8-OH-DPAT

8-OH-DPAT
Clinical data
Other names8-Hydroxy-2-(dipropylamino)tetralin; 8-Hydroxy-2-(di-n-propylamino)tetralin
Drug classSerotonin 5-HT1A receptor agonist; Serotonin 5-HT7 receptor agonist; Serotonin reuptake inhibitor or releasing agent
ATC code
  • None
Identifiers
  • 7-(dipropylamino)-5,6,7,8-tetrahydronaphthalen-1-ol
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
ChEBI
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC16H25NO
Molar mass247.382 g·mol−1
3D model (JSmol)
  • CCCN(CCC)C1CCc2cccc(O)c2C1
  • InChI=1S/C16H25NO/c1-3-10-17(11-4-2)14-9-8-13-6-5-7-16(18)15(13)12-14/h5-7,14,18H,3-4,8-12H2,1-2H3 Y
  • Key:ASXGJMSKWNBENU-UHFFFAOYSA-N Y
 NY (what is this?)  (verify)

8-OH-DPAT, also known as 8-hydroxy-2-(dipropylamino)tetralin, is a serotonin 5-HT1A receptor agonist of the 2-aminotetralin family which was developed in the 1980s and has been widely used to study the function of the 5-HT1A receptor.[1][2] It was one of the first major 5-HT1A receptor full agonists to have been discovered.

Originally believed to be selective for the 5-HT1A receptor, 8-OH-DPAT was later found to act as a serotonin 5-HT7 receptor agonist and serotonin reuptake inhibitor or releasing agent as well.[3][4][5][6][7]

In animal studies, 8-OH-DPAT has been shown to possess antidepressant,[8] anxiolytic,[9] serenic (antiaggressive),[10] anorectic,[11] antiemetic,[12] hypothermic,[13] hypotensive,[14] bradycardic,[14] hyperventilative,[15][16][17] and analgesic effects.[18]

