✅ M5 - Brain & Neurology Flashcards

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1
Q

What is the basic anatomy of the brain?

A
  1. Cerebrum containing the cerebral cortex: frontal, temporal, parietal and occipital (FPOT clockwise)
    - Has grey matter (neural cell bodies) AND white matter (neural axon and dendrites)
    - Has gyrus (ridges) and sulcus (valley) -> maximise SA
  2. Cerebellum: coordinates movement posture
  3. Brainstem: cardiovascular and respiratory centre
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2
Q

What are the functions of the four lobes?

A
  1. Frontal lobe - primary motor cortex, responsible for movement, personality, and planning
  2. Parietal lobe: primary somatosensory cortex, responsible for awareness of surrounding & stereognosis (object manipulation)
  3. Temporal lobe: responsible for hearing and language.
  4. Occipital lobe: responsible for processing visual signals.
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3
Q

What are the different classifications of neurons?

A
  1. Structural:
    • Unipolar
    • Bipolar
    • Multipolar
  2. Functional:
    • Afferent (from receptor)
    • Efferent (to muscle)
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4
Q

What parts are the neuron consist of?

A
  1. Soma (cell body)
  2. Dendrites
  3. Axon (tend to have myelin sheath & nodes of ranvier)
  4. Axon terminal (synapse)
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5
Q

What are different neuroglia and their functions?

A
  1. Astrocytes (‘star’)
    - Provide physical support for neurons in CNS
    - Help form blood-brain barrier (allows nutrition to comes in)
    - Clean up debris & regulate neural environment
  2. Oligodendrocyte: produce the myelin sheath to protect axon in neurons in CNS (multiple neurons at once)
  3. Muller: provide structural and metabolic (nutrition) support for neurons (mainly in the retina)
  4. Schwann: produces myelin sheath for neuron in PNS (one neuron at a time)
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6
Q

Describe the process of depolarisation - action potential - hypepolarisation in neural communication?

A

Axon has a selectively permeable membrane: allow some things through & stops others
-> Has ion channels (e.g. Na+ and K+ channels)

Neuron/Axon at rest:
- Na+ channels close
- Some K+ channels open
- Maintain in-axon potential at -70mV (RESTING MEMBRANE POTENTIAL)

Depolarisation (-ve to +ve)
- Reach threshold of excitation -> open Na+ channel AND change potential from -70mV to 40mV
- All Na+ channel open
- K+ channels close

Action potential/Repolarisation (+ve to -ve)
- K+ channel opens
- Na+ channel is blocked when 40mV is reached
=> reset the membrane potential to -70mV

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7
Q

Features of neural transmission?

A
  1. Saltatory conduction: action potential only occurs in nodes of ranvier, between myelin sheaths of axon => faster and save energy
  2. All-or-nothing: in order for an action potential to happen to pass electrical signals along the axon and between neurons, the membrane potential needs to exceed the threshold.
  3. Diffusion: movement of ions between outside and inside of the axon depends on diffusion (movement from high conc. to low conc. down the concentration gradient)
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8
Q

Describe the process of neural transmission between neurons? (mostly in chemical synapses)

A
  1. Action potential reaches axon terminal
  2. Vesicles containing neurotransmitters fuse with the pre-synaptic membrane.
  3. Release of the neurotransmitter into the synaptic cleft (exocytosis)
  4. The neurotransmitter binds to receptor on post-synaptic membrane (key-lock mechanism)
  5. Excitatory effect or an inhibitory effect on post-synaptic neuron -> leading or preventing an action potential to occur.
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9
Q

What are the structures in CNS and PNS?

A
  1. Central Nervous System (CNS):
    - Brain (head)
    - Spinal cord (rest of body)
  2. Peripheral Nervous system (PNS):
    - Cranial nerves (head)
    - Spinal nerves (rest of body)
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10
Q

How is seizure defined?

A
  • Same as convulsion
  • Transient abnormal event resulting from discharge of cerebral neuron.
  • Epilepsy is the continued tendency to have such seizures.
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11
Q

What are the features of seizures?

