Partial agonist

{{Short description|Agonist drug having partial efficacy at a receptor}} class=skin-invert-image|thumb|Relationship between percentage activity and concentration of full agonists and partial agonists In pharmacology, '''partial agonists''' are drugs that bind to and activate a given receptor, but have only partial efficency at the receptor relative to a full agonist. They may also be considered ligands which display both agonistic and antagonistic effects—when both a full agonist and partial agonist are present, the partial agonist actually acts as a competitive antagonist,<ref>{{cite book |last1=Waller |first1=Derek |last2=Sampson |first2=Anthony P. |title=Medical pharmacology & therapeutics |date=2018 |publisher=Elsevier |location=Edinburgh |isbn=978-0-7020-7167-6 |page=18 |edition=Fifth}}</ref> competing with the full agonist for receptor occupancy and producing a net decrease in the receptor activation observed with the full agonist alone.<ref>{{cite book |first1=Norman |last1=Calvey |first2=Norton |last2=Williams | name-list-style = vanc |year=2009 |chapter=Partial agonists |chapter-url=https://books.google.com/books?id=lnRlU12Q4h8C&pg=PA62 |page=62 |title=Principles and Practice of Pharmacology for Anaesthetists |publisher=John Wiley & Sons |isbn=978-1-4051-9484-6}}</ref> Clinically, partial agonists can be used to activate receptors to give a desired submaximal response when inadequate amounts of the endogenous ligand are present, or they can reduce the overstimulation of receptors when excess amounts of the endogenous ligand are present.<ref>{{cite journal | vauthors = Zhu BT | title = Mechanistic explanation for the unique pharmacologic properties of receptor partial agonists | journal = Biomedicine & Pharmacotherapy | volume = 59 | issue = 3 | pages = 76–89 | date = April 2005 | pmid = 15795100 | doi = 10.1016/j.biopha.2005.01.010 }}</ref>

Some currently common drugs that have been classed as partial agonists at particular receptors include buspirone, aripiprazole, buprenorphine, clobazam, nordazepam, nalmefene and norclozapine. Examples of ligands activating peroxisome proliferator-activated receptor gamma as partial agonists are honokiol and falcarindiol.<ref>{{cite journal | vauthors = Atanasov AG, Wang JN, Gu SP, Bu J, Kramer MP, Baumgartner L, Fakhrudin N, Ladurner A, Malainer C, Vuorinen A, Noha SM, Schwaiger S, Rollinger JM, Schuster D, Stuppner H, Dirsch VM, Heiss EH | title = Honokiol: a non-adipogenic PPARγ agonist from nature | journal = Biochimica et Biophysica Acta (BBA) - General Subjects | volume = 1830 | issue = 10 | pages = 4813–9 | date = October 2013 | pmid = 23811337 | pmc = 3790966 | doi = 10.1016/j.bbagen.2013.06.021 }}</ref><ref>{{cite journal | vauthors = Atanasov AG, Blunder M, Fakhrudin N, Liu X, Noha SM, Malainer C, Kramer MP, Cocic A, Kunert O, Schinkovitz A, Heiss EH, Schuster D, Dirsch VM, Bauer R | title = Polyacetylenes from Notopterygium incisum--new selective partial agonists of peroxisome proliferator-activated receptor-gamma | journal = PLOS ONE | volume = 8 | issue = 4 | article-number = e61755 | year = 2013 | pmid = 23630612 | pmc = 3632601 | doi = 10.1371/journal.pone.0061755 | bibcode = 2013PLoSO...861755A | doi-access = free }}</ref> Delta 9-tetrahydrocannabivarin (THCV) is a partial agonist at CB2 receptors and this activity might be implicated in ∆9-THCV-mediated anti-inflammatory effects.<ref>{{Cite web|url=http://insubriaspace.cineca.it/bitstream/10277/269/1/Phd_thesis_bolognini_completa.pdf|title=PHARMACOLOGICAL PROPERTIES OF THE PHYTOCANNABINOIDS ∆9-TETRAHYDROCANNABIVARIN AND CANNABIDIOL - Phd thesis of: Dr. Daniele Bolognini - PDF|date=2010|access-date=2017-12-14|archive-date=2017-12-15|archive-url=https://web.archive.org/web/20171215000348/http://insubriaspace.cineca.it/bitstream/10277/269/1/Phd_thesis_bolognini_completa.pdf}}</ref> Additionally, Delta-9-Tetrahydrocannabinol (THC) is a partial agonist at both the CB1 and CB2 receptors, with the former being responsible for its psychoactive effects.

== References == {{reflist}}

Category:Pharmacodynamics