DRUG RECEPTOR INTERACTIONS
Roselyn Aperocho-NaranjoPharmacy InstructorUniversity of Southern Philippines Foundationwww.roselynnaranjo.vze.com
Definition of Terms
Receptors – are chemicals which binds to the drug to exert a pharmacologic effect.
Formula:
D + R = D-R ------ Drug Response
Note: Binding of a drug to the receptor is usually reversible
A Receptor is analogous to
a switch in that it has two
configurations: “ON” and “OFF”
Definition of Terms
Receptor
Four Primary Receptor Families 1. Cell-membrane embedded proteins
2. Ligand-gated Ion Channel
3. G –protein coupled Receptor Systems
4. Transcription Factors
Definition of Terms
Agonist – are molecules that activates receptors.
- a drug that has both affinity and high intrinsic activity.
Many drugs produce their effects by acting as an agonist. For example:
DOBUTAMINE - it mimics the action of norephenephrine at the receptors on the
heart. Thereby causing the heart to contract and increase the heart beat.
Definition of Terms
Affinity – allows the agonist to bind to receptors.
Intrinsic Activity – allows the bound agonist to
activate or turn on its receptor
function.
Definition of Terms
Antagonist – molecules that acts against and blocks
drug action
Types of Antagonism
Chemical Antagonism Interaction of drug (agonist) with another
chemical (antagonist) outside of receptor to form an inactive complex.
Competitive Antagonism Drug (agonist) is displaced from drug-receptor
binding by another chemical (antagonist). It is reversible and depends on actual drug and
antagonist concentration in the biophase. Law of mass action
Types of Antagonism
Partial Antagonism Antagonist has high affinity but low
intrinsic activity
Non-equilibrium Antagonism Antagonist forms irreversible receptor
binding
Noncompetitive Antagonism Agonist and antagonist bind to different
receptors and have opposite pharmacologic actions
Types of Pharmacologic Action of the Drugs Structural Non-specific Drugs
- drugs which do not depend its pharmacologic action to the chemical structure of the drug.
- only its structure affects its physicochemical property.
- slight modification of its structure does not produce a change in its pharmacologic action.
Types of Pharmacologic Action of the Drugs Structural Specific Drugs
- drugs in which the pharmacologic action directly depend on its chemical structure
- it attaches itself to a receptor in the biophase
Three Prerequisites of the binding of drug to the receptor
1. chemical reactivity2. presence of functional group3. electronic distribution4. mirror-like image of the receptor
Drug-Receptor Theories
Hypothesis of Clark
“ The Pharmacologic effect of the drug depends on the percentage of the receptors occupied”
If receptors are occupied, maximum effect is obtained.
Chemical binding follow the Law of Mass Action.
Drug-Receptor Theories
Hypothesis of Ariens and Stephenson“ Effectiveness of a drug lasts as long as the
receptor is occupied. Many substance possess different effect , some have high affinity for the receptor, some have low affinity and some are not effective, and those ineffective substances block or inhibit the receptor.”
It is also called Occupation Theory.
Drug-Receptor Theories
Hypothesis of Paton
“ Effectiveness of a drug does not depend on the actual occupation of the receptor but by obtaining proper stimulus”
This is also known as the Rate Theory.
Drug-Receptor Theories
Lock and Key Hypothesis
“ The drug molecule must fit into the receptor like a key fits into the lock”
Known as the Intrinsic Activity.
GOOD LUCK
and
Prepare ½ crosswise….