Pharmacodynamicslibvolume2.xyz/biotechnology/semester6/clinicalandpharmaceuticalbiotechnology/...Pharmacodynamics...
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Pharmacodynamics
Prof. Dr. Öner SüzerCerrahpaşa Medical Faculty
Department of Pharmacology and Clinical Pharmacologywww.onersuzer.com
Last updated: 13.05.2010
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English Pharmacology Textbooks
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Contents of the lecturePharmacodynamics deals with what drugs do for humanbody.Subjects to be discussed:Mechanisms of drug actionsDrug-receptor interactionDose (concentration) - effect relationshipFactors that modify drug actions and drug interactionsAdverse drug reactions (drug toxicology)
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Molecular targets for drugs IEnzymes such as: Acetylcholine esterase, choline acetyltransferase, cyclooxygenase, xanthine oxidase, angiotensin-convertingenzyme, carbonic anhydrase, HMG-CoA reductase, Dopadecarboxylase, monoamine oxidase, dihydrofolatereductase, DNA polymerase…
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Molecular targets for drugs IITransport proteins such as:Choline transporter at terminal neuron, vesicularnorepinefrine uptake, norepinefrine reuptake1, proximaltubular secretion (for weak acids), Na+/K+/2Cl- cotransportat loop of Henle, Na+/K+-ATPase pump, proton pump at gastric mucosa...
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Molecular targets for drugs IIIIon channels such as:Receptor or voltage gated Na+, K+, Ca2+, Cl- channels.
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Molecular targets for drugs IVReceptors such as:Acetylcholine receptors, adrenergic receptors, histaminereceptors, opioid receptors, serotonine receptors, dopaminreceptors, prokineticin receptors, insulin receptors, estrogen receptors, progesterone receptors, ryanodinereceptors…
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ReceptorsThe effects of most drugs result from their interaction with macromolecular components of the organism. These interactions alter the function of the pertinent component and thereby initiate the biochemical and physiological changes that are characteristic of the response to the drug.The term receptor denotes the component of the organism with which the chemical agent is presumed to interact.For recent and updated information please referhttp://iuphar-db.org
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The concept of drugs acting on receptors generally is credited to John Langley (1878). While studying the antagonistic effects of atropine against pilocarpine -induced salivation, Langley observed, "There is some substance or substances in the nerve ending or gland cell with which both atropine and pilocarpine are capable of forming compounds." He later referred to this factor as a "receptive substance." The word receptor was introduced in 1909 by Paul Ehrlich. Ehrlich postulated that a drug could have a therapeutic effect only if it has the "right sort of affinity." Ehrlich defined a receptor in functional terms: "… that combining group of the protoplasmic molecule to which the introduced group is anchored will hereafter be termed receptor."
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Drug-Receptor Binding and Agonism IA receptor can exist in at least two conformational states, active (Ra), and inactive (Ri). If these states are in equilibrium and the inactive state predominates in the absence of drug, then the basal signal output will be low.The extent to which the equilibrium is shifted toward the active state is determined by the relative affinity of the drug for the two conformations.
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Drug-Receptor Binding and Agonism IIA drug that has a higher affinity for the active conformation than for the inactive conformation will drive the equilibrium to the active state and thereby activate the receptor. Such a drug will be an agonist.A full agonist is sufficiently selective for the active conformation that at a saturating concentration it will drive the receptor essentially completely to the active state.
Goodman & Gilman Pharmacology, 11th edition
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Drug-Receptor Binding and Agonism IIIIf a different but perhaps structurally similar compound binds to the same site on R but with only moderately greater affinity for Ra than for Ri , its effect will be less, even at saturating concentrations.A drug that displays such intermediate effectiveness is referred to as a partial agonist because it cannot promote a full biological response at any concentration.In an absolute sense, all agonists are partial; selectivity for Ra over Ri cannot be total.
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AntagonismA drug that binds with equal affinity to either conformation will not alter the activation equilibrium and will act as a competitive antagonist of any compound, agonist or antagonist, that does.A drug with preferential affinity for Ri actually will produce an effect opposite to that of an agonist; examples of such inverse agonists at G protein-coupled receptors (GPCRs) do exist (e.g., famotidine, losartan, metoprolol, and risperidone).
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Receptor types
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Type 1. Ligand-gated ion channelsThese receptors are located at the membrane. Their celulareffects are mediated via ion channels coupled directly (e.g. Na+, K+, Ca2+, Cl- channels).Effect occurs in miliseconds.Examples: nicotinic acetylcholine receptors, GABAAreceptor, NMDA receptor.
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Ligand-gated ion channels
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Type 2. G-protein coupled receptors (GPCR)
These receptors are located at the membrane. Their celulareffects are mediated via G-protein coupled secondmessengers.Effect occurs in seconds.Examples: muscarinic acetylcholine receptors, adrenergicreceptors, GABAB receptor, metabotropic glutamatereceptor.
