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词条 5-HT receptor
释义

  1. Classification

     Families  Subtypes 

  2. Expression patterns

  3. 5-HT{{sub|1}}-like

  4. References

  5. External links

5-hydroxytryptamine receptors or 5-HT receptors, or serotonin receptors, are a group of G protein-coupled receptor and ligand-gated ion channels found in the central and peripheral nervous systems.[1][2][3] They mediate both excitatory and inhibitory neurotransmission. The serotonin receptors are activated by the neurotransmitter serotonin, which acts as their natural ligand.

The serotonin receptors modulate the release of many neurotransmitters, including glutamate, GABA, dopamine, epinephrine / norepinephrine, and acetylcholine, as well as many hormones, including oxytocin, prolactin, vasopressin, cortisol, corticotropin, and substance P, among others. The serotonin receptors influence various biological and neurological processes such as aggression, anxiety, appetite, cognition, learning, memory, mood, nausea, sleep, and thermoregulation. The serotonin receptors are the target of a variety of pharmaceutical and recreational drugs, including many antidepressants, antipsychotics, anorectics, antiemetics, gastroprokinetic agents, antimigraine agents, hallucinogens, and entactogens.[4]

Serotonin receptors are found in almost all animals and are even known to regulate longevity and behavioral aging in the primitive nematode, Caenorhabditis elegans.[5][6]

Classification

5-hydroxytryptamine receptors or 5-HT receptors, or serotonin receptors are found in the central and peripheral nervous systems.[1][2]

They can be divided into 7 families of G protein-coupled receptors except for the 5-HT3 receptor, a ligand-gated ion channel, which activate an intracellular second messenger cascade to produce an excitatory or inhibitory response.

In 2014, a novel 5-HT receptor was isolated from the small white butterfly, Pieris rapae, and named pr5-HT8. It does not occur in mammals and shares relatively low similarity to the known 5-HT receptor classes.[7]

Families

Family Type Mechanism Potential
5-HT1 Gi/Go-protein coupled. Decreasing cellular levels of cAMP. Inhibitory
5-HT2 Gq/G11-protein coupled. Increasing cellular levels of IP3 and DAG. Excitatory
5-HT3 Ligand-gated Na+ and K+ cation channel. Depolarizing plasma membrane. Excitatory
5-HT4 Gs-protein coupled. Increasing cellular levels of cAMP. Excitatory
5-HT5 Gi/Go-protein coupled.[8] Decreasing cellular levels of cAMP. Inhibitory
5-HT6 Gs-protein coupled. Increasing cellular levels of cAMP. Excitatory
5-HT7 Gs-protein coupled. Increasing cellular levels of cAMP. Excitatory

Subtypes

The 7 general serotonin receptor classes include a total of 14 known serotonin receptors.[9] The specific types have been characterized as follows:[10][11][12]

