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BMY 7378 is an agonist at 5-HT1A receptors mediating hypotension and renal sympatho-inhibition in anaesthetised cats.

Abstract
The putative 5-HT1A receptor antagonist BMY 7378 (3-100 micrograms.kg-1 i.v.) caused reductions in blood pressure, heart rate and efferent renal nerve activity in anaesthetised cats. Similar effects were produced by the selective 5-HT1A receptor agonist, 8-hydroxy-2(di-n-propylamino)tetralin (8-OH-DPAT 1-10 micrograms.kg-1 i.v.). The sympatho-inhibitory effects of BMY 7378 and 8-OH-DPAT, but not those of clonidine were reversed by the non-selective 5-HT1A receptor antagonist, spipirone (1 mg.kg-1 i.v.). It is concluded that BMY 7378 is an agonist at 5-HT1A receptors mediating hypotension and renal sympatho-inhibition in anaesthetised cats.
AuthorsC M Stubbs, H E Connor, W Feniuk
JournalEuropean journal of pharmacology (Eur J Pharmacol) Vol. 197 Issue 1 Pg. 113-6 (May 02 1991) ISSN: 0014-2999 [Print] Netherlands
PMID1832639 (Publication Type: Journal Article)
Chemical References
  • Piperazines
  • Receptors, Serotonin
  • Sympatholytics
  • Tetrahydronaphthalenes
  • Spiperone
  • 8-Hydroxy-2-(di-n-propylamino)tetralin
  • BMY 7378
Topics
  • 8-Hydroxy-2-(di-n-propylamino)tetralin
  • Anesthesia
  • Animals
  • Blood Pressure (drug effects)
  • Cats
  • Female
  • Heart Rate (drug effects)
  • Kidney (drug effects, innervation)
  • Male
  • Piperazines (pharmacology)
  • Receptors, Serotonin (drug effects)
  • Spiperone (pharmacology)
  • Sympathetic Nervous System (drug effects)
  • Sympatholytics (pharmacology)
  • Tetrahydronaphthalenes (pharmacology)

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