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Adrenergic antagonist

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Visual definition of an antagonist, where it compared to agonists and reverse agonists.

An adrenergic antagonist is a drug that inhibits the function of adrenergic receptors. There are five adrenergic receptors, which are divided into two groups. The first group of receptors are the beta (β) adrenergic receptors. There are β1, β2, and β3 receptors. The second group contains the alpha (α) adrenoreceptors. There are only α1 and α2 receptors. Adrenergic receptors are located near the heart, kidneys, lungs, and gastrointestinal tract.[1] There are also α-adreno receptors that are located on vascular smooth muscle.[2]

Antagonists reduce or block the signals of agonists. They can be drugs, which are added to the body for therapeutic reasons, or endogenous ligands. The α-adrenergic antagonists have different effects from the β-adrenergic antagonists.

Pharmacology

Adrenergic ligands are endogenous proteins that modulate and evoke specific cardiovascular effects. Adrenergic antagonists reverse the natural cardiovascular effect, based on the type of adrenoreceptor being blocked. For example, if the natural activation of the α1-adrenergic receptor leads to vasoconstriction, an α1-adrenergic antagonist will result in vasodilation.[3]

Some adrenergic antagonists, mostly β antagonists, passively diffuse from the gastrointestinal tract. From there, they bind to albumin and α1-acid glycoprotein in the plasma, allowing for a wide spread through the body. From there, the lipophilic antagonists are metabolized in the liver and eliminated with urine while the hydrophilic ones are eliminated unchanged.[4]

Mechanisms of action

There are three different types of antagonists.

Competitive

While only a few α-adrenergic antagonists are competitive, all β-adrenergic antagonists are competitive antagonists.[5][6] Competitive antagonists are a type of reversible antagonists. A competitive antagonist will attach itself to the same binding site of the receptor that the agonist will bind to. Even though it is in activator region, the antagonist will not activate the receptor. This type of binding is reversible as increasing the concentration of agonist will outcompete the concentration of antagonist, resulting in receptor activation.[7]

Adrenergic competitive antagonists are shorter lasting than the other two types of antagonists. While the antagonists for alpha and beta receptors are usually different compounds, there has been recent drug development that effects both types of the adrenoreceptors.

Phentolamine, an adrenergic antagonist

Examples

Two examples of competitive adrenergic antagonists are propranolol and phentolamine. Phentolamine is a competitive and nonselective α-adrenoreceptor antagonist. Propranolol is a β-adrenoreceptor antagonist.[8]

Non-competitive

While competitive antagonists bind to the agonist or ligand binding site of the receptor reversibly, non-competitive antagonists can either bind to the ligand site or other site called the allosteric site. A receptor's agonist does not bind to its allosteric binding site. The binding of a non-competitive antagonist is irreversible. If the non-competitive antagonist binds to the allosteric site and an agonist binds to the ligand site, the receptor will remain unactivated.[9][10]

An example of an adrenergic non competitive antagonists is phenoxybenzamine. This drug is a non-selective α-adrenergic antagonist, which means it binds to both alpha receptors.[11]

Uncompetitive

There were few if any adrenergic uncompetitive antagonists. An uncompetitive antagonist is slightly different from the other two types of antagonists. The action of an uncompetitive antagonist is dependent on the receptor's prior activation. This means only after the agonist binds to the receptor can the antagonist block the receptor's function.[12]

Examples

Alpha blockers

Beta blockers

Mixed action

Major effects

Major complications of persistent high blood pressure, which can be attenuated by adrenergic antagonists.

Adrenergic antagonists have inhibitory or opposing effects on the receptors in the adrenergic system. The adrenergic system modulates the fight-or-flight response. Since this response, which is mostly seen as an increase in blood pressure, is produced by the release of the endogenous adrenergic ligands, administration of an adrenergic antagonist results a decrease in blood pressure, which is controlled by both heart rate and vasculature tone.[14] Administration of an adrenergic antagonist that specifically targets the beta receptors, results in this decrease in blood pressure by slowing or reducing cardiac output.[15]

Medical uses

Adrenergic antagonists are mostly used for cardiovascular disease. The adrenergic antagonists are widely used for lowering blood pressure and relieving hypertension.[16] These antagonists have a been proven to relieve the pain caused by myocardial infarction, and also the infarction size, which correlates with heart rate.[17]

There are few non-cardiovascular uses for adrenergic antagonists. Alpha-adrenergic antagonists are also used for treatment of ureteric stones, pain and panic disorders, withdrawal, and anesthesia.[18][2]

Limitations

While these adrenergic antagonists are used for treating cardiovascular disease, mainly hypertension, they can evoke harmful cardiac events through prolongation of the QT interval. Some adrenergic antagonists have a diminished ability to reduce stroke compared to placebo drugs.[19][needs update]

Side effects and toxicity

While adrenergic antagonists have been used for years, there are multiple issues with using this class of drug. When overused, adrenergic antagonists can result in bradycardia, hypotension, hyperglycemia and even hypodynamic shock. This is because adrenergic stimulation by agonists results in normal calcium channel regulation. If these adrenergic receptors are blocked too often, there will be an excess in calcium channel inhibition, which causes most of these problems.[20]

