Singh, Priyanka and Kadam, Nagesh Y and Panigrahi, Rajlaxmi and Mehrotra, Arpit and Upadhayay, Krishna and Dey, Madhumita and Tyagi, Arpit and Aquib, Muhammad and Nielsen, Janni and Kleijwegt, Giulia and Singh, Prashant and Sharma, Abhishek and Rao, Alka and Otzen, Daniel E and Kumar, Ashutosh and Sharma, Deepak (2025) Sulfamerazine as a potential modulator against α-synuclein aggregation and associated toxicity. ACS Chem. Neurosci., 16 (5). pp. 880-894.
Full text not available from this repository.Abstract
Parkinson's disease (PD) is the second most prevalent neurodegenerative disorder. The presence of Lewy bodies, primarily consisting of amyloid aggregates of the protein α-synuclein (α-Syn), is a common feature seen in dopaminergic neurons in (PD) patients. In the present study, we screened 2320 FDA-approved drugs and found 3 lead molecules, sulfamerazine, lathosterol, and tamoxifen, that reproducibly inhibited α-Syn fibrillation. Dose-response studies showed that sulfamerazine and lathosterol are relatively more potent than tamoxifen in inhibiting α-Syn aggregation. Among the lead compounds, sulfamerazine showed a significant reduction in α-Syn aggregation and associated toxicity in Caenorhabditis elegans model of PD. Sulfamerazine also reduced the accumulation of α-Syn aggregates in neuronal SH-SY5Y cells. Microscale thermophoresis confirmed the binding of sulfamerazine to α-Syn. NMR studies corroborated the binding of sulfamerazine with α-Syn and show that upon interaction, α-Syn is sequestered into large soluble dispersed assemblies, which is similar to as seen in transmission electron microscopy. We conclude that sulfamerazine and its derivatives hold promise as therapeutic agents against Parkinson's disease.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | Caenorhabditis elegans model of PD; Parkinson's disease; SH-SY5Y cells; amyloid aggregates; sulfamerazine; α-synuclein |
| Depositing User: | Dr. K.P.S.Sengar |
| Date Deposited: | 01 Feb 2026 13:42 |
| Last Modified: | 01 Feb 2026 13:42 |
| URI: | http://crdd.osdd.net/open/id/eprint/3272 |
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