Overview of serotonin receptors
ReceptorFirst clonedGene(s)DistributionFunctionAgonistsAntagonistsUses of drugs that act on this receptor
Blood vessels CNS GI Tract Platelets PNS Smooth Muscle
5-HT1A1987
  • {{Gene|HTR1A}}
{{Yes}} {{Yes}} {{No}} {{No}} {{No}} {{No}}
  • Addiction [13][14][15]
  • Aggression[16]
  • Anxiety[17]
  • Appetite[18]
  • Autoreceptor
  • Blood Pressure[19][20]
  • Cardiovascular Function[21]
  • Emesis[22]
  • Heart Rate[19][20]
  • Impulsivity[23]
  • Memory[24][25]
  • Mood[26]
  • Nausea[22]
  • Nociception[27]
  • Penile Erection[28]
  • Pupil Dilation[29]
  • Respiration[30]
  • Sexual Behavior[31]
  • Sleep[32]
  • Sociability[33]
  • Thermoregulation[34]
  • Vasoconstriction[35]
Selective (for 5-HT1A over other 5-HT receptors)
  • Vilazodone (Viibryd)
  • F-15,599 (research compound, highly potent and selective for 5-HT1A)
  • Flesinoxan (potent, EC50 = 24 nM)
  • Gepirone (partial agonist, Ki = 70 nM)
  • Haloperidol
  • Ipsapirone (partial agonist, Ki = 12.1 nM)
  • Quetiapine
  • Trazodone (SARI, selective in the sense that on all other 5-HT receptors it acts as either an antagonist or has no action. Kd = 78nM)
  • Yohimbine (unselective partial agonist)
  • Tandospirone (potent and selective partial agonist)
Nonselective
  • 5-CT (potent - Ki = 250±50 pM)
  • 8-OH-DPAT (potent)
  • Aripiprazole (atypical antipsychotic)
  • Asenapine (atypical antipsychotic)
  • Buspirone[36] (partial agonist)
  • Vortioxetine (high-efficacy partial agonist)[37]
  • Ziprasidone (Partial agonist, Ki = 3.4 nM)
  • Methylphenidate (weak agonist)
  • BMY 7378
  • Cyanopindolol
  • Iodocyanopindolol
  • Lecozotan
  • Methiothepin
  • Methysergide[38]
  • NAN-190
  • Nebivolol
  • Nefazodone
  • WAY-100,135
  • WAY-100,635
  • Mefway
  • Analgesics (agonists)
  • Antidepressants (post-synaptic receptor agonists and pre-synaptic autoreceptor antagonists serve as antidepressants)
  • Anxiolytics[39] (antagonist)
5-HT1B1992
  • {{Gene|HTR1B}}
{{Yes}} {{Yes}} {{No}} {{No}} {{No}} {{No}}
  • Addiction [40]
  • Aggression[16]
  • Anxiety[41][42][43]
  • Autoreceptor
  • Learning[44]
  • Locomotion[45]
  • Memory[44]
  • Mood[43]
  • Penile Erection[28]
  • Sexual Behavior[31]
  • Vasoconstriction
  • 5-CT
  • CGS-12066A
  • CP-93,129
  • CP-94,253
  • Dihydroergotamine
  • Eltoprazine
  • Ergotamine
  • Methysergide
  • RU 24969
  • TFMPP
  • Triptans[36] (antimigraine[36])
    • Zolmitriptan
    • Eletriptan
    • Sumatriptan
  • Vortioxetine (partial agonist, Ki = 33 nM)[37]
  • Alprenolol
  • AR-A000002
  • Asenapine
  • Cyanopindolol
  • GR-127,935
  • Iodocyanopindolol
  • Isamoltane
  • Metergoline
  • Methiothepin
  • Oxprenolol
  • Pindolol
  • Propranolol
  • SB-216,641
  • Yohimbine
  • Migraines (e.g. triptans)
5-HT1D1991
  • {{Gene|HTR1D}}
{{Yes}} {{Yes}} {{No}} {{No}} {{No}} {{No}}
  • Anxiety[46][47]
  • Autoreceptor
  • Locomotion[45]
  • Vasoconstriction
  • 5-CT
  • CP-135,807
  • Dihydroergotamine
  • Ergotamine
  • Methysergide
  • Triptans[36] (antimigraine[36])
    • Almotriptan
    • Eletriptan
    • Frovatriptan
    • Naratriptan
    • Rizatriptan
    • Sumatriptan
    • Zolmitriptan
