Loading…

Upregulation of Orai Channels Contributes to Aging-Related Vascular Alterations in Rat Coronary Arteries

Vascular territories display heterogeneous sensitivity to the impacts of aging. The relevance of the STIM/Orai system to vascular function depends on the vascular bed. We aimed to evaluate the contribution of the STIM/Orai system to aging-related vascular dysfunction in rat coronary circulation. Vas...

Full description

Saved in:
Bibliographic Details
Published in:International journal of molecular sciences 2023-09, Vol.24 (17), p.13402
Main Authors: Angulo, Javier, Fernández, Argentina, Sevilleja-Ortiz, Alejandro, Sánchez-Ferrer, Alberto, Rodríguez-Mañas, Leocadio, El Assar, Mariam
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c526t-d0bbab5255c72ec21540895b60760af32f75af658cdc8f19b16e6ddfb2e8b3043
cites cdi_FETCH-LOGICAL-c526t-d0bbab5255c72ec21540895b60760af32f75af658cdc8f19b16e6ddfb2e8b3043
container_end_page
container_issue 17
container_start_page 13402
container_title International journal of molecular sciences
container_volume 24
creator Angulo, Javier
Fernández, Argentina
Sevilleja-Ortiz, Alejandro
Sánchez-Ferrer, Alberto
Rodríguez-Mañas, Leocadio
El Assar, Mariam
description Vascular territories display heterogeneous sensitivity to the impacts of aging. The relevance of the STIM/Orai system to vascular function depends on the vascular bed. We aimed to evaluate the contribution of the STIM/Orai system to aging-related vascular dysfunction in rat coronary circulation. Vascular function was evaluated according to myography in coronary arteries from young (three-month-old) and older (twenty-month-old) rats. The effects of aging and STIM/Orai inhibition on the contraction and relaxation of the coronary arteries and on the protein expression of STIM-1, Orai1, and Orai3 in these vessels were determined. Aging-related hypercontractility to serotonin and endothelin-1 in arteries from male rats was reversed by STIM/Orai inhibition with YM-58483 or by specifically blocking the Orai1 channel with Synta66. The inhibitory effects of Synta66 on coronary vasoconstriction were also observed in older female rats. YM-58483 relaxed serotonin- but not KCl-contracted arteries from males. STIM/Orai inhibition improved defective endothelial vasodilations in aged arteries, even in the presence of NO synthase and cyclooxygenase inhibitors, but not in KCl-contracted segments. YM-58483 significantly enhanced relaxations to calcium-activated potassium channel stimulation in aged vessels. Increased protein expression of Orai1 and Orai3 was detected in arterial homogenates and sections from older rats. Upregulation of the Orai channel contributes to aging-related coronary dysfunction, revealing a potential target in reducing CVD risk.
doi_str_mv 10.3390/ijms241713402
format article
fullrecord <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_9b3a6cd0b675415e8ecd8fd4a25d4502</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A764266323</galeid><doaj_id>oai_doaj_org_article_9b3a6cd0b675415e8ecd8fd4a25d4502</doaj_id><sourcerecordid>A764266323</sourcerecordid><originalsourceid>FETCH-LOGICAL-c526t-d0bbab5255c72ec21540895b60760af32f75af658cdc8f19b16e6ddfb2e8b3043</originalsourceid><addsrcrecordid>eNptUk1v1DAQjRCIloUjd0tcuKT4O8kJrVZ8VKpUqaJcLcceZ71K7MVOKvHvcboVsAj5YGvmvTczz1NVbwm-YqzDH_xhypSThjCO6bPqknBKa4xl8_yv90X1KucDxpRR0b2sLlgjW0mxvKz298cEwzLq2ceAokO3SXu02-sQYMxoF8OcfL_MkNEc0XbwYajvoMDBou86m8JMaDvOkB4VMvIB3em5EFMMOv1E21RyHvLr6oXTY4Y3T_emuv_86dvua31z--V6t72pjaByri3ue90LKoRpKBhKBMdtJ3qJG4m1Y9Q1QjspWmNN60jXEwnSWtdTaHuGOdtU1yddG_VBHZOfShcqaq8eAzENSqfZmxFU1zMtTakoG8GJgBaMbZ3lmgrLRTFrU308aR2XfgJroJihxzPR80zwezXEB0Uwb4vFazfvnxRS_LFAntXks4Fx1AHikhVtJaMdF90KffcP9BCXFIpXK4o2XJTf-4MadJnABxdLYbOKqm0jOZVFjxXU1X9Q5ViYvIkBnC_xM0J9IpgUc07gfg9JsFr3TJ3tGfsFypnEEA</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2862745232</pqid></control><display><type>article</type><title>Upregulation