Pavlick- Basal Nuclei and Pathways Flashcards
basal nuclei structures
primary motor cortex
caudate
putamen
globus pallidus (internus and externus)
subthalamic nuclei
substantia nigra
VL of thalamus
parts of basal nuclei that make up corpus striatum
caudate
putamen
structures of basal ganglia that make up lentiform nucleus
putamen
Globus pallidus (internus and externus)
involved with modulating voluntary movement and cognitive functions
basal nuclei
structures involved in basal nuclei pathway that release glutamate
structures involved in basal nuclei pathway that release GABA
1, 2, 3, 4
1: caudate
2: putamen
3: globus pallidus externus
4: globus pallidus internus
1, 2, 3, 4
1: caudate
2: putamen
3: globus pallidus externus
4: globus pallidus internus
Process whereby an output is permitted by reducing the inhibitory effect on it (inhibiting the inhibitor)
disinhibition
top: primary motor cortex (M1)
middle L: VL of thalamus
bottom L: putamen
top R: globus pallidus externus
middle R: globus pallidus internus
bottom R: subthalamic nucleus
the GO pathway (direct pathway) is disinhibition of _____ of the thalamus
ventrolateral nucleus
direct pathway (VL of thalamus disinhibited)
NO-GO pathway (indirect) is disinhibition of _____
subthalamic nucleus
indirect pathway (subthalamic nuclei disinhibited)
produced by substantia nigra pars compacta
dopamine
___ receptors in direct pathway—– excitatory
D1 (Gs)
____ receptors in indirect pathway—-inhibitory
D2 (Gi)
Where dopamine is produced
substantia nigra
direct pathway (VL of thalamus releasing more glutamate)
indirect pathway (VL of thalamus releasing less glutamate)
net effect of both direct and indirect pathways that are happening at the same time
net cortical facilitation (movement)
abnormal movement; can be categorized by speed and/or pattern
dyskinesia
decrease or absence of movement
hypokinetic
excess of movement
hyperkinetic
unilateral wild flinging movements of the extremities
hemiballismus
hemiballismus happens due to damage of the _______; contralateral lesion (effects contralateral muscle)
subthalamic nucleus
what happens if you knockout signal at subthalamic nucleus (of indirect pathway)
excess movement due to VL of thalamus releasing more glutamate
HEMIBALLISMUS
autosomal dominant disorder characterized by degeneration of striatum (mostly _____)
caudate nucleus
(Huntington’s)
genetic feature of codon repeat disorders that dictates an earlier age of onset in successive generations (seen in huntingtons)
anticipation
CAG repeats on chromosome 4p responsible for transcribing ______protein
Huntington
chorea (dance-like movements)
cachexia (wasting syndrome)
psychiatric sx’s
dementia
Huntington’s disease
Mean age of onset is 40 years with a disease duration of ~ 18 years
Huntington’s disease
Ages 5-15 most commonly affected with typical onset in adolescence
Sydenham’s chorea
can follow group A strep pharyngitis as part of _______
acute rheumatic heart disease (rheumatic fever)
Pancarditis
Migratory polyarthritis of large joints
Erythema marginatum of skin
sydenham’s chorea
rheumatic fever
Causes autoimmune attack on the basal nuclei
rheumatic fever
type of dystonia which follows long-term use of dopaminergic antagonists
tardive dyskinesia
antipsychotic or anti-emetic medications
dopaminergic antagonists
Symptoms include rapid movements of mouth, tongue, and limbs
tardive dyskinesia
~1/3 cases of ____continue even after discontinued use of offending medication
tardive dyskinesia
Group of movement disorders which exhibit signs and symptoms of Parkinson’s Disease
Parkinsonisms
primary parkinsonisms
PD
atypical parkinsonisms (do not respond to PD meds)
can be attributed to trauma, toxins, infections, or medications
secondary parkinsonisms
characterized by loss of dopamine-producing neurons in substantia nigra
Parkinson’s disease
SMART-D sx’s of PD
shuffling gait
mask-like facies
akinesia (bradykinesia)
rigidity
tremor (resting)
dementia (may have lewy bodies)
Lewy body (seen in dementia)
“pill-rolling” tremor
Parkinson’s disease
resting tremor
PD
hereditary disease causing insufficient copper metabolism
Wilson Disease
Copper collects in brain, eye, and liver (cirrhosis)
Wilson Disease
Wilson disease causes damage to ____
lentiform nucleus (putamen and globus pallidus)
Kayser-Flesher ring seen in Wilson Disease
K-F rings
personality/mood changes in teens
tremor (wing-beating)
rigidity
bradykinesia
Wilson disease
putamen affected
due to hand-sanitizer exposure and first batch of moon shine
chemical production
furnaces
methanol intoxication
globus pallidus affected
seen in colder months (fires, heaters, stoves)
carbon monoxide poisoning