Endothelin-1: a new target of therapeutic intervention for the treatment of heart failure
Endothelin-1 has been appreciated in animals and humans as a potential target for inhibition in patients with acutely decompensated congestive heart failure (CHF), as well as patients with a chronic low-output state. There has been intense interest in determining the effects of endothelin-1 on the c...
Gespeichert in:
Veröffentlicht in: | Current opinion in cardiology 2000-05, Vol.15 (3), p.136-140 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 140 |
---|---|
container_issue | 3 |
container_start_page | 136 |
container_title | Current opinion in cardiology |
container_volume | 15 |
creator | Duchman, Stanley M Thohan, Vinay Kalra, Dinesh Torre-Amione, Guillermo |
description | Endothelin-1 has been appreciated in animals and humans as a potential target for inhibition in patients with acutely decompensated congestive heart failure (CHF), as well as patients with a chronic low-output state. There has been intense interest in determining the effects of endothelin-1 on the cardiovascular system. Elevated plasma levels of endothelin-1 in patients with CHF portend a poorer prognosis than similar patients without elevated levels. Endothelin-1 levels correlate inversely with maximum oxygen consumption, and inhibition of the myocardial endothelin pathway in rats with CHF improves survival. An association between endothelin-1 and the development of CHF has recently been supported. Selectively inhibiting the endothelin A receptors in dogs with CHF produced hemodynamic improvement. Similarly, in rabbits, a structural advantage was demonstrated. Benefits in cardiac remodeling have been demonstrated in several models of CHF by nonselectively antagonizing endothelin receptors. In human trials using nonselective endothelin-1 inhibitors, researchers have demonstrated hemodynamic benefit and improvement in cardiac function in patients with decompensated CHF. Inhibition of endothelin-1 in patients with CHF appears to have potential therapeutic value, and ongoing clinical trials will further investigate the safety, efficacy, and role of this new potential therapeutic target for the treatment of CHF. |
doi_str_mv | 10.1097/00001573-200005000-00003 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71762970</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71762970</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3563-1751c342740f8b8789bed323e01771ac7b0e9d64ca8f021b2ba69cbbff2d7ea3</originalsourceid><addsrcrecordid>eNp1kUtLxDAQgIMo7rr6FyQnb9E82qb1JosvWPCyF08hbSduNW3XJHXx35vaVbwYCBlmvpmBLwhhRi8ZLeQVjYelUhA-Rmm8ZAzEAZqzVDAiaU4P0ZzyLCeJpOkMnXj_GgleFNkxmsUhKU9YPkfPt13dhw3YpiPsGmvcwQ4H7V4g4N7gWHF6C0NoKtx0AdwHdKHpO2x6NxZxcKBDG5MjvQHtAja6sYODU3RktPVwtn8XaH13u14-kNXT_ePyZkUqkWaCMJmySiRcJtTkZS7zooRacAGUScl0JUsKRZ0llc4N5azkpc6KqiyN4bUELRboYhq7df37AD6otvEVWKs76AevJJMZLySNYD6Bleu9d2DU1jWtdp-KUTVaVT9W1a_V75SIref7HUPZQv2ncdIYgWQCdr2NkvybHXbgVPRhw0b991viC1DkgjU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>71762970</pqid></control><display><type>article</type><title>Endothelin-1: a new target of therapeutic intervention for the treatment of heart failure</title><source>MEDLINE</source><source>Journals@Ovid Complete</source><creator>Duchman, Stanley M ; Thohan, Vinay ; Kalra, Dinesh ; Torre-Amione, Guillermo</creator><creatorcontrib>Duchman, Stanley M ; Thohan, Vinay ; Kalra, Dinesh ; Torre-Amione, Guillermo</creatorcontrib><description>Endothelin-1 has been appreciated in animals and humans as a potential target for inhibition in patients with acutely decompensated congestive heart failure (CHF), as well as patients with a chronic low-output state. There has been intense interest in determining the effects of endothelin-1 on the cardiovascular system. Elevated plasma levels of endothelin-1 in patients with CHF portend a poorer prognosis than similar patients without elevated levels. Endothelin-1 levels correlate inversely with maximum oxygen consumption, and inhibition of the myocardial endothelin pathway in rats with CHF improves survival. An association between endothelin-1 and the development of CHF has recently been supported. Selectively inhibiting the endothelin A receptors in dogs with CHF produced hemodynamic improvement. Similarly, in rabbits, a structural advantage was demonstrated. Benefits in cardiac remodeling have been demonstrated in several models of CHF by nonselectively antagonizing endothelin receptors. In human trials using nonselective endothelin-1 inhibitors, researchers have demonstrated hemodynamic benefit and improvement in cardiac function in patients with decompensated CHF. Inhibition of endothelin-1 in patients with CHF appears to have potential therapeutic value, and ongoing clinical trials will further investigate the safety, efficacy, and role of this new potential therapeutic target for the treatment of CHF.