Go to:
Logótipo
Comuta visibilidade da coluna esquerda
Você está em: Start > Publications > View > Selective ETB1 stimulation relaxes the iris sphincter muscle.
Publication

Publications

Selective ETB1 stimulation relaxes the iris sphincter muscle.

Title
Selective ETB1 stimulation relaxes the iris sphincter muscle.
Type
Summary of Presentation in an International Conference
Year
2004
Authors
Rocha-Sousa A
(Author)
FMUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page View ORCID page
Saraiva I
(Author)
Other
The person does not belong to the institution. The person does not belong to the institution. The person does not belong to the institution. Without AUTHENTICUS Without ORCID
Falcão-Reis F
(Author)
FMUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page View ORCID page
Leite Moreira AF
(Author)
FMUP
View Personal Page You do not have permissions to view the institutional email. Search for Participant Publications View Authenticus page View ORCID page
Conference proceedings International
Initial page: 145
European Association for Vision and Eye research (EVER).
Vilamoura, Portugal, 24 27 de Setembro de 2004
Scientific classification
FOS: Medical and Health sciences > Other medical sciences
Other information
Resumo (PT): Purpose: Endothelin–1 (ET-1) effects are mediated by two different receptors (ETA and ETB). The later include ETB1 (endothelial) and ETB2 (muscular) subtypes. ETB1 stimulation promotes NO release and Pg production. The present study investigated, in rabbit iris sphincter muscles, the effects of selective ETB stimulation. Methods: Rabbit iris sphincter muscles (n=46) were dissected and attached to a force transducer, on a vertical organ bath containing a modified Krebs-Ringer solution (1.8 mM Ca2+; 35ºC).The effects of ETB stimulation by Sarafotoxin (SRTX; 2*10e-7 M) were studied alone (n=10) or in presence of: (i) a selective ETA receptor antagonist, (BQ-123; 10e-5 M ; n=7); (ii) a selective ETB2 antagonist, (BQ 788; 10e-5 M; n=7); (iii) a NOS inhibitor (LNA; 10e-4 M; n=7) (iv) and a COX inhibitor (Indomethacin; 10e-5 M; n=7). Finally the effects of a selective ETB1 agonist (IRL-1620 10e-6 M; n=8) were evaluated. All effects were recorded and analysed after an isometric contraction elicited by Carbachol (10e-4 M). Only significant results (mean±SE, p<0.05) are given, expressed as % changes from control. Results: When compared to control, SRTX promoted a 4,8±1,6% decrease in isometric tension, 2’ 30’’ after its addition to the bathing solution, an effect that disappeared at 10’. This effect was not affected by BQ-788 (tension decreased 4.0±1.7%), BQ-123 (4.3±0.8%) or L-NA (5.6±1.5%), but was slightly but not significantly attenuated by INDO (3.5±0.9%); yet it was increased by selective ETB1 stimulation with IRL-1620 (tension decreased 6.9±1.6%). Conclusions: ETB stimulation relaxes the iris sphincter muscle, an effect that seems to be mediated by the ETB1 subtype.
Language: English
Type (Professor's evaluation): Scientific
Notes: European Association for Vision and Eye research (EVER), published in journal, Ophthalmic Research. 2004; 36(Suppl.1):145.
Documents
We could not find any documents associated to the publication.
Related Publications

Of the same authors

Obestatin potentiates the carbachol-elicited contraction of the iris sphincter muscle. (2006)
Summary of Presentation in an International Conference
Rocha-Sousa A; Alves-Faria P; Saraiva I; Falcão-Reis F; Leite-Moreira AF
Ghrelin relaxes the iris sphincter muscle through a GHSR-1a independent pathway. (2004)
Summary of Presentation in an International Conference
Rocha-Sousa A; Saraiva I; Gonzaga S; Correia-Pinto J; Falcão-Reis F; Leite-Moreira AF
Recommend this page Top
Copyright 1996-2025 © Faculdade de Direito da Universidade do Porto  I Terms and Conditions  I Acessibility  I Index A-Z
Page created on: 2025-08-06 at 03:41:06 | Privacy Policy | Personal Data Protection Policy | Whistleblowing