Lompat ke isi

Reseptor serotonin

Dari Wikipedia bahasa Indonesia, ensiklopedia bebas
The 5-HT1B adalah salah satu contoh reseptor serotonin metabotropik. Ini adalah struktur kristalografi dalam representasi pita

.

Reseptor serotonin atau juga dikenal sebagai reseptor 5-hidroksitriptamin atau reseptor 5-HT adalah kelompok dari reseptor terhubung-protein G dan reseptor kanal ion (ligand-gated ion channels, LGIC) yang ditemukan pada sistem saraf pusat dan sistem saraf tepi.[1][2] Reseptor serotonin memperantarai neurotransmisi eksitatori (pemicuan) dan inhibitori (penghambatan) yang beraksi terhadap ligan alaminya.

Klasifikasi

[sunting | sunting sumber]

Dengan pengecualian dari reseptor 5-HT3, semua reseptor serotonin termasuk dalam reseptor terhubung-protein G yang mengaktifkan kaskade kurir kedua untuk menghasilkan respons eksitatori atau inhibitori (penghambatan). Pada tahun 2014 sebuah reseptor 5-HT novel dideskripsikan yang diisolasi dari kupu-kupu putih kecil, Pieris rapae, dan diberi nama pr5-HT8. Kesamaan relatif antara reseptor ini dengan kelas reseptor 5-HT lainnya bersifat rendah dan tidak terdapat pada mamalia.[3]

Famili

[sunting | sunting sumber]
Famili Tipe Mekanisme Respon
5-HT1 Gi/Go-protein coupled. Menurunkan level cAMP seluler. Inhibitori
5-HT2 Gq/G11-protein coupled. Meningkatkan level IP3 dan DAG. Eksitatori
5-HT3 Ligand-gated Na+ and K+ cation channel. depolariisasi membran plasma. Eksitatori
5-HT4 Gs-protein coupled. Meningkatkan level cAMP seluler. Eksitatori
5-HT5 Gi/Go-protein coupled.[4] Menurunkan level cAMP seluler. Inhibitori
5-HT6 Gs-protein coupled. Meningkatkan level cAMP seluler. Eksitatori
5-HT7 Gs-protein coupled. Meningkatkan level cAMP seluler. Eksitatori

Subtipe

[sunting | sunting sumber]

Tujuh kelas reseptor serotonin mencakup total 14 reseptor serotonin dikenal.[5] Jenis tertentu telah ditandai sebagai berikut:[6][7][8]

Gambaran Reseptor Serotonin
Reseptor Kloning pertama kali Gen Distribusi Fungsi Agonis Antagonis reseptor Obat-obat yang beraksi pada reseptor
Pembuluh darah SSP Saluran GI Platelet PNS Otot polos
5-HT1A 1987 Yes Yes Tidak Tidak Tidak Tidak

Selektif (untuk 5-HT1A lebih dari reseptor 5-HT lainnya)

Nonselektif

5-HT1B 1992 Yes Yes Tidak Tidak Tidak Tidak
5-HT1D 1991 Yes Yes Tidak Tidak Tidak Tidak
5-HT1E 1992 Yes Yes Tidak Tidak Tidak Tidak
  • Tidak diketahui
5-HT1F 1993 Tidak Yes Tidak Tidak Tidak Tidak
  • Migrain
  • Tidak diketahui
5-HT2A 1988 Yes Yes Yes Yes Yes Yes
  • Addiksi (modulasi secara potensial)[44]
  • Ansietas[45]
  • Nafsu makan
  • Kognisi
  • Imajinasi
  • Belajar
  • Memori
  • Mood
  • Persepsi
  • Perilaku seksual[46]
  • Tidur[47]
  • Thermoregulasi[48]
  • Vasokonstriksi[49]
5-HT2B 1992 Yes Yes Yes Yes Yes Yes
5-HT2C 1988 Yes Yes Yes Yes Yes Yes
5-HT3 1993 Tidak Yes Yes Tidak Yes Tidak
  • Addiksi
  • Asietas
  • Emesis
  • Motilitas GI[66]
  • Belajar[67]
  • Memori[67]
  • Muntah
5-HT4 1995 Tidak Yes Yes Tidak Yes Tidak
5-HT5A 1994 Tidak Yes Tidak Tidak Tidak Tidak
  • Tidak ada selama ini
5-HT5B 1993 Tidak Tidak Tidak Tidak Tidak Tidak

Functions in rodents,
pseudogene in humans

  • tidak ada selama ini
5-HT6 1993 Tidak Yes Tidak Tidak Tidak Tidak
5-HT7 1993 Yes Yes Yes Tidak Tidak Tidak