of Orai Channels Contributes to Aging-Related Vascular Alterations in Rat Coronary Arteries</title><source>Open Access: PubMed Central</source><source>ProQuest Publicly Available Content database</source><creator>Angulo, Javier ; Fernández, Argentina ; Sevilleja-Ortiz, Alejandro ; Sánchez-Ferrer, Alberto ; Rodríguez-Mañas, Leocadio ; El Assar, Mariam</creator><creatorcontrib>Angulo, Javier ; Fernández, Argentina ; Sevilleja-Ortiz, Alejandro ; Sánchez-Ferrer, Alberto ; Rodríguez-Mañas, Leocadio ; El Assar, Mariam</creatorcontrib><description>Vascular territories display heterogeneous sensitivity to the impacts of aging. The relevance of the STIM/Orai system to vascular function depends on the vascular bed. We aimed to evaluate the contribution of the STIM/Orai system to aging-related vascular dysfunction in rat coronary circulation. Vascular function was evaluated according to myography in coronary arteries from young (three-month-old) and older (twenty-month-old) rats. The effects of aging and STIM/Orai inhibition on the contraction and relaxation of the coronary arteries and on the protein expression of STIM-1, Orai1, and Orai3 in these vessels were determined. Aging-related hypercontractility to serotonin and endothelin-1 in arteries from male rats was reversed by STIM/Orai inhibition with YM-58483 or by specifically blocking the Orai1 channel with Synta66. The inhibitory effects of Synta66 on coronary vasoconstriction were also observed in older female rats. YM-58483 relaxed serotonin- but not KCl-contracted arteries from males. STIM/Orai inhibition improved defective endothelial vasodilations in aged arteries, even in the presence of NO synthase and cyclooxygenase inhibitors, but not in KCl-contracted segments. YM-58483 significantly enhanced relaxations to calcium-activated potassium channel stimulation in aged vessels. Increased protein expression of Orai1 and Orai3 was detected in arterial homogenates and sections from older rats. Upregulation of the Orai channel contributes to aging-related coronary dysfunction, revealing a potential target in reducing CVD risk.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms241713402</identifier><identifier>PMID: 37686206</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Aging ; arterial hypercontractility ; Arteries ; coronary artery ; Coronary vessels ; endothelial function ; Endothelin ; Endothelium ; Gerontology ; Orai channel ; Serotonin ; Smooth muscle ; vascular aging ; Veins &amp; arteries</subject><ispartof>International journal of molecular sciences, 2023-09, Vol.24 (17), p.13402</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-d0bbab5255c72ec21540895b60760af32f75af658cdc8f19b16e6ddfb2e8b3043</citedby><cites>FETCH-LOGICAL-c526t-d0bbab5255c72ec21540895b60760af32f75af658cdc8f19b16e6ddfb2e8b3043</cites><orcidid>0000-0002-6551-1333 ; 0000-0002-3789-9465</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2862745232/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2862745232?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids></links><search><creatorcontrib>Angulo, Javier</creatorcontrib><creatorcontrib>Fernández, Argentina</creatorcontrib><creatorcontrib>Sevilleja-Ortiz, Alejandro</creatorcontrib><creatorcontrib>Sánchez-Ferrer, Alberto</creatorcontrib><creatorcontrib>Rodríguez-Mañas, Leocadio</creatorcontrib><creatorcontrib>El Assar, Mariam</creatorcontrib><title>Upregulation of Orai Channels Contributes to Aging-Related Vascular Alterations in Rat Coronary Arteries</title><title>International journal of molecular sciences</title><description>Vascular territories display heterogeneous sensitivity to the impacts of aging. The relevance of the STIM/Orai system to vascular function depends on the vascular bed. We aimed to evaluate the contribution of the STIM/Orai system to aging-related vascular dysfunction in rat coronary circulation. Vascular function was