“Functional selectivity”的意思、由来-开放百科全书

Functional selectivity has been proposed to broaden conventional definitions of pharmacology.

Traditional pharmacology posits that a ligand can be either classified as an agonist (full or partial), antagonist or more recently an inverse agonist through a specific receptor subtype, and that this characteristic will be consistent with all effector (second messenger) systems coupled to that receptor. While this dogma has been the backbone of ligand-receptor interactions for decades now, more recent data indicates that this classic definition of ligand-protein associations does not hold true for a number of compounds; such compounds may be termed as mixed agonist-antagonists.

Functional selectivity posits that a ligand may inherently produce a mix of the classic characteristics through a single receptor isoform depending on the effector pathway coupled to that receptor. For instance, a ligand can not easily be classified as an agonist or antagonist, because it can be a little of both, depending on its preferred signal transduction pathways. Thus, such ligands must instead be classified on the basis of their individual effects in the cell, instead of being either an agonist or antagonist to a receptor.

It is also important to note that these observations were made in a number of different expression systems and therefore functional selectivity is not just an epiphenomenon of one particular expression system.

Examples

One notable example of functional selectivity occurs with the 5-HT_2A receptor, as well as the 5-HT_2C receptor. Serotonin, the main endogenous ligand of 5-HT receptors, is a functionally selective agonist at this receptor, activating phospholipase C (which leads to inositol triphosphate accumulation), but does not activate phospholipase A2, which would result in arachidonic acid signalling. However, the other endogenous compound dimethyltryptamine activates arachidonic acid signaling at the 5-HT_2A receptor, as do many exogenous hallucinogens such as DOB and lysergic acid diethylamide (LSD). Notably, LSD does not activate IP₃ signaling through this receptor to any significant extent. Oligomers; specifically 5-HT_2A–{{abbrlink|mGluR2|metabotropic glutamate receptor 2}} heteromers mediate this effect. This may explain why some direct 5-HT₂ receptor agonists have psychedelic effects, whereas compounds that indirectly increase serotonin signalling at the 5-HT₂ receptors, such as selective serotonin reuptake inhibitors (SSRIs) and monoamine oxidase inhibitors (MAOIs), generally do not; nor do 5HT_2A receptor agonists without constitutive activity at the mGluR dimer, such as lisuride.^[5]

See also

References

1. ^¹{{Cite journal|last=Smith|first=Jeffrey S.|last2=Lefkowitz|first2=Robert J.|last3=Rajagopal|first3=Sudarshan|date=2018-01-05|title=Biased signalling: from simple switches to allosteric microprocessors|journal=Nature Reviews. Drug Discovery|volume=17|issue=4|pages=243–260|doi=10.1038/nrd.2017.229|issn=1474-1784|pmid=29302067|pmc=5936084}}
2. ^{{cite journal | author = Simmons MA | title = Functional selectivity, ligand-directed trafficking, conformation-specific agonism: what's in a name? | journal = Mol. Interv. | volume = 5 | issue = 3 | pages = 154–7 |date=June 2005 | pmid = 15994454 | doi = 10.1124/mi.5.3.4 }}
3. ^{{Cite journal|last=Manglik|first=Aashish|last2=Lin|first2=Henry|last3=Aryal|first3=Dipendra K.|last4=McCorvy|first4=John D.|last5=Dengler|first5=Daniela|last6=Corder|first6=Gregory|last7=Levit|first7=Anat|last8=Kling|first8=Ralf C.|last9=Bernat|first9=Viachaslau|date=8 September 2016|title=Structure-based discovery of opioid analgesics with reduced side effects|journal=Nature|volume=537|issue=7619|pages=185–190|doi=10.1038/nature19112|issn=1476-4687|pmc=5161585|pmid=27533032}}
4. ^{{Cite journal|last=Smith|first=Jeffrey S.|last2=Nicholson|first2=Lowell T.|last3=Suwanpradid|first3=Jutamas|last4=Glenn|first4=Rachel A.|last5=Knape|first5=Nicole M.|last6=Alagesan|first6=Priya|last7=Gundry|first7=Jaimee N.|last8=Wehrman|first8=Thomas S.|last9=Atwater|first9=Amber Reck|date=2018-11-06|title=Biased agonists of the chemokine receptor CXCR3 differentially control chemotaxis and inflammation|journal=Science Signaling|volume=11|issue=555|pages=eaaq1075|doi=10.1126/scisignal.aaq1075|issn=1937-9145|pmid=30401786|pmc=6329291}}
5. ^{{cite journal |vauthors=Urban JD, Clarke WP, von Zastrow M, Nichols DE, Kobilka B, Weinstein H, Javitch JA, Roth BL, Christopoulos A, Sexton PM, Miller KJ, Spedding M, Mailman RB | title = Functional selectivity and classical concepts of quantitative pharmacology | journal = J. Pharmacol. Exp. Ther. | volume = 320 | issue = 1 | pages = 1–13 |date=January 2007 | pmid = 16803859 | doi = 10.1124/jpet.106.104463 }}
6. ^{{cite journal | vauthors = Samuels BA, Nautiyal KM, Kruegel AC, Levinstein MR, Magalong VM, Gassaway MM, Grinnell SG, Han J, Ansonoff MA, Pintar JE, Javitch JA, Sames D, Hen R | title = The Behavioral Effects of the Antidepressant Tianeptine Require the Mu Opioid Receptor | journal = Neuropsychopharmacology | volume = 42| issue = 10| pages = 2052–2063| year = 2017 | pmid = 28303899 | pmc = 5561344 | doi = 10.1038/npp.2017.60 | url = }}
7. ^{{cite journal|last1=Cavalla|first1=D|last2=Chianelli|first2=F|title=Tianeptine prevents respiratory depression without affecting analgesic effect of opiates in conscious rats.|journal=European Journal of Pharmacology|volume=761|pages=268–272|date=August 2015|doi=10.1016/j.ejphar.2015.05.067|pmid=26068549}}

Functional vs. traditional selectivity

Examples

See also

References

Further reading