Loading…

The vascular effects of peppermint ( Mentha longifolia. L) on aorta in a mouse model: an ex-vivo and computational study

The present study examined the vascular effects of peppermint or mint ( ) using an abdominal aortic rings model. Concentration-response curves for mint oil were generated after precontracting isolated mouse aorta with phenylephrine. The effect of different receptor antagonists and ion channel or enz...

Full description

Saved in:
Bibliographic Details
Published in:Journal of biomolecular structure & dynamics 2024-12, p.1-16
Main Authors: Alkharfy, Khalid M, Ahmad, Ajaz, Almuaijel, Saleh, Bin Hashim, Abdullah, Raish, Mohammad, Jan, Basit L, Rehman, Najeeb Ur, Anwar, Farooq, Rehman, Md Tabish, Alajmi, Mohamad F
Format: Article
Language:English
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c187t-8a0b944609992f984d4d52d71121b7bf67b0ee1fa8a1cd751742249e4d99ab623
container_end_page 16
container_issue
container_start_page 1
container_title Journal of biomolecular structure & dynamics
container_volume
creator Alkharfy, Khalid M
Ahmad, Ajaz
Almuaijel, Saleh
Bin Hashim, Abdullah
Raish, Mohammad
Jan, Basit L
Rehman, Najeeb Ur
Anwar, Farooq
Rehman, Md Tabish
Alajmi, Mohamad F
description The present study examined the vascular effects of peppermint or mint ( ) using an abdominal aortic rings model. Concentration-response curves for mint oil were generated after precontracting isolated mouse aorta with phenylephrine. The effect of different receptor antagonists and ion channel or enzyme inhibitors on the vasorelaxant potential of mint oil were studied. Molecular docking studies were conducted using computational techniques to investigate the potential interactions between the bioactive constituents of mint oil and key vascular targets. The tension of aortic rings, which had been contracted by phenylephrine, relaxed as a function of the concentration of mint oil (0.0002-2 mg/mL). Pretreatment of the rings with the nitric oxide synthase inhibitor (L-NAME), a nonselective β-blocker (propranolol), and a muscarinic receptor blocker (atropine) didn't show significant resistance to the vasodilatory effects of the mint oil. The vasodilatory effects of mint oil were significantly diminished when the rings were pretreated with glibenclamide, an inhibitor of ATP-sensitive K channels. In addition, indomethacin, a cyclooxygenase (COX) inhibitor, did influence mint oil's tension in the preparations precontracted with phenylephrine. The present findings imply that ATP-sensitive K channels activation, blocking of Ca channels, and inhibition of COX play a role in mediating the mint oil-induced vasorelaxation. Molecular docking studies of mint oil constituents showed that β-Elemene and Aromadendrene can interact with K and Ca channels through various hydrophobic interactions with key amino acid residues. Additional work is needed to confirm the possible beneficial application of mint oil or its constituents in regulating the vascular tone.
