Literature DB >> 22746536

Targeting Nrf2-mediated gene transcription by extremely potent synthetic triterpenoids attenuate dopaminergic neurotoxicity in the MPTP mouse model of Parkinson's disease.

Navneet Ammal Kaidery1, Rebecca Banerjee, Lichuan Yang, Natalya A Smirnova, Dmitry M Hushpulian, Karen T Liby, Charlotte R Williams, Masayuki Yamamoto, Thomas W Kensler, Rajiv R Ratan, Michael B Sporn, M Flint Beal, Irina G Gazaryan, Bobby Thomas.   

Abstract

UNLABELLED: Although the etiology of Parkinson's disease (PD) remains unclear, ample empirical evidence suggests that oxidative stress is a major player in the development of PD and in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) neurotoxicity. Nuclear factor E2-related factor 2 (Nrf2) is a redox-sensitive transcription factor that upregulates a battery of antioxidant response element (ARE)-driven antioxidative and cytoprotective genes that defend against oxidative stress. AIMS: We evaluated whether the strategy of activation of Nrf2 and its downstream network of cytoprotective genes with small molecule synthetic triterpenoids (TP) attenuate MPTP-induced PD in mice.
RESULTS: We show that synthetic TP are thus far the most potent and direct activators of the Nrf2 pathway using a novel Neh2-luciferase reporter. They upregulate several cytoprotective genes, including those involved in glutathione biosynthesis in vitro. Oral administration of TP that were structurally modified to penetrate the brain-induced messenger RNA and protein levels for a battery of Nrf2-dependent cytoprotective genes reduced MPTP-induced oxidative stress and inflammation, and ameliorated dopaminergic neurotoxicity in mice. The neuroprotective effect of these TP against MPTP neurotoxicity was dependent on Nrf2, since treatment with TP in Nrf2 knockout mice failed to block against MPTP neurotoxicity and induce Nrf2-dependent cytoprotective genes. INNOVATION: Extremely potent synthetic TP that are direct activators of the Nrf2 pathway block dopaminergic neurodegeneration in the MPTP mouse model of PD.
CONCLUSION: Our results indicate that activation of Nrf2/antioxidant response element (ARE) signaling by synthetic TP is directly associated with their neuroprotective effects against MPTP neurotoxicity and suggest that targeting the Nrf2/ARE pathway is a promising approach for therapeutic intervention in PD.

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Year:  2012        PMID: 22746536      PMCID: PMC3514006          DOI: 10.1089/ars.2011.4491

Source DB:  PubMed          Journal:  Antioxid Redox Signal        ISSN: 1523-0864            Impact factor:   8.401


  52 in total

1.  Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.

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2.  Identification and characterization of novel Nrf2 inducers designed to target the intervening region of Keap1.

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3.  Neuroprotective effect of Nrf2/ARE activators, CDDO ethylamide and CDDO trifluoroethylamide, in a mouse model of amyotrophic lateral sclerosis.

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8.  Activation of NRF2 by nitrosative agents and H2O2 involves KEAP1 disulfide formation.

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10.  Neuroprotective effects of the triterpenoid, CDDO methyl amide, a potent inducer of Nrf2-mediated transcription.

Authors:  Lichuan Yang; Noel Y Calingasan; Bobby Thomas; Rajnish K Chaturvedi; Mahmoud Kiaei; Elizabeth J Wille; Karen T Liby; Charlotte Williams; Darlene Royce; Renee Risingsong; Eric S Musiek; Jason D Morrow; Michael Sporn; M Flint Beal
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  65 in total

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4.  Distinct Nrf2 Signaling Mechanisms of Fumaric Acid Esters and Their Role in Neuroprotection against 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine-Induced Experimental Parkinson's-Like Disease.

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Review 5.  Antioxidant gene therapy against neuronal cell death.

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Review 6.  Current perspective of mitochondrial biology in Parkinson's disease.

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7.  Methylene blue upregulates Nrf2/ARE genes and prevents tau-related neurotoxicity.

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