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Pharmacodynamics-I
Dr. Pravin Prasad
M.B.B.S., MD Clinical Pharmacology
Lecturer, Lumbini Medical College & TH
11 December, 2018 (25 Mangsir, 2075),
Tuesday
By the end of the class, MBBS
Ist year students will be able to:
Explain the term pharmacodynamics and its
components
List the common drug targets involved in drug
action with examples
Appraise the different types of:
Drug enzyme interaction
Drug receptor interaction
Introduction
Introduction
Pharmacodynamics is the study of the
biochemical cellular and physiological effects of
drugs and their mechanisms of action
Pharmacodynamics:
What drugs do?
• Effects
How drugs do it?
• Mechanism
Components of
Pharmacodynamics
Principles of Drug action
Stimulation:
Selective enhancement of the level of
activity of specialized cells
Acetylcholine on salivary glands
• Increases secretion of saliva
Principles of Drug action
Depression:
Selective diminution of the level of activity of
specialized cells
Salbutamol on uterine muscles
• Contraction of uterus decreased
Principles of Drug action
Irritation:
Non-selective, often noxious effect on less
specialized cells
• Capsaicin in herpetic neuralgia
Strong irritation  inflammation, necrosis,
morphological damage
• Local alcohol injection in refractory
neuralgia
Principles of Drug action
Replacement:
Use of natural metabolites, hormones, or
their congeners in deficiency states
• Iron supplementation in Iron deficiency
anaemia
• Insulin in Diabetes mellitus
Principles of Drug action
Cytotoxic Action:
Selective cytotoxic action on invading
microbes
• Penicillin, cephalosporins
Selective cytotoxic action on cancer cells
• Methotrexate, Cisplatin
Mechanism of Action of Drugs
By virtue of physical property:
Isaphgula Laxatives
Dimethicone Ulcer dressing
Para-amino benzoic acid Sunscreen
Activated charcoal Drug overdose
131I radioisotopes Hyperthyroidism
Mechanism of Action of Drugs
By virtue of chemical property:
Antacids Hyper-acidity
Potassium permanganate Antibacterial
Chelating agents Heavy metal
poisoning
Cholestyramine
Hypercholesterolemi
a
Mechanism of Action of Drugs
By interacting with protein molecules:
Colchicine
Vinca alkaloids
Taxanes
By interacting with nucleic acids:
Alkylating agents
Sulfonamides
By interacting with macromolecular functional
proteins:
Ion channels
Transporters (Carriers)
Enzymes
Receptors
Drug targets
Cellular macromolecule or macromolecular
complex with which the drug interacts to elicit a
cellular or systemic response.
Mechanism of Action of Drugs
RIC
E
Drug Targets- Ion channels
Drug Targets- Ion channels
Ion channels-
Modify the intracellular ionic composition of
cells
Drugs can be used to modify their
conductance
Can be:
Ligand gated
G-protein gated
Receptors
Drug Targets- Ion channels
Drug Ion channel Use
Quinidine
Myocardial Na+
channels
Arrhythmia
Amiodarone
Myocardial K+
channels
Arrhythmia
Sulfonylurea
s
Pancreatic K+
channels
Insulin
Phenytoin
Neuronal Na+
channels
Epilepsy
Drug Targets- Transporters
(Carriers)
Drug Targets- Transporters
Carrier Transports Blockers
Norepinephrine
transporters
Noradrenaline
(Norepinephrine)
Desipramine,
Cocaine
Gamma butyric
acid transporter
(GAT1)
GABA Tiagabine
Na+ - K+ - 2Cl-
co-transporter
Na+, K+, Cl- Furosemide
Serotonin
Transporter
Serotonin Fluoxetine
Drug Targets- Enzymes
Enzymes:
Optimises the rate of chemical reaction in
our body
Can be stimulated or inhibited using drugs
Increase in activity can also occur by
enzyme induction
Drug Targets- Enzymes
Enzyme stimulation:
Thiamine, Pyridoxine: increase decarboxylase
activity
• Directly stimulated
• Metabolism of formaldehyde, formic acid
enhanced
Adrenaline: increases hepatic glycogen
phosphorylase
• Stimulated through beta receptors
• Increased glycogen breakdown
Drug Targets- Enzymes
Enzyme inhibition:
Nonselective inhibition
• Denature proteins
• Heavy metal salts, strong acids and alkalis
Selective inhibition
• Competitive (equilibrium, non-equilibrium
type)
• Non-competitive
Drug Targets- Receptors
Receptors:
Are the macromolecule or binding site
located on the surface or inside the effector
cell
that serves to recognise the signal
molecule/drug, and
initiate a response to it,
but itself has no other function
Drug Targets- Receptors
Has two sites
Ligand binding domain
• Recognition of physiological molecules/
drugs
Effector domain
• Undergoes functional conformational
changes
Drug Targets- Receptors
Site 1
Site
2
Drug Targets- Receptors
Types (Based on intracellular signalling
molecules)
G-protein Coupled receptors
Ion channel receptors
Transmembrane-enzyme linked receptors
Transmembrane JAK-STAT binding
receptors
Intracellular receptors (cytoplasmic/nuclear)
Drug Targets- Receptors
G-protein coupled receptors (GPCRs)