Referensi

[sunting | sunting sumber]
  1. ^ Hoyer D, Clarke DE, Fozard JR, Hartig PR, Martin GR, Mylecharane EJ, Saxena PR, Humphrey PP (1994). "International Union of Pharmacology classification of receptors for 5-hydroxytryptamine (Serotonin)". Pharmacol. Rev. 46 (2): 157–203. PMID 7938165. 
  2. ^ Frazer A, Hensler JG (1999). "Chapter 13: Serotonin Receptors". Dalam Siegel GJ, Agranoff BW, Albers RW, Fisher SK, Uhler MD. Basic Neurochemistry: Molecular, Cellular, and Medical Aspects. Philadelphia: Lippincott-Raven. hlm. 263–292. ISBN 0-397-51820-X. Diakses tanggal 2008-04-11. 
  3. ^ Qi YX, Xia RY, Wu YS, Stanley D, Huang J, Ye GY (2014). "Larvae of the small white butterfly, Pieris rapae, express a novel serotonin receptor". J. Neurochem. 131: 767–77. doi:10.1111/jnc.12940. PMID 25187179. 
  4. ^ Francken BJ, Jurzak M, Vanhauwe JF, Luyten WH, Leysen JE (1998). "The human 5-ht5A receptor couples to Gi/Go proteins and inhibits adenylate cyclase in HEK 293 cells". Eur J Pharmacol. 361 (2–3): 299–309. doi:10.1016/S0014-2999(98)00744-4. PMID 9865521. 
  5. ^ Malenka RC, Nestler EJ, Hyman SE (2009). Sydor A, Brown RY, ed. Molecular Neuropharmacology: A Foundation for Clinical Neuroscience (edisi ke-2nd). New York: McGraw-Hill Medical. hlm. 4. ISBN 978-0-07-148127-4. Similarly, little is known about which of serotonin’s 14 known receptors must be activated to achieve an antidepressant response. 
  6. ^ Glennon RA, Dukat M, Westkaemper RB (2000-01-01). "Serotonin Receptor Subtypes and Ligands". American College of Neurophyscopharmacology. Diarsipkan dari versi asli tanggal 21 April 2008. Diakses tanggal 2008-04-11. 
  7. ^ "5-Hydroxytryptamine Receptors". IUPHAR Receptor Database. International Union of Basic and Clinical Pharmacology. Diakses tanggal 2008-04-11. 
  8. ^ Wesolowska A (2002). "In the search for selective ligands of 5-HT5, 5-HT6 and 5-HT7 serotonin receptors" (PDF). Polish Journal of Pharmacology. 54 (4): 327–41. PMID 12523486. 
  9. ^ Tomkins DM, Higgins GA, Sellers EM (1994). "Low doses of the 5-HT1A agonist 8-hydroxy-2-(di-n-propylamino)-tetralin (8-OH DPAT) increase ethanol intake". Psychopharmacology (Berl). 115 (1–2): 173–9. doi:10.1007/BF02244769. PMID 7862892. 
  10. ^ Müller CP, Carey RJ, Huston JP, De Souza Silva MA (2007). "Serotonin and psychostimulant addiction: focus on 5-HT1A-receptors". Prog Neurobiol. 81 (3): 133–78. doi:10.1016/j.pneurobio.2007.01.001. PMID 17316955. 
  11. ^ Carey RJ, DePalma G, Damianopoulos E, Shanahan A, Müller CP, Huston JP (2005). "Evidence that the 5-HT1A autoreceptor is an important pharmacological target for the modulation of cocaine behavioral stimulant effects". Brain Res. 1034 (1–2): 162–71. doi:10.1016/j.brainres.2004.12.012. PMID 15713268. 
  12. ^ a b de Boer SF, Koolhaas JM (2005). "5-HT1A and 5-HT1B receptor agonists and aggression: a pharmacological challenge of the serotonin deficiency hypothesis". Eur J Pharmacol. 526 (1–3): 125–39. doi:10.1016/j.ejphar.2005.09.065. PMID 16310183. 
  13. ^ Parks CL, Robinson PS, Sibille E, Shenk T, Toth M (1998). "Increased anxiety of mice lacking the serotonin1A receptor". Proceedings of the National Academy of Sciences of the United States of America. 195 (18): 10734–9. doi:10.1073/pnas.95.18.10734. PMC 27964 alt=Dapat diakses gratis. PMID 9724773. 
  14. ^ Ebenezer IS, Arkle MJ, Tite RM (1998). "8-Hydroxy-2-(di-n-propylamino)-tetralin inhibits food intake in fasted rats by an action at 5-HT1A receptors". Methods Find Exp Clin Pharmacol. 29 (4): 269–72. doi:10.1358/mf.2007.29.4.1075362. PMID 17609739. 
