Receptor antagonist

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This article is about the biochemistry term. For other uses, see Antagonist (disambiguation).
File:Antagonist.png
Antagonists will block the binding of an agonist at a receptor molecule, inhibiting the signal produced by a receptor-agonist coupling.

A receptor antagonist is a type of receptor ligand or drug that does not provoke a biological response itself upon binding to a receptor, but blocks or dampens agonist-mediated responses.[1] In pharmacology, antagonists have affinity but no efficacy for their cognate receptors, and binding will disrupt the interaction and inhibit the function of an agonist or inverse agonist at receptors. Antagonists mediate their effects by binding to the active site or to allosteric sites on receptors, or they may interact at unique binding sites not normally involved in the biological regulation of the receptor's activity. Antagonist activity may be reversible or irreversible depending on the longevity of the antagonist–receptor complex, which, in turn, depends on the nature of antagonist receptor binding. The majority of drug antagonists achieve their potency by competing with endogenous ligands or substrates at structurally-defined binding sites on receptors.[2]

Receptors

Main article: Receptor (biochemistry)

Biochemical receptors are large protein molecules that can be activated by the binding of a ligand (such as a hormone or drug).[3] Receptors can be membrane-bound, occurring on the cell membrane of cells, or intracellular, such as on the nucleus or mitochondrion. Binding occurs as a result of noncovalent interaction between the receptor and its ligand, at locations called the binding site on the receptor. A receptor may contain one or more binding sites for different ligands. Binding to the active site on the receptor regulates receptor activation directly.[3] The activity of receptors can also be regulated by the binding of a ligand to other sites on the receptor, as in allosteric binding sites.[4] Antagonists mediate their effects through receptor interactions by preventing agonist-induced responses. This may be accomplished by binding to the active site or the allosteric site.[5] In addition, antagonists may interact at unique binding sites not normally involved in the biological regulation of the receptor's activity to exert their effects.[5][6][7]

The term antagonist was originally coined to describe different profiles of drug effects.[8] The biochemical definition of a receptor antagonist was introduced by Ariens[9] and Stephenson[10] in the 1950s. The current accepted definition of receptor antagonist is based on the receptor occupancy model. It narrows the definition of antagonism to consider only those compounds with opposing activities at a single receptor. Agonists were thought to turn "on" a single cellular response by binding to the receptor, thus initiating a biochemical mechanism for change within a cell. Antagonists were thought to turn "off" that response by 'blocking' the receptor from the agonist. This definition also remains in use for physiological antagonists, substances that have opposing physiological actions, but act at different receptors. For example, histamine lowers arterial pressure through vasodilation at the histamine H1 receptor, while adrenaline raises arterial pressure through vasoconstriction mediated by β-adrenergic receptor activation.

Our understanding of the mechanism of drug-induced receptor activation and receptor theory and the biochemical definition of a receptor antagonist continues to evolve. The two-state model of receptor activation has given way to multistate models with intermediate conformational states.[11] The discovery of functional selectivity and that ligand-specific receptor conformations occur and can affect interaction of receptors with different second messenger systems may mean that drugs can be designed to activate some of the downstream functions of a receptor but not others.[12] This means efficacy may actually depend on where that receptor is expressed, altering the view that efficacy at a receptor is receptor-independent property of a drug.[12]

Pharmacodynamics

Main article: Pharmacodynamics

Efficacy and potency

By definition, antagonists display no efficacy[10] to activate the receptors they bind. Antagonists do not maintain the ability to activate a receptor. Once bound, however, antagonists inhibit the function of agonists, inverse agonists, and partial agonists. In functional antagonist assays, a dose-response curve measures the effect of the ability of a range of concentrations of antagonists to reverse the activity of an agonist.[3] The potency of an antagonist is usually defined by its IC50 value. This can be calculated for a given antagonist by determining the concentration of antagonist needed to elicit half inhibition of the maximum biological response of an agonist. Elucidating an IC50 value is useful for comparing the potency of drugs with similar efficacies, however the dose-response curves produced by both drug antagonists must be similar.[13] The lower the IC50 the greater the potency of the antagonist, and the lower the concentration of drug that is required to inhibit the maximum biological response. Lower concentrations of drugs may be associated with fewer side-effects.[14]

