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dc.contributor.author
Gonzalez, Susana Laura  
dc.date.available
2021-10-03T01:29:48Z  
dc.date.issued
2020-04  
dc.identifier.citation
Gonzalez, Susana Laura; Progesterone for the treatment of central nervous system disorders: the many signaling roads for a single molecule; Chinese Association of Rehabilitation Medicine; Neural Regeneration Research; 15; 10; 4-2020; 1846-1847  
dc.identifier.issn
1673-5374  
dc.identifier.uri
http://hdl.handle.net/11336/142382  
dc.description.abstract
Central nervous system (CNS) injuries and neurodegenerative diseases show a broad spectrum of common pathophysiological processes, including oxidative stress, neuroinflammation, excitotoxicity, demyelination and neurotransmission dysfunctions. Over the past decades, valuable experimental investigations have helped to clarify the role and timing of these multiple molecular and cellular mechanisms in each of these particular disorders, which usually overlap and critically contribute to long-term disability. However, up to now, no definite cures or effective disease-modifying therapies are available for any of these conditions. This has led to an active search of novel therapeutic approaches, including the repositioning of existing drugs for new indications, as a valid approach to promptly move candidate molecules to clinical trials. Progesterone, a steroid with a crucial role in the reproductive function in mammals, stands as one of these promising repositioning molecules to modulate the complex array of cellular and molecular events observed in several of these central nervous system diseases (Stein and Sayeed, 2019). Indeed, a great number of preclinical studies have provided solid basis for supporting a protective effect of progesterone in stroke, traumatic brain injury, spinal cord trauma, central and peripheral neuropathies, multiple sclerosis, and Alzheimer’s and Parkinson’s disease (González et al., 2019, 2020). Notwithstanding this remarkable number of studies exploring the beneficial effects of progesterone in CNS disorders, few of them offer a deeper look at the different receptors and complex signaling cascades involved. This perspective aims at expanding our view on the variety of receptors and signaling pathways that might be involved in progesterone-mediated actions in the nervous system as part of a rational strategy to promote a successful translation of steroid-based therapies for the treatment of neurological diseases.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Chinese Association of Rehabilitation Medicine  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
PROGESTERONE  
dc.subject
PROGESTERONE RECEPTORS  
dc.subject
NEUROLOGICAL DISEASES  
dc.subject
STEROID-BASED THERAPIES  
dc.subject
SIGNALING PATHWAYS  
dc.subject.classification
Neurociencias  
dc.subject.classification
Medicina Básica  
dc.subject.classification
CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Progesterone for the treatment of central nervous system disorders: the many signaling roads for a single molecule  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2021-09-20T14:35:51Z  
dc.identifier.eissn
1876-7958  
dc.journal.volume
15  
dc.journal.number
10  
dc.journal.pagination
1846-1847  
dc.journal.pais
China  
dc.description.fil
Fil: Gonzalez, Susana Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Bioquímica Humana; Argentina  
dc.journal.title
Neural Regeneration Research  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.nrronline.org/article.asp?issn=1673-5374;year=2020;volume=15;issue=10;spage=1846;epage=1847;aulast=Gonzalez  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.4103/1673-5374.280314