  15. ^ a b Wouters W, Tulp MT, Bevan P (1998). "Flesinoxan lowers blood pressure and heart rate in cats via 5-HT1A receptors". Eur J Pharmacol. 149 (3): 213–23. doi:10.1016/0014-2999(88)90651-6. PMID 2842163. 
  16. ^ a b Horiuchi J, McDowall LM, Dampney RA (2008). "Role of 5-HT(1A) receptors in the lower brainstem on the cardiovascular response to dorsomedial hypothalamus activation". Auton Neurosci. 142 (1–2): 71–6. doi:10.1016/j.autneu.2008.06.004. PMID 18667366. 
  17. ^ Nalivaiko E, Ootsuka Y, Blessing WW (2005). "Activation of 5-HT1A receptors in the medullary raphe reduces cardiovascular changes elicited by acute psychological and inflammatory stresses in rabbits". Am J Physiol Regul Integr Comp Physiol. 289 (2): R596–R604. doi:10.1152/ajpregu.00845.2004. PMID 15802554. 
  18. ^ a b Lucot JB. (1994). "Antiemetic effects of flesinoxan in cats: comparisons with 8-hydroxy-2-(di-n-propylamino)tetralin". Eur J Pharmacol. 253 (1–2): 53–60. doi:10.1016/0014-2999(94)90756-0. PMID 8013549. 
  19. ^ Winstanley CA, Theobald DE, Dalley JW, Robbins TW (2005). "Interactions between serotonin and dopamine in the control of impulsive choice in rats: therapeutic implications for impulse control disorders". Neuropsychopharmacology. 30 (4): 669–682. doi:10.1038/sj.npp.1300610. PMID 15688093. 
  20. ^ Ogren SO, Eriksson TM, Elvander-Tottie E, D'Addario C, Ekström JC, Svenningsson P, Meister B, Kehr J, Stiedl O (2008). "The role of 5-HT(1A) receptors in learning and memory". Behav. Brain Res. 195 (1): 54–77. doi:10.1016/j.bbr.2008.02.023. PMID 18394726. 
  21. ^ Yasuno F, Suhara T, Nakayama T, Ichimiya T, Okubo Y, Takano A, Ando T, Inoue M, Maeda J, Suzuki K (2003). "Inhibitory effect of hippocampal 5-HT1A receptors on human explicit memory". Am J Psychiatry. 160 (2): 334–40. doi:10.1176/appi.ajp.160.2.334. PMID 12562581. 
  22. ^ Kennett GA, Dourish CT, Curzon G (1987). "Antidepressant-like action of 5-HT1A agonists and conventional antidepressants in an animal model of depression". Eur J Pharmacol. 134 (3): 265–74. doi:10.1016/0014-2999(87)90357-8. PMID 2883013. 
  23. ^ Bardin L, Tarayre JP, Malfetes N, Koek W, Colpaert FC (2003). "Profound, non-opioid analgesia produced by the high-efficacy 5-HT(1A) agonist F 13640 in the formalin model of tonic nociceptive pain". Pharmacology. 67 (4): 182–194. doi:10.1159/000068404. PMID 12595749. 
  24. ^ a b Millan MJ, Perrin-Monneyron S (1997). "Potentiation of fluoxetine-induced penile erections by combined blockade of 5-HT1A and 5-HT1B receptors". Eur J Pharmacol. 321 (3): 11–3. doi:10.1016/S0014-2999(97)00050-2. PMID 9085055. 
  25. ^ Prow MR, Martin KF, Heal DJ (1996). "8-OH-DPAT-induced mydriasis in mice: a pharmacological characterisation". Eur J Pharmacol. 317 (1): 21–8. doi:10.1016/S0014-2999(96)00693-0. PMID 8982715. 
  26. ^ a b Meyer LC, Fuller A, Mitchell D (February 2006). "Zacopride and 8-OH-DPAT reverse opioid-induced respiratory depression and hypoxia but not catatonic immobilization in goats". American Journal of Physiology. Regulatory, Integrative and Comparative Physiology. 290 (2): R405–13. doi:10.1152/ajpregu.00440.2005. PMID 16166206. 
  27. ^ a b Popova NK, Amstislavskaya TG (2002). "Involvement of the 5-HT(1A) and 5-HT(1B) serotonergic receptor subtypes in sexual arousal in male mice". Psychoneuroendocrinology. 27 (5): 609–18. doi:10.1016/S0306-4530(01)00097-X. PMID 11965359. 
  28. ^ Monti JM, Jantos H (1992). "Dose-dependent effects of the 5-HT1A receptor agonist 8-OH-DPAT on sleep and wakefulness in the rat". J Sleep Res. 1 (3): 169–175. doi:10.1111/j.1365-2869.1992.tb00033.x. PMID 10607047. 