A

Two types of seizures: generalised (originate from one part, the spread to all parts of the brain) and partial seizure (only remain in one place)

  1. Generalised seizure
    - Tonic clonic (grand mal): two phases, loss of body control (tonic phase) & body convulsion (clonic phase)
    - Absence (petit mal): blanking/zoning out for few seconds
    - Myoclonic: sudden, brief muscle jerks or twitches.
  2. Partial seizure
    - Induced aura: a sensory/perceptual experience prior to a seizure (warning sign).
    - Jacksonian seizure (motor cortex): localized jerking movements in body
    - Todd’s paralysis: temporary weakness or paralysis that occurs after a seizure
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12
Q

What are the causes of seizure?

A
  1. Trauma: Depressed skull fracture, penetrating brain injury, cerebral contusion, dural tear
  2. Cerebrovascular: Following cerebral infarction (stroke) -> abrupt loss of bloodflow to the brain
  3. Alcohol induced: Hypoglycaemia (low blood sugar levels) -> coma
  4. Others including pyrexia (high fever) and brain tumours.

=> In 2/3rds of cases, no definite cause is found.

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13
Q

What is Parkinson’s Disease, its causes and features?

A
  1. Overview: a neurodegenerative disorder, affecting 145,000 people in the UK
  2. Caused by genetic (10%) and environmental factors
    - Genetic basis: associative genes (LRRK2, PARK2, SNCA, etc.)
    - Environmental: reduced risk - coffee and smoking, increased risk - living in rural area and well-water
  3. Features: motor symptoms
    - Akinesia (impairment of voluntary movements)
    - Resting tremor
    - Rigidity
    - Stooped posture and shuffling gait
    - Other symptoms include: Loss of smell, Sleep disorders, Constipation, Depression & Anxiety, Mask-like face
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14
Q

What causes motor symptoms in Parkinson’s disease? (brain)

A
  1. Motor control in brain:
    - Basal ganglia: subconscious control & coordination of learned movement => within the grey matter.
    - Substantia nigra: moderates the activity of the basal ganglia with dopamine (neurotransmitter).
  2. Why motor symptoms occur in Parkinson’s disease?
    - Loss of dopamine producing neurones in the substantia nigra
    - Lewy bodies within neurons disrupting normal neuronal functioning
    - α-synuclein (regulating synaptic functions) is main constituent in Lewy bodies -> potential biomarkers
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15
Q

What is the diagnosis and treatment for Parkinson’s Disease?

A
  1. Diagnosis (clinical)
    - Patients live ~10-15 years from diagnosis
    - Death usually caused by bronchopneumonia
  2. Treatment:
    - Can give dopamine agonists (e.g. levodopa) => produce initial striking improvements
    - No drugs alter the course of the disease (no cure)
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16
Q

What is Alzheimer’s Disease?

A
  1. Overview
    - A degenerative brain disease & the most common cause of dementia.
    - 520000 people in the UK have it.
  2. Effects on brain tissue:
    - enlarged ventricles
    - neural loss
    - reduce SA for parts that control language and memory
    => Cognitive and functional decline

Extra info: Dementia is a collective terms for degenerating cognitive abilities (e.g. memory, problem solving, etc.)

17
Q

What are the causes of dementia?

A
  1. Degenerative causes: Alzheimers (62%), lewy body dementia
  2. Vascular: multi infarct dementia
  3. Infective: CJD or ‘mad-cow disease’, AIDs, syphilis
  4. Metabolic: Vitamin B12 & folate deficiency, hypoglycaemia
  5. Toxic: alcohol/drugs
  6. Space occupying lesion: tumour, chronic haematoma
18
Q

What are the biological expression/hallmarks of Alzheimer’s Disease?

A
  1. Biological change (potential biomarkers):
    - β-amyloid plaques outside neurones
    - protein tau (tangles) inside neurones
    -> block communication at synapses
    -> block transport of nutrients into neurones
  2. Risk factors:
    - Genetic (APP, presenilin 1&2)
    - Down syndrome
    - Age
    - Education
19
Q

What is the diagnosis and treatment for Alzheimers Disease?

A
  1. Diagnosis (clinical)
    - Input from close friends & family, medical history
    - Cognitive tests, neurological examination
    - Blood tests to rule out other causes (e.g. B12 deficiency, cancers)
  2. Treatment:
    - Aim is to maintain quality of life
    - Acetylcholinerase inhibitor drugs (to keep neurotransmitter in synapse for longer)
  3. Prevention - modifiable risk factors:
    - having good cardiovascular health protects against dementia (e.g. diet)
    - brain health is affected by heart health