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1.
Phytochem Anal ; 30(1): 89-94, 2019 Jan.
Article in English | MEDLINE | ID: mdl-30216583

ABSTRACT

INTRODUCTION: L-Dopa, a key neurotransmitter used to treat neural disorders such as Parkinson's disease, is found in the seeds of the genus Mucuna at a sufficient concentration for possible commercial use. OBJECTIVE: To develop a simple and reliable method to extract L-Dopa from M. pruriens seeds in an aqueous medium and then quantitate this compound using a 1 H qNMR method (internal standard); and also to evaluate the accuracy and reproducibility of this method with an NMR calibration curve. METHODOLOGY: The extraction method of L-Dopa from M. pruriens was optimized. The quantitation with single point quantitative NMR (qNMR) and NMR calibration curve was based on the resonance properties of the main functional groups of the L-Dopa molecule, in particular the signals of the three aromatic protons, which were compared with the signal of an internal standard such as syringic acid. The accuracy (precision and trueness) and reproducibility of both NMR techniques were evaluated. RESULTS: The methods of single point qNMR and NMR calibration curve, applied to the seeds of two M. pruriens varieties, gave very similar L-Dopa contents: 3.0-3.2% and 3.0-3.1%, respectively. CONCLUSION: The statistical analysis confirmed the accuracy and reproducibility of this single point qNMR method (internal standard) for determining L-Dopa, as well as other commercial preparations of this species, without performing an NMR calibration curve.


Subject(s)
Levodopa/analysis , Mucuna/embryology , Proton Magnetic Resonance Spectroscopy/methods , Seeds/chemistry , Gallic Acid/analogs & derivatives , Gallic Acid/chemistry , Gallic Acid/standards , Levodopa/isolation & purification , Mucuna/classification , Reference Standards , Species Specificity , Water
3.
Science ; 304(5674): 1158-60, 2004 May 21.
Article in English | MEDLINE | ID: mdl-15087508

ABSTRACT

Parkinson's disease (PD) is a neurodegenerative disorder characterized by degeneration of dopaminergic neurons in the substantia nigra. We previously mapped a locus for a rare familial form of PD to chromosome 1p36 (PARK6). Here we show that mutations in PINK1 (PTEN-induced kinase 1) are associated with PARK6. We have identified two homozygous mutations affecting the PINK1 kinase domain in three consanguineous PARK6 families: a truncating nonsense mutation and a missense mutation at a highly conserved amino acid. Cell culture studies suggest that PINK1 is mitochondrially located and may exert a protective effect on the cell that is abrogated by the mutations, resulting in increased susceptibility to cellular stress. These data provide a direct molecular link between mitochondria and the pathogenesis of PD.


Subject(s)
Mitochondria/metabolism , Mutation , Parkinson Disease/genetics , Protein Kinases/genetics , Protein Kinases/metabolism , Amino Acid Sequence , Animals , Apoptosis , COS Cells , Cell Line, Tumor , Codon, Nonsense , Exons , Humans , Leupeptins/pharmacology , Membrane Potentials , Mitochondria/enzymology , Molecular Sequence Data , Mutation, Missense , Neurons/metabolism , Neurons/physiology , Oxidative Stress , Parkinson Disease/enzymology , Parkinson Disease/metabolism , Protein Kinases/chemistry , Protein Structure, Tertiary , Transfection
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