  29. ^ Thompson MR, Callaghan PD, Hunt GE, Cornish JL, McGregor IS (2007). "A role for oxytocin and 5-HT(1A) receptors in the prosocial effects of 3,4 methylenedioxymethamphetamine ("ecstasy")". Neuroscience. 146 (2): 509–14. doi:10.1016/j.neuroscience.2007.02.032. PMID 17383105. 
  30. ^ Gudelsky GA, Koenig JI, Meltzer HY (1986). "Thermoregulatory responses to serotonin (5-HT) receptor stimulation in the rat. Evidence for opposing roles of 5-HT2 and 5-HT1A receptors". Neuropharmacology. 25 (12): 1307–13. doi:10.1016/0028-3908(86)90101-2. PMID 2951611. 
  31. ^ Ootsuka Y, Blessing WW (2006). "Activation of 5-HT1A receptors in rostral medullary raphé inhibits cutaneous vasoconstriction elicited by cold exposure in rabbits". Brain Res. 1073–1074: 252–61. doi:10.1016/j.brainres.2005.12.031. PMID 16455061. 
  32. ^ a b c d e f g h i j k l m n o p q r s Pharmacology Corner > Serotonin (5-HT): receptors, agonists and antagonists By Flavio Guzmán, M.D. on 9/08/09
  33. ^ a b c d e "BRINTELLIX™ (vortioxetine) tablets for oral use. Full Prescribing Information, Section 12.2 (Pharmacodynamics)." Takeda Pharmaceuticals America Inc. and Lundbeck, 2013. Revised September 2013. [1] Diarsipkan 2019-09-18 di Wayback Machine.
  34. ^ Saxena, PR; Lawang, A (Oct 1985). "A comparison of cardiovascular and smooth muscle effects of 5-hydroxytryptamine and 5-carboxamidotryptamine, a selective agonist of 5-HT1 receptors". Archives Internationales de Pharmacodynamie et de Thérapie. 277 (2): 235–52. PMID 2933009. 
  35. ^ Cao BJ, Rodgers RJ (October 1998). "Comparative effects of novel 5-HT1A receptor ligands, LY293284, LY315712 and LY297996, on plus-maze anxiety in mice". Psychopharmacology. 139 (3): 185–94. doi:10.1007/s002130050703. PMID 9784072. 
  36. ^ Harrison AA, Parsons LH, Koob GF, Markou A (1999). "RU 24969, a 5-HT1A/1B agonist, elevates brain stimulation reward thresholds: an effect reversed by GR 127935, a 5-HT1B/1D antagonist". Psychopharmacology (Berl). 141 (3): 242–50. doi:10.1007/s002130050831. PMID 10027505. 
  37. ^ Chojnacka-Wójcik E, Klodzinska A, Tatarczynska E (2005). "The anxiolytic-like effect of 5-HT1B receptor ligands in rats: a possible mechanism of action". J Pharm Pharmacol. 57 (2): 253–7. doi:10.1211/0022357055399. PMID 15720791. 
  38. ^ Lin D, Parsons LH (2002). "Anxiogenic-like effect of serotonin(1B) receptor stimulation in the rat elevated plus-maze". Pharmacol Biochem Behav. 71 (4): 581–7. doi:10.1016/S0091-3057(01)00712-2. PMID 11888549. 
  39. ^ a b Tatarczynska E, Klodzinska A, Stachowicz K, Chojnacka-Wójcik E (2004). "Effects of a selective 5-HT1B receptor agonist and antagonists in animal models of anxiety and depression". Behav Pharmacol. 15 (8): 523–34. doi:10.1097/00008877-200412000-00001. PMID 15577451. 
  40. ^ a b Eriksson TM, Madjid N, Elvander-Tottie E, Stiedl O, Svenningsson P, Ogren SO (2008). "Blockade of 5-HT 1B receptors facilitates contextual aversive learning in mice by disinhibition of cholinergic and glutamatergic neurotransmission". Neuropharmacology. 54 (7): 1041–50. doi:10.1016/j.neuropharm.2008.02.007. PMID 18394658. 
  41. ^ a b McCreary AC, Bankson MG, Cunningham KA (1999). "Pharmacological studies of the acute and chronic effects of (+)-3, 4-methylenedioxymethamphetamine on locomotor activity: role of 5-hydroxytryptamine(1A) and 5-hydroxytryptamine(1B/1D) receptors". J Pharmacol Exp Ther. 290 (3): 965–73. PMID 10454466. 