Affinity

The affinity of an antagonist for its binding site (Ki), i.e. its ability to bind to a receptor, will determine the duration of inhibition of agonist activity. The affinity of an antagonist can be determined experimentally using Schild regression or for competitive antagonists in radioligand binding studies using the Cheng-Prusoff equation. Schild regression can be used to determine the nature of antagonism as beginning either competitive or non-competitive and Ki determination is independent of the affinity, efficacy or concentration of the agonist used. However, it is important that equilibrium has been reached. The effects of receptor desensitization on reaching equilibrium must also be taken into account. The affinity constant of antagonists exhibiting two or more effects, such as in competitive neuromuscular-blocking agents that also block ion channels as well as antagonising agonist binding, cannot be analyzed using Schild regression.[15][16] Schild regression involves comparing the change in the dose ratio, the ratio of the EC50 of an agonist alone compared to the EC50 in the presence of a competitive antagonist as determined on a dose response curve. Altering the amount of antagonist used in the assay can alter the dose ratio. In Schild regression, a plot is made of the log(dose ratio-1) versus the log concentration of antagonist for a range of antagonist concentrations.[17] The affinity or Ki is where the line cuts the x-axis on the regression plot. Whereas, with Schild regression, antagonist concentration is varied in experiments used to derive Ki values from the Cheng-Prusoff equation, agonist concentrations are varied. Affinity for competitive agonists and antagonists is related by the Cheng-Prusoff factor used to calculate the Ki (affinity constant for an antagonist) from the shift in IC50 that occurs during competitive inhibition.[18] The Cheng-Prusoff factor takes into account the effect of altering agonist concentration and agonist affinity for the receptor on inhibition produced by competitive antagonists.[14]

Types

Competitive

Competitive antagonists (also known as surmountable antagonists) reversibly bind to receptors at the same binding site (active site) as the endogenous ligand or agonist, but without activating the receptor. Agonists and antagonists "compete" for the same binding site on the receptor. Once bound, an antagonist will block agonist binding. The level of activity of the receptor will be determined by the relative affinity of each molecule for the site and their relative concentrations. High concentrations of a competitive agonist will increase the proportion of receptors that the agonist occupies, higher concentrations of the antagonist will be required to obtain the same degree of binding site occupancy.[14] In functional assays using competitive antagonists, a parallel rightward shifts of agonist dose–response curves with no alteration of the maximal response is observed.[19] The interleukin-1 receptor antagonist, IL-1Ra is an example of a competitive antagonist.[20] The effects of a competitive antagonist may be overcome by increasing the concentration of agonist. Often (though not always) these antagonists possess a very similar chemical structure to that of the agonist.

Non-competitive

Non-competitive antagonists (sometimes called non-surmountable antagonists) are allosteric antagonists. These antagonists bind to a distinctly separate binding site from the agonist, exerting their action to that receptor via the other binding site. Cyclothiazide has been shown to act as a reversible non-competitive antagonist of mGluR1 receptor.[21] Non-competitive antagonists do not compete with agonists for binding. The bound antagonists may prevent conformational changes in the receptor required for receptor activation after the agonist binds.[22] No amount of agonist can completely overcome the inhibition once it has been established. In functional assays of non-competitive antagonists, depression of the maximal response of agonist dose-response curves, and in some cases, rightward shifts, is produced.[19] The rightward shift will occur as a result of a receptor reserve[10] and inhibition of the agonist response will only occur when this reserve is depleted.

Uncompetitive

Uncompetitive antagonists differ from non-competitive antagonists in that they require receptor activation by an agonist before they can bind to a separate allosteric binding site. This type of antagonism produces a kinetic profile in which "the same amount of antagonist blocks higher concentrations of agonist better than lower concentrations of agonist".[23] Memantine, used in the treatment of Alzheimer's disease, is an uncompetitive antagonist of the NMDA receptor.[24]

Silent antagonists

Silent antagonists are competitive receptor antagonists that have zero intrinsic activity for activating a receptor. They are true antagonists, so to speak. The term was created to distinguish fully inactive antagonists from weak partial agonists or inverse agonists.

