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High Glucosylceramides and Low Anandamide Contribute to Sensory Loss and Pain in Parkinson's Disease

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Pain as a Nonmotor Symptom of Parkinson Disease

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Evolution of Prodromal Clinical Markers of Parkinson Disease in a GBA Mutation–Positive Cohort

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Comparison of Parkinson Risk in Ashkenazi Jewish Patients With Gaucher Disease andGBAHeterozygotes

inferredcites →https://doi.org/10.1001/jamaneurol.2016.1593openalex-snapshot

High Frequency of GBA Gene Mutations in Dementia With Lewy Bodies Among Ashkenazi Jews

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‘Wind‐up’ in Parkinson's disease: A functional magnetic resonance imaging study

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Effect of medical cannabis on thermal quantitative measurements of pain in patients with Parkinson's disease

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Contribution of genetic variants to pain susceptibility in P arkinson disease

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Survey on cannabis use in Parkinson's disease: Subjective improvement of motor symptoms

inferredcites →https://doi.org/10.1002/mds.20629openalex-snapshot

Effect of levodopa on pain threshold in Parkinson's disease: A clinical and positron emission tomography study

inferredcites →https://doi.org/10.1002/mds.22172openalex-snapshot

Lesions outside the CNS in Parkinson's disease

inferredcites →https://doi.org/10.1002/mds.870010106openalex-snapshot

Pain in Parkinson's disease

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Glycosphingolipids and Insulin Resistance

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A role for sphingolipids in the pathophysiology of obesity-induced inflammation

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Spread of aggregates after olfactory bulb injection of α-synuclein fibrils is associated with early neuronal loss and is reduced long term

inferredcites →https://doi.org/10.1007/s00429-013-0651-2openalex-snapshot

α-Synuclein in the olfactory system in Parkinson’s disease: role of neural connections on spreading pathology

inferredcites →https://doi.org/10.1016/0304-3959(94)00172-bopenalex-snapshot

The role of the basal ganglia in nociception and pain

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Chemosensitivity of human colon cancer cells is influenced by a p53-dependent enhancement of ceramide synthase 5 and induction of autophagy

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Gaucher Disease Glucocerebrosidase and α-Synuclein Form a Bidirectional Pathogenic Loop in Synucleinopathies

inferredcites →https://doi.org/10.1016/j.clinph.2010.03.055openalex-snapshot

Reproducibility and influence of test modality order on thermal perception and thermal pain thresholds in quantitative sensory testing

inferredcites →https://doi.org/10.1016/j.jns.2008.09.023openalex-snapshot

Hyperalgesia and laser evoked potentials alterations in hemiparkinson: Evidence for an abnormal nociceptive processing

inferredcites →https://doi.org/10.1016/j.metabol.2019.04.002openalex-snapshot

Targeted lipidomics reveal derangement of ceramides in major depression and bipolar disorder

inferredcites →https://doi.org/10.1016/j.neuint.2017.12.014openalex-snapshot

Pathological role of lipid interaction with α-synuclein in Parkinson's disease

inferredcites →https://doi.org/10.1016/j.neurobiolaging.2013.08.018openalex-snapshot

Reduced functional connectivity in early-stage drug-naive Parkinson's disease: a resting-state fMRI study

inferredcites →https://doi.org/10.1016/j.neuron.2017.01.018openalex-snapshot

The Complicated Relationship between Gaucher Disease and Parkinsonism: Insights from a Rare Disease

inferredcites →https://doi.org/10.1016/j.neuron.2017.12.012openalex-snapshot

Reversible Conformational Conversion of α-Synuclein into Toxic Assemblies by Glucosylceramide

inferredcites →https://doi.org/10.1016/j.neuropharm.2013.03.021openalex-snapshot

Anandamide deficiency and heightened neuropathic pain in aged mice

inferredcites →https://doi.org/10.1016/j.pain.2006.01.041openalex-snapshot

Quantitative sensory testing in the German Research Network on Neuropathic Pain (DFNS): Standardized protocol and reference values

inferredcites →https://doi.org/10.1016/j.pain.2007.06.022openalex-snapshot

Abnormal processing of the nociceptive input in Parkinson’s disease: A study with CO2 laser evoked potentials

inferredcites →https://doi.org/10.1016/j.pain.2008.12.004openalex-snapshot

Pain in Parkinson’s disease: Prevalence and characteristics

inferredcites →https://doi.org/10.1016/j.pain.2010.05.002openalex-snapshot

Quantitative sensory testing in the German Research Network on Neuropathic Pain (DFNS): Somatosensory abnormalities in 1236 patients with different neuropathic pain syndromes

inferredcites →https://doi.org/10.1016/j.pain.2014.02.004openalex-snapshot

Quantitative sensory testing in the German Research Network on Neuropathic Pain (DFNS): Reference data for the trunk and application in patients with chronic postherpetic neuralgia

inferredcites →https://doi.org/10.1016/j.prostaglandins.2017.06.002openalex-snapshot