  • Yohimbine
  • BRL-15572
  • GR-127,935
  • Ketanserin
  • Metergoline
  • Methiothepin
  • Rauwolscine
  • Ritanserin
  • Vortioxetine (Ki = 54 nM)[37]
  • Ziprasidone
  • Migraines (e.g. triptans)
5-HT1E1992
  • {{Gene|HTR1E}}
{{Yes}} {{Yes}} {{No}} {{No}} {{No}} {{No}}
  • BRL-54443
  • None known
5-HT1F1993
  • {{Gene|HTR1F}}
{{No}} {{Yes}} {{No}} {{No}} {{No}} {{No}}
  • Migraine
  • BRL-54443
  • Lasmiditan
  • LY-334,370
  • Naratriptan
  • Eletriptan
  • None known
5-HT2A1988
  • {{Gene|HTR2A}}
{{Yes}} {{Yes}} {{Yes}} {{Yes}} {{Yes}} {{Yes}}
  • Addiction (potentially modulating) [48]
  • Anxiety[49]
  • Appetite
  • Cognition
  • Imagination
  • Learning
  • Memory
  • Mood
  • Perception
  • Sexual Behavior[50]
  • Sleep[51]
  • Thermoregulation[52]
  • Vasoconstriction[53]
  • 25I-NBOMe (Full agonist)
  • 2C-B
  • 5-MeO-DMT
  • BZP
  • Bufotenin
  • DMT
  • DOM
  • Ergonovine
  • Lisuride
  • LSD
  • Mescaline
  • Myristicin
  • PNU-22394 (Partial agonist)[54][55][56]
  • Psilocin
  • Psilocybin
  • TFMPP (partial agonist or antagonist)
  • Atypical antipsychotics
    • Clozapine[36]
    • Olanzapine
    • Quetiapine
    • Risperidone
    • Ziprasidone
  • Aripiprazole
  • Asenapine
  • Amitriptyline
  • Clomipramine
  • Cyproheptadine
  • Eplivanserin
  • Etoperidone
  • Haloperidol
  • Hydroxyzine
  • Iloperidone
  • Ketanserin[36] (antihypertensive[36])
  • Methysergide
  • Mianserin
  • Mirtazapine
  • Nefazodone
  • Pimavanserin
  • Pizotifen
  • Ritanserin
  • Trazodone
  • Yohimbine
  • Atypical antipsychotics (antagonist)
  • Psychedelics (agonists)
  • NaSSAs (antidepressants and anxiolytics; they serve as antagonists at this site)
  • Treating serotonin syndrome (antagonists; e.g. cyproheptadine)
  • Sleeping aid (antagonists; e.g. trazodone)
5-HT2B1992
  • {{Gene|HTR2B}}
{{Yes}} {{Yes}} {{Yes}} {{Yes}} {{Yes}} {{Yes}}
  • Anxiety[57][58][59]
  • Appetite[60]
  • Cardiovascular Function
  • GI Motility[61]
  • Sleep[51]
  • Vasoconstriction
  • 6-APB (full agonist)
  • BW-723C86
  • Fenfluramine
  • MDMA
  • Norfenfluramine
  • PNU-22394 (Partial agonist)[54][55][56]
  • Ro60-0175
  • Methylphenidate (weak agonist)
  • Agomelatine
  • Asenapine
  • BZP
  • Ketanserin
  • Methysergide
  • Ritanserin
  • RS-127,445
  • Tegaserod
  • Yohimbine
  • Migraines (antagonists)
5-HT2C1988
  • {{Gene|HTR2C}}
{{Yes}} {{Yes}} {{Yes}} {{Yes}} {{Yes}} {{Yes}}
  • Addiction. (potentially modulating)[48]
  • Anxiety[62][63][64]
  • Appetite
  • GI Motility[65]
  • Heteroreceptor for norepinephrine and dopamine
  • Locomotion
  • Mood[63][64]
  • Penile Erection[66][67]
  • Sexual Behavior[50]
  • Sleep[68]
  • Thermoregulation[52]
  • Vasoconstriction
  • A-372,159
  • AL-38022A
  • Aripiprazole
  • Ergonovine
  • Lorcaserin
  • PNU-22394 (Full agonist)[54][55][56]
  • Ro60-0175
  • TFMPP
  • Trazodone[36] (hypnotic[36])
  • YM-348
  • Agomelatine[36] (antidepressant[36])
  • Amitriptyline
  • Asenapine
  • Clomipramine
  • Clozapine[36] (antipsychotic[36])
  • Cyproheptadine
  • Dimebolin
  • Eltoprazine
  • Etoperidone
  • Fluoxetine
  • Haloperidol
  • Iloperidone
  • Ketanserin[36] (antihypertensive[36])