evaluated according to myography in coronary arteries from young (three-month-old) and older (twenty-month-old) rats. The effects of aging and STIM/Orai inhibition on the contraction and relaxation of the coronary arteries and on the protein expression of STIM-1, Orai1, and Orai3 in these vessels were determined. Aging-related hypercontractility to serotonin and endothelin-1 in arteries from male rats was reversed by STIM/Orai inhibition with YM-58483 or by specifically blocking the Orai1 channel with Synta66. The inhibitory effects of Synta66 on coronary vasoconstriction were also observed in older female rats. YM-58483 relaxed serotonin- but not KCl-contracted arteries from males. STIM/Orai inhibition improved defective endothelial vasodilations in aged arteries, even in the presence of NO synthase and cyclooxygenase inhibitors, but not in KCl-contracted segments. YM-58483 significantly enhanced relaxations to calcium-activated potassium channel stimulation in aged vessels. Increased protein expression of Orai1 and Orai3 was detected in arterial homogenates and sections from older rats. Upregulation of the Orai channel contributes to aging-related coronary dysfunction, revealing a potential target in reducing CVD risk.</description><subject>Aging</subject><subject>arterial hypercontractility</subject><subject>Arteries</subject><subject>coronary artery</subject><subject>Coronary vessels</subject><subject>endothelial function</subject><subject>Endothelin</subject><subject>Endothelium</subject><subject>Gerontology</subject><subject>Orai channel</subject><subject>Serotonin</subject><subject>Smooth muscle</subject><subject>vascular aging</subject><subject>Veins &amp; arteries</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1v1DAQjRCIloUjd0tcuKT4O8kJrVZ8VKpUqaJcLcceZ71K7MVOKvHvcboVsAj5YGvmvTczz1NVbwm-YqzDH_xhypSThjCO6bPqknBKa4xl8_yv90X1KucDxpRR0b2sLlgjW0mxvKz298cEwzLq2ceAokO3SXu02-sQYMxoF8OcfL_MkNEc0XbwYajvoMDBou86m8JMaDvOkB4VMvIB3em5EFMMOv1E21RyHvLr6oXTY4Y3T_emuv_86dvua31z--V6t72pjaByri3ue90LKoRpKBhKBMdtJ3qJG4m1Y9Q1QjspWmNN60jXEwnSWtdTaHuGOdtU1yddG_VBHZOfShcqaq8eAzENSqfZmxFU1zMtTakoG8GJgBaMbZ3lmgrLRTFrU308aR2XfgJroJihxzPR80zwezXEB0Uwb4vFazfvnxRS_LFAntXks4Fx1AHikhVtJaMdF90KffcP9BCXFIpXK4o2XJTf-4MadJnABxdLYbOKqm0jOZVFjxXU1X9Q5ViYvIkBnC_xM0J9IpgUc07gfg9JsFr3TJ3tGfsFypnEEA</recordid><startdate>20230901</startdate><enddate>20230901</enddate><creator>Angulo, Javier</creator><creator>Fernández, Argentina</creator><creator>Sevilleja-Ortiz, Alejandro</creator><creator>Sánchez-Ferrer, Alberto</creator><creator>Rodríguez-Mañas, Leocadio</creator><creator>El Assar, Mariam</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-6551-1333</orcidid><orcidid>https://orcid.org/0000-0002-3789-9465</orcidid></search><sort><creationdate>20230901</creationdate><title>Upregulation of Orai Channels Contributes to Aging-Related Vascular Alterations in Rat Coronary Arteries</title><author>Angulo, Javier ; Fernández, Argentina ; Sevilleja-Ortiz, Alejandro ; Sánchez-Ferrer, Alberto ; Rodríguez-Mañas, Leocadio ; El Assar, Mariam</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-d0bbab5255c72ec21540895b60760af32f75af658cdc8f19b16e6ddfb2e8b3043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Aging</topic><topic>arterial hypercontractility</topic><topic>Arteries</topic><topic>coronary artery</topic><topic>Coronary vessels</topic><topic>endothelial function</topic><topic>Endothelin</topic><topic>Endothelium</topic><topic>Gerontology</topic><topic>Orai channel</topic><topic>Serotonin</topic><topic>Smooth muscle</topic><topic>vascular aging</topic><topic>Veins &amp; arteries</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Angulo, Javier</creatorcontrib><creatorcontrib>Fernández, Argentina</creatorcontrib><creatorcontrib>Sevilleja-Ortiz, Alejandro</creatorcontrib><creatorcontrib>Sánchez-Ferrer, Alberto</creatorcontrib><creatorcontrib>Rodríguez-Mañas, Leocadio</creatorcontrib><creatorcontrib>El