Pscyhopharm exam 1 Flashcards

(28 cards)

1
Q

Pharmacology

A
  • Study of drug actions and effects on living organisms
  • Includes synthetic and natural substances
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2
Q

Neuropharmacology

A
  • Focused on drug-induced changes in cell functioning in nervous system
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3
Q

Psychopharmacology

A

Drug-induced changes in mood, thinking, and behavior

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4
Q

Neuropsychopharmacology

A

Focused on identification of chemical substances that alter nervous system and alter behaviors changed by injury, disease or environmental factors

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5
Q

Drug

A

Any substance that brings about change in biologic function through its chemical actions

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6
Q

Drug action

A

Specific molecular changes caused by a drug when it binds to specific target or receptor

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7
Q

Drug effects

A
  • Widespread alterations in physiological or psychological functioning.
  • Site where these effects can be different
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8
Q

Therapeutic effects

A
  • Interaction between drug and receptor results in desired change, physical or behavioral
  • Not all drugs have therapeutic effects
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9
Q

Side Effects

A
  • Unwanted and sometimes unintentional changes caused by interaction between drug and receptor
  • All drugs have side effects
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10
Q

Nonspecific drug effects

A

Changes that occur after drug-receptor interactions due to uniqueness of the person rather than drug-site interaction

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11
Q

Liver (enzyme)

A
  • Critical for metabolism of nutrients
  • Increased serum levels of liver enzymes indicate
    • Alcoholic hepatitis
    • Active viral hepatitis (A, B, C)
    • Drug-induced hepatitis
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12
Q

Cytochrome P450

A
  • Proteins with a heme (taxi carrier blood brain barrier) group
  • Involves various intracellular electron transfers
  • Oxidation reactions
  • In liver
  • Involves in drug metabolism
  • Leads to drug-drug interactions
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13
Q

Pharmacodynamics

A
  • Pharmacodynamics: Study of what the drug does to the body
    • Other drugs present
    • Chemical interactions
    • Disorders
      • Genetic mutation
      • Malnutrition
      • Parkinson’s disease
    • Affected by physiologic changes
    • Post-receptor effects
    • Aging
    • Receptor binding
  • Up-regulation
    • Receptor numbers increase
    • Due to drug effects
  • Down-regulations
    • Receptor numbers decrease
    • Due to drug effects
  • Potency
    • Amount of drug necessary to achieve desired behavioral effect
  • Tolerance
    • Diminished response to specific drug after repeated exposure
      • Cross-tolerance: drug interaction
      • Acute tolerance: single administration
      • Pharmacodynamic tolerance: changes in cell function compensate for presence of drug
      • Behavioral tolerance: Involves learning
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14
Q

Pharmacokinetics

A

Pharmacokinetics: Study of what the body does to the drug

  • Determines onset, duration and intensity of the drug’s effect

Four factors:

  • Absorption: How body “takes in” the drug?
    • Determined by drug’s physiochemical properties, formulation and route of administration
    • Routes of administration:
      • Oral (pills, liquid): First-pass metabolism, Involves liver
      • Intramuscular (IM, shot): Slower then IV, faster than oral, Drugs can be suspended in oil
      • Subcutaneous (under the skin):
      • Inhalant (breathe in): Absorbed into blood via lungs, Very rapid, Get to brain quickly
      • Intravenously (IV, shot): Most rapid, Accurate, Quick onset of drug action can be dangerous
  • Distribution: How body releases the drug?
  • Biotransformation: What body does to the drug?
  • Excretion: How body gets rid of the drug?
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15
Q

Absorption

A
  • Crossing the blood-brain barrier
    • Passive Transport:
      • Easily moves through membrane
      • Smaller chemical
      • More likely lipophilic
    • Active Transport:
      • Requires higher expenditure of energy
      • Drugs likely endogenous (vitamins, sugars, amino acids)
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16
Q