  42. ^ Amital D, Fostick L, Sasson Y, Kindler S, Amital H, Zohar J (2005). "Anxiogenic effects of Sumatriptan in panic disorder: a double-blind, placebo-controlled study". Eur Neuropsychopharmacol. 15 (3): 279–82. doi:10.1016/j.euroneuro.2004.12.002. PMID 15820416. 
  43. ^ Feuerstein TJ, Hüring H, van Velthoven V, Lücking CH, Landwehrmeyer GB (1996). "5-HT1D-like receptors inhibit the release of endogenously formed [3H]GABA in human, but not in rabbit, neocortex". Neurosci Lett. 209 (3): 210–4. doi:10.1016/0304-3940(96)12637-9. PMID 8736648. 
  44. ^ a b [2] Bubar MJ, Cunningham KA. Serotonin 5-HT2A and 5-HT2C receptors as potential targets for modulation of psychostimulant use and dependence. Curr Top Med Chem. 2006;6(18):1971-85.
  45. ^ Schreiber R, Melon C, De Vry J (1998). "The role of 5-HT receptor subtypes in the anxiolytic effects of selective serotonin reuptake inhibitors in the rat ultrasonic vocalization test". Psychopharmacology (Berl). 135 (4): 383–91. doi:10.1007/s002130050526. PMID 9539263. 
  46. ^ a b Popova NK, Amstislavskaya TG (2002). "5-HT2A and 5-HT2C serotonin receptors differentially modulate mouse sexual arousal and the hypothalamo-pituitary-testicular response to the presence of a female". Neuroendocrinology. 76 (1): 28–34. doi:10.1159/000063681. PMID 12097814. 
  47. ^ a b Popa D, Léna C, Fabre V, Prenat C, Gingrich J, Escourrou P, Hamon M, Adrien J (2005). "Contribution of 5-HT2 receptor subtypes to sleep-wakefulness and respiratory control, and functional adaptations in knock-out mice lacking 5-HT2A receptors". J Neurosci. 25 (49): 11231–8. doi:10.1523/JNEUROSCI.1724-05.2005. PMID 16339018. 
  48. ^ a b Mazzola-Pomietto P, Aulakh CS, Tolliver T, Murphy DL (1997). "Functional subsensitivity of 5-HT2A and 5-HT2C receptors mediating hyperthermia following acute and chronic treatment with 5-HT2A/2C receptor antagonists". Psychopharmacology (Berl). 130 (2): 144–51. doi:10.1007/s002130050222. PMID 9106912. 
  49. ^ Blessing WW, Seaman B (2003). "5-hydroxytryptamine(2A) receptors regulate sympathetic nerves constricting the cutaneous vascular bed in rabbits and rats". Neuroscience. 117 (4): 939–948. doi:10.1016/S0306-4522(02)00810-2. PMID 12654345. 
  50. ^ a b c McCall, R. B.; Franklin, S. R.; Hyslop, D. K.; Knauer, C. S.; Chio, C. L.; Haber, C. L.; Fitzgerald, L. W. (2001). "PNU-22394, a 5-HT2C receptor agonist, reduced feeding in rodents and produces weight loss in humans" (Online). 27 (309.2). Presentation Number 309.2. Convention Center Exhibit Hall, Poster Board TT-45, San Diego, CA: Society for Neuroscience Abstracts. Diakses tanggal 18 July 2014. 
  51. ^ a b c Garfield AS, Heisler LK (2009). "Pharmacological targeting of the serotonergic system for the treatment of obesity". The Journal of Physiology. 587 (1): 49–60. doi:10.1113/jphysiol.2008.164152. PMC 2670022 alt=Dapat diakses gratis. PMID 19029184. 
  52. ^ a b c Jensen, Anders A.; Plath, Niels; Pedersen, Martin Holst Friborg; Isberg, Vignir; et al. (2013). "Design, Synthesis, and Pharmacological Characterization of N- and O-Substituted 5,6,7,8-Tetrahydro-4H-isoxazolo[4,5-d]azepin-3-ol Analogues: Novel 5-HT2A/5-HT2C Receptor Agonists with Pro-Cognitive Properties". Journal of Medicinal Chemistry. 56 (3): 1211–1227. doi:10.1021/jm301656h. ISSN 0022-2623. 
  53. ^ Kennett GA, Bright F, Trail B, Baxter GS, Blackburn TP (1996). "Effects of the 5-HT2B receptor agonist, BW 723C86, on three rat models of anxiety". Br J Pharmacol. 117 (7): 1443–8. doi:10.1111/j.1476-5381.1996.tb15304.x. PMC 1909458 alt=Dapat diakses gratis. PMID 8730737. 
