protein misfolding diseases and could be further used to design effective antiamyloidosis compounds.
- Published
- 2021