Partial agonists

Partial agonists are defined as drugs that, at a given receptor, might differ in the amplitude of the functional response that they elicit after maximal receptor occupancy. Although they are agonists, partial agonists can act as a competitive antagonist in the presence of a full agonist, as it competes with the full agonist for receptor occupancy, thereby producing a net decrease in the receptor activation as compared to that observed with the full agonist alone.[25][26] Clinically, their usefulness is derived from their ability to enhance deficient systems while simultaneously blocking excessive activity. Exposing a receptor to a high level of a partial agonist will ensure that it has a constant, weak level of activity, whether its normal agonist is present at high or low levels. In addition, it has been suggested that partial agonism prevents the adaptive regulatory mechanisms that frequently develop after repeated exposure to potent full agonists or antagonists.[27][28] Buprenorphine, a partial agonist of the μ-opioid receptor, binds with weak morphine-like activity and is used clinically as an analgesic in pain management and in reversing morphine addiction as an alternative to methodone in the treatment of drug addiction.[29]

Inverse agonists

An inverse agonist can have effects similar to those of an antagonist, but causes a distinct set of downstream biological responses. Constitutively active receptors that exhibit intrinsic or basal activity can have inverse agonists, which not only block the effects of binding agonists like a classical antagonist but also inhibit the basal activity of the receptor. Many drugs previously classified as antagonists are now beginning to be reclassified as inverse agonists because of the discovery of constitutive active receptors.[30][31] Antihistamines, originally classified as antagonists of histamine H1 receptors have been reclassified as inverse agonists.[32]

Reversibility

Many antagonists are reversible antagonists that, like most agonists, will bind and unbind a receptor at rates determined by receptor-ligand kinetics.

Irreversible antagonists covalently bind to the receptor target and, in general, cannot be removed; inactivating the receptor for the duration of the antagonist effects is determined by the rate of receptor turnover, the rate of synthesis of new receptors. Phenoxybenzamine is an example of an irreversible alpha blocker—it permanently binds to α adrenergic receptors, preventing adrenaline and noradrenaline from binding.[33] Inactivation of receptors normally results in a depression of the maximal response of agonist dose-response curves and a right shift in the curve occurs where there is a receptor reserve similar to non-competitive antagonists. A washout step in the assay will usually distinguish between non-competitive and irreversible antagonist drugs, as effects of non-competitive antagonists are reversible and activity of agonist will be restored.[19]

Irreversible competitive antagonists also involve competition between the agonist and antagonist of the receptor, but the rate of covalent bonding differs and depends on affinity and reactivity of the antagonist.[13] For some antagonist, there may be a distinct period during which they behave competitively (regardless of basal efficiacy), and freely associate to and dissociate from the receptor, determined by receptor-ligand kinetics. But, once irreversible bonding has taken place, the receptor is deactivated and degraded. As for non-competitive antagonists and irreversible antagonists in functional assays with irreversible competitive antagonist drugs, there may be a shift in the log concentration–effect curve to the right, but, in general, both a decrease in slope and a reduced maximum are obtained.[13]