doi_str_mv 10.1080/07391102.2024.2439616
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3146654054</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3146654054</sourcerecordid><originalsourceid>FETCH-LOGICAL-c187t-8a0b944609992f984d4d52d71121b7bf67b0ee1fa8a1cd751742249e4d99ab623</originalsourceid><addsrcrecordid>eNo9kE1PwzAMhiMEYmPwE0A5jkNHnKZpww0hvqQhLuNcpY3DitqmNOm0_Xs6sXGxfXhe23oIuQa2AJaxO5bGCoDxBWdcLLiIlQR5QqaQxFnEeCJOyXTPRHtoQi68_2aMA6RwTiYjLGMZsynZrtZIN9qXQ617itZiGTx1lnbYddg3VRvonL5jG9aa1q79qqyrK72gy1vqWqpdHzStxoE2bvA4VoP1PdUtxW20qTZuHA0tXdMNQYfKtbqmPgxmd0nOrK49Xh36jHw-P60eX6Plx8vb48MyKiFLQ5RpVighJFNKcasyYYRJuEkBOBRpYWVaMESwOtNQmjSBVHAuFAqjlC4kj2dk_re3693PgD7kTeVLrGvd4vhxHoOQMhEsESOa_KFl77zv0eZdXzW63-XA8r30_Cg930vPD9LH3M3hxFA0aP5TR8vxL2_ZfB0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3146654054</pqid></control><display><type>article</type><title>The vascular effects of peppermint ( Mentha longifolia. L) on aorta in a mouse model: an ex-vivo and computational study</title><source>Taylor and Francis Science and Technology Collection</source><creator>Alkharfy, Khalid M ; Ahmad, Ajaz ; Almuaijel, Saleh ; Bin Hashim, Abdullah ; Raish, Mohammad ; Jan, Basit L ; Rehman, Najeeb Ur ; Anwar, Farooq ; Rehman, Md Tabish ; Alajmi, Mohamad F</creator><creatorcontrib>Alkharfy, Khalid M ; Ahmad, Ajaz ; Almuaijel, Saleh ; Bin Hashim, Abdullah ; Raish, Mohammad ; Jan, Basit L ; Rehman, Najeeb Ur ; Anwar, Farooq ; Rehman, Md Tabish ; Alajmi, Mohamad F</creatorcontrib><description>The present study examined the vascular effects of peppermint or mint ( ) using an abdominal aortic rings model. Concentration-response curves for mint oil were generated after precontracting isolated mouse aorta with phenylephrine. The effect of different receptor antagonists and ion channel or enzyme inhibitors on the vasorelaxant potential of mint oil were studied. Molecular docking studies were conducted using computational techniques to investigate the potential interactions between the bioactive constituents of mint oil and key vascular targets. The tension of aortic rings, which had been contracted by phenylephrine, relaxed as a function of the concentration of mint oil (0.0002-2 mg/mL). Pretreatment of the rings with the nitric oxide synthase inhibitor (L-NAME), a nonselective β-blocker (propranolol), and a muscarinic receptor blocker (atropine) didn't show significant resistance to the vasodilatory effects of the mint oil. The vasodilatory effects of mint oil were significantly diminished when the rings were pretreated with glibenclamide, an inhibitor of ATP-sensitive K channels. In addition, indomethacin, a cyclooxygenase (COX) inhibitor, did influence mint oil's tension in the preparations precontracted with phenylephrine. The present findings imply that ATP-sensitive K channels activation, blocking of Ca channels, and inhibition of COX play a role in mediating the mint oil-induced vasorelaxation. Molecular docking studies of mint oil constituents showed that β-Elemene and Aromadendrene can interact with K and Ca channels through various hydrophobic interactions with key amino acid residues. Additional work is needed to confirm the possible beneficial application of mint oil or its constituents in regulating the vascular tone.</description><identifier>ISSN: 0739-1102</identifier><identifier>ISSN: 1538-0254</identifier><identifier>EISSN: 1538-0254</identifier><identifier>DOI: 10.1080/07391102.2024.2439616</identifier><identifier>PMID: 39663630</identifier><language>eng</language><publisher>England</publisher><ispartof>Journal of biomolecular structure &amp; dynamics, 2024-12, p.1-16</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c187t-8a0b944609992f984d4d52d71121b7bf67b0ee1fa8a1cd751742249e4d99ab623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39663630$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alkharfy, Khalid M</creatorcontrib><creatorcontrib>Ahmad, Ajaz</creatorcontrib><creatorcontrib>Almuaijel, Saleh</creatorcontrib><creatorcontrib>Bin Hashim, Abdullah</creatorcontrib><creatorcontrib>Raish, Mohammad</creatorcontrib><creatorcontrib>Jan, Basit