5-HT5A receptor

{{Short description|Protein-coding gene in the species Homo sapiens}}

{{DISPLAYTITLE:5-HT5A receptor}}

{{Infobox_gene}}

5-Hydroxytryptamine (serotonin) receptor 5A, also known as HTR5A, is a protein that in humans is encoded by the HTR5A gene.{{cite web | title = Entrez Gene: HTR5A 5-hydroxytryptamine (serotonin) receptor 5A| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=3361}}{{cite journal | vauthors = Rees S, den Daas I, Foord S, Goodson S, Bull D, Kilpatrick G, Lee M | title = Cloning and characterisation of the human 5-HT5A serotonin receptor | journal = FEBS Letters | volume = 355 | issue = 3 | pages = 242–246 | date = December 1994 | pmid = 7988681 | doi = 10.1016/0014-5793(94)01209-1 | s2cid = 36425845 | doi-access = free }} Agonists and antagonists for 5-HT receptors, as well as serotonin uptake inhibitors, present promnesic (memory-promoting) and/or anti-amnesic effects under different conditions, and 5-HT receptors are also associated with neural changes.

Function

The gene described in this record is a member of 5-hydroxytryptamine receptor family and encodes a multi-pass membrane protein that functions as a receptor for 5-hydroxytryptamine and couples to G proteins, negatively influencing cAMP levels via Gi and Go.{{cite journal | vauthors = Francken BJ, Jurzak M, Vanhauwe JF, Luyten WH, Leysen JE | title = The human 5-ht5A receptor couples to Gi/Go proteins and inhibits adenylate cyclase in HEK 293 cells | journal = European Journal of Pharmacology | volume = 361 | issue = 2–3 | pages = 299–309 | date = November 1998 | pmid = 9865521 | doi = 10.1016/S0014-2999(98)00744-4 }} This protein has been shown to function in part through the regulation of intracellular Ca2+ mobilization. The 5-HT5A receptor has been shown to be functional in a native expression system.{{cite journal | vauthors = Goodfellow NM, Bailey CD, Lambe EK | title = The native serotonin 5-HT(5A) receptor: electrophysiological characterization in rodent cortex and 5-HT(1A)-mediated compensatory plasticity in the knock-out mouse | journal = The Journal of Neuroscience | volume = 32 | issue = 17 | pages = 5804–5809 | date = April 2012 | pmid = 22539842 | pmc = 4644074 | doi = 10.1523/JNEUROSCI.4849-11.2012 }}

Rodents have been shown to possess two functional 5-HT5 receptor subtypes, 5-HT5A and 5-HT5B,{{cite journal | vauthors = Matthes H, Boschert U, Amlaiky N, Grailhe R, Plassat JL, Muscatelli F, Mattei MG, Hen R | display-authors = 6 | title = Mouse 5-hydroxytryptamine5A and 5-hydroxytryptamine5B receptors define a new family of serotonin receptors: cloning, functional expression, and chromosomal localization | journal = Molecular Pharmacology | volume = 43 | issue = 3 | pages = 313–319 | date = March 1993 | pmid = 8450829 | url = http://molpharm.aspetjournals.org/cgi/reprint/43/3/313 }} however while humans possess a gene coding for the 5-HT5B subtype, its coding sequence is interrupted by stop codons, making the gene non-functional, and so only the 5-HT5A subtype is expressed in human brain.{{cite journal | vauthors = Nelson DL | title = 5-HT5 receptors | journal = Current Drug Targets. CNS and Neurological Disorders | volume = 3 | issue = 1 | pages = 53–58 | date = February 2004 | pmid = 14965244 | doi = 10.2174/1568007043482606 }}

It also appears to serve as a presynaptic serotonin autoreceptor.{{cite journal | vauthors = Thomas DR, Soffin EM, Roberts C, Kew JN, de la Flor RM, Dawson LA, Fry VA, Coggon SA, Faedo S, Hayes PD, Corbett DF, Davies CH, Hagan JJ | display-authors = 6 | title = SB-699551-A (3-cyclopentyl-N-[2-(dimethylamino)ethyl]-N-[(4'-{[(2-phenylethyl)amino]methyl}-4-biphenylyl)methyl]propanamide dihydrochloride), a novel 5-ht5A receptor-selective antagonist, enhances 5-HT neuronal function: Evidence for an autoreceptor role for the 5-ht5A receptor in guinea pig brain | journal = Neuropharmacology | volume = 51 | issue = 3 | pages = 566–577 | date = September 2006 | pmid = 16846620 | doi = 10.1016/j.neuropharm.2006.04.019 | s2cid = 543423 }}

