Literature DB >> 18267255

Mechanisms of neurodegeneration in idiopathic Parkinson's disease.

Jörg B Schulz1.   

Abstract

The discovery of mutations in hereditary forms of Parkinson's disease has implicated aggregation of a-synuclein, dysfunction of protein turnover and mitochondrial dysfunction as important mediators in the pathogenesis of Parkinson's disease. Subsequent studies have shown that these factors also represent hallmarks of idiopathic Parkinson's disease. Cell death mechanisms include excitotoxicity, calcium overload, apoptosis and autophagia. Here, I will briefly review the molecular mechanisms of neurodegeneration in Parkinson's disease and point out potential treatment options.

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Year:  2007        PMID: 18267255     DOI: 10.1016/S1353-8020(08)70021-X

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN: 1353-8020            Impact factor:   4.891


  20 in total

1.  Hyperexcitable substantia nigra dopamine neurons in PINK1- and HtrA2/Omi-deficient mice.

Authors:  Matthew W Bishop; Subhojit Chakraborty; Gillian A C Matthews; Antonios Dougalis; Nicholas W Wood; Richard Festenstein; Mark A Ungless
Journal:  J Neurophysiol       Date:  2010-10-06       Impact factor: 2.714

Review 2.  Protein misfolding and retinal degeneration.

Authors:  Radouil Tzekov; Linda Stein; Shalesh Kaushal
Journal:  Cold Spring Harb Perspect Biol       Date:  2011-11-01       Impact factor: 10.005

3.  Early involvement of lysosome dysfunction in the degeneration of cerebral cortical neurons caused by the lipid peroxidation product 4-hydroxynonenal.

Authors:  Shi Zhang; Erez Eitan; Mark P Mattson
Journal:  J Neurochem       Date:  2017-02-16       Impact factor: 5.372

Review 4.  Therapeutic potential of targeting group III metabotropic glutamate receptors in the treatment of Parkinson's disease.

Authors:  Susan Duty
Journal:  Br J Pharmacol       Date:  2010-09       Impact factor: 8.739

5.  Parkinson's disease: is it a toxic syndrome?

Authors:  Seham A Gad Elhak; Abdel Aziz A Ghanem; Hassan Abdelghaffar; Sahar El Dakroury; Mohamed M Salama
Journal:  Neurol Res Int       Date:  2010-09-05

6.  Axonopathy in an α-synuclein transgenic model of Lewy body disease is associated with extensive accumulation of C-terminal-truncated α-synuclein.

Authors:  Dora Games; Peter Seubert; Edward Rockenstein; Christina Patrick; Margarita Trejo; Kiren Ubhi; Benjamin Ettle; Majid Ghassemiam; Robin Barbour; Dale Schenk; Silke Nuber; Eliezer Masliah
Journal:  Am J Pathol       Date:  2013-01-09       Impact factor: 4.307

7.  Septin 4, the drosophila ortholog of human CDCrel-1, accumulates in parkin mutant brains and is functionally related to the Nedd4 E3 ubiquitin ligase.

Authors:  Verónica Muñoz-Soriano; Rocío Nieto-Arellano; Nuria Paricio
Journal:  J Mol Neurosci       Date:  2012-05-06       Impact factor: 3.444

8.  Acidic Ca2+ stores in neurodegeneration.

Authors:  Emyr Lloyd-Evans
Journal:  Messenger (Los Angel)       Date:  2016-06-01

9.  Pathogenic mutation in VPS35 impairs its protection against MPP(+) cytotoxicity.

Authors:  Fangfang Bi; Fang Li; Cao Huang; Hongxia Zhou
Journal:  Int J Biol Sci       Date:  2013-01-26       Impact factor: 6.580

10.  Drosophila models of Parkinson's disease: discovering relevant pathways and novel therapeutic strategies.

Authors:  Verónica Muñoz-Soriano; Nuria Paricio
Journal:  Parkinsons Dis       Date:  2011-03-03
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