  • Lisuride
  • Methysergide[69]
  • Mianserin
  • Mirtazapine
  • Nefazodone
  • Olanzapine
  • Paroxetine
  • Quetiapine
  • Risperidone
  • Ritanserin
  • SB-242084
  • Tramadol
  • Trazodone
  • Ziprasidone
  • Antidepressant (antagonists; e.g. agomelatine, fluoxetine, mirtazapine)
  • Orexigenic (e.g. mirtazapine, clozapine and olanzapine; antagonists)
  • Anorectic (Lorcaserin; agonist)
  • Antipsychotic (Vabicaserin; agonists)
5-HT31993
  • {{Gene|HTR3A}}
  • {{Gene|HTR3B}}
  • {{Gene|HTR3C}}
  • {{Gene|HTR3D}}
  • {{Gene|HTR3E}}
{{No}} {{Yes}} {{Yes}} {{No}} {{Yes}} {{No}}
  • Addiction
  • Anxiety
  • Emesis
  • GI Motility[70]
  • Learning[71]
  • Memory[71]
  • Nausea
  • 2-Methyl-5-HT
  • BZP
  • Quipazine
  • RS-56812
  • Alosetron
  • Several antiemetics[36]
    • Dolasetron
    • Ondansetron[36]
    • Granisetron
    • Tropisetron
  • Clozapine
  • Memantine
  • Metoclopramide
  • Mianserin
  • Mirtazapine
  • Olanzapine
  • Quetiapine
  • Vortioxetine (Ki = 3.7 nM)[37]
  • Antiemetic
5-HT41995
  • {{Gene|HTR4}}
{{No}} {{Yes}} {{Yes}} {{No}} {{Yes}} {{No}}
  • Anxiety[72][73]
  • Appetite[74][75]
  • GI Motility
  • Learning[76][77]
  • Memory[76][77][78]
  • Mood[79][80]
  • Respiration[81]
  • 5-MT
  • BIMU-8
  • Cinitapride
  • Cisapride[36] (gastroprokinetic)
  • Dazopride
  • Metoclopramide
  • Mosapride
  • Prucalopride
  • RS-67333
  • Renzapride
  • Tegaserod
  • Zacopride
  • L-Lysine[72]
  • Piboserod
  • Gastroprokinetics (e.g. Tegaserod)
5-HT5A1994
  • {{Gene|HTR5A}}
{{No}} {{Yes}} {{No}} {{No}} {{No}} {{No}}
  • Autoreceptor
  • Locomotion[82]
  • Sleep[83]
  • 5-CT
  • Ergotamine
  • Valerenic Acid (partial agonist)[83]
  • Asenapine
  • Dimebolin
  • Methiothepin
  • Ritanserin
  • SB-699,551
  • SB-699,551-A
  • None thus far
5-HT5B1993
  • {{Gene|HTR5BP}}
{{No}} {{No}} {{No}} {{No}} {{No}} {{No}}Functions in rodents,
pseudogene in humans
  • None thus far
5-HT61993
  • {{Gene|HTR6}}
{{No}} {{Yes}} {{No}} {{No}} {{No}} {{No}}
  • Anxiety[84][85]
  • Cognition[86]
  • Learning[87]
  • Memory[87]
  • Mood[85][88]
  • EMD-386,088
  • EMDT
  • Amitriptyline
  • Aripiprazole
  • Asenapine
  • Clomipramine
  • Clozapine
  • Dimebolin
  • EGIS-12233
  • Haloperidol
  • Iloperidone
  • MS-245
  • Olanzapine
  • Ro04-6790
  • SB-258,585
  • SB-271,046[89]
  • SB-357,134
  • SB-399,885
  • Antidepressant (antagonists and agonists)
  • Anxiolytic (antagonists and agonist)
  • Nootropic (antagonists)
  • Anorectic (antagonists)
5-HT71993
  • {{Gene|HTR7}}
{{Yes}} {{Yes}} {{Yes}} {{No}} {{No}} {{No}}
  • Anxiety[90][91]
  • Autoreceptor
  • Memory[92][93]
  • Mood[90][91]
  • Respiration[30][94]
  • Sleep[90][94][95]
  • Thermoregulation
  • Vasoconstriction
  • 5-CT
  • 8-OH-DPAT
  • Aripiprazole (weak partial agonist)[96]
  • AS-19
  • E-55888
  • RA-7
  • Amitriptyline
  • Asenapine
  • Clomipramine
  • Clozapine
  • EGIS-12233
  • Haloperidol
  • Iloperidone
  • Imipramine
  • Ketanserin
  • Mirtazapine
  • Olanzapine
  • Ritanserin
  • Risperidone
  • SB-269,970
  • Vortioxetine (Ki = 19 nM)[37]
  • Antidepressant (antagonists)
  • Anxiolytics (antagonists)
  • Nootropic (antagonists)

