Evidence of calpain/cdk5 pathway inhibition by lithium in 3-nitropropionic acid toxicity in vivo and in vitro
Abstract
Lithium reduced striatal neurodegeneration induced in rats by 3-nitropropionic acid inhibiting calpain activation. Lithium prevented an increase in cdk5 activity, as shown by the levels of the co-activator p35. Myocite enhancer factor 2 (MEF2), a downstream substrate for cdk5 with pro-survival activity, showed increased phosphorylation. In primary cultures of neurons treated with 3-NP, lithium also reduced protease activity mediated by calpain, cdk5 activation and cellular death. These observations indicate that lithium has a neuroprotective effect. Lithium treatment also reduced the intracellular increase in calcium induced by 3-NP. The finding that lithium mediates the modulation of the calpain/cdk5 pathway further supports its use in the treatment of neurodegenerative diseases. (c) 2008 Elsevier Ltd. All rights reserved.
Más información
Título según WOS: | ID WOS:000263454200011 Not found in local WOS DB |
Título de la Revista: | NEUROPHARMACOLOGY |
Volumen: | 56 |
Número: | 2 |
Editorial: | PERGAMON-ELSEVIER SCIENCE LTD |
Fecha de publicación: | 2009 |
Página de inicio: | 422 |
Página final: | 428 |
DOI: |
10.1016/j.neuropharm.2008.09.012 |
Notas: | ISI |