Module 3: Understanding the Biological Components of Mental Illness Flashcards

1
Q

Prefrontal cortex

A

front part of brain; very important for executive functioning; take in the environment; prioritize; make decisions

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2
Q

Amygdala, hippocampus, hypothalamus

A

very important for regulation of emotions and behavior

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3
Q

Function of Brainstem

A
  • Core–regulates internal organs and vital functions
  • Hypothalamus–basic drives and link between thought and emotion and function of internal organs
  • Brainstem–processing center for sensory information coming from all areas of the body
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4
Q

Function of Cerebellum

A
  • Regulates skeletal muscle

- Coordination and contraction of major muscle groups

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5
Q

Functions of Cerebrum

A
  • At very base of brain–responsible for mental activities.
  • Conscious–sense of being
  • Emotional status
  • Memory
  • Control of skeletal muscles–movement
  • Language and communication–difficulties with cerebrum will affect patients language.
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6
Q

Dendrites within the brain

A
  • network of neurons
  • neurons: smallest component of nerves within brain
  • pass signals to various areas of brain
  • neurotransmitters: vehicle for passing these signals
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7
Q

Neuronal cleft

A
  • presynaptic membrane at top
  • postsynaptic membrane at bottom
  • neurotransmitters lie in the neuronal cleft where signals are transferred from neuron to neuron
  • at times there is a lack of neurotransmitters within the cleft (one of the major theories of depression)
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8
Q

Neurotransmitters

A
  • vehicles responsible for carrying signals for neuron to neuron
  • GABA: responsible for psychotic thoughts
  • Serotonin: responsible for depression and depressive disorders (lack of serotonin in neuronal cleft)
  • Norepinephrine
  • Dopamine
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9
Q

Anti-anxiety Medication

Anxiolytics

A
  1. Benzodiazepines (Ativan, Klonopin, Valium)–very short half life; can create tolerance = risk of abuse.
  2. Buspar (non-benzodiazepine)–takes 2-4 wks to start working; useful for patients with chemical dependency issues who can’t take benzos and for children on autism spectrum.
  3. Antidepressants–used as anti-anxiety med for patients with long-standing and chronic anxiety; SSRIs (prozac, paxil, zoloft)
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10
Q

Pharmacodynamics

A

understanding medications impact on the body

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11
Q

Pharmacokinesics

A

understanding the impact of the individuals body on the medication

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12
Q

Treating the elderly

A
  • complicated livers
  • slowed metabolism
  • break up of medication in liver slowly
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13
Q

Anti-depressants

A
  • SSRI (selective serotonin reuptake inhibitors)–introduced as first non-tricyclic antidepressant; Prozac, zoloft, paxil, celexa (lexapro)
  • Tricyclic–older generation; a lot of side effects; not used as much anymore; Amitryptaline, imipramine, nortryptyline
  • Venlafexine–blocks reuptake of serotonin and norepinephrine; newer generation; fewer side effects
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14
Q

Side Effects of Anti-depressants

A
  • TCAs (tricyclic)–sedation, dry mouth, orthostatic hypotension
  • SSRIs–weight gain (esp. Paxil), sedation, sexual dysfunction (men: erectile dysfunction; women: inorgasmia)
  • Venlafaxine (Effexor)–anxiety, nausea, dry mouth
  • Buproprion (Wellbutrin)–contraindicated in individuals w/ seizure hx because it lowers seizure threshold.
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15
Q

Mood Stabilizers

A
  • First introduced in 1970s
  • Lithium
  • Anticonvulsant drugs (depakoate, tegretol, lamictal)
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16
Q

Lithium

A
  • mood stabilizer
  • metabolized and excreted through kidneys
  • people with Lithium toxicity will have damage to their kidneys
  • important to educate patients about salt intake, dehydration that can lead to lithium toxicity
17
Q

Anticonvulsant drugs

depakoate, tegretol, lamictal

A
  • often used for bipolar 1 manic depressive d/o w/ mania (depakoate and tegretol)
  • mood stabilizer for patients of bipolar 2 (lamictal)
  • serious side effects
  • stevens johnson syndrome (necrotizing skin condition; patient looks sunburnt, sloughing off of skin)
  • educate when beginning medication
  • look for rashes that appear on trunk and face (esp. within 1st 8 wks)
18
Q

Antipsychotics

A
  • Conventional Antipsychotics

- Atypical 2nd generational, 3rd generational

19
Q

Conventional Antipsychotics

A

-Phenothiazines
(Thorazine–rarely used now, Haldol, Prolixin)
-Strong blockers of dopamine, ACH, norepinephrine, and histamine–important to consider when talking about side effects

20
Q

Side Effects for Conventional Antipsychotics

A
  1. Dopamine blocade = motor disturbances
    (TD–tardive dyskinesia–permanent reaction to med; dyskinesia–sudden onset of spasms of muscles–psychiatric emergency, treat w/ benadryl; parkinsonism–pt has mask like face, shuffling gait; akathesia–feeling that you just can’t sit still)
  2. Anticholinergic blockade = ACH side effects
    (blurred vision, dry mouth, constipation)
  3. Norepinephrine blockade = vasodilation, orthostatic hypotension
  4. H1 receptor blockade = sedation, weight gain
21
Q

Atypical/Second Generation Antipsychotics

A
  • bind with dopamine in the limbic system vs. basal ganglia
  • largest and most problematic side effect–weight gain and metabolic syndrome (weight gain, increased abdominal girth, diabetes type 2, hypercholesterolemia)
22
Q

Clozapine

A

atypical/3rd generation antipsychotic

  • side effect = agranulocytosis (elimination of WBCs)
  • used as a last resort
  • tightly regulated
  • 2 wk supply dispensed with WBC counts every 2 wks
23
Q

Zyprexa

A

side effect of excessive weight gain