CD200 selectively upregulates prostaglandin E2 and D2 synthesis in LPS-treated bone marrow-derived macrophages

inferredcites →https://doi.org/10.1016/j.tiv.2015.11.004openalex-snapshot

The neuroprotection of cannabidiol against MPP + -induced toxicity in PC12 cells involves trkA receptors, upregulation of axonal and synaptic proteins, neuritogenesis, and might be relevant to Parkinson's disease

inferredcites →https://doi.org/10.1016/j.ymgme.2017.11.001openalex-snapshot

Glucocerebrosidase haploinsufficiency in A53T α-synuclein mice impacts disease onset and course

inferredcites →https://doi.org/10.1016/s0304-3959(96)03188-0openalex-snapshot

Sensory dysfunction in fibromyalgia patients with implications for pathogenic mechanisms

inferredcites →https://doi.org/10.1038/mp.2014.164openalex-snapshot

Molecular mechanisms of placebo responses in humans

inferredcites →https://doi.org/10.1038/nn1916openalex-snapshot

Cannabinoids mediate analgesia largely via peripheral type 1 cannabinoid receptors in nociceptors

inferredcites →https://doi.org/10.1038/nrneurol.2012.54openalex-snapshot

Pains in Parkinson disease—many syndromes under one umbrella

inferredcites →https://doi.org/10.1038/nrneurol.2012.80openalex-snapshot

Olfactory dysfunction in Parkinson disease

inferredcites →https://doi.org/10.1038/s41598-018-33077-8openalex-snapshot

Machine-learning based lipid mediator serum concentration patterns allow identification of multiple sclerosis patients with high accuracy

inferredcites →https://doi.org/10.1056/nejmoa0901281openalex-snapshot

Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

inferredcites →https://doi.org/10.1073/pnas.1700465115openalex-snapshot

GBA1 deficiency negatively affects physiological α-synuclein tetramers and related multimers

inferredcites →https://doi.org/10.1084/jem.20160368openalex-snapshot

Widespread transneuronal propagation of α-synucleinopathy triggered in olfactory bulb mimics prodromal Parkinson’s disease

inferredcites →https://doi.org/10.1093/brain/122.9.1651openalex-snapshot

Sensory processing in Parkinson's and Huntington's disease

inferredcites →https://doi.org/10.1093/brain/awn102openalex-snapshot

Sensory deficit in Parkinson's disease: evidence of a cutaneous denervation

inferredcites →https://doi.org/10.1093/brain/awt367openalex-snapshot

Reduced glucocerebrosidase is associated with increased α-synuclein in sporadic Parkinson’s disease

inferredcites →https://doi.org/10.1093/brain/awv179openalex-snapshot

Glucocerebrosidase activity in Parkinson’s disease with and without GBA mutations

inferredcites →https://doi.org/10.1093/ecco-jcc/jjw056openalex-snapshot

Tetrahydrobiopterin Attenuates DSS-evoked Colitis in Mice by Rebalancing Redox and Lipid Signalling

inferredcites →https://doi.org/10.1093/hmg/ddq038openalex-snapshot

Extensive enteric nervous system abnormalities in mice transgenic for artificial chromosomes containing Parkinson disease-associated α-synuclein gene mutations precede central nervous system changes

inferredcites →https://doi.org/10.1093/hmg/ddv372openalex-snapshot

Glucocerebrosidase deficiency accelerates the accumulation of proteinase K-resistant α-synuclein and aggravates neurodegeneration in aDrosophilamodel of Parkinson's disease

inferredcites →https://doi.org/10.1093/hmg/ddw185openalex-snapshot

Autophagic lysosome reformation dysfunction in glucocerebrosidase deficient cells: relevance to Parkinson disease

inferredcites →https://doi.org/10.1097/00002508-200112000-00005openalex-snapshot

Quantitative Sensory Testing in Fibromyalgia Patients and in Healthy Subjects: Identification of Subgroups

inferredcites →https://doi.org/10.1097/ajp.0000000000000437openalex-snapshot

Pain in Extrapyramidal Neurodegenerative Diseases

inferredcites →https://doi.org/10.1097/j.pain.0000000000000300openalex-snapshot

Quality assurance for Quantitative Sensory Testing laboratories

inferredcites →https://doi.org/10.1097/j.pain.0000000000000433openalex-snapshot

Quantitative sensory testing using DFNS protocol in Europe

inferredcites →https://doi.org/10.1097/j.pain.0000000000000588openalex-snapshot

Symptom profiles in the painDETECT Questionnaire in patients with peripheral neuropathic pain stratified according to sensory loss in quantitative sensory testing

inferredcites →https://doi.org/10.1097/j.pain.0000000000000923openalex-snapshot

Altered neural responses to heat pain in drug-naive patients with Parkinson disease

