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1
Q

Each hemisphere is divided into what four lobes?

A

Frontal. Parietal - top of the brain. Occipital - back of the brain. Temporal - sides.

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2
Q

How are the infoldings and bumps on the brain lobes called?

A

Infoldings - sulcus (sulci).

Bumps - gyrus (gyri).

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3
Q

What ion causes depolarisation (more positive)? What ion causes hyperpolarisation (even more negative)?

A

Depolarisation - Na+. Excitatory post-synaptic potential.

Hyperpolarisation - Cl-. Inhibitory post-synaptic potential.

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4
Q

What is signal integration ?

A

Sum of all the individual EPSPs and IPSPs.

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5
Q

Motor output comes from the motor cortex, which projects through X to Y, where it synapses with Z. What’s X, Y, and Z?

A

Pyramidal Tracts.
Spinal Cord.
Peripheral Motor Neurons. Other pathways run parallel from cortex, basal ganglia, and cerebellum via brainstem and spinal cord - called extrapyramidal system.

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6
Q

Motor control systems in the cortex are … ?

A
  1. Primary motor cortex - source of pyramidal tract neurons.
  2. Supplementary motor cortex - conception or initiation of movement. Lesions cause deficits in voluntary movement or speech.
  3. Premotor cortex - important in motor coordination. Lesions cause impairments in stability of stance and gait.
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7
Q

What does basal ganglia do ?

A

It basically modulates motor activity patterns.

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8
Q

Where are the sound waves converted into vibration ? Organ of … ?

A

Basilar membrane ?

Organ of Corti.

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9
Q

Deafness causes (three) ?

A
  1. Sensorineural - inability of the auditory nerve fibres to be excited in the normal manner.
  2. Conduction - disorders of the outer or middle ear, which prevent sound vibrations reaching the cochlea.
  3. Central - damage in the brain.
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10
Q

What is analgesia ? Where in brain is it believed to be a pain perception “centre” ?

A

It is the modulation of pain/nociception.

Probably cingulate cortex.

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11
Q

What molecule blocks analgesia ?

A

Naloxone.

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12
Q

Three types of opioid analgesia .. ?

A

I. Spinal - delta and kappa receptors - enkephalins, dynorphins.
II. Subraspinal - opioid receptor activation in the brain stem. mu receptors - morphine and endorphins.
III. Hormonal - adrenal, etc.

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13
Q

Non opioid-analgesia .. ?

A

i. Brain stem - noradrenaline and 5HT (serotonin)
ii. Spinal cord - noradrenaline blocks response to noxious stimuli, 5HT is analgesic.
iii. Periphery - anti-histamines and anti-inflammatories reduce impact of the injury, local anaesthetics.
iv. Others can include - stress, TENS, acupuncture, hypnosis, cognitive, placebo.

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14
Q

What is longitudinal fissure and corpus callosum ?

A

Longitudinal fissure “splits” brain in two and they communicate through the corpus callosum (large tract of neurones connecting two sides).

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15
Q

What part of the brain is responsible for circadian rhythm ?

A

Superchiasmatic Nucleus, which is located above optic chasm.

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16
Q

Where is it believed that sleep is modulated in the brain ?

A

Probably midbrain.

17
Q

Three dominating theories of mental disorders … ?

A
  1. Psychodynamic - unconscious.
  2. Behavioural - reinforcement/punishment.
  3. Cognitive - interacting with the world.
  4. Humanistic - pursueing own values and goals.
18
Q

OCD is usually treated with … ?

A

Selective Serotonin Reuptake Inhibitors and Cognitive Behavioural Therapy.

19
Q

Types of Schizophrenia.

A

I. Disorganized Schizophrenia: disorganized speech and behaviours, less occurence.
II. Catatonic Schizophrenia: dramatic reduction in activity, voluntary movement might even stop.
III. Paranoid Schizophrenia: delusions, hallucinations.

20
Q

What is borderline personality disorder.

A

BPD is a pervasive pattern of instability in interpersonal relationships, self-image, and emotion as well as marked impulsivity beginning by early adulthood and present in a variety of contexts, as indicated by five (or more) of these criteria:
fear of abandonment – unstable interpersonal relationships – identity disturbance – impulsive behaviour – emotional instability – suicidal behaviour – emptiness – anger – dissociative symptoms or paranoia.

21
Q

Stress response hormone ? all chain of them

A

Firstly a release of corticotrophin releasing factor (CRF), then corticotrophin release, release of stress hormones (glucocorticoids (which ultimately stops release of CRF) and adrenaline) from the adrenal cortex.

22
Q

Explain: tricyclic antideppresants vs. monoamine oxidase inhibitors.

A

MAOI prevent the breakdown of dopamine, 5HT and noradrenaline.
Tricyclics prevent the reuptake of serotonin and noradrenaline.

23
Q

What is natural motivation pathway in human ?

A

Dopaminergic mesolimbi pathway.

24
Q

Necrosis can happen because 1, 2, and 3 ?

A
  1. Excitotoxicity.
  2. Oxidative Stress.
  3. Toxicity from external sources.
25
Q

Alzheimer’s disease - X plaques and neurofibrilallary Y. What’s X and Y?

A

X - amyloid. Y - tangles

26
Q

Two types of strokes .. ?

A

Ischaemic - blockage of blood vessel.

Haemorrhagic - burst of blood vessel.

27
Q

Extinction vs generalisation in CLASSICAL CONDITIONING.

A

Generalisation - generalising fairly similar unconditioned stimulus to the response.
Extinction - eliminating of original learning of conditioned stimulus/response. (it comes back after some time)

28
Q

Types of long-term memory.

A

i. Episodic - personal events that happened in the past - like first time trying to swim.
ii. Semantic - general knowledge of the world - like what is a swimming pool.
iii. Procedural - how to do things - how to swim.
i and ii are explicit (declarative) memory which is conscious and can be explained, whereas iii is implicit and unconscious, very hard or impossible to explain in words.

29
Q

Proactive vs retroactive interference.

A

Proactive - older events interact with newer events.
Retroactive - newer events interact with older events.
The greater the similarity between the two, the greater the chance of interference to occur.