Pscyhopharm exam 1 Flashcards
(28 cards)
Pharmacology
- Study of drug actions and effects on living organisms
- Includes synthetic and natural substances
Neuropharmacology
- Focused on drug-induced changes in cell functioning in nervous system
Psychopharmacology
Drug-induced changes in mood, thinking, and behavior
Neuropsychopharmacology
Focused on identification of chemical substances that alter nervous system and alter behaviors changed by injury, disease or environmental factors
Drug
Any substance that brings about change in biologic function through its chemical actions
Drug action
Specific molecular changes caused by a drug when it binds to specific target or receptor
Drug effects
- Widespread alterations in physiological or psychological functioning.
- Site where these effects can be different
Therapeutic effects
- Interaction between drug and receptor results in desired change, physical or behavioral
- Not all drugs have therapeutic effects
Side Effects
- Unwanted and sometimes unintentional changes caused by interaction between drug and receptor
- All drugs have side effects
Nonspecific drug effects
Changes that occur after drug-receptor interactions due to uniqueness of the person rather than drug-site interaction
Liver (enzyme)
- Critical for metabolism of nutrients
- Increased serum levels of liver enzymes indicate
- Alcoholic hepatitis
- Active viral hepatitis (A, B, C)
- Drug-induced hepatitis
Cytochrome P450
- 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
Pharmacodynamics
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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
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Up-regulation
- Receptor numbers increase
- Due to drug effects
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Down-regulations
- Receptor numbers decrease
- Due to drug effects
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Potency
- Amount of drug necessary to achieve desired behavioral effect
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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
- Diminished response to specific drug after repeated exposure
Pharmacokinetics
Pharmacokinetics: Study of what the body does to the drug
- Determines onset, duration and intensity of the drug’s effect
Four factors:
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Absorption: How body “takes in” the drug?
- Determined by drug’s physiochemical properties, formulation and route of administration
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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?
Absorption
- Crossing the blood-brain barrier
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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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Passive Transport:
Blood-Brain Barrier
- Dense network of blood vessels
- Supplies brain with nutrients
- Keeps out toxins
- Cerebrospinal fluid created by choroid plexus (lateral ventricle)
Distribution
- How drug is distributed to body tissues
- Usually uneven
- Distribution is slow to muscles and lipids
First-order kinetics
Half-life
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First-order kinetics
- Drug clearance
- How much gets through in the first pass
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Half-life
- The amount of time required for 50% of a drug to be eliminated from the body
Binding
- 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
Steady State plasma level
Zero-order kinetics
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Steady State plasma level:
- Desired blood concentration of drug in order to have therapeutic effects
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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
Biotransformation
- 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
Excretion
- The process of elimination of drug
- Through the kidneys
- If hydrophilic
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Other routes include:
- GI tract
- Lungs
- Sweat
- Saliva
- Breast milk
Half LIfe
- 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
Why Side Effects
- Symptoms occur because of chemical reactions
- Medications effect chemicals all over body
- Thus we have side effects
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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.
- Many molecules bind to more than one receptor