See also

References

  1. ^ Glennon RA (1992). "Concepts for the design of 5-HT 1A serotonin agonists and antagonists". Drug Development Research. 26 (3): 251–274. doi:10.1002/ddr.430260306. ISSN 0272-4391. Retrieved 19 November 2025.
  2. ^ Shulgin A, Manning T, Daley P (2011). The Shulgin Index, Volume One: Psychedelic Phenethylamines and Related Compounds. Vol. 1. Berkeley: Transform Press. ISBN 978-0-9630096-3-0.
  3. ^ Larsson LG, Rényi L, Ross SB, Svensson B, Angeby-Möller K (February 1990). "Different effects on the responses of functional pre- and postsynaptic 5-HT1A receptors by repeated treatment of rats with the 5-HT1A receptor agonist 8-OH-DPAT". Neuropharmacology. 29 (2): 85–91. doi:10.1016/0028-3908(90)90047-U. PMID 1691832. S2CID 39066002.
  4. ^ Sprouse J, Reynolds L, Li X, Braselton J, Schmidt A (January 2004). "8-OH-DPAT as a 5-HT7 agonist: phase shifts of the circadian biological clock through increases in cAMP production". Neuropharmacology. 46 (1): 52–62. doi:10.1016/j.neuropharm.2003.08.007. PMID 14654097. S2CID 41623573.
  5. ^ "IUPHAR DATABASE - 5-Hydroxytryptamine receptors - 5-HT7". Archived from the original on 2016-03-03. Retrieved 2009-09-23.
  6. ^ Assié MB, Koek W (November 1996). "Possible in vivo 5-HT reuptake blocking properties of 8-OH-DPAT assessed by measuring hippocampal extracellular 5-HT using microdialysis in rats". British Journal of Pharmacology. 119 (5): 845–850. doi:10.1111/j.1476-5381.1996.tb15749.x. PMC 1915946. PMID 8922730.
  7. ^ Wölfel R, Graefe KH (February 1992). "Evidence for various tryptamines and related compounds acting as substrates of the platelet 5-hydroxytryptamine transporter". Naunyn-Schmiedeberg's Archives of Pharmacology. 345 (2): 129–136. doi:10.1007/BF00165727. PMID 1570019. S2CID 2984583.
  8. ^ Luscombe GP, Martin KF, Hutchins LJ, Gosden J, Heal DJ (March 1993). "Mediation of the antidepressant-like effect of 8-OH-DPAT in mice by postsynaptic 5-HT1A receptors". British Journal of Pharmacology. 108 (3): 669–677. doi:10.1111/j.1476-5381.1993.tb12859.x. PMC 1908013. PMID 8467355.
  9. ^ Schreiber R, De Vry J (November 1993). "Neuronal circuits involved in the anxiolytic effects of the 5-HT1A receptor agonists 8-OH-DPAT ipsapirone and buspirone in the rat". European Journal of Pharmacology. 249 (3): 341–351. doi:10.1016/0014-2999(93)90531-L. PMID 7904566.
  10. ^ de Boer SF, Koolhaas JM (December 2005). "5-HT1A and 5-HT1B receptor agonists and aggression: a pharmacological challenge of the serotonin deficiency hypothesis". European Journal of Pharmacology. 526 (1–3): 125–139. doi:10.1016/j.ejphar.2005.09.065. PMID 16310183.
  11. ^ Dourish CT, Hutson PH, Curzon G (October 1985). "Characteristics of feeding induced by the serotonin agonist 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT)". Brain Research Bulletin. 15 (4): 377–384. doi:10.1016/0361-9230(85)90005-X. PMID 2933126. S2CID 11047288.
  12. ^ Lucot JB (February 1994). "Antiemetic effects of flesinoxan in cats: comparisons with 8-hydroxy-2-(di-n-propylamino)tetralin". European Journal of Pharmacology. 253 (1–2): 53–60. doi:10.1016/0014-2999(94)90756-0. PMID 8013549.
  13. ^ O'Connell MT, Sarna GS, Curzon G (July 1992). "Evidence for postsynaptic mediation of the hypothermic effect of 5-HT1A receptor activation". British Journal of Pharmacology. 106 (3): 603–609. doi:10.1111/j.1476-5381.1992.tb14382.x. PMC 1907559. PMID 1387027.
  14. ^ a b Fozard JR, Mir AK, Middlemiss DN (March 1987). "Cardiovascular response to 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT) in the rat: site of action and pharmacological analysis". Journal of Cardiovascular Pharmacology. 9 (3): 328–347. doi:10.1097/00005344-198703000-00010. PMID 2437400. S2CID 24327371.
  15. ^ Sahibzada N, Ferreira M, Wasserman AM, Taveira-DaSilva AM, Gillis RA (February 2000). "Reversal of morphine-induced apnea in the anesthetized rat by drugs that activate 5-hydroxytryptamine(1A) receptors". The Journal of Pharmacology and Experimental Therapeutics. 292 (2): 704–713. doi:10.1016/S0022-3565(24)35342-X. PMID 10640309.
  16. ^ 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–R413. doi:10.1152/ajpregu.00440.2005. PMID 16166206. S2CID 224414.
  17. ^ Guenther U, Manzke T, Wrigge H, Dutschmann M, Zinserling J, Putensen C, et al. (April 2009). "The counteraction of opioid-induced ventilatory depression by the serotonin 1A-agonist 8-OH-DPAT does not antagonize antinociception in rats in situ and in vivo". Anesthesia and Analgesia. 108 (4): 1169–1176. doi:10.1213/ane.0b013e318198f828. PMID 19299781. S2CID 25951835.
  18. ^ Xu W, Qiu XC, Han JS (June 1994). "Serotonin receptor subtypes in spinal antinociception in the rat". The Journal of Pharmacology and Experimental Therapeutics. 269 (3): 1182–1189. doi:10.1016/S0022-3565(25)38857-9. PMID 8014862.
This article is issued from Wikipedia. The text is available under Creative Commons Attribution-Share Alike 4.0 unless otherwise noted. Additional terms may apply for the media files.