Positive Lusitropic Effect of Quercetin on Isolated Ventricular Myocardia from Normal and Streptozotocin-Induced Diabetic Mice

The lusitropic effect of quercetin was examined on isolated ventricular myocardial tissue preparations from normal and streptozotocin-induced diabetic mice. The time required for 90% relaxation of the myocardium, which was prolonged in the diabetic mice, was shortened by quercetin in both normal and...

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Veröffentlicht in:Biological & pharmaceutical bulletin 2021/12/01, Vol.44(12), pp.1894-1897
Hauptverfasser: Hamaguchi, Shogo, Abe, Kohei, Komatsu, Momoka, Kainuma, Jun, Namekata, Iyuki, Tanaka, Hikaru
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container_end_page 1897
container_issue 12
container_start_page 1894
container_title Biological & pharmaceutical bulletin
container_volume 44
creator Hamaguchi, Shogo
Abe, Kohei
Komatsu, Momoka
Kainuma, Jun
Namekata, Iyuki
Tanaka, Hikaru
description The lusitropic effect of quercetin was examined on isolated ventricular myocardial tissue preparations from normal and streptozotocin-induced diabetic mice. The time required for 90% relaxation of the myocardium, which was prolonged in the diabetic mice, was shortened by quercetin in both normal and diabetic myocardia. This effect of quercetin was completely inhibited by cyclopiazonic acid but not by SEA0400. These results indicated that quercetin accelerates myocardial relaxation through activation of the sarco–endoplasmic reticulum Ca2+-ATPase.
doi_str_mv 10.1248/bpb.b21-00580
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The time required for 90% relaxation of the myocardium, which was prolonged in the diabetic mice, was shortened by quercetin in both normal and diabetic myocardia. This effect of quercetin was completely inhibited by cyclopiazonic acid but not by SEA0400. These results indicated that quercetin accelerates myocardial relaxation through activation of the sarco–endoplasmic reticulum Ca2+-ATPase.</description><identifier>ISSN: 0918-6158</identifier><identifier>EISSN: 1347-5215</identifier><identifier>DOI: 10.1248/bpb.b21-00580</identifier><identifier>PMID: 34853274</identifier><language>eng</language><publisher>Japan: The Pharmaceutical Society of Japan</publisher><subject>Adenosine triphosphatase ; Adenosine Triphosphatases - metabolism ; Aniline Compounds - pharmacology ; Animals ; Ca2+-transporting ATPase ; Calcium (reticular) ; Calcium - metabolism ; Cyclopiazonic acid ; Diabetes ; Diabetes mellitus ; Diabetes Mellitus, Experimental - drug therapy ; Diabetes Mellitus, Experimental - metabolism ; Diabetes Mellitus, Experimental - physiopathology ; Endoplasmic Reticulum ; Enzyme Inhibitors ; Heart Ventricles - metabolism ; Heart Ventricles - physiopathology ; Indoles - pharmacology ; lusitropy ; Male ; Mice ; Myocardial Contraction - drug effects ; Myocardium ; Myocardium - metabolism ; Myocardium - pathology ; Phenyl Ethers - pharmacology ; Plant Extracts - pharmacology ; Plant Extracts - therapeutic use ; Plants, Edible - chemistry ; Quercetin ; Quercetin - pharmacology ; Quercetin - therapeutic use ; Reference Values ; Rodents ; sarco–endoplasmic reticulum Ca2+-ATPase ; Streptozocin ; Ventricle ; Ventricular Dysfunction, Left - etiology ; Ventricular Pressure</subject><ispartof>Biological and Pharmaceutical Bulletin, 2021/12/01, Vol.44(12), pp.1894-1897</ispartof><rights>2021 The Pharmaceutical Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c659t-cea636dac82e02042b4e8fd7d5d81044d042b0a874729d6fa8bd11147888a60d3</citedby><cites>FETCH-LOGICAL-c659t-cea636dac82e02042b4e8fd7d5d81044d042b0a874729d6fa8bd11147888a60d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,1877,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34853274$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hamaguchi, Shogo</creatorcontrib><creatorcontrib>Abe, Kohei</creatorcontrib><creatorcontrib>Komatsu, Momoka</creatorcontrib><creatorcontrib>Kainuma, Jun</creatorcontrib><creatorcontrib>Namekata, Iyuki</creatorcontrib><creatorcontrib>Tanaka, Hikaru</creatorcontrib><creatorcontrib>Department of Pharmacology</creatorcontrib><creatorcontrib>Toho University Faculty of Pharmaceutical Sciences</creatorcontrib><title>Positive Lusitropic Effect of Quercetin on Isolated Ventricular Myocardia from Normal and Streptozotocin-Induced Diabetic Mice</title><title>Biological &amp; pharmaceutical bulletin</title><addtitle>Biol Pharm Bull</addtitle><description>The lusitropic effect of quercetin was examined on isolated ventricular myocardial tissue preparations from normal and streptozotocin-induced diabetic mice. The time required for 90% relaxation of the myocardium, which was prolonged in the diabetic mice, was shortened by quercetin in both normal and diabetic myocardia. This effect of quercetin was completely inhibited by cyclopiazonic acid but not by SEA0400. These results indicated that quercetin accelerates myocardial relaxation through activation of the sarco–endoplasmic reticulum Ca2+-ATPase.