</description><identifier>ISSN: 0268-4705</identifier><identifier>EISSN: 1531-7080</identifier><identifier>DOI: 10.1097/00001573-200005000-00003</identifier><identifier>PMID: 10952418</identifier><language>eng</language><publisher>United States: Lippincott Williams & Wilkins, Inc</publisher><subject>Animals ; Disease Models, Animal ; Disease Progression ; Dogs ; Drug Evaluation, Preclinical ; Endothelin-1 - antagonists & inhibitors ; Endothelin-1 - drug effects ; Endothelin-1 - physiology ; Heart Failure - drug therapy ; Heart Failure - etiology ; Heart Failure - metabolism ; Heart Failure - physiopathology ; Hemodynamics - drug effects ; Humans ; Oxygen Consumption ; Prognosis ; Pyridines - pharmacology ; Pyridines - therapeutic use ; Rabbits ; Rats ; Survival Analysis ; Tetrazoles - pharmacology ; Tetrazoles - therapeutic use</subject><ispartof>Current opinion in cardiology, 2000-05, Vol.15 (3), p.136-140</ispartof><rights>2000 Lippincott Williams & Wilkins, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3563-1751c342740f8b8789bed323e01771ac7b0e9d64ca8f021b2ba69cbbff2d7ea3</citedby><cites>FETCH-LOGICAL-c3563-1751c342740f8b8789bed323e01771ac7b0e9d64ca8f021b2ba69cbbff2d7ea3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10952418$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Duchman, Stanley M</creatorcontrib><creatorcontrib>Thohan, Vinay</creatorcontrib><creatorcontrib>Kalra, Dinesh</creatorcontrib><creatorcontrib>Torre-Amione, Guillermo</creatorcontrib><title>Endothelin-1: a new target of therapeutic intervention for the treatment of heart failure</title><title>Current opinion in cardiology</title><addtitle>Curr Opin Cardiol</addtitle><description>Endothelin-1 has been appreciated in animals and humans as a potential target for inhibition in patients with acutely decompensated congestive heart failure (CHF), as well as patients with a chronic low-output state. There has been intense interest in determining the effects of endothelin-1 on the cardiovascular system. Elevated plasma levels of endothelin-1 in patients with CHF portend a poorer prognosis than similar patients without elevated levels. Endothelin-1 levels correlate inversely with maximum oxygen consumption, and inhibition of the myocardial endothelin pathway in rats with CHF improves survival. An association between endothelin-1 and the development of CHF has recently been supported. Selectively inhibiting the endothelin A receptors in dogs with CHF produced hemodynamic improvement. Similarly, in rabbits, a structural advantage was demonstrated. Benefits in cardiac remodeling have been demonstrated in several models of CHF by nonselectively antagonizing endothelin receptors. In human trials using nonselective endothelin-1 inhibitors, researchers have demonstrated hemodynamic benefit and improvement in cardiac function in patients with decompensated CHF. Inhibition of endothelin-1 in patients with CHF appears to have potential therapeutic value, and ongoing clinical trials will further investigate the safety, efficacy, and role of this new potential therapeutic target for the treatment of CHF.</description><subject>Animals</subject><subject>Disease Models, Animal</subject><subject>Disease Progression</subject><subject>Dogs</subject><subject>Drug Evaluation, Preclinical</subject><subject>Endothelin-1 - antagonists & inhibitors</subject><subject>Endothelin-1 - drug effects</subject><subject>Endothelin-1 - physiology</subject><subject>Heart Failure - drug therapy</subject><subject>Heart Failure - etiology</subject><subject>Heart Failure - metabolism</subject><subject>Heart Failure - physiopathology</subject><subject>Hemodynamics - drug effects</subject><subject>Humans</subject><subject>Oxygen Consumption</subject><subject>Prognosis</subject><subject>Pyridines - pharmacology</subject><subject>Pyridines - therapeutic use</subject><subject>Rabbits</subject><subject>Rats</subject><subject>Survival Analysis</subject><subject>Tetrazoles - pharmacology</subject><subject>Tetrazoles - therapeutic use</subject><issn>0268-4705</issn><issn>1531-7080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUtLxDAQgIMo7rr6FyQnb9E82qb1JosvWPCyF08hbSduNW3XJHXx35vaVbwYCBlmvpmBLwhhRi8ZLeQVjYelUhA-Rmm8ZAzEAZqzVDAiaU4P0ZzyLCeJpOkMnXj_GgleFNkxmsUhKU9YPkfPt13dhw3YpiPsGmvcwQ4H7V4g4N7gWHF6C0NoKtx0AdwHdKHpO2x6NxZxcKBDG5MjvQHtAja6sYODU3RktPVwtn8XaH13u14-kNXT_ePyZkUqkWaCMJmySiRcJtTkZS7zooRacAGUScl0JUsKRZ0llc4N5azkpc6KqiyN4bUELRboYhq7df37AD6otvEVWKs76AevJJMZLySNYD6Bleu9d2DU1jWtdp-KUTVaVT9W1a_V75SIref7HUPZQv2ncdIYgWQCdr2NkvybHXbgVPRhw0b991viC1DkgjU</recordid><startdate>200005</startdate><enddate>200005</enddate><creator>Duchman, Stanley M</creator><creator>Thohan, Vinay</creator><creator>Kalra, Dinesh</creator><creator>Torre-Amione, Guillermo</creator><general>Lippincott Williams & Wilkins, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200005</creationdate><title>Endothelin-1: a new target of therapeutic intervention for the treatment of heart failure</title><author>Duchman, Stanley