Examples: α, β receptors, muscarinic
receptors
Consists of 7 transmembrane helices
Linked to various effectors
Action seen in seconds
Coupled to G-protein ( α, β and γ)
Drug Targets- Receptors
G-protein coupled receptors (GPCRs)
Coupled to different transducer mechanisms
• Gs  cAMP, Gi  cAMP
• Gq  Phospholipase C, Go  Ca2+ channel
β and γ subunits:
• As chaperone
• Receptor operated K+ channels
• Voltage gated Ca2+ channels
• GPCR desensitization
Drug Targets- Receptors
β
Gα
Gγ
cAMP
Phospholipase C Ca2+ channels
K+, Ca2+ channels
Drug Targets- Receptors
Ion channel receptors
Examples: nicotinic ACh receptors, GABAA
receptors
Two types:
• G-protein gated
• Ligand gated
Encloses ion selective channels within their
molecules
Drug Targets- Receptors
Agonist
binding Site
α
Na+, K+, Ca2+, Cl-
Drug Targets- Receptors
Transmembrane enzyme-linked receptors
Examples: insulin, epidermal growth factors,
transforming growth factors
Extracellular and intracellular subunits
connected with single transmembrane helix
Intracellular subunit has enzymatic activity
• Tyrosine, serine/threonine
Response seen in minutes to hours
Drug Targets- Receptors
Agonist
binding site
Intracellular
subunit having
enzymatic
activity
t
Drug Targets- Receptors
Transmembrane JAK-STAT binding receptors
Examples: cytokines, growth factors,
prolactin
Extracellular and intracellular subunits
connected with single transmembrane helix
Intracellular subunit has no enzymatic
activity
• On activation, binds to cytosolic protein
Janus Kinase (has enzymatic activity)
Drug Targets- Receptors
Agonist
binding site
Intracellular
subunit with NO
enzymatic
activity
t
Drug Targets- Receptors
Intracellular receptors
Examples: glucocorticoids, androgens,
thyroxine, vitamin D
Can be present in cytoplasm or within
nucleus
Ligand binding domain- carboxy terminus
Effector domain – N-terminus
Response generated by modification of
Drug Targets- Receptors
Ligand
binding
domain
Effector
domain
Conclusion
Pharmacodynamics:
What drug does, How it does and
modification of drug action by another drug
Five principles of drug action
Drug Targets: mainly proteins (RICE)
Other drug targets do exists
Next class…
Tomorrow (10-11 am)
Topics:
Intracellular signaling mechanism, Dose
Response Curve, Therapeutic index,
Therapeutic Window
Any queries?
Thank you!

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Pharmacodynamics part 1

  • 1. Pharmacodynamics-I Dr. Pravin Prasad M.B.B.S., MD Clinical Pharmacology Lecturer, Lumbini Medical College & TH 11 December, 2018 (25 Mangsir, 2075), Tuesday
  • 2. By the end of the class, MBBS Ist year students will be able to: Explain the term pharmacodynamics and its components List the common drug targets involved in drug action with examples Appraise the different types of: Drug enzyme interaction Drug receptor interaction
  • 4. Introduction Pharmacodynamics is the study of the biochemical cellular and physiological effects of drugs and their mechanisms of action Pharmacodynamics: What drugs do? • Effects How drugs do it? • Mechanism
  • 6. Principles of Drug action Stimulation: Selective enhancement of the level of activity of specialized cells Acetylcholine on salivary glands • Increases secretion of saliva
  • 7. Principles of Drug action Depression: Selective diminution of the level of activity of specialized cells Salbutamol on uterine muscles • Contraction of uterus decreased
  • 8. Principles of Drug action Irritation: Non-selective, often noxious effect on less specialized cells • Capsaicin in herpetic neuralgia Strong irritation  inflammation, necrosis, morphological damage • Local alcohol injection in refractory neuralgia
  • 9. Principles of Drug action Replacement: Use of natural metabolites, hormones, or their congeners in deficiency states • Iron supplementation in Iron deficiency anaemia • Insulin in Diabetes mellitus
  • 10. Principles of Drug action Cytotoxic Action: Selective cytotoxic action on invading microbes • Penicillin, cephalosporins Selective cytotoxic action on cancer cells • Methotrexate, Cisplatin
  • 11. Mechanism of Action of Drugs By virtue of physical property: Isaphgula Laxatives Dimethicone Ulcer dressing Para-amino benzoic acid Sunscreen Activated charcoal Drug overdose 131I radioisotopes Hyperthyroidism
  • 12. Mechanism of Action of Drugs By virtue of chemical property: Antacids Hyper-acidity Potassium permanganate Antibacterial Chelating agents Heavy metal poisoning Cholestyramine Hypercholesterolemi a
  • 13. Mechanism of Action of Drugs By interacting with protein molecules: Colchicine Vinca alkaloids Taxanes By interacting with nucleic acids: Alkylating agents Sulfonamides
