| Grant number: | 10/17272-5 |
| Support Opportunities: | Regular Research Grants |
| Start date: | April 01, 2011 |
| End date: | March 31, 2013 |
| Field of knowledge: | Biological Sciences - Morphology - Histology |
| Principal Investigator: | Anselmo Sigari Moriscot |
| Grantee: | Anselmo Sigari Moriscot |
| Host Institution: | Instituto de Ciências Biomédicas (ICB). Universidade de São Paulo (USP). São Paulo , SP, Brazil |
| City of the host institution: | São Paulo |
Abstract
Glucorticoids, have been largely used as antinflammatory and immunosupressor agents in the control of inflammatory related disorders. Artrite, asma, vascular disease, alergies, skin diseases, transpants are among the most common conditions in which glucorticoids are systematically used. Although indubitably efficient, collateral effects emerge, significantly affecting quality of life. Therefore the development of new compounds that maximize therapeutic effects and minimize collateral effects is of obvious benefit. New compounds named L5 and L7 (glucorticoid analogs and derivate from arylpyrazole) have been developed and seem to retain potent antinflammatory effects. Since glucorticoids have a notorious effect upon skeletal muscle mass loss, the aim of the present study was to investigate the impact of such compounds in structural, functional and molecular aspects of skeletal muscle. (AU)
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