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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...
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Published in: | Journal of biomolecular structure & dynamics 2024-12, p.1-16 |
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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 |
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) 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 & 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 & 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 & 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 & 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> |
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title | The vascular effects of peppermint ( Mentha longifolia. L) on aorta in a mouse model: an ex-vivo and computational study |
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