  54. ^ Duxon MS, Kennett GA, Lightowler S, Blackburn TP, Fone KC (1997). "Activation of 5-HT2B receptors in the medial amygdala causes anxiolysis in the social interaction test in the rat". Neuropharmacology. 36 (4–5): 601–8. doi:10.1016/S0028-3908(97)00042-7. PMID 9225285. 
  55. ^ Kennett GA, Trail B, Bright F (1998). "Anxiolytic-like actions of BW 723C86 in the rat Vogel conflict test are 5-HT2B receptor mediated". Neuropharmacology. 37 (12): 1603–10. doi:10.1016/S0028-3908(98)00115-4. PMID 9886683. 
  56. ^ Kennett GA, Ainsworth K, Trail B, Blackburn TP (1997). "BW 723C86, a 5-HT2B receptor agonist, causes hyperphagia and reduced grooming in rats". Neuropharmacology. 36 (2): 233–9. doi:10.1016/S0028-3908(96)00171-2. PMID 9144661. 
  57. ^ Borman RA, Tilford NS, Harmer DW, Day N, Ellis ES, Sheldrick RL, Carey J, Coleman RA, Baxter GS (2002). "5-HT(2B) receptors play a key role in mediating the excitatory effects of 5-HT in human colon in vitro". Br J Pharmacol. 135 (5): 1144–1151. doi:10.1038/sj.bjp.0704571. PMC 1573235 alt=Dapat diakses gratis. PMID 11877320. 
  58. ^ Kennett GA, Wood MD, Bright F, Trail B, Riley G, Holland V, Avenell KY, Stean T, Upton N, Bromidge S, Forbes IT, Brown AM, Middlemiss DN, Blackburn TP (1997). "SB 242084, a selective and brain penetrant 5-HT2C receptor antagonist". Neuropharmacology. 36 (4–5): 609–20. doi:10.1016/S0028-3908(97)00038-5. PMID 9225286. 
  59. ^ a b Millan MJ, Brocco M, Gobert A, Dekeyne A (2005). "Anxiolytic properties of agomelatine, an antidepressant with melatoninergic and serotonergic properties: role of 5-HT2C receptor blockade". Psychopharmacology (Berl). 177 (4): 448–58. doi:10.1007/s00213-004-1962-z. PMID 15289999. 
  60. ^ a b Millan MJ, Brocco M, Gobert A, Dekeyne A (2008). "S32006, a novel 5-HT2C receptor antagonist displaying broad-based antidepressant and anxiolytic properties in rodent models". Psychopharmacology (Berl). 199 (4): 549–68. doi:10.1007/s00213-008-1177-9. PMID 18523738. 
  61. ^ Fujitsuka N, Asakawa A, Hayashi M, Sameshima M, Amitani H, Kojima S, Fujimiya M, Inui A (2009). "Selective serotonin reuptake inhibitors modify physiological gastrointestinal motor activities via 5-HT2c receptor and acyl ghrelin". Biol Psychiatry. 65 (9): 748–759. doi:10.1016/j.biopsych.2008.10.031. PMID 19058784. 
  62. ^ Millan MJ, Peglion JL, Lavielle G, Perrin-Monneyron S (1997). "5-HT2C receptors mediate penile erections in rats: actions of novel and selective agonists and antagonists". Eur J Pharmacol. 325 (1): 9–12. doi:10.1016/S0014-2999(97)89962-1. PMID 9151932. 
  63. ^ Stancampiano R, Melis MR, Argiolas A (1994). "Penile erection and yawning induced by 5-HT1C receptor agonists in male rats: relationship with dopaminergic and oxytocinergic transmission". Eur J Pharmacol. 261 (1–2): 149–55. doi:10.1016/0014-2999(94)90313-1. PMID 8001637. 
  64. ^ Frank MG, Stryker MP, Tecott LH (2002). "Sleep and sleep homeostasis in mice lacking the 5-HT2c receptor". Neuropsychopharmacology. 27 (5): 869–73. doi:10.1016/S0893-133X(02)00353-6. PMC 2452994 alt=Dapat diakses gratis. PMID 12431861. 
  65. ^ Rang, H. P. (2003). Pharmacology. Edinburgh: Churchill Livingstone. ISBN 0-443-07145-4.  Page 187
  66. ^ Michel K, Zeller F, Langer R, Nekarda H, Kruger D, Dover TJ, Brady CA, Barnes NM, Schemann M (May 2005). "Serotonin excites neurons in the human submucous plexus via 5-HT3 receptors". National Center for Biotechnology Information. Diakses tanggal 10 October 2014. 
