Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Olfactory bulb in multiple system atrophy.

Tibor Kovács1, Mátyás I Papp, Nigel J Cairns

  • 1Department of Neurology, Semmelweis University, Faculty of General Medicine, Budapest, Hungary. tibor@neur.sote.hu

Movement Disorders : Official Journal of the Movement Disorder Society
|July 31, 2003
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Basic Science and Pathogenesis.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2025
Same author

Identification of small molecule dimethyoxyphenyl piperazine inhibitors of alpha-synuclein fibril growth.

Scientific reports·2025
Same author

Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's disease.

Genome biology·2025
Same author

Identification of Small Molecule Dimethyoxyphenyl Piperazine Inhibitors of Alpha-Synuclein Fibril Growth.

bioRxiv : the preprint server for biology·2025
Same author

Elevated levels of tritium in surface water collected in the immediate aftermath of the Fukushima accident.

Environmental pollution (Barking, Essex : 1987)·2025
Same author

Role of Hemocytes in the Aging of Drosophila Male Germline.

Cells·2025
Same journal

Gene Therapy for Amino Acid Decarboxylase Deficiency: Clinical and Imaging Outcomes in a French Cohort.

Movement disorders : official journal of the Movement Disorder Society·2026
Same journal

Alzheimer's Disease Cerebrospinal Fluid Biomarkers Predict Survival in Progressive Supranuclear Palsy.

Movement disorders : official journal of the Movement Disorder Society·2026
Same journal

Hyperhomocysteinemia and Vitamin B Deficiency as Potential Aggravating Factors in Huntington's Disease: A Prospective Monocentric Study.

Movement disorders : official journal of the Movement Disorder Society·2026
Same journal

Longitudinal Dynamics of Polyglutamine-Expanded ATXN3 in Biofluids of Spinocerebellar Ataxia Type 3.

Movement disorders : official journal of the Movement Disorder Society·2026
Same journal

Putamen Structural-Functional Decoupling as an Early-Stage Candidate Imaging Marker for Motor Severity in Spinocerebellar Ataxia Type 3.

Movement disorders : official journal of the Movement Disorder Society·2026
Same journal

Melanopsin-Mediated Post-Illumination Pupillary Response in Idiopathic Rapid Eye Movement (REM) Sleep Behavior Disorder and Parkinson's Disease.

Movement disorders : official journal of the Movement Disorder Society·2026
See all related articles

Olfactory dysfunction is common in Parkinson's disease (PD) and multiple system atrophy (MSA). Glial cytoplasmic inclusions in the olfactory bulb are diagnostic for MSA, while Lewy bodies are characteristic of PD.

Area of Science:

  • Neuroscience
  • Neuropathology
  • Clinical Neurology

Background:

  • Olfactory dysfunction, including hyposmia and anosmia, is a hallmark clinical feature of Parkinson's disease (PD).
  • Similar olfactory deficits are observed in multiple system atrophy (MSA), suggesting shared or distinct underlying pathologies.

Purpose of the Study:

  • To investigate and compare the neuropathological changes in the olfactory bulb (OB) and anterior olfactory nucleus (AON) in Parkinson's disease (PD) and multiple system atrophy (MSA).
  • To determine if specific pathological markers can differentiate between PD and MSA-related olfactory dysfunction.

Main Methods:

  • Histopathological examination of olfactory bulbs (OBs) and anterior olfactory nuclei (AON) from post-mortem cases of PD and MSA.
  • Microscopic analysis to identify characteristic protein aggregates such as Lewy bodies and glial cytoplasmic inclusions (GCIs).

Related Experiment Videos

  • Assessment of neuronal loss in the AON for both disease cohorts.
  • Main Results:

    • Lewy bodies and significant neuronal loss in the AON were confirmed in PD olfactory bulbs.
    • Glial cytoplasmic inclusions (GCIs) were consistently identified in the OBs of all examined MSA cases.
    • Neuronal loss was also observed in the AON of MSA cases.
    • The presence of GCIs in the OB was found to be a diagnostic pathological feature for MSA.

    Conclusions:

    • The distinct pathological findings in the olfactory bulb, specifically GCIs in MSA versus Lewy bodies in PD, can serve as diagnostic markers.
    • Neuronal loss in the anterior olfactory nucleus occurs in both PD and MSA.
    • These neuropathological alterations in the olfactory system are likely responsible for the observed olfactory dysfunction in both Parkinson's disease and multiple system atrophy.