</description><subject>Adenosine triphosphatase</subject><subject>Adenosine Triphosphatases - metabolism</subject><subject>Aniline Compounds - pharmacology</subject><subject>Animals</subject><subject>Ca2+-transporting ATPase</subject><subject>Calcium (reticular)</subject><subject>Calcium - metabolism</subject><subject>Cyclopiazonic acid</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes Mellitus, Experimental - drug therapy</subject><subject>Diabetes Mellitus, Experimental - metabolism</subject><subject>Diabetes Mellitus, Experimental - physiopathology</subject><subject>Endoplasmic Reticulum</subject><subject>Enzyme Inhibitors</subject><subject>Heart Ventricles - metabolism</subject><subject>Heart Ventricles - physiopathology</subject><subject>Indoles - pharmacology</subject><subject>lusitropy</subject><subject>Male</subject><subject>Mice</subject><subject>Myocardial Contraction - drug effects</subject><subject>Myocardium</subject><subject>Myocardium - metabolism</subject><subject>Myocardium - pathology</subject><subject>Phenyl Ethers - pharmacology</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Extracts - therapeutic use</subject><subject>Plants, Edible - chemistry</subject><subject>Quercetin</subject><subject>Quercetin - pharmacology</subject><subject>Quercetin - therapeutic use</subject><subject>Reference Values</subject><subject>Rodents</subject><subject>sarco–endoplasmic reticulum Ca2+-ATPase</subject><subject>Streptozocin</subject><subject>Ventricle</subject><subject>Ventricular Dysfunction, Left - etiology</subject><subject>Ventricular Pressure</subject><issn>0918-6158</issn><issn>1347-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkUmP1DAQhSMEYpqBI1dkiQuXDN4SO0c0Gy31sIjlajl2BdxK7B7bQZo58NtxuodG4lK2XF-9evKrqpcEnxHK5dt-15_1lNQYNxI_qlaEcVE3lDSPqxXuiKxb0siT6llKW4yxwJQ9rU4Ylw2jgq-q359Cctn9ArSZyyWGnTPochjAZBQG9HmGaCA7j4JH6xRGncGi7-BzdGYedUQ3d8HoaJ1GQwwT-hDipEekvUVfcoRdDvchB-N8vfZ2NmX4wum-KBp04ww8r54Mekzw4uE8rb5dXX49f19vPl6vz99tatM2Xa4N6Ja1VhtJAVPMac9BDlbYxkqCObfLE9ZScEE72w5a9pYQwoWUUrfYstPqzUF3F8PtDCmrySUD46g9hDkp2uKmxaQRpKCv_0O3YY6-uNtTjDLSykLVB8rEkFKEQe2im3S8UwSrJRhVglElGLUPpvCvHlTnfgJ7pP8mUYDrA1C6zugx-NF5-LfbJNG7MAZF8V6Uc0JVcayI7PhSBOsoYXRZdXFQ2qasf8BxlY7l10fYG-NlhC716PDYNj91VODZHwEOuHM</recordid><startdate>20211201</startdate><enddate>20211201</enddate><creator>Hamaguchi, Shogo</creator><creator>Abe, Kohei</creator><creator>Komatsu, Momoka</creator><creator>Kainuma, Jun</creator><creator>Namekata, Iyuki</creator><creator>Tanaka, Hikaru</creator><general>The Pharmaceutical Society of Japan</general><general>Pharmaceutical Society of Japan</general><general>Japan Science and Technology Agency</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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20211201</creationdate><title>Positive Lusitropic Effect of Quercetin on Isolated Ventricular Myocardia from Normal and Streptozotocin-Induced Diabetic Mice</title><author>Hamaguchi, Shogo ; 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The time required for 90% relaxation of the myocardium, which was prolonged in the diabetic mice, was shortened by quercetin in both normal and diabetic myocardia. This effect of quercetin was completely inhibited by cyclopiazonic acid but not by SEA0400. These results indicated that quercetin accelerates myocardial relaxation through activation of the sarco–endoplasmic reticulum Ca2+-ATPase.</abstract><cop>Japan</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>34853274</pmid><doi>10.1248/bpb.b21-00580</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
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subjects Adenosine triphosphatase
Adenosine Triphosphatases - metabolism
Aniline Compounds - pharmacology
Animals
Ca2+-transporting ATPase
Calcium (reticular)
Calcium - metabolism
Cyclopiazonic acid
Diabetes
Diabetes mellitus
Diabetes Mellitus, Experimental - drug therapy
Diabetes Mellitus, Experimental - metabolism
Diabetes Mellitus, Experimental - physiopathology
Endoplasmic Reticulum
Enzyme Inhibitors
Heart Ventricles - metabolism
Heart Ventricles - physiopathology
Indoles - pharmacology
lusitropy
Male
Mice
Myocardial Contraction - drug effects
Myocardium
Myocardium - metabolism
Myocardium - pathology
Phenyl Ethers - pharmacology
Plant Extracts - pharmacology
Plant Extracts - therapeutic use
Plants, Edible - chemistry
Quercetin
Quercetin - pharmacology
Quercetin - therapeutic use
Reference Values
Rodents
sarco–endoplasmic reticulum Ca2+-ATPase
Streptozocin
Ventricle
Ventricular Dysfunction, Left - etiology
Ventricular Pressure
title Positive Lusitropic Effect of Quercetin on Isolated Ventricular Myocardia from Normal and Streptozotocin-Induced Diabetic Mice
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