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Rapid biphasic arteriolar dilations induced by skeletal muscle contraction are dependent on stimulation characteristics
To test the hypothesis that measurable changes in microvasculature dilation occur in response to a single short-duration tetanic contraction, we contracted three to five skeletal muscle fibres of the hamster cremaster muscle microvascular preparation (in situ) and evaluated the response of an arteri...
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Published in: | Canadian journal of physiology and pharmacology 2004-04, Vol.82 (4), p.282-287 |
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description | To test the hypothesis that measurable changes in microvasculature dilation occur in response to a single short-duration tetanic contraction, we contracted three to five skeletal muscle fibres of the hamster cremaster muscle microvascular preparation (in situ) and evaluated the response of an arteriole overlapping the active muscle fibres. Arteriolar diameter (baseline diameter = 16.4 ± 0.9 µm, maximum diameter = 34.7 ± 1.2 µm) was measured before and after a single contraction resulting from a range of stimulus frequencies (4, 10, 20, 30, 40, 60, and 80 Hz) within a 250- or 500-ms train. Four and 10 Hz produced a significant dilation at 2.9 ± 0.4 and 6.5 ± 2.8 s, respectively, within a 250-ms train and 3.0 ± 0.2 and 6.1 ± 1.3 s, respectively, within a 500-ms train. Biphasic dilations were observed within a 250-ms train at 20 Hz (at 3.9 ± 0.9 and 22.1 ± 4.3 s), 30 Hz (at 2.7 ± 0.3 and 17.5 ± 2.9 s), and 40 Hz (at 3.8 ± 0.4 and 23.2 ± 2.6 s) and within a 500-ms train at 20 Hz (at 4.8 ± 0.4 and 31.9 ± 3.8 s) and 30 Hz (at 3.4 ± 0.3 and 27.6 ± 3.0 s). A single dilation was observed within a 250-ms train at 60 Hz (at 5.1 ± 0.7 s) and 80 Hz (at 14.2 ± 3.3 s) and within a 500-ms train at 40 Hz (at 9.9 ± 3.2 s), 60 Hz (at 7.9 ± 2.1 s), and 80 Hz (at 13.4 ± 4.0 s). We have shown that a single contraction ranging from a single twitch (4 Hz, 250 ms) to fused tetanic contractions produces significant arteriolar dilations and that the pattern of dilation is dependent on the stimulus frequency and train duration.Key words: arteriole, skeletal muscle, hyperaemia, vasodilation, stimulus frequency. |
doi_str_mv | 10.1139/y04-016 |
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Arteriolar diameter (baseline diameter = 16.4 ± 0.9 µm, maximum diameter = 34.7 ± 1.2 µm) was measured before and after a single contraction resulting from a range of stimulus frequencies (4, 10, 20, 30, 40, 60, and 80 Hz) within a 250- or 500-ms train. Four and 10 Hz produced a significant dilation at 2.9 ± 0.4 and 6.5 ± 2.8 s, respectively, within a 250-ms train and 3.0 ± 0.2 and 6.1 ± 1.3 s, respectively, within a 500-ms train. Biphasic dilations were observed within a 250-ms train at 20 Hz (at 3.9 ± 0.9 and 22.1 ± 4.3 s), 30 Hz (at 2.7 ± 0.3 and 17.5 ± 2.9 s), and 40 Hz (at 3.8 ± 0.4 and 23.2 ± 2.6 s) and within a 500-ms train at 20 Hz (at 4.8 ± 0.4 and 31.9 ± 3.8 s) and 30 Hz (at 3.4 ± 0.3 and 27.6 ± 3.0 s). A single dilation was observed within a 250-ms train at 60 Hz (at 5.1 ± 0.7 s) and 80 Hz (at 14.2 ± 3.3 s) and within a 500-ms train at 40 Hz (at 9.9 ± 3.2 s), 60 Hz (at 7.9 ± 2.1 s), and 80 Hz (at 13.4 ± 4.0 s). We have shown that a single contraction ranging from a single twitch (4 Hz, 250 ms) to fused tetanic contractions produces significant arteriolar dilations and that the pattern of dilation is dependent on the stimulus frequency and train duration.Key words: arteriole, skeletal muscle, hyperaemia, vasodilation, stimulus frequency.</description><identifier>ISSN: 0008-4212</identifier><identifier>EISSN: 1205-7541</identifier><identifier>DOI: 10.1139/y04-016</identifier><identifier>PMID: 15181467</identifier><identifier>CODEN: CJPPA3</identifier><language>eng</language><publisher>Ottawa, Canada: NRC Research Press</publisher><subject>Animals ; Arterioles - physiology ; Biological and medical sciences ; Blood vessels and receptors ; Cricetinae ; Drug Evaluation, Preclinical - methods ; Electric Stimulation - methods ; Fundamental and applied biological sciences. Psychology ; Male ; Microcirculation - anatomy & histology ; Microcirculation - physiology ; Muscle Contraction - physiology ; Muscle Fibers, Skeletal - physiology ; Muscle, Skeletal - physiology ; Time Factors ; Vasodilation - physiology ; Vertebrates: cardiovascular system</subject><ispartof>Canadian journal of physiology and pharmacology, 