Lecture 15 - antidepressants Flashcards

1
Q

what is unipolar depression?

A
  • mood swings always in the same direction
  • reactive (75%) associated with stressful life and accompanied by anxiety, agitation.
  • endogenous (25%) is unrelated to external stress
  • both treated same way
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2
Q

what is bipolar disorder?

A
  • depression alternates with mania characterised by excessive exuberance, enthusiasm, self-confidence is combined with irritability, impatience and aggression.
  • bipolar is hereditary
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3
Q

symptoms of depression?

A
  • low mood (anhedonia), negative thoughts, misery
  • apathy (loss of interest in daily activities)
  • severe weight loss/gain
  • low self-esteem
  • sleep disturbance
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4
Q

what is the diagnosis for depression?

A
  • caused by stressful life events and genetic risk (40%)
  • secondary to illness (cushing’s) side effect of a drug
  • patients have depressed behaviour for more than 2 weeks
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5
Q

what brain regions have an antidepressant effect?

A

deep brain stimulation of subgenual cingulate cortex or nucleus accumbens has an antidepressant effect on individuals after treatment. Mediated by inhibiting activity of these regions

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6
Q

action of brain-derived neurotrophic factor (BDNF)

A

BDNF within mesolimbic dopamine circuit mediates social stress, through activation of transcription factor CREB through phosphorylation

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7
Q

what is the importance of the amygdala?

A

shown to be important limbic node for processing emotionally salient stimuli like fearful faces

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8
Q

what does stress cause?

A

decreases concentrations of neurotrophins (BDNF). decreased activity of CREB result from high levels of cortisol which is the stress hormone released from adrenal cortex

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9
Q

what does metabolic hormones produce?

A

ghrelin and leptin produce mood-related changes through their effects on hypothalamus and several limbic regions

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10
Q

what is the effect of postnatal depression?

A

happens shortly after giving birth and the children of the mother are more likely to have depression

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11
Q

what is the acute stress animal model of depression?

A
  • behaviours caused by some conditions that trigger human depression.
  • forced-swim test quantifies immobility in a water bath. antidepressants increase escape behaviour.
  • model used for coping behaviours
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12
Q

what is the chronic stress animal for depression?

A
  • shows structural, transcriptional and epigenetic changes in several brain changes.
  • learned helplessness is where rodents are exposed to repeated inescapable foot shock resulting in failure to escape and depression.
  • animals have stressful stimuli over a 2 week period
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13
Q

what is the monoamine hypothesis?

A

depletion of monoamine transmitters (noradrenaline and serotonin) causes depression. drugs like reserpine can cause this.

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14
Q

what neurotransmitters promote neurogenesis?

A

serotonin and noradrenaline through their 5HT1A receptors and alpha2 adrenoreceptors via BDNF. BDNF binds to TrkB receptors

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15
Q

what does over activation of glutamatergic NMDA cause?

A

neuronal degeneration

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16
Q

how does iproniazid support the monoamine hypothesis?

A

first specific anti-depressant, acting as a monoamine oxidase inhibitor and increases central noradrenergic and serotonergic transmission

17
Q

how does reserpine support monoamine hypothesis?

A

produces depression and parkinsonism, depletes stores of monoamine transmitters

18
Q

antidepressant drugs

A
  • monoamine oxidase inhibitors e.g. phenylazine
  • tricyclic antidepressants (TCA) e,g, imipramine
  • selective serotonin reuptake inhibitors e.g. fluoxetine
19
Q

action of MAO inhibitors

A

type A (NA and serotonin) produces anti-depressant effect
type B is useful in parkinson’s
- produce rapid and sustained increase of serotonin

20
Q

what are the side effects of MAO inhibitors?

A

cause postural hypotension because of the noradrenaline depletion in sympathetic terminals

21
Q

what causes the hypertension?

A

combined with dietary sources of tyramine (cheese,wine) is not being broken down by MAO because of MAOIs. this problem avoided by reversible MAO inhibitor moclobemide.

22
Q

what are the dangers of tricyclic antidepressants (TCA)

A

in overdose causes excitement, convulsions and then a coma with respiratory depression (increased by alcohol), cardiotoxicity due to block of HERG channels

23
Q

action of antidepressants (TCA)

A

inhibit neural reuptake of NA and serotonin

24
Q

side effects of TCA

A

associated with anticholinergic (dry mouth, blurred vision and constipation.
in adrenergic system the side effects are postural hypotension and histaminergic causing sedation

25
Q

what does excessive central stimulation of noradrenergic pathways in CNS cause?

A

leads to tremors, excitement, insomnia and in overdose convulsions happen
side effects are increased appetite and weight

26
Q

what is the precursor to serotonin?

A

tryptophan - an essential amino acid in protein rich foods and chocolate as well as dietary supplements

27
Q

what are the side effects of SSRI’s?

A

nausea, insomnia and sexual dysfunction but there is less sedative effects then TCA’s and less antimuscarinic effects

28
Q

what serotonin receptor is the only ligand gated?

A

5HT3

29
Q

what serotonin receptors are Gi(inhibitory)

A

5HT1 and 5HT5

30
Q

what serotonin receptors are Gq (phosphorylation)

A

5HT2

31
Q

what serotonin receptors are Gs?

A

5HT4,6 and 7

32
Q

what is the action of SSRIs?

A

bind to p glycoprotein - molecule in BBB to transport drugs back into bloodstream. they inhibit neurotransmitter release by serotonin