| Grant number: | 16/06879-2 |
| Support Opportunities: | Regular Research Grants |
| Start date: | December 01, 2016 |
| End date: | November 30, 2018 |
| Field of knowledge: | Biological Sciences - Physiology - Physiology of Organs and Systems |
| Principal Investigator: | Carla Alessandra Scorza Bahi |
| Grantee: | Carla Alessandra Scorza Bahi |
| Host Institution: | Escola Paulista de Medicina (EPM). Universidade Federal de São Paulo (UNIFESP). Campus São Paulo. São Paulo , SP, Brazil |
| City of the host institution: | São Paulo |
| Associated researchers: | Antônio Carlos Guimarães de Almeida ; Ésper Abrão Cavalheiro |
Abstract
Isquemic stroke is a major cause of death in the world and a leading cause of disability. In the first month after the stroke the risk of death is about 10% reaching up to 40% in the first year. After an hypoxic-ischemic insult, a multi-faceted complex cascade of events occurs. In addition to vascular injury and neurodegeneration, which are typical hallmarks of stroke, the most conspicuous features are the marked neuroinflammatory response, marked glia cell activation and the blood-brain barrier breakdown. Furthermore, the neuronal electrical activity, which is an essential physiological attribute of the nervous tissue, is also greatly affected. In this scenario, when homeostatic events are drastically disturbed, the dysfunctional compensatory events may result in pathological maladaptive plasticity, a topic of extreme interest. In recent years, our laboratory has been studying Proechimys, a rodent from Amazon forest which exhibits huge resistance to the epileptogenic insults. Since stroke is a clinically important epileptogenic event, Proechimys rodents may be a valuable tool to investigate the impact of cortical ischemic stroke in the brain. To do so, this project was designed to evaluate the acute phase and long-term brain response of the Neotropical rodents Proechimys to ischemic stroke and to compare these findings to those found in the Wistar rats. The findings of the study may provide new research on pathophysiological mechanisms of ischemic stroke and in the search for new therapeutic targets. (AU)
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