2004-04, Vol.82 (4), p.282-287</ispartof><rights>2004 INIST-CNRS</rights><rights>Copyright National Research Council of Canada Apr 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c332t-b3c5c2be2e316874b085cbfa1291daa232000156e3c6106b0bee8686adf60e813</citedby><cites>FETCH-LOGICAL-c332t-b3c5c2be2e316874b085cbfa1291daa232000156e3c6106b0bee8686adf60e813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15860576$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15181467$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mihok, Marika L</creatorcontrib><creatorcontrib>Murrant, Coral L</creatorcontrib><title>Rapid biphasic arteriolar dilations induced by skeletal muscle contraction are dependent on stimulation characteristics</title><title>Canadian journal of physiology and pharmacology</title><addtitle>Revue canadienne de physiologie et pharmacologie</addtitle><description>To test the hypothesis that measurable changes in microvasculature dilation occur in response to a single short-duration tetanic contraction, we contracted three to five skeletal muscle fibres of the hamster cremaster muscle microvascular preparation (in situ) and evaluated the response of an arteriole overlapping the active muscle fibres. Arteriolar diameter (baseline diameter = 16.4 ± 0.9 µm, maximum diameter = 34.7 ± 1.2 µm) was measured before and after a single contraction resulting from a range of stimulus frequencies (4, 10, 20, 30, 40, 60, and 80 Hz) within a 250- or 500-ms train. Four and 10 Hz produced a significant dilation at 2.9 ± 0.4 and 6.5 ± 2.8 s, respectively, within a 250-ms train and 3.0 ± 0.2 and 6.1 ± 1.3 s, respectively, within a 500-ms train. Biphasic dilations were observed within a 250-ms train at 20 Hz (at 3.9 ± 0.9 and 22.1 ± 4.3 s), 30 Hz (at 2.7 ± 0.3 and 17.5 ± 2.9 s), and 40 Hz (at 3.8 ± 0.4 and 23.2 ± 2.6 s) and within a 500-ms train at 20 Hz (at 4.8 ± 0.4 and 31.9 ± 3.8 s) and 30 Hz (at 3.4 ± 0.3 and 27.6 ± 3.0 s). A single dilation was observed within a 250-ms train at 60 Hz (at 5.1 ± 0.7 s) and 80 Hz (at 14.2 ± 3.3 s) and within a 500-ms train at 40 Hz (at 9.9 ± 3.2 s), 60 Hz (at 7.9 ± 2.1 s), and 80 Hz (at 13.4 ± 4.0 s). We have shown that a single contraction ranging from a single twitch (4 Hz, 250 ms) to fused tetanic contractions produces significant arteriolar dilations and that the pattern of dilation is dependent on the stimulus frequency and train duration.Key words: arteriole, skeletal muscle, hyperaemia, vasodilation, stimulus frequency.</description><subject>Animals</subject><subject>Arterioles - physiology</subject><subject>Biological and medical sciences</subject><subject>Blood vessels and receptors</subject><subject>Cricetinae</subject><subject>Drug Evaluation, Preclinical - methods</subject><subject>Electric Stimulation - methods</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Male</subject><subject>Microcirculation - anatomy & histology</subject><subject>Microcirculation - physiology</subject><subject>Muscle Contraction - physiology</subject><subject>Muscle Fibers, Skeletal - physiology</subject><subject>Muscle, Skeletal - physiology</subject><subject>Time Factors</subject><subject>Vasodilation - physiology</subject><subject>Vertebrates: cardiovascular system</subject><issn>0008-4212</issn><issn>1205-7541</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNp90duK1TAUBuAgirNnFN9AguAIQjWHNk0vZXBUGBBEr8NqssrOmKY1aZH99qbsgiLoVcjKlz-HRcgzzt5wLru3J1ZXjKsH5MAFa6q2qflDcmCM6aoWXFyQy5zvy1RpqR-TC95wzWvVHsjPLzB7R3s_HyF7SyEtmPwUIFHnAyx-ipn66FaLRZ1o_o4BFwh0XLMNSO0UlwR2c2UvUoczRodxoaWQFz-u5xBqj7C5El6qNj8hjwYIGZ_u4xX5dvv-683H6u7zh0837-4qK6VYql7axooeBUqudFv3TDe2H4CLjjsAIUV5FG8USqs4Uz3rEbXSCtygGGour8j1OXdO048V82JGny2GABGnNZuWd10txAZf_AXvpzXFcjdTlgtrWVfQqzOyaco54WDm5EdIJ8OZ2RphSiNMaUSRz_e4tR_R_Xb7zxfwcgeQLYQhQbQ-_-G0Yk27Bb0-u5hswoyQ7PE_p17_G-_IzG6QvwBID60w</recordid><startdate>20040401</startdate><enddate>20040401</enddate><creator>Mihok, Marika L</creator><creator>Murrant, Coral L</creator><general>NRC Research Press</general><general>National Research Council of Canada</general><general>Canadian Science Publishing NRC Research Press</general><scope>IQODW</scope><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>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FQ</scope><scope>8FV</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M3G</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20040401</creationdate><title>Rapid biphasic arteriolar dilations induced by skeletal muscle contraction are dependent on stimulation