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Summary Cognitive psychologie II, slides + nota's+ voorbeelden, geslaagd eerste zit

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Samenvatting bevat slides aangevuld met nota's en voorbeelden van alle gastlessen. Geslaagd met deze samenvatting in eerste zit. Betreffende gastcolleges: Parkinson, mindfulness, eating disorders, sociale cognition and ASD, Unilateral neglect, sleep disorders and cognition.

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Parkingson’s disease
Theoretical background
Chronic Progressive Degenerative Brain Disorder

Fastest growing neurological disorder

Second-most common neurodegenerative disorder

▪ 2-3% of population ≥65 years of age

Cause: degeneration of dopamine-producing cells in the
substantia nigra of the basal ganglia

Effect: typical motor symptoms, non-motor features and neurobehavioral abnormalities

Epidemiology
Estimated global incidence: 5 to 230 new cases per 100,000 individuals yearly.

Rare before age 50

Incidence 5 to 10-fold from ages 60-90

Global prevalence estimated 0.3%

▪ Increases to >3% in >80 years

Usually: onset between ages 60-70

Genetic variant: Young Onset PD

▪ 5-20% of persons w/ PD

Male:Female distribution ± 1.5:1

Most cases: idiopathic (no known cause)

Most likely a combination of factors:

• Age

• Environmental (toxins, pesiticides, insecticides: rotenone, paraquat, MPTP)

• Dietary (pollutants)

• Genetic predisposition (mutations in ⍺-synuclein, LRRK2, GBA)

• Brain trauma, stroke, viral inflammation

• Oxidative stress destroys mitochondria → apoptosis (cell death) of dopaminergic cells.

Pathophysiology
Characteristic features:

1. Loss of dopaminergic neurons in the pars compacta of the substantia nigra


1

,NO general macroscopic atrophy of the brain, but degeneration in certain types of neurons within
particular brain regions.
E.g. early-stage PD: loss of dopaminergic neurons restricted to VL substantia nigra
end-stage PD: more widespread loss

➔ resulting in a reduction of the neurotransmitter dopamine in the basal ganglia



Panels A and B represent the human
postmortem bilateral midbrain of normal
and Parkinsonian subjects, respectively




2. Widespread protein (⍺-synuclein) accumulation (“Lewy Bodies”) in neurons




The basal ganglia
Anatomy
5 interconnected sub-cortical nuclei:

I. Nucleus Caudatus
II. Putamen
III. Globus Pallidus
IV. Nucleus Subthalamicus
V. Substantia Nigra

Function
• Motor control

• Cognitive processes

• Emotional/behavioral processes

➔ Control of global-directed and habitual actions

Basal ganglia disorders are manifested by abnormal movement and a number of neuropsychiatric
disorders




2

,Connectivity
Input Nuclei of the BG:

• Nucleus Caudatus

• Putamen

• Subthalamic Nucleus

Output Nuclei of the BG:

• Globus Pallidus (pars interna)

• Substantia Nigra (pars reticulata)

Cortico-Basal-Ganglia-Thalamo-Cortical Loop = CBGTC Loop

Connections with other cerebral structures




The frontostriatal network
Evolutionary interpretation
Organisms are in need of two systems for circuits
behavioral control:

1. Routine responses to known
environmental stimuli: pre-
programmed behavior, stimulus-
based, procedural, automatic, fast
(walking, shaving, typing)

➔ BASAL GANGLIA

2. Reflective, problem-solving behavior in
new situations, more attention
needed

➔ FRONTAL CORTEX
These two systems are integrated in the FRONTOSTRIATAL NETWORK= involved in motor
cognitive func: thinking,….

3

, Direct Pathway




Netto excitation effect on cortex

Indirect pathway




Netto: inhibitory effect on cortex: keeps indirect movements
from appearing.

Imbalance in neuronal circuits in PD
DIRECT PATHWAY (netto = excitation of cortex)

cortex – striatum – globus pallidus pars interna – thalamus - cortex

INDIRECT PATHWAY (netto = inhibition of cortex)

cortex – striatum – globus pallidus pars externa – nucleus subthalamicus – globus pallidus pars
interna – thalamus – cortex

PD: Dopamine depletion causes imbalance between direct (excitatory) and indirect (inhibitory)
pathways
➔ thalamus is inhibited
➔ movement disorders

4

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