  • 14. By interacting with macromolecular functional proteins: Ion channels Transporters (Carriers) Enzymes Receptors Drug targets Cellular macromolecule or macromolecular complex with which the drug interacts to elicit a cellular or systemic response. Mechanism of Action of Drugs RIC E
  • 15. Drug Targets- Ion channels
  • 16. Drug Targets- Ion channels Ion channels- Modify the intracellular ionic composition of cells Drugs can be used to modify their conductance Can be: Ligand gated G-protein gated Receptors
  • 17. Drug Targets- Ion channels Drug Ion channel Use Quinidine Myocardial Na+ channels Arrhythmia Amiodarone Myocardial K+ channels Arrhythmia Sulfonylurea s Pancreatic K+ channels Insulin Phenytoin Neuronal Na+ channels Epilepsy
  • 19. Drug Targets- Transporters Carrier Transports Blockers Norepinephrine transporters Noradrenaline (Norepinephrine) Desipramine, Cocaine Gamma butyric acid transporter (GAT1) GABA Tiagabine Na+ - K+ - 2Cl- co-transporter Na+, K+, Cl- Furosemide Serotonin Transporter Serotonin Fluoxetine
  • 20. Drug Targets- Enzymes Enzymes: Optimises the rate of chemical reaction in our body Can be stimulated or inhibited using drugs Increase in activity can also occur by enzyme induction
  • 21. Drug Targets- Enzymes Enzyme stimulation: Thiamine, Pyridoxine: increase decarboxylase activity • Directly stimulated • Metabolism of formaldehyde, formic acid enhanced Adrenaline: increases hepatic glycogen phosphorylase • Stimulated through beta receptors • Increased glycogen breakdown
  • 22. Drug Targets- Enzymes Enzyme inhibition: Nonselective inhibition • Denature proteins • Heavy metal salts, strong acids and alkalis Selective inhibition • Competitive (equilibrium, non-equilibrium type) • Non-competitive
  • 23. Drug Targets- Receptors Receptors: Are the macromolecule or binding site located on the surface or inside the effector cell that serves to recognise the signal molecule/drug, and initiate a response to it, but itself has no other function
  • 24. Drug Targets- Receptors Has two sites Ligand binding domain • Recognition of physiological molecules/ drugs Effector domain • Undergoes functional conformational changes
  • 26. Drug Targets- Receptors Types (Based on intracellular signalling molecules) G-protein Coupled receptors Ion channel receptors Transmembrane-enzyme linked receptors Transmembrane JAK-STAT binding receptors Intracellular receptors (cytoplasmic/nuclear)
  • 27. Drug Targets- Receptors G-protein coupled receptors (GPCRs) Examples: α, β receptors, muscarinic receptors Consists of 7 transmembrane helices Linked to various effectors Action seen in seconds Coupled to G-protein ( α, β and γ)
  • 28. Drug Targets- Receptors G-protein coupled receptors (GPCRs) Coupled to different transducer mechanisms • Gs  cAMP, Gi  cAMP • Gq  Phospholipase C, Go  Ca2+ channel β and γ subunits: • As chaperone • Receptor operated K+ channels • Voltage gated Ca2+ channels • GPCR desensitization
  • 29. Drug Targets- Receptors β Gα Gγ cAMP Phospholipase C Ca2+ channels K+, Ca2+ channels
  • 30. Drug Targets- Receptors Ion channel receptors Examples: nicotinic ACh receptors, GABAA receptors Two types: • G-protein gated • Ligand gated Encloses ion selective channels within their molecules
  • 31. Drug Targets- Receptors Agonist binding Site α Na+, K+, Ca2+, Cl-
  • 32. Drug Targets- Receptors Transmembrane enzyme-linked receptors Examples: insulin, epidermal growth factors, transforming growth factors Extracellular and intracellular subunits connected with single transmembrane helix Intracellular subunit has enzymatic activity • Tyrosine, serine/threonine Response seen in minutes to hours
  • 33. Drug Targets- Receptors Agonist binding site Intracellular subunit having enzymatic activity t
  • 34. Drug Targets- Receptors Transmembrane JAK-STAT binding receptors Examples: cytokines, growth factors, prolactin Extracellular and intracellular subunits connected with single transmembrane helix Intracellular subunit has no enzymatic activity • On activation, binds to cytosolic protein Janus Kinase (has enzymatic activity)
  • 35. Drug Targets- Receptors Agonist binding site Intracellular subunit with NO enzymatic activity t
  • 36. Drug Targets- Receptors Intracellular receptors Examples: glucocorticoids, androgens, thyroxine, vitamin D Can be present in cytoplasm or within nucleus Ligand binding domain- carboxy terminus Effector domain – N-terminus Response generated by modification of
  • 38. Conclusion Pharmacodynamics: What drug does, How it does and modification of drug action by another drug Five principles of drug action Drug Targets: mainly proteins (RICE) Other drug targets do exists
  • 39. Next class… Tomorrow (10-11 am) Topics: Intracellular signaling mechanism, Dose Response Curve, Therapeutic index, Therapeutic Window Any queries? Thank you!