Page last updated: 2024-10-19

inositol and Parkinson Disease

inositol has been researched along with Parkinson Disease in 15 studies

Inositol: An isomer of glucose that has traditionally been considered to be a B vitamin although it has an uncertain status as a vitamin and a deficiency syndrome has not been identified in man. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1379) Inositol phospholipids are important in signal transduction.
inositol : Any cyclohexane-1,2,3,4,5,6-hexol.
1D-chiro-inositol : Belonging to the inositol family of compounds, D-chiro-inositol (DCI) is an isomer of glucose. It is an important secondary messenger in insulin signal transduction.
muco-inositol : An inositol that is cyclohexane-1,2,3,4,5,6-hexol having a (1R,2R,3r,4R,5S,6r)-configuration.

Parkinson Disease: A progressive, degenerative neurologic disease characterized by a TREMOR that is maximal at rest, retropulsion (i.e. a tendency to fall backwards), rigidity, stooped posture, slowness of voluntary movements, and a masklike facial expression. Pathologic features include loss of melanin containing neurons in the substantia nigra and other pigmented nuclei of the brainstem. LEWY BODIES are present in the substantia nigra and locus coeruleus but may also be found in a related condition (LEWY BODY DISEASE, DIFFUSE) characterized by dementia in combination with varying degrees of parkinsonism. (Adams et al., Principles of Neurology, 6th ed, p1059, pp1067-75)

Research Excerpts

ExcerptRelevanceReference
"myo-Inositol was raised by about 15%, again uniformly throughout the brain, but there was no evidence for changed levels of choline."2.41A comprehensive review of proton magnetic resonance spectroscopy studies in dementia and Parkinson's disease. ( Firbank, MJ; Harrison, RM; O'Brien, JT, 2002)
"Although no difference was found between groups with RBD and IPD without dream enactment behavior in demographic characteristics, duration of disease, mean levodopa dosage and duration of levodopa use, all UPDRS scores (total, motor and cognitive) were worse in RBD group (p<0."1.33Brainstem 1H-MR spectroscopy in patients with Parkinson's disease with REM sleep behavior disorder and IPD patients without dream enactment behavior. ( Dincer, A; Hanoglu, L; Meral, H; Ozer, F, 2006)

Research

Studies (15)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (26.67)29.6817
2010's9 (60.00)24.3611
2020's2 (13.33)2.80

Authors

AuthorsStudies
Ruz, C1
Alcantud, JL1
Vives, F1
Arrebola, F1
Hardy, J1
Lewis, PA1
Manzoni, C1
Duran, R1
Cengiz, S1
Arslan, DB1
Kicik, A1
Erdogdu, E1
Yildirim, M1
Hatay, GH1
Tufekcioglu, Z1
Uluğ, AM1
Bilgic, B1
Hanagasi, H1
Demiralp, T1
Gurvit, H1
Ozturk-Isik, E1
Ren, X1
Hinchie, A1
Swomley, A1
Powell, DK1
Butterfield, DA1
Waragai, M1
Moriya, M1
Nojo, T1
Papadopoulos, VE1
Nikolopoulou, G1
Antoniadou, I1
Karachaliou, A1
Arianoglou, G1
Emmanouilidou, E1
Sardi, SP1
Stefanis, L2
Vekrellis, K1
Kuo, CL1
Kallemeijn, WW1
Lelieveld, LT1
Mirzaian, M1
Zoutendijk, I1
Vardi, A1
Futerman, AH1
Meijer, AH1
Spaink, HP1
Overkleeft, HS1
Aerts, JMFG1
Artola, M1
Dermentzaki, G1
Dimitriou, E1
Xilouri, M1
Michelakakis, H1
Ginns, EI1
Mak, SK1
Ko, N1
Karlgren, J1
Akbarian, S1
Chou, VP1
Guo, Y1
Lim, A1
Samuelsson, S1
LaMarca, ML1
Vazquez-DeRose, J1
Manning-Boğ, AB1
Adams, BT1
Niccoli, S1
Chowdhury, MA1
Esarik, AN1
Lees, SJ1
Rempel, BP1
Phenix, CP1
Almuqbel, M1
Melzer, TR1
Myall, DJ1
MacAskill, MR1
Pitcher, TL1
Livingston, L1
Wood, KL1
Keenan, RJ1
Dalrymple-Alford, JC1
Anderson, TJ1
Yap, TL1
Gruschus, JM1
Velayati, A1
Westbroek, W1
Goldin, E1
Moaven, N1
Sidransky, E1
Lee, JC1
Firbank, MJ1
Harrison, RM1
O'Brien, JT1
Hanoglu, L1
Ozer, F1
Meral, H1
Dincer, A1
Prestel, J1
Gempel, K1
Hauser, TK1
Schweitzer, K1
Prokisch, H1
Ahting, U1
Freudenstein, D1
Bueltmann, E1
Naegele, T1
Berg, D1
Klopstock, T1
Gasser, T1
Lucetti, C1
Del Dotto, P1
Gambaccini, G1
Bernardini, S1
Bianchi, MC1
Tosetti, M1
Bonuccelli, U1

Reviews

1 review available for inositol and Parkinson Disease

ArticleYear
A comprehensive review of proton magnetic resonance spectroscopy studies in dementia and Parkinson's disease.
    Dementia and geriatric cognitive disorders, 2002, Volume: 14, Issue:2

