Abstract:
:The guinea pig ileum possesses NK-1 and NK-3 tachykinin receptors. As expected, [Pro9]SP and senktide, which are selective agonists of NK-1 and NK-3 receptors, respectively, were found to be highly potent in contracting the guinea pig ileum. Surprisingly, similar observations were made with septide, SP-O-CH3, [Apa9-10]SP, or [Pro9,10]SP although, in contrast to [Pro9]SP, these four peptides showed a low affinity for 3H-[Pro9]SP-specific NK-1 binding sites on membranes from the guinea pig ileum. They were also devoid of affinity for NK-2 and NK-3 binding sites. GR 71251, a compound which has been described as a NK-1 antagonist, was more potent in inhibiting the septide- than the [Pro9]SP-evoked contracting response. Altogether, these results suggest that septide, [Apa9-10]SP, and [Pro9,10]SP exert their high contracting activity in the guinea pig ileum by acting on a new subtype of tachykinin receptors.
journal_name
Peptidesjournal_title
Peptidesauthors
Petitet F,Saffroy M,Torrens Y,Lavielle S,Chassaing G,Loeuillet D,Glowinski J,Beaujouan JCdoi
10.1016/0196-9781(92)90125-msubject
Has Abstractpub_date
1992-03-01 00:00:00pages
383-8issue
2eissn
0196-9781issn
1873-5169pii
0196-9781(92)90125-Mjournal_volume
13pub_type
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