Artículo

Progesterone Neuroprotection in traumatic CNS injury and motoneuron degeneration

de Nicola, Alejandro Federico Icon; Labombarda, Maria Florencia Icon; Gonzalez Deniselle, Maria Claudia Icon; Gonzalez, Susana Laura Icon; Garay, Laura Ines Icon; Meyer, Maria Icon; Gargiulo Monachelli, Gisella Mariana Icon; Guennoun, Rachida ; Schummacher, Michale

Otros responsables

Fecha

2009

Editorial

Elsevier

Revista

Frontiers In Neuroendocrinology

Título del libro

Nombre del evento

Fecha del evento

Institución organizadora

ISSN

0091-3022

eISSN

1090-2430

ISBN

Idioma

Inglés

Tipo del evento

Resumen

Studies on the neuroprotective and promyelinating effects of progesterone in the nervous system are of great interest due to their potential clinical connotations. In peripheral neuropathies, progesterone and reduced derivatives promote remyelination, axonal regeneration and the recovery of function. In traumatic brain injury (TBI), progesterone has the ability to reduce edema and inflammatory cytokines, prevent neuronal loss and improve functional outcomes. Clinical trials have shown that short-and long-term progesterone treatment induces a significant improvement in the level of disability among patients with brain injury. In experimental spinal cord injury (SCI), molecular markers of functional motoneurons become impaired, including brain-derived neurotrophic factor (BDNF) mRNA, Na,K-ATPase mRNA, microtubule- associated protein 2 and choline acetyltransferase (ChAT). SCI also produces motoneuron chromatolysis. Progesterone treatment restores the expression of these molecules while chromatolysis subsided. SCI also causes oligodendrocyte loss and demyelination. In this case, a short progesterone treatment enhances proliferation and differentiation of oligodendrocyte progenitors into mature myelin-producing cells, whereas prolonged treatment increases a transcription factor (Olig1) needed to repair injuryinduced demyelination. Progesterone neuroprotection has also been shown in motoneuron  neurodegeneration. In Wobbler mice spinal cord, progesterone reverses the impaired expression of BDNF, ChAT and Na,K-ATPase, prevents vacuolar motoneuron degeneration and the development of mitochondrial abnormalities, while functionally increases muscle strength and the survival of Wobbler mice. Multiple mechanisms contribute to these progesterone effects, and the role played by classical nuclear receptors, extra nuclear receptors, membrane receptors, and the reduced metabolites of progesterone in neuroprotection and myelin formation remain an exciting field worth of exploration.

Colecciones

Aprobación

Revisión

Complementado por

Referenciado por

Licencia Creative Commons

Excepto donde se indique lo contrario, la licencia de este ítem se describe como by-nc-sa