characteristics</title><author>Mihok, Marika L ; Murrant, Coral L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c332t-b3c5c2be2e316874b085cbfa1291daa232000156e3c6106b0bee8686adf60e813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Arterioles - physiology</topic><topic>Biological and medical sciences</topic><topic>Blood vessels and receptors</topic><topic>Cricetinae</topic><topic>Drug Evaluation, Preclinical - methods</topic><topic>Electric Stimulation - methods</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Male</topic><topic>Microcirculation - anatomy & histology</topic><topic>Microcirculation - physiology</topic><topic>Muscle Contraction - physiology</topic><topic>Muscle Fibers, Skeletal - physiology</topic><topic>Muscle, Skeletal - physiology</topic><topic>Time Factors</topic><topic>Vasodilation - physiology</topic><topic>Vertebrates: cardiovascular system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mihok, Marika L</creatorcontrib><creatorcontrib>Murrant, Coral L</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Canadian Business & Current Affairs Database</collection><collection>Canadian Business & Current Affairs Database (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Science Database</collection><collection>CBCA Reference & Current Events</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</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 China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Canadian journal of physiology and pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mihok, Marika L</au><au>Murrant, Coral L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid biphasic arteriolar dilations induced by skeletal muscle contraction are dependent on stimulation characteristics</atitle><jtitle>Canadian journal of physiology and pharmacology</jtitle><addtitle>Revue canadienne de physiologie et pharmacologie</addtitle><date>2004-04-01</date><risdate>2004</risdate><volume>82</volume><issue>4</issue><spage>282</spage><epage>287</epage><pages>282-287</pages><issn>0008-4212</issn><eissn>1205-7541</eissn><coden>CJPPA3</coden><abstract>To test the hypothesis that measurable changes in microvasculature dilation occur in response to a single short-duration tetanic contraction, we contracted three to five skeletal muscle fibres of the hamster cremaster muscle microvascular preparation (in situ) and evaluated the response of an arteriole overlapping the active muscle fibres. Arteriolar diameter (baseline diameter = 16.4 ± 0.9 µm, maximum diameter = 34.7 ± 1.2 µm) was measured before and after a single contraction resulting from a range of stimulus frequencies (4, 10, 20, 30, 40, 60, and 80 Hz) within a 250- or 500-ms train. Four and 10 Hz produced a significant dilation at 2.9 ± 0.4 and 6.5 ± 2.8 s, respectively, within a 250-ms train and 3.0 ± 0.2 and 6.1 ± 1.3 s, respectively, within a 500-ms train. Biphasic dilations were observed within a 250-ms train at 20 Hz (at 3.9 ± 0.9 and 22.1 ± 4.3 s), 30 Hz (at 2.7 ± 0.3 and 17.5 ± 2.9 s), and 40 Hz (at 3.8 ± 0.4 and 23.2 ± 2.6 s) and within a 500-ms train at 20 Hz (at 4.8 ± 0.4 and 31.9 ± 3.8 s) and 30 Hz (at 3.4 ± 0.3 and 27.6 ± 3.0 s). A single dilation was observed within a 250-ms train at 60 Hz (at 5.1 ± 0.7 s) and 80 Hz (at 14.2 ± 3.3 s) and within a 500-ms train at 40 Hz (at 9.9 ± 3.2 s), 60 Hz (at 7.9 ± 2.1 s), and 80 Hz (at 13.4 ± 4.0 s). We have shown that a single contraction ranging from a single twitch (4 Hz, 250 ms) to fused tetanic contractions produces significant arteriolar dilations and that the pattern of dilation is dependent on the stimulus frequency and train duration.Key words: arteriole, skeletal muscle, hyperaemia, vasodilation, stimulus frequency.</abstract><cop>Ottawa, Canada</cop><pub>NRC Research Press</pub><pmid>15181467</pmid><doi>10.1139/y04-016</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Arterioles - physiology Biological and medical sciences Blood vessels and receptors Cricetinae Drug Evaluation, Preclinical - methods Electric Stimulation - methods Fundamental and applied biological sciences. Psychology Male Microcirculation - anatomy & histology Microcirculation - physiology Muscle Contraction - physiology Muscle Fibers, Skeletal - physiology Muscle, Skeletal - physiology Time Factors Vasodilation - physiology Vertebrates: cardiovascular system |
title | Rapid biphasic arteriolar dilations induced by skeletal muscle contraction are dependent on stimulation characteristics |
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