    Topics: Alzheimer Disease; Aspartic Acid; Brain; Choline; Humans; Inositol; Magnetic Resonance Spectroscopy;

2002

Other Studies

14 other studies available for inositol and Parkinson Disease

ArticleYear
Seventy-Two-Hour LRRK2 Kinase Activity Inhibition Increases Lysosomal GBA Expression in H4, a Human Neuroglioma Cell Line.
    International journal of molecular sciences, 2022, Jun-22, Volume: 23, Issue:13

    Topics: Cell Line; Cell Line, Tumor; Enzyme Inhibitors; Glioma; Glucosylceramidase; Humans; Inositol; Leucin

2022
Identification of metabolic correlates of mild cognitive impairment in Parkinson's disease using magnetic resonance spectroscopic imaging and machine learning.
    Magma (New York, N.Y.), 2022, Volume: 35, Issue:6

    Topics: Cognitive Dysfunction; Creatine; Humans; Inositol; Machine Learning; Magnetic Resonance Imaging; Mag

2022
Profiles of brain oxidative damage, ventricular alterations, and neurochemical metabolites in the striatum of PINK1 knockout rats as functions of age and gender: Relevance to Parkinson disease.
    Free radical biology & medicine, 2019, 11-01, Volume: 143

    Topics: Animals; Aspartic Acid; Biomarkers; Brain; Corpus Striatum; Disease Models, Animal; Female; Gene Kno

2019
Decreased N-Acetyl Aspartate/Myo-Inositol Ratio in the Posterior Cingulate Cortex Shown by Magnetic Resonance Spectroscopy May Be One of the Risk Markers of Preclinical Alzheimer's Disease: A 7-Year Follow-Up Study.
    Journal of Alzheimer's disease : JAD, 2017, Volume: 60, Issue:4

    Topics: Aged; Aged, 80 and over; Alzheimer Disease; Aspartic Acid; Biomarkers; Cognitive Dysfunction; Diseas

2017
Modulation of β-glucocerebrosidase increases α-synuclein secretion and exosome release in mouse models of Parkinson's disease.
    Human molecular genetics, 2018, 05-15, Volume: 27, Issue:10

    Topics: alpha-Synuclein; Animals; Brain; Disease Models, Animal; Exosomes; Glucosylceramidase; Humans; Inosi

2018
In vivo inactivation of glycosidases by conduritol B epoxide and cyclophellitol as revealed by activity-based protein profiling.
    The FEBS journal, 2019, Volume: 286, Issue:3

    Topics: Animals; beta-Glucosidase; Brain; Cyclohexanols; Disease Models, Animal; Enzyme Assays; Glucosylcera

2019
Loss of β-glucocerebrosidase activity does not affect alpha-synuclein levels or lysosomal function in neuronal cells.
    PloS one, 2013, Volume: 8, Issue:4

    Topics: alpha-Synuclein; Animals; Autophagy; Cell Differentiation; Cell Line; Gaucher Disease; Glucosylceram

2013
Neuroinflammation and α-synuclein accumulation in response to glucocerebrosidase deficiency are accompanied by synaptic dysfunction.
    Molecular genetics and metabolism, 2014, Volume: 111, Issue:2

    Topics: alpha-Synuclein; Animals; Corpus Striatum; Disease Models, Animal; Dopamine; Evoked Potentials, Moto

2014
N-Alkylated aziridines are easily-prepared, potent, specific and cell-permeable covalent inhibitors of human β-glucocerebrosidase.
    Chemical communications (Cambridge, England), 2015, Jul-21, Volume: 51, Issue:57

    Topics: Alkylation; Aziridines; Enzyme Inhibitors; Gaucher Disease; Glucosylceramidase; HeLa Cells; Humans;

2015
Metabolite ratios in the posterior cingulate cortex do not track cognitive decline in Parkinson's disease in a clinical setting.
    Parkinsonism & related disorders, 2016, Volume: 22

    Topics: Aged; Aged, 80 and over; Aspartic Acid; Bayes Theorem; Case-Control Studies; Choline; Cognitive Dysf

2016
Alpha-synuclein interacts with Glucocerebrosidase providing a molecular link between Parkinson and Gaucher diseases.
    The Journal of biological chemistry, 2011, Aug-12, Volume: 286, Issue:32

    Topics: alpha-Synuclein; Amino Acid Substitution; Cell Line, Tumor; Enzyme Inhibitors; Gaucher Disease; Gluc

2011
Brainstem 1H-MR spectroscopy in patients with Parkinson's disease with REM sleep behavior disorder and IPD patients without dream enactment behavior.
    Clinical neurology and neurosurgery, 2006, Volume: 108, Issue:2

    Topics: Aged; Aspartic Acid; Brain Stem; Case-Control Studies; Choline; Creatine; Female; Humans; Inositol;

2006
Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutation.
    Journal of neurology, 2008, Volume: 255, Issue:5

    Topics: Adult; Aged; Basal Ganglia; Biomarkers; Cell Line; DNA Mutational Analysis; Energy Metabolism; Femal

2008
Proton magnetic resonance spectroscopy (1H-MRS) of motor cortex and basal ganglia in de novo Parkinson's disease patients.
    Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2001, Volume: 22, Issue:1

    Topics: Aged; Aspartic Acid; Basal Ganglia; Brain Chemistry; Choline; Creatine; Female; Humans; Inositol; Ma

2001