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Related Concept Videos

Parkinson Disease ll: Pathophysiology01:24

Parkinson Disease ll: Pathophysiology

Parkinson disease (PD) is a progressive neurodegenerative disorder primarily affecting movement, with additional non-motor features. Its pathophysiology involves complex interactions among genetic susceptibility, environmental exposures, and cellular dysfunction, including dopaminergic neuron loss, protein aggregation, and mitochondrial impairment.Selective NeurodegenerationA key feature is the degeneration of dopaminergic neurons in the substantia nigra pars compacta, leading to reduced...
Parkinson Disease l: Introduction01:24

Parkinson Disease l: Introduction

Parkinson’s disease is a chronic, progressive neurodegenerative disorder that primarily affects movement. It is characterized by motor symptoms such as resting tremors, muscle rigidity, bradykinesia (slowness of movement), and postural instability. Patients may notice hand tremors at rest, stiffness during movement, or a shuffling gait. In addition to motor features, non-motor symptoms include sleep disturbances, mood and behavioral changes, constipation, and cognitive impairment, all of which...
Parkinson's Disease: Overview01:15

Parkinson's Disease: Overview

Neurodegenerative disorders are progressive diseases that cause irreversible damage and loss to neurons in specific brain areas. Examples of these disorders include Parkinson's disease, Alzheimer's disease, Multiple Sclerosis (MS), and Amyotrophic Lateral Sclerosis (ALS). These disorders share characteristics such as proteinopathies, selective neuronal vulnerability, and a complex interplay between genetic and environmental factors. The primary therapeutic goal for these conditions is to...
Parkinson's Disease: Treatment01:24

Parkinson's Disease: Treatment

Neurodegenerative disorders, such as Parkinson's Disease (PD), involve the gradual and irreversible destruction of neurons in particular brain areas. These disorders exhibit standard features like proteinopathies, selective vulnerability of some neurons, and an interaction of intrinsic properties, genetics, and environmental influences in neural injury.
Parkinson's Disease is primarily a result of the loss of dopaminergic neurons in the substantia nigra pars compacta. The cornerstone of its...
Neural Regulation01:37

Neural Regulation

Digestion begins with a cephalic phase that prepares the digestive system to receive food. When our brain processes visual or olfactory information about food, it triggers impulses in the cranial nerves innervating the salivary glands and stomach to prepare for food.
Alterations in Muscle Tone lll01:11

Alterations in Muscle Tone lll

Rigidity and myotonia are distinct abnormalities of muscle tone that affect resistance and relaxation during movement. Although both involve altered muscle contraction, they arise from different neurological and muscular mechanisms.CharacteristicsRigidity is characterized by uniform resistance to passive movement across the entire range, independent of speed, affecting flexors and extensors equally. It may appear as lead-pipe rigidity (smooth, constant resistance) or cogwheel rigidity...

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Histological Examination of Mitochondrial Morphology in a Parkinson's Disease Model
06:07

Histological Examination of Mitochondrial Morphology in a Parkinson's Disease Model

Published on: June 23, 2023

Striatal shape in Parkinson's disease.

Nicholas W Sterling1, Guangwei Du, Mechelle M Lewis

  • 1Department of Neurology, Pennsylvania State University-Milton S Hershey Medical Center, Hershey, PA 17033-0850, USA.

Neurobiology of Aging
|July 4, 2013
PubMed
Summary

Parkinson's disease (PD) causes significant striatal atrophy, particularly in the caudal putamen and caudate head. This brain atrophy pattern in PD patients correlates with dopamine depletion.

Keywords:
CaudateMagnetic resonance imaging (MRI)MorphologyParkinson's diseasePutamenShapeStriatumStructureVolume

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Published on: February 14, 2012

Area of Science:

  • Neuroscience
  • Neurology
  • Radiology

Background:

  • Parkinson's disease (PD) is characterized by the loss of dopaminergic neurons in the nigrostriatal pathway.
  • Previous research indicates reduced striatal volume and caudate head atrophy in PD patients.
  • The precise spatial distribution of putaminal atrophy in PD remains uncharacterized.

Purpose of the Study:

  • To precisely map the locations of atrophy within the putamen and caudate nuclei in Parkinson's disease.
  • To investigate the spatial relationship between striatal volume changes and the known pattern of dopamine depletion in PD.

Main Methods:

  • Structural brain magnetic resonance imaging (MRI) using T1- and T2-weighted sequences was performed on 40 PD patients and 40 age- and gender-matched controls without dementia.
  • Advanced shape analysis techniques were applied to doubly segmented regions of interest within the putamen and caudate.
  • Statistical comparisons were made to quantify differences in volume and surface contraction magnitudes between PD subjects and controls.

Main Results:

  • PD subjects exhibited significantly reduced volumes in both the putamen (p = 0.0003) and caudate (p = 0.0003) compared to controls.
  • The greatest surface contraction magnitudes, indicative of atrophy, were observed in the caudal putamen and the head and dorsal body of the caudate nucleus (p ≤ 0.005).
  • These findings reveal a specific spatial pattern of striatal atrophy in PD.

Conclusions:

  • The observed pattern of striatal atrophy in Parkinson's disease, concentrated in the caudal putamen and caudate head/dorsal body, aligns with the known distribution of dopamine depletion.
  • This spatial correlation suggests that striatal atrophy in PD may be a consequence of widespread cellular remodeling processes linked to dopaminergic neurodegeneration.