Neurological Disorders Flashcards

1
Q

what changes in the brain lead to brain disorders

A

changes in information processing and transmission leading to changes in thoughts, behavior and feelings

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2
Q

old framework that is too simplistic of brain disorders

A

too much or too little neurotransmitter in the brain

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3
Q

how can we treat certain neurological disorders

A

targeting treatment to specific circuits and networks altered by the disorder

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4
Q

2 types of brain disorders

A

mental and neurological

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5
Q

general neural mech of different disorders

A

disorders are linked to specific brain circuits

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6
Q

types of non invasive treatments

A

cognitive interventions, transcranial magnetic stimulation, transcranial current stimulation

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7
Q

cognitive intervention

A

talk therapy; sensing, thinking and acting to activate specific circuits

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8
Q

transcranial magnetic stimulation

A

use magnetic fields (from coil on scalp) to affect cells

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9
Q

transcranial current stimulation

A

uses electric currents (electrones on head) to affect cells

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10
Q

limitation of non invasive transcranial magnetic and current stimulation techniques

A

poor spatial resolution (the ability of a technique to distinguish between two different locations in the brain)

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11
Q

types of invasive treatments

A

cell transplantation, deep brain stimulation, pharmacogenetics, optogenetics

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12
Q

cell transplantation treatment

A

replace damaged cells using embryonic or stem cells

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13
Q

deep brain stimulation

A

electrical stimulation; can perturb or enhance activity in a brain area

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14
Q

pharmacogenetics treatment

A

targeted delivery of specific genes to re-program cells

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15
Q

optogenetics treatment

A

use virus with light sensitive proteins to introduce light sensitive ion channels into cells; neuron activity can be manipulated by light

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16
Q

what class of disease is parkinson’s disease

A

movement and cerebellar disorder; motor system disorder

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17
Q

parkinson’s disease symptoms (4 main motor symptoms)

A
  • tremor (arms, hands, legs, jaw, face)
  • rigidity (limbs and trunk)
  • bradykinesia (slow movements)
    -postural instability (poor balance and coordination)
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18
Q

additional parkinson’s symptoms

A

emotional disturbances like depression, difficulty talking chewing and swallowing,, constipation, urinary problems, sleep disruptions, skin problems

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19
Q

what demographic does parkinson’s usually effect

A

people over 50

20
Q

cause of parkinson’s disease

A

loss of dopamine producing cells (pars compacta)

21
Q

part of brain that degenerates in parkinson’s disease

A

substantia nigra in basal ganglia

22
Q

2 parts of substantia nigra and their functions

A

-pars reticulata (projects to thalamus in cortex -> substantia nigra -> thalamus pathway)
-pars compacta (synthesises dopamine; degeneration leads to parkinson’s)

23
Q

what brain area is targeted by electrodes for deep brain stimulation for parkinson’s disease

A

subthalamic nucleus in basal ganglia

24
Q

2 types of deep brain stimulation

A

constant deep brain stimulation and adaptive deep brain stimulation

25
adaptive deep brain stimulation
send electrical signal when beta amplitude of beta oscillations is atypical; mimicking natural brain rhythms and adapting to changing needs
26
pharmacogenetic treatment for parkinson's disease
input genetic info (via virus) that introduce enzymes necessary for dopamine synthesis into neurons in striatum; *cells that could not make dopamine before not can synthesise it to counteract loss of dopamine from degeneration for diseases
27
optogenetic treatment for parkinson disease
optical/light high and low frequency stimulation in subthalamic nucleus
28
effects of optical high frequency stimulation in STN
inhibit spiking activity -> therapeutic benefits
29
effects of optical low frequency stimulation in STN
increase spiking activity -> made pathological condition worse
30
major depressive disorder
severe symptoms that interfere with work, sleep, eating and enjoying life; 1 or more episodes
31
persistent depressive disorder
depressed mood lasting for at least 2 years
32
psychotic depression
severe depression present with a form of psychosis (delusions, hallucinations, etc.)
33
postpartum depression
depression after childbirth which can make caring for a child overwhelming
34
seasonal affective depression
depression onset during winter where there is less sunlight (usually lifts during spring/ summer)
35
bipolar disorder
mood changes cycle from mania to depression
36
5 or more of what list of symptoms is used to diagnose major depressive disorder
-depressed mood most of the day nearly every day -diminished intrest/ pleasure in activities -significant weight loss or gain/ appetite changes -insomnia or hypersomnia (sleep patterns) -psychomotor agitation or retardation -fatigue/ loss of energy -worthlessness/ inappropriate guilt -cognitive imparement -suicidal thoughts
37
what do major depressive disorder symptoms lead to
impairment in social/ occupational and other important areas of functioning
38
brain regions involved in emotional experience
insula, orbitofrontal cortex, ventromedial frontal cortex, anterior cingulate cortex, posterior cingulate cortex, amygdala
39
role of ventromedial prefrontal cortex
emotional decision making/ reward based processing
40
what brain area has increased activation in major depressive disorder patients
are 25 (congulate cortex)
41
where is deep brain stimulation targeted for patients with major depressive disorder
white matter tracts around area 25 (area 25 input and output pathways) to decrease area 25 activity
42
result of DBS of area 25
effective for some patients but not others
43
why may DBS in area 25 only help some patients with major depressive disorder
pathway being targeted may not be the pathway resulting in that person's major depressive disorder symptoms
44
precision medicine
identify specific perturbed pathway (via fmri, diffusion mri, etc) and target intervention to that affected pathway
45
what circuit is impaired in major depressive disorder
circuit involving anterior cingulate/ ventromedial PFC