STRUCTURE-ACTIVITY-RELATIONSHIPS OF ENDOTHELIN-1 ANALOGS

Detalhes bibliográficos
Autor(a) principal: Miasiro, N. [UNIFESP]
Data de Publicação: 1995
Outros Autores: Decastiglione, R., Paiva, Antonio Cechelli de Mattos [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://journals.lww.com/cardiovascularpharm/Abstract/1995/06263/Structure_Activity_Relationships_of_Endothelin_1.96.aspx
http://repositorio.unifesp.br/handle/11600/44222
Resumo: The importance of residues 9 and 10 for endothelin-1 (ET-1) biologic activity was assessed by studying the responses of the guinea pig ileum to [Ala(9)]-ET-1 and [Ala(10)]-ET-1. Both analogues induced relaxation followed by contraction. [Ala(9)]-ET-1 showed similar ED(50) value and maximal response to those of ET-1, whereas [Ala(10)]-ET-1 had a larger ED(50) value and was a partial agonist, as was IRL1620. ET-1 and [Ala(10)]-ET-1 induced similar degrees of tachyphylaxis, whereas [Ala(9)]-ET-1 induced very little tachyphylaxis, indicating that Lys(9) is important for inducing tachyphylaxis. BQ-123, an ET(A) antagonist, did not inhibit the relaxation. It did inhibit [Ala(9)]-ET-1- and ET-1-induced contractions but not [Ala(10)]-ET-1- and IRL1620-induced contractions. Cross-tachyphylaxis and additivity studies indicated that [Ala(9)]-ET-1, like ET-1, acts at the ET(A) receptor, whereas [Ala(10)]-ET-1 behaved as an ET(B) receptor agonist, like sarafotoxin S6c. Therefore, the residue at position 10 plays a significant role in receptor activation and is a candidate for further exploration of receptor antagonism. FCE27037 (cycle [D-Cys(11)-Cys(15)]-ET-1[8-21]) inhibited the contractile but not the relaxant component of the response induced by IRL1620. These results indicate that FCE27037 is a new ET(B) antagonist and a useful tool that can discriminate pharmacologically the functionally distinct ET(B) receptors present in the guinea pig ileum.
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spelling STRUCTURE-ACTIVITY-RELATIONSHIPS OF ENDOTHELIN-1 ANALOGSENDOTHELINALANINE ANALOGSRECEPTOR SUBTYPESGUINEA PIG ILEUMTACHYPHYLAXISANTAGONISTSThe importance of residues 9 and 10 for endothelin-1 (ET-1) biologic activity was assessed by studying the responses of the guinea pig ileum to [Ala(9)]-ET-1 and [Ala(10)]-ET-1. Both analogues induced relaxation followed by contraction. [Ala(9)]-ET-1 showed similar ED(50) value and maximal response to those of ET-1, whereas [Ala(10)]-ET-1 had a larger ED(50) value and was a partial agonist, as was IRL1620. ET-1 and [Ala(10)]-ET-1 induced similar degrees of tachyphylaxis, whereas [Ala(9)]-ET-1 induced very little tachyphylaxis, indicating that Lys(9) is important for inducing tachyphylaxis. BQ-123, an ET(A) antagonist, did not inhibit the relaxation. It did inhibit [Ala(9)]-ET-1- and ET-1-induced contractions but not [Ala(10)]-ET-1- and IRL1620-induced contractions. Cross-tachyphylaxis and additivity studies indicated that [Ala(9)]-ET-1, like ET-1, acts at the ET(A) receptor, whereas [Ala(10)]-ET-1 behaved as an ET(B) receptor agonist, like sarafotoxin S6c. Therefore, the residue at position 10 plays a significant role in receptor activation and is a candidate for further exploration of receptor antagonism. FCE27037 (cycle [D-Cys(11)-Cys(15)]-ET-1[8-21]) inhibited the contractile but not the relaxant component of the response induced by IRL1620. These results indicate that FCE27037 is a new ET(B) antagonist and a useful tool that can discriminate pharmacologically the functionally distinct ET(B) receptors present in the guinea pig ileum.PHARM FARMITALIA CARLO ERBA,NERVIANO,ITALYWeb of ScienceLippincott-raven PublPHARM FARMITALIA CARLO ERBAUniversidade Federal de São Paulo (UNIFESP)Miasiro, N. [UNIFESP]Decastiglione, R.Paiva, Antonio Cechelli de Mattos [UNIFESP]2018-06-15T17:53:07Z2018-06-15T17:53:07Z1995-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionS320-S321http://journals.lww.com/cardiovascularpharm/Abstract/1995/06263/Structure_Activity_Relationships_of_Endothelin_1.96.aspxJournal Of Cardiovascular Pharmacology. Philadelphia: Lippincott-raven Publ, v. 26, p. S320-S321, 1995.0160-2446http://repositorio.unifesp.br/handle/11600/44222WOS:A1995TH91200096engJournal Of Cardiovascular Pharmacologyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-05-02T15:51:55Zoai:repositorio.unifesp.br/:11600/44222Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-05-02T15:51:55Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv STRUCTURE-ACTIVITY-RELATIONSHIPS OF ENDOTHELIN-1 ANALOGS
title STRUCTURE-ACTIVITY-RELATIONSHIPS OF ENDOTHELIN-1 ANALOGS
spellingShingle STRUCTURE-ACTIVITY-RELATIONSHIPS OF ENDOTHELIN-1 ANALOGS
Miasiro, N. [UNIFESP]
ENDOTHELIN
ALANINE ANALOGS
RECEPTOR SUBTYPES
GUINEA PIG ILEUM
TACHYPHYLAXIS
ANTAGONISTS
title_short STRUCTURE-ACTIVITY-RELATIONSHIPS OF ENDOTHELIN-1 ANALOGS
title_full STRUCTURE-ACTIVITY-RELATIONSHIPS OF ENDOTHELIN-1 ANALOGS
title_fullStr STRUCTURE-ACTIVITY-RELATIONSHIPS OF ENDOTHELIN-1 ANALOGS
title_full_unstemmed STRUCTURE-ACTIVITY-RELATIONSHIPS OF ENDOTHELIN-1 ANALOGS
title_sort STRUCTURE-ACTIVITY-RELATIONSHIPS OF ENDOTHELIN-1 ANALOGS
author Miasiro, N. [UNIFESP]
author_facet Miasiro, N. [UNIFESP]
Decastiglione, R.