Blood-Brain Barrier

A
  • Dense network of blood vessels
  • Supplies brain with nutrients
  • Keeps out toxins
  • Cerebrospinal fluid created by choroid plexus (lateral ventricle)
17
Q

Distribution

A
  • How drug is distributed to body tissues
  • Usually uneven
  • Distribution is slow to muscles and lipids
18
Q

First-order kinetics

Half-life

A
  • First-order kinetics
    • Drug clearance
    • How much gets through in the first pass
  • Half-life
    • The amount of time required for 50% of a drug to be eliminated from the body
19
Q

Binding

A
  • How the chemical “sticks” to proteins
  • “free”drug: unbound (not stuck)
    • Can diffuse to tissue sites where drug effects occur
    • Free” drug amount causes drug effects
  • Albumin
    • Critical plasma protein for mental health drugs
    • Acidic drugs bind to albumin
20
Q

Steady State plasma level

Zero-order kinetics

A
  • Steady State plasma level:
    • Desired blood concentration of drug in order to have therapeutic effects
  • Zero-order kinetics:
    • Drug molecules are cleared at constant rate regardless of drug concentration
    • Drug levels are high and receptors are bound
    • Zero clearance: receptors are busy
21
Q

Biotransformation

A
  • Process by which any substance that enters body is changed
    • From hydrophobic or lipophilic
    • to hydrophilic or lipophobic
    • This is done to facilitate the elimination from the body.
  • Metabolizing the chemical
  • Occurs in the liver, primarily
    • Caused by enzymes
    • Produces by-products: metabolites
      • Helpful to reduce symptoms
  • Toxicity
    • Can occur when biotransformation is not working correctly
22
Q

Excretion

A
  • The process of elimination of drug
  • Through the kidneys
    • If hydrophilic
  • Other routes include:
    • GI tract
    • Lungs
    • Sweat
    • Saliva
    • Breast milk
23
Q

Half LIfe

A
  • How long drug stays in body
  • “amount of time required for the serum concentration to be reduced by 50%
  • Used to determine dosage amount and intervals
  • Steady State
    • When drug concentrations in the blood to reach a plateau so the amount administered is equal to the amount being eliminated
24
Q

Why Side Effects

A
  • Symptoms occur because of chemical reactions
  • Medications effect chemicals all over body
  • Thus we have side effects
  • The mechanisms:
    • Many molecules bind to more than one receptor
      • Antipsychotics can bind to DA receptor and Ach muscurinic receptors causing side effects
    • A molecule can bind to receptors in more than one system
      • DA receptors in limbic system and gut.
25
Common Side Effects
* **Anticholinergic Effects** * Dry mouth * Urinary retention * Blurred vision * Headaches * **Orthostasis** * Especially problematic with elderly * **Akathesia** * restlessness
26
Serious Side Effects
* **Dystonic reactions** * Painful muscle spasms * Young males most at risk * Larnygospasm (can’t breathe) is fatal type * **Pseudoparkinson symptoms** * Elderly more at risk * **Tardive Dyskinesia** * Tremors, tongue thrusting, facial movements * Must stop drug * Occurs more with typical antipsychotics * **Agranulocytosis** * Symptoms include fever, easy bruising, mouth sores, flu-like * Decrease in white blood cells * Must stop medica6on immediately * Clozaril has the highest risk
27
Interactions
* Drugs interact with each other as well as foods * Charbroiled foods and cigareqe smoke * These interactions can increase or decrease drug levels * Many psychotropics are used for treating chronic pain * Can interact with each other as well as with medications used for treating mental disorders
28
Medications used for Neuropathic Pain
* Anticonvulsants * Neurontin (gabapentin) * Valproate * Carbamazepine * Clonazepam * Topiramate * Antidepressants: lower doses used than for depression * Elavil (amitriptyline) * Despiramine * Nortriptyline * First choice for pain * Paxil (paroxetine) * Celexa (citalopram)