Literature DB >> 16806180

Wld(S) mice are protected against the Parkinsonian mimetic MPTP.

Daphne M Hasbani1, Karen L O'Malley.   

Abstract

The progressive loss of the nigrostriatal pathway is a distinguishing feature of Parkinson's disease. Because terminal field loss appears to precede cell body loss, we tested whether the mouse mutant Wld(S), which delays axonal degeneration in a variety of disorders, would ameliorate nigrostriatal degeneration following treatment with the Parkinsonian mimetic 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). The present findings show that the Wld(S) gene product enhances survival, prevents nigrostriatal axon degeneration, and attenuates neurotransmitter loss but does not rescue cell bodies. As MPTP is thought to impair mitochondrial energy production, these data suggest that disease pathology due to metabolic dysfunction could be improved by the Wld(S) gene product. These results suggest new therapeutic avenues for Parkinson's disease.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16806180     DOI: 10.1016/j.expneurol.2006.05.017

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  39 in total

Review 1.  Axon degeneration in Parkinson's disease.

Authors:  Robert E Burke; Karen O'Malley
Journal:  Exp Neurol       Date:  2012-01-18       Impact factor: 5.330

Review 2.  Wallerian degeneration, wld(s), and nmnat.

Authors:  Michael P Coleman; Marc R Freeman
Journal:  Annu Rev Neurosci       Date:  2010       Impact factor: 12.449

Review 3.  Axon Self-Destruction: New Links among SARM1, MAPKs, and NAD+ Metabolism.

Authors:  Josiah Gerdts; Daniel W Summers; Jeffrey Milbrandt; Aaron DiAntonio
Journal:  Neuron       Date:  2016-02-03       Impact factor: 17.173

Review 4.  Emergence of SARM1 as a Potential Therapeutic Target for Wallerian-type Diseases.

Authors:  Heather S Loring; Paul R Thompson
Journal:  Cell Chem Biol       Date:  2019-11-21       Impact factor: 8.116

5.  The parkinsonian mimetic, MPP+, specifically impairs mitochondrial transport in dopamine axons.

Authors:  Jeong Sook Kim-Han; Jo Ann Antenor-Dorsey; Karen L O'Malley
Journal:  J Neurosci       Date:  2011-05-11       Impact factor: 6.167

Review 6.  Wld(S), Nmnats and axon degeneration--progress in the past two decades.

Authors:  Yan Feng; Tingting Yan; Zhigang He; Qiwei Zhai
Journal:  Protein Cell       Date:  2010-02-23       Impact factor: 14.870

7.  Synaptic protection in the brain of WldS mice occurs independently of age but is sensitive to gene-dose.

Authors:  Ann K Wright; Thomas M Wishart; Cali A Ingham; Thomas H Gillingwater
Journal:  PLoS One       Date:  2010-11-29       Impact factor: 3.240

8.  The Wallerian degeneration slow (Wld(s)) gene does not attenuate disease in a mouse model of spinal muscular atrophy.

Authors:  Ferrill F Rose; Philip W Meehan; Tristan H Coady; Virginia B Garcia; Michael L Garcia; Christian L Lorson
Journal:  Biochem Biophys Res Commun       Date:  2008-08-03       Impact factor: 3.575

9.  Maintaining energy homeostasis is an essential component of Wld(S)-mediated axon protection.

Authors:  Hua Shen; Krzysztof L Hyrc; Mark P Goldberg
Journal:  Neurobiol Dis       Date:  2013-07-24       Impact factor: 5.996

10.  Expression of the neuroprotective slow Wallerian degeneration (WldS) gene in non-neuronal tissues.

Authors:  Thomas M Wishart; David G Brownstein; Derek Thomson; Anca M Tabakova; Katherine M Boothe; Jack W Tsao; Thomas H Gillingwater
Journal:  BMC Neurosci       Date:  2009-12-16       Impact factor: 3.288

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.