dc.creatorPerez Lloret, Santiago
dc.creatorCardinali, Daniel Pedro
dc.date.accessioned2022-08-12T11:08:23Z
dc.date.accessioned2022-10-15T03:58:47Z
dc.date.available2022-08-12T11:08:23Z
dc.date.available2022-10-15T03:58:47Z
dc.date.created2022-08-12T11:08:23Z
dc.date.issued2021-04
dc.identifierPerez Lloret, Santiago; Cardinali, Daniel Pedro; Melatonin as a Chronobiotic and Cytoprotective Agent in Parkinson's Disease; Frontiers Media; Frontiers in Pharmacology; 12; 4-2021; 1-16
dc.identifier1663-9812
dc.identifierhttp://hdl.handle.net/11336/165321
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4342916
dc.description.abstractThis article discusses the role that melatonin may have in the prevention and treatment of Parkinson’s disease (PD). In parkinsonian patients circulating melatonin levels are consistently disrupted and the potential therapeutic value of melatonin on sleep disorders in PD was examined in a limited number of clinical studies using 2–5 mg/day melatonin at bedtime. The low levels of melatonin MT1 and MT2 receptor density in substantia nigra and amygdala found in PD patients supported the hypothesis that the altered sleep/wake cycle seen in PD could be due to a disrupted melatonergic system. Motor symptomatology is seen in PD patients when about 75% of the dopaminergic cells in the substantia nigra pars compacta region degenerate. Nevertheless, symptoms like rapid eye movement (REM) sleep behavior disorder (RBD), hyposmia or depression may precede the onset of motor symptoms in PD for years and are index of worse prognosis. Indeed, RBD patients may evolve to an α-synucleinopathy within 10 years of RBD onset. Daily bedtime administration of 3–12 mg of melatonin has been demonstrated effective in RDB treatment and may halt neurodegeneration to PD. In studies on animal models of PD melatonin was effective to curtail symptomatology in doses that allometrically projected to humans were in the 40–100 mg/day range, rarely employed clinically. Therefore, double-blind, placebo-controlled clinical studies are urgently needed in this respect.
dc.languageeng
dc.publisherFrontiers Media
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.3389/fphar.2021.650597
dc.rightshttps://creativecommons.org/licenses/by/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAGING
dc.subjectGLYMPHATIC SYSTEM
dc.subjectMELATONIN
dc.subjectNEURODEGENERATION
dc.subjectOXIDATIVE STRESS
dc.subjectPARKINSON’S DISEASE
dc.subjectSLEEP
dc.titleMelatonin as a Chronobiotic and Cytoprotective Agent in Parkinson's Disease
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


Este ítem pertenece a la siguiente institución