A Composition Comprising Glucoraphanin, Myrosinase and a Buffered Solution for Use in the Treatment of Neurodegenerative Diseases
Glucosinolates (GLs) are phytocompounds mainly found in the Cruciferae (Brassicacea) and Moringa oleifera plants. The hydrolysis of GLs by myrosinase led to the production of isothiocyanate (ITCs). ITCs consumption was associated with different health promoting effects, including to neuroprotective, anti-oxidant and anti-inflammatory capacities. In particular, they showed neuroprotective effects in experimental models of neurodegenerative diseases, including multiple sclerosis (MS) and Parkinson's disease (PD). From different GLs, different ITCs are originated. In particular, from glucoraphanin (GRA) the ITC sulforaphane (SFN) is obtained. The PI of the project is one of the proprietor of a patent (EP2908850B1) for the application of (Rs)-GRA with myrosinase in a buffered solution for the treatment of neurodegenerative diseases. The aim of this project is to evaluate the effects of the administration of bioactivated GRA in different cohorts of adult patients, affected by MS and PD, but also a cohort of pediatric patients affected by neuromuscolar and degenerative diseases. The effects of bioactivated (Rs)-GRA administration will be evaluated with a combination of clinical evaluations and a multiomic (metabolomic, genomic) approach.
• Male or female patients aged between 45-75 years old.
• Clinical diagnosis of PD according to UK Brain Bank Criteria.
• 3 months of clinical stability before study enrolment.
• Anti-parkinsonian medication is fixed for at least 3 months prior to study entry.
• Male or female patients 18 years old or older.
• Diagnosis of RR-MS according to McDonald criteria.
• Expanded Disability Status Scale(EDSS) lower or equal to 5.5.
• Stable disease for at least 30 days prior to study entry.
• Stable disease-modifying therapy for at least 3 months prior to study entry.
⁃ Common inclusion criteria for MS and PD:
• No changes in drug treatment during 6 months-study treatment.
• Patients understand and comply with the study procedure and are able to complete tests and examinations required by the project.
• Written informed consent.
• Eligible patients are those clinically stable;
• Age range from 1 to 10, between 5 and 30 kg.
• Patients not involved in other clinical trials.