L</creatorcontrib><creatorcontrib>Rehman, Najeeb Ur</creatorcontrib><creatorcontrib>Anwar, Farooq</creatorcontrib><creatorcontrib>Rehman, Md Tabish</creatorcontrib><creatorcontrib>Alajmi, Mohamad F</creatorcontrib><title>The vascular effects of peppermint ( Mentha longifolia. L) on aorta in a mouse model: an ex-vivo and computational study</title><title>Journal of biomolecular structure &amp; dynamics</title><addtitle>J Biomol Struct Dyn</addtitle><description>The present study examined the vascular effects of peppermint or mint ( ) using an abdominal aortic rings model. Concentration-response curves for mint oil were generated after precontracting isolated mouse aorta with phenylephrine. The effect of different receptor antagonists and ion channel or enzyme inhibitors on the vasorelaxant potential of mint oil were studied. Molecular docking studies were conducted using computational techniques to investigate the potential interactions between the bioactive constituents of mint oil and key vascular targets. The tension of aortic rings, which had been contracted by phenylephrine, relaxed as a function of the concentration of mint oil (0.0002-2 mg/mL). Pretreatment of the rings with the nitric oxide synthase inhibitor (L-NAME), a nonselective β-blocker (propranolol), and a muscarinic receptor blocker (atropine) didn't show significant resistance to the vasodilatory effects of the mint oil. The vasodilatory effects of mint oil were significantly diminished when the rings were pretreated with glibenclamide, an inhibitor of ATP-sensitive K channels. In addition, indomethacin, a cyclooxygenase (COX) inhibitor, did influence mint oil's tension in the preparations precontracted with phenylephrine. The present findings imply that ATP-sensitive K channels activation, blocking of Ca channels, and inhibition of COX play a role in mediating the mint oil-induced vasorelaxation. Molecular docking studies of mint oil constituents showed that β-Elemene and Aromadendrene can interact with K and Ca channels through various hydrophobic interactions with key amino acid residues. Additional work is needed to confirm the possible beneficial application of mint oil or its constituents in regulating the vascular tone.</description><issn>0739-1102</issn><issn>1538-0254</issn><issn>1538-0254</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kE1PwzAMhiMEYmPwE0A5jkNHnKZpww0hvqQhLuNcpY3DitqmNOm0_Xs6sXGxfXhe23oIuQa2AJaxO5bGCoDxBWdcLLiIlQR5QqaQxFnEeCJOyXTPRHtoQi68_2aMA6RwTiYjLGMZsynZrtZIN9qXQ617itZiGTx1lnbYddg3VRvonL5jG9aa1q79qqyrK72gy1vqWqpdHzStxoE2bvA4VoP1PdUtxW20qTZuHA0tXdMNQYfKtbqmPgxmd0nOrK49Xh36jHw-P60eX6Plx8vb48MyKiFLQ5RpVighJFNKcasyYYRJuEkBOBRpYWVaMESwOtNQmjSBVHAuFAqjlC4kj2dk_re3693PgD7kTeVLrGvd4vhxHoOQMhEsESOa_KFl77zv0eZdXzW63-XA8r30_Cg930vPD9LH3M3hxFA0aP5TR8vxL2_ZfB0</recordid><startdate>20241211</startdate><enddate>20241211</enddate><creator>Alkharfy, Khalid M</creator><creator>Ahmad, Ajaz</creator><creator>Almuaijel, Saleh</creator><creator>Bin Hashim, Abdullah</creator><creator>Raish, Mohammad</creator><creator>Jan, Basit L</creator><creator>Rehman, Najeeb Ur</creator><creator>Anwar, Farooq</creator><creator>Rehman, Md Tabish</creator><creator>Alajmi, Mohamad F</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20241211</creationdate><title>The vascular effects of peppermint ( Mentha longifolia. L) on aorta in a mouse model: an ex-vivo and computational study</title><author>Alkharfy, Khalid M ; Ahmad, Ajaz ; Almuaijel, Saleh ; Bin Hashim, Abdullah ; Raish, Mohammad ; Jan, Basit L ; Rehman, Najeeb Ur ; Anwar, Farooq ; Rehman, Md Tabish ; Alajmi, Mohamad F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c187t-8a0b944609992f984d4d52d71121b7bf67b0ee1fa8a1cd751742249e4d99ab623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alkharfy, Khalid M</creatorcontrib><creatorcontrib>Ahmad, Ajaz</creatorcontrib><creatorcontrib>Almuaijel, Saleh</creatorcontrib><creatorcontrib>Bin Hashim, Abdullah</creatorcontrib><creatorcontrib>Raish, Mohammad</creatorcontrib><creatorcontrib>Jan, Basit