Psychopharmacology
Factors influencing drug effects:
Biological factors: inherited differences in reactions to drugs- initial sensitivity, gender, weight, age
Psychological factors: personality (sensation seeking); “addictive personality”; drug expectancies and beliefs
Social and environmental factors:
Setting: influences effects of alcohol, marijuana, hallucinogenic drugs; whether using alone or with others
Tolerance:
Dispositional tolerance: Increase in the rate of metabolizing a drug with regular use (how fast does your body metabolize it)
Functional tolerance: decreased behavioral effects of a drug with regular use
Acute tolerance: a type of functional tolerance occurring within a single drug dose (tolerance in a short period time, ex: cigarettes)
Protracted tolerance: a type of functional tolerance occurring over 2 or more drug doses
Behavioral tolerance: adjustment of behavior through experience in using a drug (learned tolerance, change in behavior)
Cross-tolerance: tolerance to a drug never taken before resulting from protracted use of other drugs
Explanations of tolerance:
Cell adaptation theory or homeostasis hypothesis
Plasticity of CNS
Reduced synthesis of neurotransmitter
Reduced number of receptor sites = down regulation
Drug compensatory reactions and learning
Biological homeostatic counterreactions
Conditioned stimuli may elicit compensatory reactions
Body tries to keep homeostasis, so it over compensates before you take the drug, so after taking it you are still in homeostasis
Behavioral pharmacology:
Reinforcement and punishment
Operant principles and drug dependence
Drug discrimination study
Conflict paradigm
Animal models and human drug use:
Causal relationship established between drugs and functioning
Ethical issues:
Strict federal regulations guide treatment of animals
Three Rs in research planning:
Reduce the number of animals used to a minimum
Replace use of animals with alternatives if possible
Refine experimental methods to minimize potential pain or distress
Human behavioral pharmacology:
Responsible, voluntary, informed consent of human participants
Placebo controls: control group, enables placebo control (to rule out placebo effects)
Argument that its unethical to give ill people placebos
But only placebo control groups establish that the chemical action of the drug being tested is responsible for the effects
New drug development: Need clinical trials, and FDA approval
Three ways new drugs are found:
Rediscovery of traditional uses of naturally occurring products
Accidental observation of an unexpected drug effect
Synthesizing of known or novel compounds
Three phases of clinical trials
Phase 1: healthy human volunteers, to determine safety
Phase 2: human diagnosed with target disease, to determine efficacy
Phase 3: expands phase 2 with more patients, less controlled trials
Commercial status: drug is given a chemical name, brand name, generic name
Drug companies usually have sole rights to market a drug for 20 years after filing a patent
Generic drugs come out after the 20 years
Drug companies object to generics after all the time, and money spent making it
Generic drugs are equivalent in effect to brand names, but cost 50% less
Generic drugs lower the cost of health care