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G-protein-coupled receptors
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Effectors controlled by G-proteins I
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Effectors controlled by G-proteins II
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Effectors controlled by G-proteins III
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G-protein coupled celular events
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Type 3. kinase-linked receptorsThese receptors are located at the membrane. Their celulareffects are mediated via tyrosine kinase or guanylatecyclase.Effect occurs in minutes (sometimes in hours).Examples: Tyrosine kinase-linked, insulin receptor, cytokine and growth factor (e.g. epidermal and plateletderived growth factors) receptors; guanylate cyclaselinked, atrial natriuretic factor (ANF) receptor.Guanylate cyclase related events are mediated via protein kinase G (PKG).
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Tyrosine kinase mediated secondmessengers
Insulin receptor (when activated tyrosine kinase initiatesvarious celular events and intracelular cAMP decreases)Ras/Raf/Mek/MAP kinase pathway is stimulated via growthfactors which are important for cell division anddifferentiationJak/Stat pathway is stimulated via cytokines which areresponsible for synthesis and release of manyinflammatory mediators
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Kinase-linked receptors
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Growth factor (Ras/Raf) pathway
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Cytokine (Jak/Stat) pathway
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Type 4. Cytoplasmic or nuclear receptorsSteroid hormon, vitamine D and retinoic acid receptors arelocated at the cytoplasm. These hormons effect on gene transcription on DNA via (heat shock proteins, HSP).Tyroid hormon receptors are located at the nucleus.Effect depends on new protein synthesis and occurs in hours. Synthesis of effector proteins controlled via complexcontrol cascades.
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Steroid receptors
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Dose-response relationshipQuantal dose-response relationship: Effect of drug is “allor none” (action is either present or absent).Graded dose-response relationship: Effect of drug is enhanced with increasing concentration/dosage.
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Graded dose-response relationship
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Drug antagonismChemical antagonism: Antagonist binds to agonist anddeactivates/neutralizes. Most of the chemical antagonistsare antidotes.Pharmacological antagonism: Agonist and antagonisteffects directly or indirectly on the same receptor. It can be competetive or non-competetive.Physiological antagonism: Antagonist effects on a physiological mechanism that is antagonist to the pathwaythat agonist effects.Pharmacokinetic antagonism: Interaction of antagonist on absorption, distribution, metabolism, and elimination(ADME) of agonist.
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Quantifying antagonismCharacteristic patterns of antagonism are associated with certain mechanisms of blockade of receptors. One is simple competitive antagonism, whereby a drug that lacks intrinsic efficacy but retains affinity competes with the agonist for the binding site on the receptor. The characteristic pattern of suchantagonism is the concentration-dependent production of a parallel shift to the right of the agonist dose-response curve with no change in the maximal asymptotic response.Competitive antagonism is surmountable by a sufficiently high concentration of agonist.The magnitude of the rightward shift of the curve depends on the concentration of the antagonist and its affinity for the receptor. The affinity of a competitive antagonist for its receptor therefore can be determined according to its concentration-dependent capacity to shift the concentration-response curve for an agonist rightward, as analyzed by Schild (1957).
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Reversible competitive antagonism I
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Reversible competitive antagonism IIDose Ratio (r):The ratio=agonist concentration (dose) required to produce a givenresponse (effect) in the presence of an antagonistagonist concentration (dose) required to produce the sameresponse in the absence of an antagonist
Schild plot (regression): When logarithm of antagonistconcentration (logC) is plotted on X axis, and log(r-1) on Y axis, all points are on the same line. The line meets X axis when doseratio is 2 (i.e. log(2-1)=0). The antagonist concentration at thispoint is called KB.KB: The antagonist concentration that makes dose ratio 2 (a constant value).
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Reversible competitive antagonism IIIpA2= -logKB It determines the afinity of antagonist to a given receptor.The pA2 value is constant for a competetive antagonistbinding to the same receptor subtype on different tissues.pA10= -logX10 (X10 is the antagonist concentration thatmakes dose ratio 10).At competitive antagonism: pA2 - pA10 = log(9) = 0.95
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Noncompetitive antagonism IAn antagonist may dissociate so slowly from the receptor as to be essentially irreversible in its action. Under these circumstances, the maximal response to the agonist will be depressed at some antagonist concentrations.Operationally, this is referred to as noncompetitive antagonism, although the molecular mechanism of action really cannot be inferred unequivocally from the effect.
Goodman & Gilman Pharmacology, 11th edition
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Noncompetitive antagonism IINoncompetitive antagonism can be produced by another type of drug, referred to as an allosteric antagonist. This type of drug produces its effect by binding a site on the receptor distinct from that of the primary agonist and thereby changing the affinity of the receptor for the agonist. In the case of an allosteric antagonist, the affinity of the receptor for the agonist is decreased by the antagonist.In contrast, some allosteric effects could potentiate the effects of agonists. The interaction of benzodiazepines (anxiolytics) with the GABAA receptor to increase the receptor's affinity for GABA is an example of allostericpotentiation.
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Noncompetitive antagonism III
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Desensitization and tachyphylaxisContinued stimulation of cells with agonists generally results in a state of desensitization (also referred to as adaptation, refractoriness, or down-regulation) such that the effect that follows continued or subsequent exposure to the same concentration of drug is diminished.This phenomenon known as tachyphylaxis occurs rapidly and is very important in therapeutic situations; an example is attenuated response to the repeated use of β receptor agonists as bronchodilators for the treatment of asthma.
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Thank you