Clinical significance

The neurotransmitter serotonin (5-hydroxytryptamine, 5-HT) has been implicated in a wide range of psychiatric conditions and also has vasoconstrictive and vasodilatory effects.

Selective ligands

Few highly selective ligands are commercially available for the 5-HT5A receptor, though the field has expanded considerably in recent years.Volk B, Nagy BJ, Vas S, Kostyalik D, Simig G, Bagdy G. Medicinal chemistry of 5-HT5A receptor ligands: a receptor subtype with unique therapeutical potential. Curr Top Med Chem. 2010;10(5):554-78. {{doi|10.2174/156802610791111588}} {{pmid|20166946}}Kordylewski SK, Bugno R, Bojarski AJ, Podlewska S. Uncovering the unique characteristics of different groups of 5-HT5AR ligands with reference to their interaction with the target protein. Pharmacol Rep. 2024 Oct;76(5):1130-1146. {{doi|10.1007/s43440-024-00622-4}} {{pmid|38971919}} When selective activation of this receptor is desired in scientific research, the non-selective serotonin receptor agonist 5-Carboxamidotryptamine can be used in conjunction with selective antagonists for its other targets (principally 5-HT1A, 5-HT1B, 5-HT1D, and 5-HT7). Research in this area is ongoing.{{cite journal | vauthors = Wesołowska A | title = In the search for selective ligands of 5-HT5, 5-HT6 and 5-HT7 serotonin receptors | journal = Polish Journal of Pharmacology | volume = 54 | issue = 4 | pages = 327–341 | year = 2002 | pmid = 12523486 | url = http://www.if-pan.krakow.pl/pjp/pdf/2002/4_327.pdf }}{{cite journal | vauthors = Peters JU, Lübbers T, Alanine A, Kolczewski S, Blasco F, Steward L | title = Cyclic guanidines as dual 5-HT5A/5-HT7 receptor ligands: optimising brain penetration | journal = Bioorganic & Medicinal Chemistry Letters | volume = 18 | issue = 1 | pages = 262–266 | date = January 2008 | pmid = 18023344 | doi = 10.1016/j.bmcl.2007.10.078 }}

= Agonists =

  • LSD:(+)-lysergic acid.The RBI Handbook of Receptor Classification and Signal Transduction, page 114 (1995){{ISBN|0-9640548-1-7}} {{cite journal | vauthors = Zhang S, Chen H, Zhang C, Yang Y, Popov P, Liu J, Krumm BE, Cao C, Kim K, Xiong Y, Katritch V, Shoichet BK, Jin J, Fay JF, Roth BL | display-authors = 6 | title = Inactive and active state structures template selective tools for the human 5-HT5A receptor | journal = Nature Structural & Molecular Biology | volume = 29 | issue = 7 | pages = 677–687 | date = July 2022 | pmid = 35835867 | pmc = 9299520 | doi = 10.1038/s41594-022-00796-6 }}
  • Lisuride{{snd}} partial agonist.
  • 5-CT{{snd}} full agonist.
  • Methylergometrine{{snd}} full agonist.
  • Valerenic acid{{snd}} a component of valerian, has been shown to act as a 5HT5A partial agonist.{{cite journal | vauthors = Dietz BM, Mahady GB, Pauli GF, Farnsworth NR | title = Valerian extract and valerenic acid are partial agonists of the 5-HT5a receptor in vitro | journal = Brain Research. Molecular Brain Research | volume = 138 | issue = 2 | pages = 191–197 | date = August 2005 | pmid = 15921820 | pmc = 5805132 | doi = 10.1016/j.molbrainres.2005.04.009 }}
  • Olanzapine{{snd}} an atypical antipsychotic.Roth BL, Driscol J. "PDSP Ki Database". Psychoactive Drug Screening Program (PDSP). University of North Carolina at Chapel Hill and the United States National Institute of Mental Health. Retrieved 14 August 2017.
  • Psilocin{{cite journal | vauthors = Ray TS | title = Psychedelics and the human receptorome | journal = PLOS ONE | volume = 5 | issue = 2 | pages = e9019 | date = February 2010 | pmid = 20126400 | pmc = 2814854 | doi = 10.1371/journal.pone.0009019 | doi-access = free | bibcode = 2010PLoSO...5.9019R }}
  • Aripiprazole - an atypical antipsychotic
  • Mirtazapine - an atypical antidepressant
  • UCSF648 - selective 5-HT5A partial agonist
  • Another ligand that has been recently disclosed is shown below, claimed be a selective 5-HT5A agonist with Ki = 124 nM.{{Cite patent | inventor = Garcia-Ladona FJ, Szabo L, Steiner G, Hofmann HP | pubdate = 2004-06-15 | title = Use of 5-HT5-ligands in the treatment of neurodegenerative and neuropsychiatric disturbances | country=US |number=6750221}}