See also

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References

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Pharmacokinetics
Pharmacodynamics
Agonism and antagonism
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Types
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  1. ↑ "Pharmacology Guide: In vitro pharmacology: concentration-response curves." GlaxoWellcome. Retrieved on December 6, 2007.
  2. ↑ Hopkins AL, Groom CR (2002). "The druggable genome". Nature reviews. Drug discovery. 1 (9): 727–30. doi:10.1038/nrd892. PMID 12209152. 
  3. ↑ 3.0 3.1 3.2 T. Kenakin (2006) A Pharmacology Primer: Theory, Applications, and Methods. 2nd Edition Elsevier ISBN 0-12-370599-1
  4. ↑ May LT, Avlani VA, Sexton PM, Christopoulos A (2004). "Allosteric modulation of G protein-coupled receptors". Curr. Pharm. Des. 10 (17): 2003–13. doi:10.2174/1381612043384303. PMID 15279541. 
  5. ↑ 5.0 5.1 Christopoulos A (2002). "Allosteric binding sites on cell-surface receptors: novel targets for drug discovery". Nature reviews. Drug discovery. 1 (3): 198–210. doi:10.1038/nrd746. PMID 12120504. 
  6. ↑ Bleicher KH, Green LG, Martin RE, Rogers-Evans M (2004). "Ligand identification for G-protein-coupled receptors: a lead generation perspective". Curr Opin Chem Biol. 8 (3): 287–96. doi:10.1016/j.cbpa.2004.04.008. PMID 15183327. 
  7. ↑ Rees S, Morrow D, Kenakin T (2002). "GPCR drug discovery through the exploitation of allosteric drug binding sites". Recept. Channels. 8 (5-6): 261–8. doi:10.1080/10606820214640. PMID 12690954. 
  8. ↑ Negus SS (2006). "Some implications of receptor theory for in vivo assessment of agonists, antagonists and inverse agonists". Biochem. Pharmacol. 71 (12): 1663–70. doi:10.1016/j.bcp.2005.12.038. PMC 1866283 Freely accessible. PMID 16460689. 
  9. ↑ Ariëns EJ (1954). "Affinity and intrinsic activity in the theory of competitive inhibition. I. Problems and theory". Archives internationales de pharmacodynamie et de thérapie. 99 (1): 32–49. PMID 13229418. 
  10. ↑ 10.0 10.1 10.2 Stephenson RP (1997). "A modification of receptor theory. 1956". Br. J. Pharmacol. 120 (4 Suppl): 106–20; discussion 103–5. PMID 9142399.  Full text at PMC: 1510558 of the original article.
  11. ↑ Vauquelin G, Van Liefde I (2005). "G protein-coupled receptors: a count of 1001 conformations". Fundamental & clinical pharmacology. 19 (1): 45–56. doi:10.1111/j.1472-8206.2005.00319.x. PMID 15660959. 
  12. ↑ 12.0 12.1 Urban JD, Clarke WP, von Zastrow M; et al. (2007). "Functional selectivity and classical concepts of quantitative pharmacology". J. Pharmacol. Exp. Ther. 320 (1): 1–13. doi:10.1124/jpet.106.104463. PMID 16803859. 
  13. ↑ 13.0 13.1 13.2 Lees P, Cunningham FM, Elliott J (2004). "Principles of pharmacodynamics and their applications in veterinary pharmacology". J. Vet. Pharmacol. Ther. 27 (6): 397–414. doi:10.1111/j.1365-2885.2004.00620.x. PMID 15601436. 
  14. ↑ 14.0 14.1 14.2 Swinney DC (2004). "Biochemical mechanisms of drug action: what does it take for success?". Nature reviews. Drug discovery. 3 (9): 801–8. doi:10.1038/nrd1500. PMID 15340390. 
  15. ↑ Wyllie DJ, Chen PE (2007). "Taking the time to study competitive antagonism". Br. J. Pharmacol. 150 (5): 541–51. doi:10.1038/sj.bjp.0706997. PMC 2189774 Freely accessible. PMID 17245371. 
  16. ↑ Colquhoun D (2007). "Why the Schild method is better than Schild realised". Trends Pharmacol Sci. 28 (12): 608. doi:10.1016/j.tips.2007.09.011. PMID 18023486. 
  17. ↑ Schild HO (1975). "An ambiguity in receptor theory". Br. J. Pharmacol. 53 (2): 311. PMC 1666289 Freely accessible. PMID 1148491. 