Note that there is no 5-HT1C receptor since, after the receptor was cloned and further characterized, it was found to have more in common with the 5-HT2 family of receptors and was redesignated as the 5-HT2C receptor.[97]

Very nonselective agonists of 5-HT receptor subtypes include ergotamine (an antimigraine), which activates 5-HT1A, 5-HT1D, 5-HT1B, D2 and norepinephrine receptors.[36] LSD (a psychedelic) is a 5-HT1A, 5-HT2A, 5-HT2C, 5-HT5A, 5-HT5, 5-HT6 agonist.[36]

Expression patterns

The genes coding for serotonin receptors are expressed across the mammalian brain. Genes coding for different receptors types follow different developmental curves. Specifically, there is a developmental increase of HTR5A expression in several subregions of the human cortex, paralleled by a decreased expression of HTR1A from the embryonic period to the post-natal one.

[98]

5-HT{{sub|1}}-like

A number of receptors were classed as "5-HT{{sub|1}}-like" - by 1998 it was being argued that, since these receptors were "a heterogeneous population of 5-HT1B, 5-HT1D and 5-HT7" receptors the classification was redundant.[99]

References

1. ^{{cite journal |vauthors=Hoyer D, Clarke DE, Fozard JR, Hartig PR, Martin GR, Mylecharane EJ, Saxena PR, Humphrey PP | title = International Union of Pharmacology classification of receptors for 5-hydroxytryptamine (Serotonin) | journal = Pharmacol. Rev. | volume = 46 | issue = 2 | pages = 157–203 | year = 1994 | pmid = 7938165 | doi = | issn = | url = http://pharmrev.aspetjournals.org/cgi/content/abstract/46/2/157}}
2. ^{{cite book |vauthors=Frazer A, Hensler JG |veditors=Siegel GJ, Agranoff BW, Albers RW, Fisher SK, Uhler MD | title = Basic Neurochemistry: MolecularCellular, and Medical Aspects | publisher = Lippincott-Raven | location = Philadelphia | year = 1999| pages = 263–292| isbn = 978-0-397-51820-3 | oclc = | doi = | chapter= Chapter 13: Serotonin Receptors | chapterurl = https://www.ncbi.nlm.nih.gov/books/bv.fcgi?call=bv.View..ShowSection&rid=bnchm.section.963 }}
3. ^{{Cite journal|last=Beliveau|first=Vincent|last2=Ganz|first2=Melanie|last3=Feng|first3=Ling|last4=Ozenne|first4=Brice|last5=Højgaard|first5=Liselotte|last6=Fisher|first6=Patrick M.|last7=Svarer|first7=Claus|last8=Greve|first8=Douglas N.|last9=Knudsen|first9=Gitte M.|date=2017-01-04|title=A High-Resolution In Vivo Atlas of the Human Brain's Serotonin System|journal=Journal of Neuroscience|volume=37|issue=1|pages=120–128|doi=10.1523/jneurosci.2830-16.2016|pmid=28053035|pmc=5214625}}
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6. ^{{cite journal | pmid = 17336425 | doi=10.1016/j.neurobiolaging.2007.01.013 | volume=29 | issue=7 | title=Manipulation of serotonin signal suppresses early phase of behavioral aging in Cnorhabditis elegans | date=July 2008 | pages=1093–100 | journal=Neurobiology of Aging |vauthors=Murakami H, Bessinger K, Hellmann J, Murakami S }}
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9. ^{{cite book |vauthors=Malenka RC, Nestler EJ, Hyman SE |veditors=Sydor A, Brown RY | title = Molecular Neuropharmacology: A Foundation for Clinical Neuroscience | year = 2009 | publisher = McGraw-Hill Medical | location = New York | isbn = 9780071481274 | page = 4 | edition = 2nd |quote = Similarly, little is known about which of serotonin’s 14 known receptors must be activated to achieve an antidepressant response. }}
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36. ^10 11 12 13 14 15 16 17 18 19 20 Pharmacology Corner > Serotonin (5-HT): receptors, agonists and antagonists By Flavio Guzmán, M.D. on 9/08/09
37. ^"BRINTELLIX™ (vortioxetine) tablets for oral use. Full Prescribing Information, Section 12.2 (Pharmacodynamics)." Takeda Pharmaceuticals America Inc. and Lundbeck, 2013. Revised September 2013.  
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External links

  • {{MeshName|Serotonin+Receptors}}
  • {{cite web | url = http://www.iuphar-db.org/GPCR/ChapterMenuForward?chapterID=1288 | title = 5-Hydroxytryptamine Receptors | accessdate = | date = | format = | work = IUPHAR Database of Receptors and Ion Channels | publisher = International Union of Basic and Clinical Pharmacology | pages = | language = | quote = }}
  • {{cite web | url = http://cogprints.org/4095/ | title = Activation of G protein-coupled receptors entails cysteine modulation of agonist binding | vauthors = Rubenstein LA, Lanzara RG | accessdate = 2008-04-11 | date = 2005-02-16 | format = | website = | publisher = Cogprints | pages = | language = | quote = }}
  • {{cite journal |vauthors=Paterson LM, Kornum BR, Nutt DJ, Pike VW, Knudsen GM |title=5-HT radioligands for human brain imaging with PET and SPECT |journal=Med Res Rev |volume=33 |issue=1 |pages=54–111 |year=2013 |pmid=21674551 |pmc=4188513 |doi=10.1002/med.20245 |url=}}
{{G protein-coupled receptors}}{{Ligand-gated ion channels}}{{Serotonergics}}

1 : Serotonin receptors

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