inferredcites →https://doi.org/10.1097/j.pain.0000000000000935openalex-snapshot

Stratifying patients with peripheral neuropathic pain based on sensory profiles: algorithm and sample size recommendations

inferredcites →https://doi.org/10.1097/md.0000000000003058openalex-snapshot

Pathophysiology of Small-Fiber Sensory System in Parkinson's Disease

inferredcites →https://doi.org/10.1097/wnf.0000000000000016openalex-snapshot

Cannabis (Medical Marijuana) Treatment for Motor and Non–Motor Symptoms of Parkinson Disease

inferredcites →https://doi.org/10.1097/wnf.0000000000000246openalex-snapshot

Medical Cannabis in Parkinson Disease: Real-Life Patients' Experience

inferredcites →https://doi.org/10.1097/wnf.0b013e3180340319openalex-snapshot

The Effect of Duloxetine on Primary Pain Symptoms in Parkinson Disease

inferredcites →https://doi.org/10.1111/ene.12197openalex-snapshot

Preceding pain symptoms and P arkinson's disease: a nationwide population‐based cohort study

inferredcites →https://doi.org/10.1111/j.1460-9568.2008.06380.xopenalex-snapshot

Pain relief as an opponent process: a psychophysical investigation

inferredcites →https://doi.org/10.1111/j.1468-1331.2009.02797.xopenalex-snapshot

Somatosensory function in asymptomatic Parkin‐mutation carriers

inferredcites →https://doi.org/10.1111/jnc.13517openalex-snapshot

Parkinson's disease: acid‐glucocerebrosidase activity and alpha‐synuclein clearance

inferredcites →https://doi.org/10.1136/jnnp.2008.145995openalex-snapshot

Pain sensitivity and descending inhibition of pain in Parkinson's disease

inferredcites →https://doi.org/10.1155/2015/273019openalex-snapshot

Altered Brain Activation in Early Drug-Naive Parkinson’s Disease during Heat Pain Stimuli: An fMRI Study

inferredcites →https://doi.org/10.1159/000447450openalex-snapshot

LRRK2, GBA and SMPD1 Founder Mutations and Parkinson's Disease in Ashkenazi Jews

inferredcites →https://doi.org/10.1186/1750-1326-7-42openalex-snapshot

Exosomal cell-to-cell transmission of alpha synuclein oligomers

inferredcites →https://doi.org/10.1186/s12974-017-0928-0openalex-snapshot

Progression of pathology in PINK1-deficient mouse brain from splicing via ubiquitination, ER stress, and mitophagy changes to neuroinflammation

inferredcites →https://doi.org/10.1186/s13024-015-0010-2openalex-snapshot

Selective loss of glucocerebrosidase activity in sporadic Parkinson’s disease and dementia with Lewy bodies

inferredcites →https://doi.org/10.1186/s40478-017-0446-4openalex-snapshot

Dysregulation of lysophosphatidic acids in multiple sclerosis and autoimmune encephalomyelitis

inferredcites →https://doi.org/10.1212/01.wnl.0000130455.38550.9dopenalex-snapshot

Quantitative measurement of pain sensation in patients with Parkinson disease

inferredcites →https://doi.org/10.1212/01.wnl.0000276989.17578.02openalex-snapshot

Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease

inferredcites →https://doi.org/10.1212/01.wnl.0000295669.12443.d3openalex-snapshot

Neurophysiologic study of central pain in patients with Parkinson disease

inferredcites →https://doi.org/10.1212/wnl.0000000000000316openalex-snapshot

Skin nerve α-synuclein deposits

inferredcites →https://doi.org/10.1212/wnl.0b013e3182a9f449openalex-snapshot

α-Synuclein in cutaneous autonomic nerves

inferredcites →https://doi.org/10.1212/wnl.26.5.423openalex-snapshot

Primary sensory symptoms in parkinsonism

inferredcites →https://doi.org/10.1212/wnl.34.7.957openalex-snapshot

Sensory symptoms in Parkinson's disease

inferredcites →https://doi.org/10.1371/journal.pone.0010628openalex-snapshot

R-Flurbiprofen Reduces Neuropathic Pain in Rodents by Restoring Endogenous Cannabinoids

inferredcites →https://doi.org/10.1371/journal.pone.0017870openalex-snapshot

Relief as a Reward: Hedonic and Neural Responses to Safety from Pain

inferredcites →https://doi.org/10.3389/fnins.2018.00081openalex-snapshot

Silencing of Glucocerebrosidase Gene in Drosophila Enhances the Aggregation of Parkinson's Disease Associated α-Synuclein Mutant A53T and Affects Locomotor Activity

inferredcites →https://doi.org/10.4103/1673-5374.202934openalex-snapshot

The emerging role of autophagic-lysosomal dysfunction in Gaucher disease and Parkinson's disease

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Elevated hexosylceramides in Parkinson’s disease cause gene upregulations in neurons mimicking responses to pathogens

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