  18. ↑ Cheng Y, Prusoff WH (1973). "Relationship between the inhibition constant (K1) and the concentration of inhibitor, which causes 50 per cent inhibition (I50) of an enzymatic reaction". Biochem. Pharmacol. 22 (23): 3099–108. doi:10.1016/0006-2952(73)90196-2. PMID 4202581. 
  19. ↑ 19.0 19.1 19.2 Vauquelin G, Van Liefde I, Birzbier BB, Vanderheyden PM (2002). "New insights in insurmountable antagonism". Fundamental & clinical pharmacology. 16 (4): 263–72. doi:10.1046/j.1472-8206.2002.00095.x. PMID 12570014. 
  20. ↑ Arend WP (1993). "Interleukin-1 receptor antagonist". Adv. Immunol. 54: 167–227. doi:10.1016/S0065-2776(08)60535-0. PMID 8379462. 
  21. ↑ Surin A, Pshenichkin S, Grajkowska E, Surina E, Wroblewski JT (2007). "Cyclothiazide selectively inhibits mGluR1 receptors interacting with a common allosteric site for non-competitive antagonists". Neuropharmacology. 52 (3): 744–54. doi:10.1016/j.neuropharm.2006.09.018. PMC 1876747 Freely accessible. PMID 17095021. 
  22. ↑ D.E. Golan, A.H Tashjian Jr, E.J. Armstrong, A.W. Armstrong. (2007) Principles of Pharmacology: The Pathophysiologic Basis of Drug Therapy Lippincott Williams & Wilkins ISBN 0-7817-8355-0
  23. ↑ Lipton SA (2004). "Failures and successes of NMDA receptor antagonists: molecular basis for the use of open-channel blockers like memantine in the treatment of acute and chronic neurologic insults". NeuroRx : the journal of the American Society for Experimental NeuroTherapeutics. 1 (1): 101–10. PMC 534915 Freely accessible. PMID 15717010. 
  24. ↑ Parsons CG, Stöffler A, Danysz W (2007). "Memantine: a NMDA receptor antagonist that improves memory by restoration of homeostasis in the glutamatergic system - too little activation is bad, too much is even worse". Neuropharmacology. 53 (6): 699–723. doi:10.1016/j.neuropharm.2007.07.013. PMID 17904591. 
  25. ↑ Principles and Practice of Pharmacology for Anaesthetists By Norton Elwy Williams, Thomas Norman Calvey Published 2001 Blackwell Publishing ISBN 0-632-05605-3
  26. ↑ Patil PN (2002). "Everhardus J. Ariëns (1918–2002): a tribute". Trends Pharmacol. Sci. 23 (7): 344–5. doi:10.1016/S0165-6147(02)02068-0. 
  27. ↑ Bosier B, Hermans E (2007). "Versatility of GPCR recognition by drugs: from biological implications to therapeutic relevance". Trends Pharmacol. Sci. 28 (8): 438–46. doi:10.1016/j.tips.2007.06.001. PMID 17629964. 
  28. ↑ Pulvirenti L, Koob GF (2002). "Being partial to psychostimulant addiction therapy". Trends Pharmacol. Sci. 23 (4): 151–3. doi:10.1016/S0165-6147(00)01991-X. PMID 11931978. 
  29. ↑ Vadivelu N, Hines RL (2007). "Buprenorphine: a unique opioid with broad clinical applications". J Opioid Manag. 3 (1): 49–58. PMID 17367094. 
  30. ↑ Greasley PJ, Clapham JC (2006). "Inverse agonism or neutral antagonism at G-protein coupled receptors: a medicinal chemistry challenge worth pursuing?". Eur. J. Pharmacol. 553 (1-3): 1–9. doi:10.1016/j.ejphar.2006.09.032. PMID 17081515. 
  31. ↑ Kenakin T (2004). "Efficacy as a vector: the relative prevalence and paucity of inverse agonism". Mol. Pharmacol. 65 (1): 2–11. doi:10.1124/mol.65.1.2. PMID 14722230. 
  32. ↑ Leurs R, Church MK, Taglialatela M (2002). "H1-antihistamines: inverse agonism, anti-inflammatory actions and cardiac effects". Clin Exp Allergy. 32 (4): 489–98. doi:10.1046/j.0954-7894.2002.01314.x. PMID 11972592. 
  33. ↑ Frang H, Cockcroft V, Karskela T, Scheinin M, Marjamäki A (2001). "Phenoxybenzamine binding reveals the helical orientation of the third transmembrane domain of adrenergic receptors". J. Biol. Chem. 276 (33): 31279–84. doi:10.1074/jbc.M104167200. PMID 11395517. 
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