Brain aging and Parkinson's disease: New therapeutic approaches using drug delivery systems. (February 2016)
- Record Type:
- Journal Article
- Title:
- Brain aging and Parkinson's disease: New therapeutic approaches using drug delivery systems. (February 2016)
- Main Title:
- Brain aging and Parkinson's disease: New therapeutic approaches using drug delivery systems
- Authors:
- Rodríguez-Nogales, C.
Garbayo, E.
Carmona-Abellán, M.M.
Luquin, M.R.
Blanco-Prieto, M.J. - Abstract:
- Highlights: The etiology of Parkinson's disease (PD) is unknown, aging being the strongest risk factor for brain degeneration. The most promising therapeutic targets and strategies to delay the loss of dopaminergic neurons observed both in PD and aging are reviewed. The latest types of drug delivery system (DDS)-based strategies for PD treatment are summarized. The ongoing challenges for the discovery of new targets and the opportunities for DDS-based therapies discussed. The emerging strategies summarized in the review show promise for better therapies for PD. Abstract: The etiology and pathogenesis of Parkinson's disease (PD) is unknown, aging being the strongest risk factor for brain degeneration. Understanding PD pathogenesis and how aging increases the risk of disease would aid the development of therapies able to slow or prevent the progression of this neurodegenerative disorder. In this review we provide an overview of the most promising therapeutic targets and strategies to delay the loss of dopaminergic neurons observed both in PD and aging. Among them, handling alpha-synuclein toxicity, enhancing proteasome and lysosome clearance, ameliorating mitochondrial disruptions and modifying the glial environment are so far the most promising candidates. These new and conventional drugs may present problems related to their labile nature and to the difficulties in reaching the brain. Thus, we highlight the latest types of drug delivery system (DDS)-based strategies for PDHighlights: The etiology of Parkinson's disease (PD) is unknown, aging being the strongest risk factor for brain degeneration. The most promising therapeutic targets and strategies to delay the loss of dopaminergic neurons observed both in PD and aging are reviewed. The latest types of drug delivery system (DDS)-based strategies for PD treatment are summarized. The ongoing challenges for the discovery of new targets and the opportunities for DDS-based therapies discussed. The emerging strategies summarized in the review show promise for better therapies for PD. Abstract: The etiology and pathogenesis of Parkinson's disease (PD) is unknown, aging being the strongest risk factor for brain degeneration. Understanding PD pathogenesis and how aging increases the risk of disease would aid the development of therapies able to slow or prevent the progression of this neurodegenerative disorder. In this review we provide an overview of the most promising therapeutic targets and strategies to delay the loss of dopaminergic neurons observed both in PD and aging. Among them, handling alpha-synuclein toxicity, enhancing proteasome and lysosome clearance, ameliorating mitochondrial disruptions and modifying the glial environment are so far the most promising candidates. These new and conventional drugs may present problems related to their labile nature and to the difficulties in reaching the brain. Thus, we highlight the latest types of drug delivery system (DDS)-based strategies for PD treatment, including DDS for local and systemic drug delivery. Finally, the ongoing challenges for the discovery of new targets and the opportunities for DDS-based therapies to improve and efficacious PD therapy will be discussed. … (more)
- Is Part Of:
- Maturitas. Volume 84(2016)
- Journal:
- Maturitas
- Issue:
- Volume 84(2016)
- Issue Display:
- Volume 84, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 84
- Issue:
- 2016
- Issue Sort Value:
- 2016-0084-2016-0000
- Page Start:
- 25
- Page End:
- 31
- Publication Date:
- 2016-02
- Subjects:
- PD Parkinson's disease -- DAergic dopaminergic -- SNpc substantia nigra pars compacta -- DA dopamine -- LB lewy body -- α-syn alpha synuclein -- L-DOPA levodopa -- MAO monoamine oxidase -- CNS central nervous system -- DDS drug delivery systems -- MPs microparticles -- NPs nanoparticles -- SNCA synucleinalpha non A4 component of amyloid precursor -- PLK Polo like kinase -- LAMP lysosomal associated membrane receptor protein -- LRRK2 leucine-rich repeat kinase 2 -- MPTP 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine -- GDNF glial cell line-derived neurotrophic factor -- BBB blood–brain barrier -- VEGF vascular endothelial growth factor -- PEG polyethylen glycol -- PLGA poly(lactic-coglycolic acid)
Parkinson disease -- Aging -- Therapeutic targets -- Alpha-synuclein -- GDNF -- Drug delivery systems -- Micro/nanoparticles
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612.66 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03785122 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/03785122 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/03785122 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.maturitas.2015.11.009 ↗
- Languages:
- English
- ISSNs:
- 0378-5122
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5413.265000
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British Library HMNTS - ELD Digital store - Ingest File:
- 1922.xml