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Molecule capable of halting and reverting Parkinson's neurodegeneration identified

Date:
September 25, 2018
Source:
Universitat Autonoma de Barcelona
Summary:
The small SynuClean-D molecule interrupts the formation of the alpha-synuclein amyloid fibres responsible for the onset of Parkinson's disease, and reverts the neurodegeneration caused by the disease.
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Parkinson's disease is the second most common incurable neurodegenerative disorder after Alzheimer's disease. It is characterised by the accumulation of protein deposits in dopaminergic neurons (in charge of producing dopamine) in the form of amyloid fibres. These aggregates are formed mainly by the alpha-synuclein protein and in a very complex manner, which makes it complicated to identify molecules which could prevent or revert the process and the neurodegeneration associated with it.

A scientific collaboration led by researchers at the Institute of Biotechnology and Biomedicine (IBB) of the Universitat Autònoma de Barcelona has identified a molecule which halts and reverts this neurodegeneration. After analysing over 14,000 molecules, they found the SynuClean-D molecule, which inhibits the aggregation of the alpha-synuclein protein and breaks the already formed amyloid fibres, thus preventing the initiation of the process causing the onset of the neurodegenerative Parkinson's disease.

Through experiments conducted with the small Caenorhabditis elegans worm, one of the most commonly used animal models in neurodegenerative diseases, researchers were able to verify that by administering it through food, the molecule was capable of notably reducing alpha-synuclein aggregations, preventing the spread of toxic aggregates and therefore avoiding the degeneration of dopaminergic neurons.

"Everything seems to indicate that the molecule we identified, the SynuClean-D, may provide therapeutic applications for the treatment of neurodegenerative disases such as Parkinson's in the future," UAB researcher and coordinator of the study Salvador Ventura points out.

To identify SynuClean-D researchers developed a methodology capable of indentifying the alpha-synuclein aggregation inhibitors among thousands of molecules. Once identified, an in vitro biophysical characterisation was conducted of their inhibiting activity and tests were run to discover their behaviour with human neural cell cultures, before testing it in animal models of the disease (the Caenorhabditis elegans worm). These animals express the alpha-synuclein in the muscle or in dopaminergic neurons. The experiments demonstrated that the administration of the identified inhibitor reduced protein aggregation, improving the mobility of the animal and protecting it from neural degeneration.


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Materials provided by Universitat Autonoma de Barcelona. Note: Content may be edited for style and length.


Journal Reference:

  1. Jordi Pujols, Samuel Peña-Díaz, Diana F. Lázaro, Francesca Peccati, Francisca Pinheiro, Danilo González, Anita Carija, Susanna Navarro, María Conde-Giménez, Jesús García, Salvador Guardiola, Ernest Giralt, Xavier Salvatella, Javier Sancho, Mariona Sodupe, Tiago Fleming Outeiro, Esther Dalfó, Salvador Ventura. Small molecule inhibits α-synuclein aggregation, disrupts amyloid fibrils, and prevents degeneration of dopaminergic neurons. Proceedings of the National Academy of Sciences, 2018; 201804198 DOI: 10.1073/pnas.1804198115

Cite This Page:

Universitat Autonoma de Barcelona. "Molecule capable of halting and reverting Parkinson's neurodegeneration identified." ScienceDaily. ScienceDaily, 25 September 2018. <www.sciencedaily.com/releases/2018/09/180925110028.htm>.
Universitat Autonoma de Barcelona. (2018, September 25). Molecule capable of halting and reverting Parkinson's neurodegeneration identified. ScienceDaily. Retrieved April 25, 2024 from www.sciencedaily.com/releases/2018/09/180925110028.htm
Universitat Autonoma de Barcelona. "Molecule capable of halting and reverting Parkinson's neurodegeneration identified." ScienceDaily. www.sciencedaily.com/releases/2018/09/180925110028.htm (accessed April 25, 2024).

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