Paiva, Antonio Cechelli de Mattos [UNIFESP]
author_role author
author2 Decastiglione, R.
Paiva, Antonio Cechelli de Mattos [UNIFESP]
author2_role author
author
dc.contributor.none.fl_str_mv PHARM FARMITALIA CARLO ERBA
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Miasiro, N. [UNIFESP]
Decastiglione, R.
Paiva, Antonio Cechelli de Mattos [UNIFESP]
dc.subject.por.fl_str_mv ENDOTHELIN
ALANINE ANALOGS
RECEPTOR SUBTYPES
GUINEA PIG ILEUM
TACHYPHYLAXIS
ANTAGONISTS
topic ENDOTHELIN
ALANINE ANALOGS
RECEPTOR SUBTYPES
GUINEA PIG ILEUM
TACHYPHYLAXIS
ANTAGONISTS
description The importance of residues 9 and 10 for endothelin-1 (ET-1) biologic activity was assessed by studying the responses of the guinea pig ileum to [Ala(9)]-ET-1 and [Ala(10)]-ET-1. Both analogues induced relaxation followed by contraction. [Ala(9)]-ET-1 showed similar ED(50) value and maximal response to those of ET-1, whereas [Ala(10)]-ET-1 had a larger ED(50) value and was a partial agonist, as was IRL1620. ET-1 and [Ala(10)]-ET-1 induced similar degrees of tachyphylaxis, whereas [Ala(9)]-ET-1 induced very little tachyphylaxis, indicating that Lys(9) is important for inducing tachyphylaxis. BQ-123, an ET(A) antagonist, did not inhibit the relaxation. It did inhibit [Ala(9)]-ET-1- and ET-1-induced contractions but not [Ala(10)]-ET-1- and IRL1620-induced contractions. Cross-tachyphylaxis and additivity studies indicated that [Ala(9)]-ET-1, like ET-1, acts at the ET(A) receptor, whereas [Ala(10)]-ET-1 behaved as an ET(B) receptor agonist, like sarafotoxin S6c. Therefore, the residue at position 10 plays a significant role in receptor activation and is a candidate for further exploration of receptor antagonism. FCE27037 (cycle [D-Cys(11)-Cys(15)]-ET-1[8-21]) inhibited the contractile but not the relaxant component of the response induced by IRL1620. These results indicate that FCE27037 is a new ET(B) antagonist and a useful tool that can discriminate pharmacologically the functionally distinct ET(B) receptors present in the guinea pig ileum.
publishDate 1995
dc.date.none.fl_str_mv 1995-01-01
2018-06-15T17:53:07Z
2018-06-15T17:53:07Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://journals.lww.com/cardiovascularpharm/Abstract/1995/06263/Structure_Activity_Relationships_of_Endothelin_1.96.aspx
Journal Of Cardiovascular Pharmacology. Philadelphia: Lippincott-raven Publ, v. 26, p. S320-S321, 1995.
0160-2446
http://repositorio.unifesp.br/handle/11600/44222
WOS:A1995TH91200096
url http://journals.lww.com/cardiovascularpharm/Abstract/1995/06263/Structure_Activity_Relationships_of_Endothelin_1.96.aspx
http://repositorio.unifesp.br/handle/11600/44222
identifier_str_mv Journal Of Cardiovascular Pharmacology. Philadelphia: Lippincott-raven Publ, v. 26, p. S320-S321, 1995.
0160-2446
WOS:A1995TH91200096
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal Of Cardiovascular Pharmacology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv S320-S321
dc.publisher.none.fl_str_mv Lippincott-raven Publ
publisher.none.fl_str_mv Lippincott-raven Publ
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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