  67. ^ a b Pitsikas N, Brambilla A, Borsini F (1994). "Effect of DAU 6215, a novel 5-HT3 receptor antagonist, on scopolamine-induced amnesia in the rat in a spatial learning task". Pharmacol Biochem Behav. 47 (1): 95–99. doi:10.1016/0091-3057(94)90116-3. PMID 8115433. 
  68. ^ a b Smriga M, Torii K (2003). "L-Lysine acts like a partial serotonin receptor 4 antagonist and inhibits serotonin-mediated intestinal pathologies and anxiety in rats". Proceedings of the National Academy of Sciences of the United States of America. 100 (26): 15370–5. doi:10.1073/pnas.2436556100. PMC 307574 alt=Dapat diakses gratis. PMID 14676321. 
  69. ^ Kennett GA, Bright F, Trail B, Blackburn TP, Sanger GJ (1997). "Anxiolytic-like actions of the selective 5-HT4 receptor antagonists SB 204070A and SB 207266A in rats". Neuropharmacology. 36 (4–5): 707–12. doi:10.1016/S0028-3908(97)00037-3. PMID 9225297. 
  70. ^ Jean A, Conductier G, Manrique C, Bouras C, Berta P, Hen R, Charnay Y, Bockaert J, Compan V (2007). "Anorexia induced by activation of serotonin 5-HT4 receptors is mediated by increases in CART in the nucleus accumbens". Proceedings of the National Academy of Sciences of the United States of America. 104 (41): 16335–40. doi:10.1073/pnas.0701471104. PMC 2042207 alt=Dapat diakses gratis. PMID 17913892. 
  71. ^ Compan V; Charnay, Y; Dusticier, N; Daszuta, A; Hen, R; Bockaert, J (2004). "Feeding disorders in 5-HT4 receptor knockout mice". J Soc Biol. 198 (1): 37–49. PMID 15146954. 
  72. ^ a b Meneses A, Hong E (1997). "Effects of 5-HT4 receptor agonists and antagonists in learning". Pharmacol Biochem Behav. 56 (3): 347–51. doi:10.1016/S0091-3057(96)00224-9. PMID 9077568. 
  73. ^ a b Fontana DJ, Daniels SE, Wong EH, Clark RD, Eglen RM (1997). "The effects of novel, selective 5-hydroxytryptamine (5-HT)4 receptor ligands in rat spatial navigation". Neuropharmacology. 36 (4–5): 689–96. doi:10.1016/S0028-3908(97)00055-5. PMID 9225295. 
  74. ^ Fontana DJ, Daniels SE, Wong EH, Clark RD, Eglen RM (1998). "Role of 5-HT4 receptors in the mouse passive avoidance test". J Pharmacol Exp Ther. 286 (3): 1115–21. PMID 9732367. 
  75. ^ Lucas, G.; Rymar, V. V.; Du, J.; Mnie-Filali, O.; Bisgaard, C.; Manta, S.; Lambas-Senas, L.; Wiborg, O.; Haddjeri, N.; Piñeyro, G.; Sadikot, A. F.; Debonnel, G. (2007). "Serotonin4 (5-HT4) Receptor Agonists Are Putative Antidepressants with a Rapid Onset of Action". Neuron. 55 (5): 712–725. doi:10.1016/j.neuron.2007.07.041. PMID 17785179. 
  76. ^ Duman, R. S. (2007). "A Silver Bullet for the Treatment of Depression?". Neuron. 55 (5): 679–681. doi:10.1016/j.neuron.2007.08.011. PMID 17785173. 
  77. ^ Manzke, T. (2003). "5-HT4(a) Receptors Avert Opioid-Induced Breathing Depression Without Loss of Analgesia". Science. 301 (5630): 226–229. doi:10.1126/science.1084674. ISSN 0036-8075. PMID 12855812. 
  78. ^ Nelson DL (2004). "5-HT5 receptors". Curr Drug Targets CNS Neurol Disord. 3 (1): 53–8. doi:10.2174/1568007043482606. PMID 14965244. 
  79. ^ a b Dietz BM, Mahady GB, Pauli GF, Farnsworth NR (2005). "Valerian extract and valerenic acid are partial agonists of the 5-HT5a receptor in vitro". Brain Res Mol Brain Res. 138 (2): 191–7. doi:10.1016/j.molbrainres.2005.04.009. PMID 15921820. 
  80. ^ Wesolowska A (February 2008). "The anxiolytic-like effect of the selective 5-HT6 receptor antagonist SB-399885: the impact of benzodiazepine receptors". European Journal of Pharmacology. 580 (3): 355–60. doi:10.1016/j.ejphar.2007.11.022. PMID 18096153. 
  81. ^ a b Wesolowska A, Nikiforuk A (April 2007). "Effects of the brain-penetrant and selective 5-HT6 receptor antagonist SB-399885 in animal models of anxiety and depression". Neuropharmacology. 52 (5): 1274–83. doi:10.1016/j.neuropharm.2007.01.007. PMID 17320917. 