M ; Thohan, Vinay ; Kalra, Dinesh ; Torre-Amione, Guillermo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3563-1751c342740f8b8789bed323e01771ac7b0e9d64ca8f021b2ba69cbbff2d7ea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animals</topic><topic>Disease Models, Animal</topic><topic>Disease Progression</topic><topic>Dogs</topic><topic>Drug Evaluation, Preclinical</topic><topic>Endothelin-1 - antagonists & inhibitors</topic><topic>Endothelin-1 - drug effects</topic><topic>Endothelin-1 - physiology</topic><topic>Heart Failure - drug therapy</topic><topic>Heart Failure - etiology</topic><topic>Heart Failure - metabolism</topic><topic>Heart Failure - physiopathology</topic><topic>Hemodynamics - drug effects</topic><topic>Humans</topic><topic>Oxygen Consumption</topic><topic>Prognosis</topic><topic>Pyridines - pharmacology</topic><topic>Pyridines - therapeutic use</topic><topic>Rabbits</topic><topic>Rats</topic><topic>Survival Analysis</topic><topic>Tetrazoles - pharmacology</topic><topic>Tetrazoles - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Duchman, Stanley M</creatorcontrib><creatorcontrib>Thohan, Vinay</creatorcontrib><creatorcontrib>Kalra, Dinesh</creatorcontrib><creatorcontrib>Torre-Amione, Guillermo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Current opinion in cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Duchman, Stanley M</au><au>Thohan, Vinay</au><au>Kalra, Dinesh</au><au>Torre-Amione, Guillermo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endothelin-1: a new target of therapeutic intervention for the treatment of heart failure</atitle><jtitle>Current opinion in cardiology</jtitle><addtitle>Curr Opin Cardiol</addtitle><date>2000-05</date><risdate>2000</risdate><volume>15</volume><issue>3</issue><spage>136</spage><epage>140</epage><pages>136-140</pages><issn>0268-4705</issn><eissn>1531-7080</eissn><abstract>Endothelin-1 has been appreciated in animals and humans as a potential target for inhibition in patients with acutely decompensated congestive heart failure (CHF), as well as patients with a chronic low-output state. There has been intense interest in determining the effects of endothelin-1 on the cardiovascular system. Elevated plasma levels of endothelin-1 in patients with CHF portend a poorer prognosis than similar patients without elevated levels. Endothelin-1 levels correlate inversely with maximum oxygen consumption, and inhibition of the myocardial endothelin pathway in rats with CHF improves survival. An association between endothelin-1 and the development of CHF has recently been supported. Selectively inhibiting the endothelin A receptors in dogs with CHF produced hemodynamic improvement. Similarly, in rabbits, a structural advantage was demonstrated. Benefits in cardiac remodeling have been demonstrated in several models of CHF by nonselectively antagonizing endothelin receptors. In human trials using nonselective endothelin-1 inhibitors, researchers have demonstrated hemodynamic benefit and improvement in cardiac function in patients with decompensated CHF. Inhibition of endothelin-1 in patients with CHF appears to have potential therapeutic value, and ongoing clinical trials will further investigate the safety, efficacy, and role of this new potential therapeutic target for the treatment of CHF.</abstract><cop>United States</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>10952418</pmid><doi>10.1097/00001573-200005000-00003</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0268-4705 |
ispartof | Current opinion in cardiology, 2000-05, Vol.15 (3), p.136-140 |
issn | 0268-4705 1531-7080 |
language | eng |
recordid | cdi_proquest_miscellaneous_71762970 |
source | MEDLINE; Journals@Ovid Complete |
subjects | Animals Disease Models, Animal Disease Progression Dogs Drug Evaluation, Preclinical Endothelin-1 - antagonists & inhibitors Endothelin-1 - drug effects Endothelin-1 - physiology Heart Failure - drug therapy Heart Failure - etiology Heart Failure - metabolism Heart Failure - physiopathology Hemodynamics - drug effects Humans Oxygen Consumption Prognosis Pyridines - pharmacology Pyridines - therapeutic use Rabbits Rats Survival Analysis Tetrazoles - pharmacology Tetrazoles - therapeutic use |
title | Endothelin-1: a new target of therapeutic intervention for the treatment of heart failure |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T03%3A51%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Endothelin-1:%20a%20new%20target%20of%20therapeutic%20intervention%20for%20the%20treatment%20of%20heart%20failure&rft.jtitle=Current%20opinion%20in%20cardiology&rft.au=Duchman,%20Stanley%20M&rft.date=2000-05&rft.volume=15&rft.issue=3&rft.spage=136&rft.epage=140&rft.pages=136-140&rft.issn=0268-4705&rft.eissn=1531-7080&rft_id=info:doi/10.1097/00001573-200005000-00003&rft_dat=%3Cproquest_cross%3E71762970%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=71762970&rft_id=info:pmid/10952418&rfr_iscdi=true |