See also

References

  1. ^ Wiysonge, CS; Volmink, J; Opie, LH (2007). "Beta-blockers and the treatment of hypertension: it is time to move on". Cardiovasc J Afr. 18 (6): 351–2. PMC 4170499. PMID 18092107.
  2. ^ a b Giovannitti JA, Thoms SM, Crawford JJ (2015). "Alpha-2 adrenergic receptor agonists: a review of current clinical applications". Anesth Prog. 62 (1): 31–9. doi:10.2344/0003-3006-62.1.31. PMC 4389556. PMID 25849473.
  3. ^ The Pharmacology of Adrenergic Blockade, Nickerson, M. (1949). The pharmacology of adrenergic blockade. Pharmacological Reviews, 1(1), 27–101.
  4. ^ a b c d e f g h i j k l Stereospecific Pharmacokinetics and Pharmacodynamics of Beta-Adrenergic Blockers in Humans, Mehvar, R., & Brocks, D. R. (2001). Stereospecific pharmacokinetics and pharmacodynamics of beta-adrenergic blockers in humans.
  5. ^ Haeusler, G (1990). "Pharmacology of beta-blockers: classical aspects and recent developments". J Cardiovasc Pharmacol. 16 Suppl 5: S1-9. doi:10.1097/00005344-199006165-00002. PMID 11527109.
  6. ^ Das, Sambhunath; Kumar, Pankaj; Kiran, Usha; Airan, Balram (2017). "Alpha blockers: A relook at phenoxybenzamine". Journal of the Practice of Cardiovascular Sciences. 3 (1): 11. doi:10.4103/jpcs.jpcs_42_16. ISSN 2395-5414.
  7. ^ "In Vitro Pharmacology: concentration-response curves]". GlaxoWellcome. Retrieved October 19, 2018.
  8. ^ A review of the animal pharmacology of labtalol, a combined alpha- and beta-adrenoceptor-blocking drug, Brittain, R. T., & Levy, G. P. (1976). A review of the animal pharmacology of labetalol, a combined alpha-and beta-adrenoceptor-blocking drug. British journal of clinical pharmacology, 3(4 Suppl 3), 681–684.
  9. ^ Golan, D. E.; Tashjian, A. H.; Armstrong, E. J. (2011). Principles of Pharmacology: The Pathophysiologic Basis of Drug Therapy. Philadelphia: Lippincott Williams & Wilkins. p. 22. ISBN 978-1-60831-270-2.
  10. ^ Craig, C. R.; Stitzel, R. E. (2004). Modern Pharmacology with Clinical Applications. Philadelphia: Lippincott Williams & Wilkins. p. 18. ISBN 978-0-7817-3762-3.
  11. ^ Van der Zee, P. A.; de Boer, A. (2014). "Pheochromocytoma: a review on preoperative treatment with phenoxybenzamine or doxazosin". Netherlands Journal of Medicine. 72 (4): 190–201. PMID 24829175.
  12. ^ Bagetta, G.; Corasaniti, M. T.; Lipton, S. A. (2007). Neuroinflammation in Neuronal Death and Repair. Amsterdam: Elsevier Academic Press. p. 17. ISBN 978-0-12-373989-6.
  13. ^ a b c d e Wiysonge, Charles S.; Bradley, Hazel A.; Volmink, Jimmy; Mayosi, Bongani M.; Opie, Lionel H. (20 January 2017). "Beta-blockers for hypertension". The Cochrane Database of Systematic Reviews. 1: CD002003. doi:10.1002/14651858.CD002003.pub5. ISSN 1469-493X. PMC 5369873. PMID 28107561.
  14. ^ Lymperopoulos, A. (2015). The Cardiovascular Adrenergic System. SpringerLink. ISBN 978-3-319-13680-6.
  15. ^ Simko, Fedor; Baka, Tomas; Paulis, Ludovit; Reiter, Russel J (2016), "Elevated heart rate and nondipping heart rate as potential targets for melatonin: A review", Journal of Pineal Research, 61 (2): 127–37, doi:10.1111/jpi.12348, PMID 27264986
  16. ^ Effects of β-Blockers With and Without Vasodilating Properties on Central Blood Pressure, Pucci, G., Ranalli, M. G., Battista, F., & Schillaci, G. (2015). Effects of β-Blockers With and Without Vasodilating Properties on Central Blood Pressure. Hypertension, HYPERTENSIONAHA-115.
  17. ^ John Malcolm Cruickshank (2010). The Modern Role of Beta-Blockers in Cardiovascular Medicine. Shelton, Conn: PMPH-USA. ISBN 978-1-60795-108-7.
  18. ^ Hollingsworth JM, Canales BK, Rogers MA, Sukumar S, Yan P, Kuntz GM, Dahm P (December 2016). "Alpha blockers for treatment of ureteric stones: systematic review and meta-analysis". BMJ. 355: i6112. doi:10.1136/bmj.i6112. PMC 5131734. PMID 27908918.
  19. ^ Charles Shey, U Wiysonge; Bradley, Hazel A; Mayosi, Bongani M; Maroney, Roy T; Mbewu, Anthony; Opie, Lionel; Volmink, Jimmy (2007). Wiysonge, Charles Shey U (ed.). "Beta-blockers for hypertension". Cochrane Database of Systematic Reviews (1): CD002003. doi:10.1002/14651858.CD002003.pub2. PMC 5369873. PMID 17253471.
  20. ^ Kerns, William (2007). "Management of β-Adrenergic Blocker and Calcium Channel Antagonist Toxicity". Emergency Medicine Clinics of North America. 25 (2): 309–331. doi:10.1016/j.emc.2007.02.001. PMID 17482022.
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