Agonistic activity of SR59230A at atypical β-adrenoceptors in guinea pig gastric fundus and duodenum

  • Horinouchi T
  • Koike K
  • 3

    Readers

    Mendeley users who have this article in their library.
  • 19

    Citations

    Citations of this article.

Abstract

We have recently suggested that atypical β-adrenoceptors are present in guinea pig gastric fundus and duodenum. In the present study, we have shown that SR59230A (3-(2-ethylphenoxy)-1-[(1S)-1,2,3,4-tetrahydronaphth-1-ylamino]-(2S)- 2-propanol oxalate), a selective β3-adrenoceptor antagonist, possesses agonistic activities at atypical β-adrenoceptors in these tissues. SR59230A caused concentration-dependent relaxations. However, (±)-propranolol (1 μM) did not affect SR59230A-induced relaxations. Pretreatment of with a combination of (±)-propranolol (1 μM) and the non-selective β1-, β2-, β3- and β4-adrenoceptor antagonist, (±)-bupranolol (30 μM), significantly antagonized the relaxant effects induced by SR59230A. The results clearly indicate that SR59230A acts as an atypical β-adrenoceptor agonist on guinea pig gastric fundus and duodenum. © 2001 Elsevier Science B.V.

Author-supplied keywords

  • (±)-Bupranolol
  • Atypical
  • Duodenum
  • Gastric fundus
  • Guinea pig
  • SR59230A
  • β-adrenoceptor
  • β3-adrenoceptor

Get free article suggestions today

Mendeley saves you time finding and organizing research

Sign up here
Already have an account ?Sign in

Find this document

Authors

  • Takahiro Horinouchi

  • Katsuo Koike

Cite this document

Choose a citation style from the tabs below

Save time finding and organizing research with Mendeley

Sign up for free