  82. ^ Hirst WD, Stean TO, Rogers DC, Sunter D, Pugh P, Moss SF, Bromidge SM, Riley G, Smith DR, Bartlett S, Heidbreder CA, Atkins AR, Lacroix LP, Dawson LA, Foley AG, Regan CM, Upton N (December 2006). "SB-399885 is a potent, selective 5-HT6 receptor antagonist with cognitive enhancing properties in aged rat water maze and novel object recognition models". European Journal of Pharmacology. 553 (1–3): 109–19. doi:10.1016/j.ejphar.2006.09.049. PMID 17069795. 
  83. ^ a b Perez-García G, Meneses A (July 2005). "Oral administration of the 5-HT6 receptor antagonists SB-357134 and SB-399885 improves memory formation in an autoshaping learning task". Pharmacology, Biochemistry, and Behavior. 81 (3): 673–82. doi:10.1016/j.pbb.2005.05.005. PMID 15964617. 
  84. ^ Wesolowska A, Nikiforuk A (March 2008). "The selective 5-HT(6) receptor antagonist SB-399885 enhances anti-immobility action of antidepressants in rats". European Journal of Pharmacology. 582 (1–3): 88–93. doi:10.1016/j.ejphar.2007.12.013. PMID 18234190. 
  85. ^ "Target Schizophrenia – Possible future developments". The Association of the British Pharmaceutical Industry. Diarsipkan dari versi asli tanggal 2008-06-12. Diakses tanggal 2008-04-11. 
  86. ^ a b c Hedlund PB, Huitron-Resendiz S, Henriksen SJ, Sutcliffe JG (November 2005). "5-HT7 receptor inhibition and inactivation induce antidepressantlike behavior and sleep pattern". Biological Psychiatry. 58 (10): 831–7. doi:10.1016/j.biopsych.2005.05.012. PMID 16018977. 
  87. ^ a b Wesolowska A, Nikiforuk A, Stachowicz K, Tatarczynska E (September 2006). "Effect of the selective 5-HT7 receptor antagonist SB 269970 in animal models of anxiety and depression". Neuropharmacology. 51 (3): 578–86. doi:10.1016/j.neuropharm.2006.04.017. PMID 16828124. 
  88. ^ Gasbarri A, Cifariello A, Pompili A, Meneses A (December 2008). "Effect of 5-HT(7) antagonist SB-269970 in the modulation of working and reference memory in the rat". Behavioural Brain Research. 195 (1): 164–70. doi:10.1016/j.bbr.2007.12.020. PMID 18308404. 
  89. ^ Liy-Salmeron G, Meneses A (2008). "Effects of 5-HT drugs in prefrontal cortex during memory formation and the ketamine amnesia-model". Hippocampus. 18 (9): 965–74. doi:10.1002/hipo.20459. PMID 18570192. 
  90. ^ a b Bonaventure P, Kelly L, Aluisio L, Shelton J, Lord B, Galici R, Miller K, Atack J, Lovenberg TW, Dugovic C (2007). "Selective blockade of 5-hydroxytryptamine (5-HT)7 receptors enhances 5-HT transmission, antidepressant-like behavior, and rapid eye movement sleep suppression induced by citalopram in rodents". J Pharmacol Exp Ther. 321 (2): 690–8. doi:10.1124/jpet.107.119404. PMID 17314195. 
  91. ^ Thomas DR, Melotto S, Massagrande M, Gribble AD, Jeffrey P, Stevens AJ, Deeks NJ, Eddershaw PJ, Fenwick SH, Riley G, Stean T, Scott CM, Hill MJ, Middlemiss DN, Hagan JJ, Price GW, Forbes IT (2003). "SB-656104-A, a novel selective 5-HT7 receptor antagonist, modulates REM sleep in rats". Br J Pharmacol. 139 (4): 705–14. doi:10.1038/sj.bjp.0705290. PMC 1573887 alt=Dapat diakses gratis. PMID 12812993. 
  92. ^ Davies MA, Sheffler DJ, Roth BL. Aripiprazole: A Novel Atypical Antipsychotic Drug With a Uniquely Robust Pharmacology. CNS Drug Reviews [Internet]. 2004 [cited 2013 Aug 4];10(4):317–36. Available from: http://onlinelibrary.wiley.com/doi/10.1111/j.1527-3458.2004.tb00030.x/pdf
Diperoleh dari "https://wiki-indonesia.club/w/index.php?title=Reseptor_serotonin&oldid=23035246"