NMR metabolomics of fibroblasts with inherited mitochondrial Complex I mutation reveals treatment-reversible lipid and amino acid metabolism alterations-Reference-Cited by-同舟云学术

NMR metabolomics of fibroblasts with inherited mitochondrial Complex I mutation reveals treatment-reversible lipid and amino acid metabolism alterations

Published:2018-03-22 Issue:5 Volume:14 Page:
ISSN:1573-3882
Container-title:Metabolomics
language:en
Short-container-title:Metabolomics

Author:

Morvan Daniel^ORCID,Demidem Aicha

Publisher

Springer Science and Business Media LLC

Subject

Clinical Biochemistry,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://link.springer.com/article/10.1007/s11306-018-1345-9/fulltext.html

Reference25 articles.

1. Angebault, C., Gueguen, N., Desquiret-Dumas, V., Chevrollier, A., Guillet, V., Verny, C., et al. (2011). Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respiration. BMC Research Notes, 4, 557. https://doi.org/10.1186/1756-0500-4-557 .

2. Bayet-Robert, M., Loiseau, D., Rio, P., Demidem, A., Barthomeuf, C., Stepien, G., & Morvan, D. (2010). Quantitative two-dimensional HRMAS 1H-NMR spectroscopy-based metabolite profiling of human cancer cell lines and response to chemotherapy. Magnetic Resonance in Medicine, 63(5), 1172–1183. https://doi.org/10.1002/mrm.22303 .

3. Baykal, A. T., Jain, M. R., & Li, H. (2008). Aberrant regulation of choline metabolism by mitochondrial electron transport system inhibition in neuroblastoma cells. Metabolomics, 4(4), 347–356. https://doi.org/10.1007/s11306-008-0125-3 .

4. Bellaver, B., Bobermin, L. D., Souza, D. G., Rodrigues, M. D. N., de Assis, A. M., Wajner, M., et al. (2016). Signaling mechanisms underlying the glioprotective effects of resveratrol against mitochondrial dysfunction. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1862(9), 1827–1838. https://doi.org/10.1016/j.bbadis.2016.06.018 .

5. Beretta, S., Mattavelli, L., Sala, G., Tremolizzo, L., Schapira, A. H. V., Martinuzzi, A., et al. (2004). Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell lines. Brain: A Journal of Neurology, 127(Pt 10), 2183–2192. https://doi.org/10.1093/brain/awh258 .

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