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28 Cards in this Set

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Drug
Any chemical substance (usually excluding foods) that alter a biological process in the body; altering normal cellular function, for better or for worse.
Psychopharmacology
The study of how drugs affect the brain and behavior and how psychosocial factors affect the action and effect of drugs.
Psychoactive drug
substance that affects functioning of cells in the CNS and thereby alters psychological processes (e.g., mood, appetite, movement, learning, sleep, sensation, social behaviour etc...)
How many names do drugs have?
3 names:
Chemical name
Generic name
Trade/brand name

e.g., acetyl salacyclic acid (chemical name), A.S.A (generic name) and Asprin (brand name)
Functional Classification
deal with the net neural effects (reducing/increasing neural activity) – has nothing to do with sites and mechanism
What are the two classification schemes for psychoactive drugs?
1.) Functional classification: drugs in the class may have different chemical structures but they have the SIMILAR behavioral and conscious effects

2.) Neuro-chemical system affected: different drugs that all affect the same NT, enzyme, protein etc... (e.g., chollinergic drugs)
What are the functional Classifications of drugs with at least one example of each class?
1.) CNS depressants: " the sedatives" - ethyl alcohol, opiates, Canabis

2.) CNS Stimulates -"the psychostimulants" - cocain, caffeine

3.) Anagesics - " Pain killers" - asprin, morphine

4.) Anaesthetics - two types:
-topical (the cain's)
-systemic: general anesthetics (e.g., alcohol, barbiturates)

5.) Hallucinogens: LSD 25, MDMA

6.) Anxiolytics: relieving anxiety (sedatives) - benzo, barbiturates

7.) Anti-psychotics: "major tranqualizers" - clozapine, haldol

8.) Antidepressants: MAOI, SSRI

9.) Anti-mania drugs - Lithium chloride
What are the determinants of drug activity?
Drug : the neurochemistry of the substance which has a fairly similar reaction on everyone.

SET: psychological expectations and knowledge (correct or incorrect) about the drug and attitudes.

SETTING: psychosocial and physical context (medical setting, friends, strangers)
Single Blind
participants randomly assigned to either active or placebo group - but they dont know which one they are in during the study
Double Blind
the person administering the drug and participants dont know what group they are in
What are the drug-host-environment factors?
1.) Drug factors
2.) Person factors (individual and group differences)
3.) Environmental factors
Drug Factors
-Ease of absorption
-Method of administration
-potency/purity of drug
-interactions w/ other drugs
Person Factors
-Tolerance and dependence
-Personal experience w/ drug, attitudes, knowledge and expectations
- Reason for use
-Circadian rhythms:e.g., NT, hormones, sleep deprivation, arousal etc..
-Self medication
-explore other realities (artists)
-Background mood at the time of use
Environmental factors
-Physical surrounding : familiarity, perceived safety, lab, clinic, home ...
-social surrounding: prerscribed vs. self administered
Pharmacokinetics
-What the body does to the drug!
the movement of the drug though the body
availability of the drug
breakdown/elimination of the drug
Routes of administration
Oral
Intravenous (I.V.)
Intramuscular (I.M.)
Intraperitoneal (I.P.)
Subcuttaneous (S.C./S.Q.)
INhalation
I.C.V
Intrathecal
transdermal
intranasal
Other factors that contribute to drug activity?
lipid-solubility
ionization (pk of the drug)
food (empty stomach vs. not)
gender
size
fat content
blood brain barrier**
First order kinetics
half lives of drugs
half the drug in the body is eliminated during 1 half life
-almost all drugs have half lives
Zero order kinetics
constant clearance rate
only drug that we know does this is alcohol.... 1 ounce/100 proof per hr.
Pharmacodynamics
What the drug does to the bodu

the physiological and biochemical interaction of drug molecules with the target tissue
Categories of NT
Amino acids: GABA, Glutamate
Monoamines: Dopamine, serotonin
Protiens: Opioids
Steroids: testosterone, estradiol
Therapeutic index
TI = LD50/ED50
TI = the dose at which 50% of the pop experience fatal side effects ( respiratory depression(/ the dose at which 50% of the pop experience desired effects (reduced anxiety)
DRC (Dose response curve)
Helps us compare efficacy and potency of drugs
What the three forms of tolerance?
1.) metabolic tolerance
- upregulation of drug breaking enzymes increase (e.g., alcoholics develop in their stomach to help the liver out)

2.) pharmacological tolerance
- alter the number of proteins available to act on (e.g., cocaine:down regulation, benzo: upregulation

3.)behavioral tolerance: cool phenomenon whereby tolerance to a behavioral effect occurs ONLY if the effect has been experienced during the drug use.
Cross tolerance
Sometimes a tolerance to one drug will also cause a tolerance to other drugs
Only if the drug uses the same NT
Withdrawal effect
The withdrawal effect is exactly opposite of the drug effect

stimulant: tolerance --> withdrawal ---> depression, lethargy, exhaustion

depressant:tolerance ---> withdrawal --> hyper-stimulation, over-excitation
Side Effect
are merely real effect of the drug that you dont want at the moment
List the different drug interactions
Occlusive: one drug cancels the other
Additive: effects of the two summate linearly (1+1 =2)
Synergistic: hyperadditive effects of two drus togehr is more than equal to the sum of the two drugs taken individually (1+1 =5)
potentiating: effects of the drug is to make another, norammyl inactive, substance active (e.g., caffine w/ tylenol)