200px

= Antagonists =

  • ASP5736{{cite journal | vauthors = Yamazaki M, Okabe M, Yamamoto N, Yarimizu J, Harada K | title = Novel 5-HT5A receptor antagonists ameliorate scopolamine-induced working memory deficit in mice and reference memory impairment in aged rats | journal = Journal of Pharmacological Sciences | volume = 127 | issue = 3 | pages = 362–369 | date = March 2015 | pmid = 25837935 | doi = 10.1016/j.jphs.2015.02.006 | doi-access = free }}{{cite journal | vauthors = Yamazaki M, Harada K, Yamamoto N, Yarimizu J, Okabe M, Shimada T, Ni K, Matsuoka N | display-authors = 6 | title = ASP5736, a novel 5-HT5A receptor antagonist, ameliorates positive symptoms and cognitive impairment in animal models of schizophrenia | journal = European Neuropsychopharmacology | volume = 24 | issue = 10 | pages = 1698–1708 | date = October 2014 | pmid = 25108314 | doi = 10.1016/j.euroneuro.2014.07.009 | doi-access = free }}
  • AS-2030680
  • AS-2674723
  • MS112{{snd}} selective potent antangonist.
  • Latrepirdine (non-selective).{{cite journal | vauthors = Wu J, Li Q, Bezprozvanny I | title = Evaluation of Dimebon in cellular model of Huntington's disease | journal = Molecular Neurodegeneration | volume = 3 | issue = 1 | pages = 15 | date = October 2008 | pmid = 18939977 | pmc = 2577671 | doi = 10.1186/1750-1326-3-15 | doi-access = free }}
  • Risperidone{{snd}} (non-selective), moderate 206 nM affinity.
  • SB-699,551