L</creatorcontrib><creatorcontrib>Rehman, Najeeb Ur</creatorcontrib><creatorcontrib>Anwar, Farooq</creatorcontrib><creatorcontrib>Rehman, Md Tabish</creatorcontrib><creatorcontrib>Alajmi, Mohamad F</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biomolecular structure &amp; dynamics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alkharfy, Khalid M</au><au>Ahmad, Ajaz</au><au>Almuaijel, Saleh</au><au>Bin Hashim, Abdullah</au><au>Raish, Mohammad</au><au>Jan, Basit L</au><au>Rehman, Najeeb Ur</au><au>Anwar, Farooq</au><au>Rehman, Md Tabish</au><au>Alajmi, Mohamad F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The vascular effects of peppermint ( Mentha longifolia. L) on aorta in a mouse model: an ex-vivo and computational study</atitle><jtitle>Journal of biomolecular structure &amp; dynamics</jtitle><addtitle>J Biomol Struct Dyn</addtitle><date>2024-12-11</date><risdate>2024</risdate><spage>1</spage><epage>16</epage><pages>1-16</pages><issn>0739-1102</issn><issn>1538-0254</issn><eissn>1538-0254</eissn><abstract>The present study examined the vascular effects of peppermint or mint ( ) using an abdominal aortic rings model. Concentration-response curves for mint oil were generated after precontracting isolated mouse aorta with phenylephrine. The effect of different receptor antagonists and ion channel or enzyme inhibitors on the vasorelaxant potential of mint oil were studied. Molecular docking studies were conducted using computational techniques to investigate the potential interactions between the bioactive constituents of mint oil and key vascular targets. The tension of aortic rings, which had been contracted by phenylephrine, relaxed as a function of the concentration of mint oil (0.0002-2 mg/mL). Pretreatment of the rings with the nitric oxide synthase inhibitor (L-NAME), a nonselective β-blocker (propranolol), and a muscarinic receptor blocker (atropine) didn't show significant resistance to the vasodilatory effects of the mint oil. The vasodilatory effects of mint oil were significantly diminished when the rings were pretreated with glibenclamide, an inhibitor of ATP-sensitive K channels. In addition, indomethacin, a cyclooxygenase (COX) inhibitor, did influence mint oil's tension in the preparations precontracted with phenylephrine. The present findings imply that ATP-sensitive K channels activation, blocking of Ca channels, and inhibition of COX play a role in mediating the mint oil-induced vasorelaxation. Molecular docking studies of mint oil constituents showed that β-Elemene and Aromadendrene can interact with K and Ca channels through various hydrophobic interactions with key amino acid residues. Additional work is needed to confirm the possible beneficial application of mint oil or its constituents in regulating the vascular tone.</abstract><cop>England</cop><pmid>39663630</pmid><doi>10.1080/07391102.2024.2439616</doi><tpages>16</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0739-1102
ispartof Journal of biomolecular structure & dynamics, 2024-12, p.1-16
issn 0739-1102
1538-0254
1538-0254
language eng
recordid cdi_proquest_miscellaneous_3146654054
source Taylor and Francis Science and Technology Collection
title The vascular effects of peppermint ( Mentha longifolia. L) on aorta in a mouse model: an ex-vivo and computational study
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T22%3A52%3A39IST&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=The%20vascular%20effects%20of%20peppermint%20(%20Mentha%20longifolia.%20L)%20on%20aorta%20in%20a%20mouse%20model:%20an%20ex-vivo%20and%20computational%20study&rft.jtitle=Journal%20of%20biomolecular%20structure%20&%20dynamics&rft.au=Alkharfy,%20Khalid%20M&rft.date=2024-12-11&rft.spage=1&rft.epage=16&rft.pages=1-16&rft.issn=0739-1102&rft.eissn=1538-0254&rft_id=info:doi/10.1080/07391102.2024.2439616&rft_dat=%3Cproquest_cross%3E3146654054%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c187t-8a0b944609992f984d4d52d71121b7bf67b0ee1fa8a1cd751742249e4d99ab623%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3146654054&rft_id=info:pmid/39663630&rfr_iscdi=true