News from DCEXS-UPF
A study conducted in animals shows that epigallocatechin-3-gallate may improve cardiac and cognitive problems related to Williams-Beuren syndrome. Williams-Beuren syndrome (WBS) is a rare disease with an incidence of approximately 1 in 10,000 that involves a series of brain and heart disorders. Cardiovascular complications account for the most serious health problems for sufferers who in addition present cognitive disorders. The molecular cause is the deletion of 26 to 28 genes in the 7q11.23 chromosomal region.
In previous studies, epigallocatechin-3-gallate (EGCG), the most abundant catechin in green tea, has been associated with possible benefits in different cardiovascular and cognitive diseases. Based on these results, the scientists investigated the effects of EGCG in WBS animal models. The team led by the researcher Victoria Campuzano of the Genetics Unit at UPF, of the Biomedical Research Networking Centre on Rare Diseases (CIBERER) and of the Mar Medical Research Institute (IMIM) shows now that EGCG may improve cardiac hypertrophy and some cognitive alterations in animal models of Williams-Beuren syndrome.
“We use a mouse model that mimics the most common deletion found in patients with WBS and presents most of the neurological features of the disorder along with some cardiovascular manifestations that lead to cardiac hypertrophy”, Victoria Campuzano explains. “EGCG is a natural compound that acts by stimulating the Nrf2 pathway, and we manage to increase the expression of the organism’s endogenous antioxidants”, says Paula Ortiz-Romero, first author of the paper and a doctoral student at DCEXS-UPF.
“Altogether, our results suggest that EGCG may have a therapeutic effect and/or play a preventive role for WBS, which encourages us to continue with our research”, Victoria Campuzano concludes.
Ortiz-Romero P, Borralleras C, Bosch-Morató M, Guivernau B, Albericio G, Muñoz F, Pérez-Jurado LA, Campuzano V. Epigallocatechin-3-gallate improves cardiac hypertrophy and short-term memory deficits in a Williams-Beuren syndrome mouse model. PLOS ONE, March 2018.