See also

References

{{reflist|33em}}

Further reading

{{refbegin|33em}}

  • {{cite journal | vauthors = Raymond JR, Mukhin YV, Gelasco A, Turner J, Collinsworth G, Gettys TW, Grewal JS, Garnovskaya MN | display-authors = 6 | title = Multiplicity of mechanisms of serotonin receptor signal transduction | journal = Pharmacology & Therapeutics | volume = 92 | issue = 2–3 | pages = 179–212 | year = 2002 | pmid = 11916537 | doi = 10.1016/S0163-7258(01)00169-3 }}
  • {{cite journal | vauthors = Thomas DR | title = 5-ht5A receptors as a therapeutic target | journal = Pharmacology & Therapeutics | volume = 111 | issue = 3 | pages = 707–714 | date = September 2006 | pmid = 16516972 | doi = 10.1016/j.pharmthera.2005.12.006 }}
  • {{cite journal | vauthors = Rees S, den Daas I, Foord S, Goodson S, Bull D, Kilpatrick G, Lee M | title = Cloning and characterisation of the human 5-HT5A serotonin receptor | journal = FEBS Letters | volume = 355 | issue = 3 | pages = 242–246 | date = December 1994 | pmid = 7988681 | doi = 10.1016/0014-5793(94)01209-1 | s2cid = 36425845 | doi-access = free }}
  • {{cite journal | vauthors = Schanen NC, Scherer SW, Tsui LC, Francke U | title = Assignment of the 5-hydroxytryptamine (serotonin) receptor 5A gene (HTR5A) to human chromosome band 7q36.1 | journal = Cytogenetics and Cell Genetics | volume = 72 | issue = 2–3 | pages = 187–188 | year = 1997 | pmid = 8978771 | doi = 10.1159/000134184 | hdl-access = free | hdl = 10722/42533 }}
  • {{cite journal | title = Toward a complete human genome sequence | journal = Genome Research | volume = 8 | issue = 11 | pages = 1097–1108 | date = November 1998 | pmid = 9847074 | doi = 10.1101/gr.8.11.1097 | doi-access = free | author2 = The Washington University Genome Sequencing Cente | author1 = The Sanger Centre }}
  • {{cite journal | vauthors = Francken BJ, Josson K, Lijnen P, Jurzak M, Luyten WH, Leysen JE | title = Human 5-hydroxytryptamine(5A) receptors activate coexpressed G(i) and G(o) proteins in Spodoptera frugiperda 9 cells | journal = Molecular Pharmacology | volume = 57 | issue = 5 | pages = 1034–1044 | date = May 2000 | pmid = 10779389 }}
  • {{cite journal | vauthors = Marazziti D, Ori M, Nardini M, Rossi A, Nardi I, Cassano GB | title = mRNA expression of serotonin receptors of type 2C and 5A in human resting lymphocytes | journal = Neuropsychobiology | volume = 43 | issue = 3 | pages = 123–126 | year = 2001 | pmid = 11287788 | doi = 10.1159/000054878 | s2cid = 20724896 }}
  • {{cite journal | vauthors = Iwata N, Ozaki N, Inada T, Goldman D | title = Association of a 5-HT(5A) receptor polymorphism, Pro15Ser, to schizophrenia | journal = Molecular Psychiatry | volume = 6 | issue = 2 | pages = 217–219 | date = March 2001 | pmid = 11317225 | doi = 10.1038/sj.mp.4000829 | doi-access = free }}
  • {{cite journal | vauthors = Grailhe R, Grabtree GW, Hen R | title = Human 5-HT(5) receptors: the 5-HT(5A) receptor is functional but the 5-HT(5B) receptor was lost during mammalian evolution | journal = European Journal of Pharmacology | volume = 418 | issue = 3 | pages = 157–167 | date = April 2001 | pmid = 11343685 | doi = 10.1016/S0014-2999(01)00933-5 }}
  • {{cite journal | vauthors = Noda M, Yasuda S, Okada M, Higashida H, Shimada A, Iwata N, Ozaki N, Nishikawa K, Shirasawa S, Uchida M, Aoki S, Wada K | display-authors = 6 | title = Recombinant human serotonin 5A receptors stably expressed in C6 glioma cells couple to multiple signal transduction pathways | journal = Journal of Neurochemistry | volume = 84 | issue = 2 | pages = 222–232 | date = January 2003 | pmid = 12558985 | doi = 10.1046/j.1471-4159.2003.01518.x | s2cid = 7364018 | doi-access = free }}
  • {{cite journal | vauthors = Khorana N, Smith C, Herrick-Davis K, Purohit A, Teitler M, Grella B, Dukat M, Glennon RA | display-authors = 6 | title = Binding of tetrahydrocarboline derivatives at human 5-HT5A receptors | journal = Journal of Medicinal Chemistry | volume = 46 | issue = 18 | pages = 3930–3937 | date = August 2003 | pmid = 12930153 | doi = 10.1021/jm030080s }}
  • {{cite journal | vauthors = Dietz BM, Mahady GB, Pauli GF, Farnsworth NR | title = Valerian extract and valerenic acid are partial agonists of the 5-HT5a receptor in vitro | journal = Brain Research. Molecular Brain Research | volume = 138 | issue = 2 | pages = 191–197 | date = August 2005 | pmid = 15921820 | pmc = 5805132 | doi = 10.1016/j.molbrainres.2005.04.009 }}

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