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Effects of pharmacological agents on the lifespan phenotype of Drosophila DJ-1beta mutants.
Gene. 2010 Aug 15; 462(1-2):26-33.GENE

Abstract

Mutations in the DJ-1 gene cause autosomal recessive, early-onset Parkinsonism. The DJ-1 protein exerts a protective role against oxidative stress damage, working as a cellular oxidative stress sensor, and it seems to regulate gene expression at different levels. In Drosophila, two DJ-1 orthologs have been identified: DJ-1alpha and DJ-1beta. Several studies have shown that loss of DJ-1beta function causes Parkinson's disease (PD)-like phenotypes in flies such as age-dependent locomotor defects, reduced lifespan, and enhanced sensitivity to toxins that induce oxidative stress, like the herbicide paraquat. However, no dopaminergic neurodegeneration is observed. These results suggested that both locomotor and lifespan phenotypes could be either related to defects in oxidative stress response, or in dopaminergic physiology as proposed in mice models. In this study, we have employed pharmacological approaches to modify the lifespan phenotype of DJ-1beta mutant flies. We have assessed the effects of chronic treatments with antiparkinsonian drugs as well as with antioxidant compounds on such phenotype finding that only antioxidants show statistically significant beneficial effects on DJ-1beta mutants' lifespan. These results strongly suggest that oxidative stress plays a causal role in the lifespan phenotype of DJ-1beta mutants. Consistent with this, we find that loss of DJ-1beta function results in cellular accumulation of reactive oxygen species (ROS) in adult brains, elevated levels of lipid peroxidation and an increased catalase enzymatic activity, thus indicating the existence of high oxidative stress levels in DJ-1beta mutants and confirming the essential function of the DJ-1beta protein in protecting the organism against oxidative insults. Our study further shows that the lifespan phenotype of DJ-1beta mutant flies is amenable to pharmacological intervention, and validates Drosophila as a valuable model for testing and identifying new drugs with therapeutic potential for PD.

Authors+Show Affiliations

Departamento de Genética, University of Valencia, Valencia, Spain.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

20423725

Citation

Lavara-Culebras, Eusebio, et al. "Effects of Pharmacological Agents On the Lifespan Phenotype of Drosophila DJ-1beta Mutants." Gene, vol. 462, no. 1-2, 2010, pp. 26-33.
Lavara-Culebras E, Muñoz-Soriano V, Gómez-Pastor R, et al. Effects of pharmacological agents on the lifespan phenotype of Drosophila DJ-1beta mutants. Gene. 2010;462(1-2):26-33.
Lavara-Culebras, E., Muñoz-Soriano, V., Gómez-Pastor, R., Matallana, E., & Paricio, N. (2010). Effects of pharmacological agents on the lifespan phenotype of Drosophila DJ-1beta mutants. Gene, 462(1-2), 26-33. https://doi.org/10.1016/j.gene.2010.04.009
Lavara-Culebras E, et al. Effects of Pharmacological Agents On the Lifespan Phenotype of Drosophila DJ-1beta Mutants. Gene. 2010 Aug 15;462(1-2):26-33. PubMed PMID: 20423725.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Effects of pharmacological agents on the lifespan phenotype of Drosophila DJ-1beta mutants. AU - Lavara-Culebras,Eusebio, AU - Muñoz-Soriano,Verónica, AU - Gómez-Pastor,Rocío, AU - Matallana,Emilia, AU - Paricio,Nuria, Y1 - 2010/04/24/ PY - 2009/10/28/received PY - 2010/04/15/revised PY - 2010/04/21/accepted PY - 2010/4/29/entrez PY - 2010/4/29/pubmed PY - 2010/8/5/medline SP - 26 EP - 33 JF - Gene JO - Gene VL - 462 IS - 1-2 N2 - Mutations in the DJ-1 gene cause autosomal recessive, early-onset Parkinsonism. The DJ-1 protein exerts a protective role against oxidative stress damage, working as a cellular oxidative stress sensor, and it seems to regulate gene expression at different levels. In Drosophila, two DJ-1 orthologs have been identified: DJ-1alpha and DJ-1beta. Several studies have shown that loss of DJ-1beta function causes Parkinson's disease (PD)-like phenotypes in flies such as age-dependent locomotor defects, reduced lifespan, and enhanced sensitivity to toxins that induce oxidative stress, like the herbicide paraquat. However, no dopaminergic neurodegeneration is observed. These results suggested that both locomotor and lifespan phenotypes could be either related to defects in oxidative stress response, or in dopaminergic physiology as proposed in mice models. In this study, we have employed pharmacological approaches to modify the lifespan phenotype of DJ-1beta mutant flies. We have assessed the effects of chronic treatments with antiparkinsonian drugs as well as with antioxidant compounds on such phenotype finding that only antioxidants show statistically significant beneficial effects on DJ-1beta mutants' lifespan. These results strongly suggest that oxidative stress plays a causal role in the lifespan phenotype of DJ-1beta mutants. Consistent with this, we find that loss of DJ-1beta function results in cellular accumulation of reactive oxygen species (ROS) in adult brains, elevated levels of lipid peroxidation and an increased catalase enzymatic activity, thus indicating the existence of high oxidative stress levels in DJ-1beta mutants and confirming the essential function of the DJ-1beta protein in protecting the organism against oxidative insults. Our study further shows that the lifespan phenotype of DJ-1beta mutant flies is amenable to pharmacological intervention, and validates Drosophila as a valuable model for testing and identifying new drugs with therapeutic potential for PD. SN - 1879-0038 UR - https://www.unboundmedicine.com/medline/citation/20423725/Effects_of_pharmacological_agents_on_the_lifespan_phenotype_of_Drosophila_DJ_1beta_mutants_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0378-1119(10)00170-8 DB - PRIME DP - Unbound Medicine ER -