Statistical Model Checking no reposionamento de fármacos na Doença de Alzheimer

• Ano de defesa: 2012
• Autor(a) principal: Herbert Rausch Fernandes
• Tipo de documento: Tese
• Tipo de acesso: Acesso aberto
• Idioma: por
• Instituição de defesa: Universidade Federal de Minas Gerais; Brasil; Programa de Pós-Graduação em Bioinformatica; UFMG
• Palavras-chave em Português: Statistical Model Checking; Doença de Alzheimer; PI3K/mTOR; Bioinformática; Reposicionamento de Medicamentos; Modelagem Computacional
• Link de acesso: http://hdl.handle.net/1843/55613

Alzheimer’s disease is the most common form of dementia characterized by the gradual loss of memory and cognition of patients. There is no drug capable of curing or preventing the disease, being the discovery of an efficient treatment for the disease is of vital importance. An approach that can contribute to this purpose of reducing time and costs of new discoveries is drug repositioning and in silico techniques. Statistical Model Checking, a formal verification technique can aid in analyzing protein and drugs interactions and test pharmacological strategies, contributing for drug discovery and repurposing. In this work, we present a stochastic formal model that allows us to test different drugs, or combination of drugs, that target the PI3K/AKT/mTOR pathway and to evaluate the effect on tau protein and amyloid-beta peptide, which are two important components that contribute to the progression of Alzheimer’s disease. We have analyzed the effect of rapamycin, LY294002, and NVP-BEZ235 on those proteins. Our results have shown that rapamycin has the potential to slow down one of the biological processes that causes neuronal death. Moreover, we have identified the ideal dose of rapamycin to obtain such results. However, our findings have unveiled that LY294002 and NVP-BEZ235 can increase tau phosphorylation in all scenarios tested. This is an indication of a possible side effect of drug candidates that inhibit PI3K and need to be investigated in in vivo models. Besides that, we have shown rapamycin has not reduced this side-effect when administered together with LY294002. The methodology proposed has been able to model both the disease and drug interactions. We have analyzed three drugs and our model is flexible to test other drugs and pharmacological strategies and efficient to analyze the properties of the model generating new insights.