1. Types of known neurochemicals
2. Action sites of Neurotransmission
Neurochemicals are classified as neurotransmitters, neuromodulators and neurohormones. Neuortransmitters generally act at the synapse.
3. Drug Actions at the Synapse
Most psychoactive drugs produce their effects by acting at the synapse, including at the action sites of the above illustration. Drugs that enhance the activity of a neurochemical from the target cell are known as agonists. Drugs that reduce the activity are known as antagonists. Actions of an agonists and antagonists link a particular drug to a specific neurochemical and often to a specific receptor type of that chemical. Because neurochemicals are associated with certain brain areas, the drug action can be specifically targeted to a brain region and therefore to a particular behavior. However, no drugs acts at only one place, so there are always other drug actions or side-effects.
Review the Gross Anatomy page to link the areas in blue to their neurochemical.
•Cocaine, Amphetamines ventral tegmental area DA,NE
•Cannabis sativa,
hashish basal ganglia Anandamide
Narcotic opium,
Morphine Descending analgesic circuit Spinal
Column Endogenous Opioids or Peptides
Alcohol All over the brain
GABA
Peyote, PCP, LSD reticular activating system 5-HT
Nicotine Neuromuscular
junction Ach
4. Basic Principles of Pharmacology
In order for drugs to reach the synapse, they must first enter the brain. This process depends on how the drug is administered.
•Pharmacokinetcis =
Movement of drug in and out of the body.
•Drug Dose Ratio of mg/kg =concentration of
drug.
•You must be given two
of the three numbers to compute a drug dose mg/kg.
•“mg”= amount of drug given
• “kg” = weight of person (convert from
pounds)
•
“concentration” = unit of dose.
•Routes of
Administration
•Oral
•Injection
(subcutaneous, intramuscular, intravenous)
•Inhalation
•Others: intranasal,
sublingual and transdermal
•Drug Absorption
•Bioavailability
•Factors that
influence absorption
•Membrane barriers, drug form, size of
surface
•Drug Distribution
•Blood flow, diffusibility, fat solubility,
affinity
•Drug Elimination
•Zero-order kinetics,
first-order kinetics, half-life
•Routes of elimination
•Drug testing and metabolic byproducts
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