Assar, Mariam</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest Publicly Available Content database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Angulo, Javier</au><au>Fernández, Argentina</au><au>Sevilleja-Ortiz, Alejandro</au><au>Sánchez-Ferrer, Alberto</au><au>Rodríguez-Mañas, Leocadio</au><au>El Assar, Mariam</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Upregulation of Orai Channels Contributes to Aging-Related Vascular Alterations in Rat Coronary Arteries</atitle><jtitle>International journal of molecular sciences</jtitle><date>2023-09-01</date><risdate>2023</risdate><volume>24</volume><issue>17</issue><spage>13402</spage><pages>13402-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Vascular territories display heterogeneous sensitivity to the impacts of aging. The relevance of the STIM/Orai system to vascular function depends on the vascular bed. We aimed to evaluate the contribution of the STIM/Orai system to aging-related vascular dysfunction in rat coronary circulation. Vascular function was evaluated according to myography in coronary arteries from young (three-month-old) and older (twenty-month-old) rats. The effects of aging and STIM/Orai inhibition on the contraction and relaxation of the coronary arteries and on the protein expression of STIM-1, Orai1, and Orai3 in these vessels were determined. Aging-related hypercontractility to serotonin and endothelin-1 in arteries from male rats was reversed by STIM/Orai inhibition with YM-58483 or by specifically blocking the Orai1 channel with Synta66. The inhibitory effects of Synta66 on coronary vasoconstriction were also observed in older female rats. YM-58483 relaxed serotonin- but not KCl-contracted arteries from males. STIM/Orai inhibition improved defective endothelial vasodilations in aged arteries, even in the presence of NO synthase and cyclooxygenase inhibitors, but not in KCl-contracted segments. YM-58483 significantly enhanced relaxations to calcium-activated potassium channel stimulation in aged vessels. Increased protein expression of Orai1 and Orai3 was detected in arterial homogenates and sections from older rats. Upregulation of the Orai channel contributes to aging-related coronary dysfunction, revealing a potential target in reducing CVD risk.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>37686206</pmid><doi>10.3390/ijms241713402</doi><orcidid>https://orcid.org/0000-0002-6551-1333</orcidid><orcidid>https://orcid.org/0000-0002-3789-9465</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1422-0067
ispartof International journal of molecular sciences, 2023-09, Vol.24 (17), p.13402
issn 1422-0067
1661-6596
1422-0067
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_9b3a6cd0b675415e8ecd8fd4a25d4502
source Open Access: PubMed Central; ProQuest Publicly Available Content database
subjects Aging
arterial hypercontractility
Arteries
coronary artery
Coronary vessels
endothelial function
Endothelin
Endothelium
Gerontology
Orai channel
Serotonin
Smooth muscle
vascular aging
Veins & arteries
title Upregulation of Orai Channels Contributes to Aging-Related Vascular Alterations in Rat Coronary Arteries
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T16%3A09%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Upregulation%20of%20Orai%20Channels%20Contributes%20to%20Aging-Related%20Vascular%20Alterations%20in%20Rat%20Coronary%20Arteries&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Angulo,%20Javier&rft.date=2023-09-01&rft.volume=24&rft.issue=17&rft.spage=13402&rft.pages=13402-&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms241713402&rft_dat=%3Cgale_doaj_%3EA764266323%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c526t-d0bbab5255c72ec21540895b60760af32f75af658cdc8f19b16e6ddfb2e8b3043%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2862745232&rft_id=info:pmid/37686206&rft_galeid=A764266323&rfr_iscdi=true