Related ArticlesMetabolomic NMR studies at presymptomatic and symptomatic stages of Huntington's disease on a Drosophila model.
J Proteome Res. 2020 Sep 03;:
Authors: Bertrand M, Decoville M, Meudal H, Birman S, Landon C
Abstract
Huntington's disease (HD) is an inherited neurodegenerative disorder, for which diagnostic development and discovery of new therapeutic targets are urgently required. In this study, a model of HD in Drosophila melanogaster has been used to identify metabolic biomarkers at presymptomatic and symptomatic stages of the disease. The pan-neuronal expression of a pathogenic fragment of the human Huntingtin (HTT) protein containing a 93-repeat polyglutamine expansion (Httex1p Q93) in transgenic flies induces a neuropathology with several characteristics of the human disease. The discriminant metabolites between the diseased flies and their controls were identified by 1H-nuclear magnetic resonance (NMR) and orthogonal partial least squares discriminant multivariate analysis (OPLS-DA). The experiments carried out with 10-day-old flies allowed us to identify a set of 10 biomarkers of the presymptomatic stage: NAD+, AMP, fumarate, asparagine, dimethylamine, ?-alanine, glutamine, succinate, glutamate and ethanol. Remarkably, the experiments conducted with 16-day-old flies, when the symptoms of the disease were present, highlighted a different set of 6 biomarkers: phosphocholine, ethanolamine, 2-oxoglutarate, succinate, pyruvate and acetate. Our results provide a better understanding of the metabolic impairments in a widely used HD model and demonstrate that metabolism perturbations change dramatically during the development of the disease.
PMID: 32880177 [PubMed - as supplied by publisher]
[NMR paper] NMR spectroscopy-based metabolomics of Drosophila model of Huntington's disease suggests altered cell energetics.
NMR spectroscopy-based metabolomics of Drosophila model of Huntington's disease suggests altered cell energetics.
Related Articles NMR spectroscopy-based metabolomics of Drosophila model of Huntington's disease suggests altered cell energetics.
J Proteome Res. 2017 Sep 05;:
Authors: Singh V, Sharma RK, Athilingam T, Sinha P, Sinha N, Thakur AK
Abstract
Huntington's disease (HD) is a neurodegenerative disorder induced by aggregation of the pathological form of Huntingtin protein that has expanded polyglutamine (polyQ) repeats. In...
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[NMR paper] Quantitative Metabolomic Profiling of Plasma, Urine and Liver Extracts by 1H NMR Spectroscopy Characterizes Different Stages of Atherosclerosis in Hamsters.
Quantitative Metabolomic Profiling of Plasma, Urine and Liver Extracts by 1H NMR Spectroscopy Characterizes Different Stages of Atherosclerosis in Hamsters.
http://www.bionmr.com//www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--pubs.acs.org-images-pubmed-acspubs.jpg Related Articles Quantitative Metabolomic Profiling of Plasma, Urine and Liver Extracts by 1H NMR Spectroscopy Characterizes Different Stages of Atherosclerosis in Hamsters.
J Proteome Res. 2016 Aug 29;
Authors: Guo W, Jiang C, Yang L, Li T, Liu X, Jin M, Qu K, Chen H, Jin X, Liu H, Zhu...
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08-31-2016 02:34 PM
Scientists Observe Structure of Protein That Plays Major Role in Huntington's Disease, Opening Door to Finding Cause ... - Huntington's Disease News
Scientists Observe Structure of Protein That Plays Major Role in Huntington's Disease, Opening Door to Finding Cause ... - Huntington's Disease News
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Huntington's Disease News
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Scientists Observe Structure of Protein That Plays Major Role in Huntington's Disease, Opening Door to Finding Cause ...
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Leibniz-Institut für Molekulare Pharmakologie (FMP) researchers used a combination of nuclear magnetic...
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02-10-2016 09:28 PM
Protein Plaques in Huntington's Patients Have Distinct Structures That Hint at Disease Mechanisms - Huntington's Disease News
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Protein Plaques in Huntington's Patients Have Distinct Structures That Hint at Disease Mechanisms
Huntington's Disease News
Researchers at the University of Pittsburgh School of Medicine used advanced nuclear magnetic resonance spectroscopy to directly assess and characterize huntingtin fibrils and other polyglutamine aggregates. Results showed that, unlike what previous ...
Protein Plaques in Huntington's Patients Have Distinct Structures That Hint at Disease Mechanisms - Huntington's Disease News
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Study finding could shed light on molecular mechanisms underlying Huntington's disease - News-Medical.net
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Study finding could shed light on molecular mechanisms underlying Huntington's disease
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... the process," he said. "Using advanced nuclear magnetic resonance spectroscopy, we were able to provide an unprecedented view of the internal structure of the protein clumps that form in the disease, which we hope will one day lead to new therapies ...
Researchers Describe Brain Plaques Involved In...
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02-04-2016 11:46 AM
Structure of brain plaques in Huntington's disease described by Pitt team University of Pittsburgh Schools of the ... - EurekAlert (press release)
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Structure of brain plaques in Huntington's disease described by Pitt team University of Pittsburgh Schools of the ...
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"Using advanced nuclear magnetic resonance spectroscopy, we were able to provide an unprecedented view of the internal structure of the protein clumps that form in the disease, which we hope will one day lead to new therapies." The gene associated with ...
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Structure of brain plaques in Huntington's disease described by Pitt team University of Pittsburgh Schools of the ... - EurekAlert (press...
[NMR paper] 1H NMR metabolomic signatures in five brain regions of the A?PPswe Tg2576 mouse model of Alzheimer's disease at four ages.
1H NMR metabolomic signatures in five brain regions of the A?PPswe Tg2576 mouse model of Alzheimer's disease at four ages.
http://www.bionmr.com//www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--iospress.metapress.com-images-ios-pubmed.gif Related Articles 1H NMR metabolomic signatures in five brain regions of the A?PPswe Tg2576 mouse model of Alzheimer's disease at four ages.
J Alzheimers Dis. 2014;39(1):121-43
Authors: Lalande J, Halley H, Balayssac S, Gilard V, Déjean S, Martino R, Francés B, Lassalle JM, Malet-Martino M
Abstract
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