| Grant number: | 15/25595-2 |
| Support Opportunities: | Scholarships in Brazil - Master |
| Start date: | March 01, 2016 |
| End date: | February 28, 2018 |
| Field of knowledge: | Health Sciences - Medicine - Psychiatry |
| Principal Investigator: | Tatiana Rosado Rosenstock |
| Grantee: | Luiz Felipe Souza e Silva |
| Host Institution: | Faculdade de Ciências Médicas da Santa Casa de São Paulo (FCMSCSP). São Paulo , SP, Brazil |
Abstract The goal of this project is to investigate the role of sirtuins (SIRTs), specifically sirtuin 1, nuclear, and 3, mitochondrial, in mitochondrial dysfunction due to hypoxia in different animal and cellular models of Schizophrenia (SHZ): astrocytes exposed to CoCl2 and from spontaneous hypertensive rats, SHR. The significant value of this project is the fact that it is known that one of the main reasons leading to SHZ is fetal hypoxia; hypoxia is nominated as diminish in body flow oxygenation, or part of it, due to a decrease in oxygen tension. Namely mitochondria, which are close related to cellular metabolism and consume between 85 to 90% of O2 to ATP production, react to hypoxia changing its metabolism and dynamics. In fact, mitochondria are organelles able to modify constantly their shape and size, to mix their metabolites, as well as mitochondrial DNA copies (DNAmt) in an attempt to adapt to the energy demand. Therefore, the unbalance between all these processes, as occur during hypoxia, can affect negatively mitochondrial function and cellular proliferation, migration and differentiation, in addition to the formation of new synapses and neural viability. However, the relation between hypoxia versus SHZ is not clear yet. Recently, the theory that genetic and/or epigenetic modifications prejudice the prevalence and/or settle an augmentation of sensibility to external factor to SHZ, as hypoxia, is becoming the center of attention. Hence, the modulation of sirtuins, a lysine deacetylase which regulates transcription factor and proteins related to energy metabolism, would be a new therapeutic strategy against SHZ. (AU) | |
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