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Mass spectrometry imaging reveals brain-region specific changes in metabolism and acetylcholine levels in experimental Parkinson’s disease and L-DOPA-induced dyskinesia

Fridjonsdottir, Elva (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Medical mass spectrometry imaging
Vallianatou, Theodosia (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
Aerts, Jordan T. (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Medical mass spectrometry imaging
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Mantas, Ioannis (author)
Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden
Nilsson, Anna (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Science for Life Laboratory, SciLifeLab,Medical mass spectrometry imaging
Shariatgorji, Mohammadreza (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Science for Life Laboratory, SciLifeLab,Medical mass spectrometry imaging
Jansson, Erik T. (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Medical mass spectrometry imaging
Svenningsson, Per (author)
Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden
Bezard, Erwan (author)
Université de Bordeaux, Institut des Maladies Neurodégénératives, Bordeaux, France.; CNRS, Institut des Maladies Neurodégénératives, Bordeaux, France.; Motac Neuroscience, Manchester, M15 6WE, United Kingdom.
Andrén, Per E., Professor, 1957- (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Science for Life Laboratory, SciLifeLab
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 (creator_code:org_t)
English.
  • Other publication (other academic/artistic)
Abstract Subject headings
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  • There is evidence that cholinergic alterations are linked to various motor and non-motor symptoms of Parkinson’s disease. We therefore used mass spectrometry imaging to investigate regional changes in acetylcholine abundance in the brain of a non-human primate model of Parkinson’s disease (PD) and L-DOPA-induced dyskinesia (LID). We also present an experimental design for performing untargeted analysis using MALDI-MSI with multiple experiments incorporating quality control samples to monitor experimental variability. We observed that MPTP treatment (i) led to reductions in putaminal acetylcholine levels that persisted after L-DOPA treatment and (ii) appeared to induce a shift of choline metabolism from α-glycerophosphocholine towards betaine. LID animals exhibited reduced levels of various metabolites important for brain homeostasis including S-adenosylmethionine, glutathione, adenosine monophosphate, and acylcarnitines. The vasculature marker heme B was upregulated in the putamen of LID animals, suggesting increased blood-flow in the dyskinetic putamen. These results provide new insights into pathological choline-related metabolic changes in PD and LID.  

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

Acetylcholine
Parkinson's disease
L-DOPA-induced dyskinesia
MALDI
Mass spectrometry imaging
Farmaceutisk vetenskap
Pharmaceutical Science

Publication and Content Type

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