Voltage Gated K+ Channel Expression in Arteries of Wistar–Kyoto and Spontaneously Hypertensive Rats
Background We have previously demonstrated differences in the gene expression of voltage-gated K v1.X channel α-subunits in arteries from Wistar–Kyoto rats (WKYs) and spontaneously hypertensive rats (SHRs). The purpose of this study was to test the hypothesis that these differences are also present...
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description | Background We have previously demonstrated differences in the gene expression of voltage-gated K v1.X channel α-subunits in arteries from Wistar–Kyoto rats (WKYs) and spontaneously hypertensive rats (SHRs). The purpose of this study was to test the hypothesis that these differences are also present at the protein level. Methods Proteins were isolated from the aorta, mesenteric (MAs) and tail arteries (TAs) of 12- to 15-week-old male WKY and SHR, and analyzed by immunoblotting. Kv currents were recorded from MA myocytes by patch clamp methods. Results Expression of Kv1.2, Kv1.5, and Kv2.1 was higher in MAs but was not different in aortas of SHRs as compared to WKYs. In the TA, expression of Kv1.2 and Kv1.5 was higher while that of Kv2.1 was lower in SHR compared to WKY. In the MA, the larger expression of an 80 kDa species of Kv1.2 in SHRs was associated with a lower expression of a 60 kDa species. Kv2.1 gene expression was larger in MAs from SHRs but not different in TAs. Kv currents associated with Kv1.X and Kv2.1 channels were both larger in MA myocytes from SHRs but less than expected based upon differences in Kv α-subunit protein expression. Conclusions For the MA, Kv protein expression and current components between WKYs and SHRs were qualitatively consistent, but differences in gene and protein expression were not closely correlated. The higher expression of Kv subunits in small mesenteric arteries (SMAs) of SHR would tend to maintain normal myogenic activity and vasoconstrictor reserve, and could be viewed as a form of homeostatic remodeling. |
doi_str_mv | 10.1038/ajh.2007.44 |
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The purpose of this study was to test the hypothesis that these differences are also present at the protein level. Methods Proteins were isolated from the aorta, mesenteric (MAs) and tail arteries (TAs) of 12- to 15-week-old male WKY and SHR, and analyzed by immunoblotting. Kv currents were recorded from MA myocytes by patch clamp methods. Results Expression of Kv1.2, Kv1.5, and Kv2.1 was higher in MAs but was not different in aortas of SHRs as compared to WKYs. In the TA, expression of Kv1.2 and Kv1.5 was higher while that of Kv2.1 was lower in SHR compared to WKY. In the MA, the larger expression of an 80 kDa species of Kv1.2 in SHRs was associated with a lower expression of a 60 kDa species. Kv2.1 gene expression was larger in MAs from SHRs but not different in TAs. Kv currents associated with Kv1.X and Kv2.1 channels were both larger in MA myocytes from SHRs but less than expected based upon differences in Kv α-subunit protein expression. Conclusions For the MA, Kv protein expression and current components between WKYs and SHRs were qualitatively consistent, but differences in gene and protein expression were not closely correlated. The higher expression of Kv subunits in small mesenteric arteries (SMAs) of SHR would tend to maintain normal myogenic activity and vasoconstrictor reserve, and could be viewed as a form of homeostatic remodeling.</description><identifier>ISSN: 0895-7061</identifier><identifier>EISSN: 1941-7225</identifier><identifier>EISSN: 1879-1905</identifier><identifier>DOI: 10.1038/ajh.2007.44</identifier><identifier>PMID: 18174882</identifier><identifier>CODEN: AJHYE6</identifier><language>eng</language><publisher>New York, NY: Oxford University Press</publisher><subject>Animals ; Antibody Specificity ; Arterial hypertension. Arterial hypotension ; Biological and medical sciences ; Blood and lymphatic vessels ; Cardiology. Vascular system ; CHO Cells ; Cricetinae ; Cricetulus ; Experimental diseases ; Gene Expression - physiology ; Humans ; Hypertension - genetics ; Hypertension - physiopathology ; Kidney - cytology ; Kv1.2 Potassium Channel - genetics ; Kv1.2 Potassium Channel - immunology ; Kv1.2 Potassium Channel - physiology ; Kv1.5 Potassium Channel - genetics ; Kv1.5 Potassium Channel - immunology ; Kv1.5 Potassium Channel - physiology ; Male ; Medical sciences ; Mesenteric Arteries - physiology ; Monocytes - physiology ; Patch-Clamp Techniques ; Potassium Channels, Voltage-Gated - genetics ; Potassium Channels, Voltage-Gated - immunology ; Potassium Channels, Voltage-Gated - physiology ; Rats ; Rats, Inbred SHR ; Rats, Inbred WKY ; Shab Potassium Channels - genetics ; Shab Potassium Channels - immunology ; Shab Potassium Channels - physiology ; Tail - blood supply ; Thoracic Arteries - physiology</subject><ispartof>American journal of hypertension, 2008-02, Vol.21 (2), p.213-218</ispartof><rights>American Journal of Hypertension, Ltd. © 2008 by the American Journal of Hypertension, Ltd. 2008</rights><rights>2008 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Feb 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-9b30f704257a75f798f1e85bbdb26df112ebb5015123ab1c6d4ee486f58f64673</citedby><cites>FETCH-LOGICAL-c451t-9b30f704257a75f798f1e85bbdb26df112ebb5015123ab1c6d4ee486f58f64673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20184891$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18174882$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cox, Robert H.</creatorcontrib><creatorcontrib>Fromme, Samantha J.</creatorcontrib><creatorcontrib>Folander, Kimberly L.</creatorcontrib><creatorcontrib>Swanson, Richard J.</creatorcontrib><title>Voltage Gated K+ Channel Expression in Arteries of Wistar–Kyoto and Spontaneously Hypertensive Rats</title><title>American journal of hypertension</title><addtitle>AJH</addtitle><description>Background We have previously demonstrated differences in the gene expression of voltage-gated K v1.X channel α-subunits in arteries from Wistar–Kyoto rats (WKYs) and spontaneously hypertensive rats (SHRs). The purpose of this study was to test the hypothesis that these differences are also present at the protein level. Methods Proteins were isolated from the aorta, mesenteric (MAs) and tail arteries (TAs) of 12- to 15-week-old male WKY and SHR, and analyzed by immunoblotting. Kv currents were recorded from MA myocytes by patch clamp methods. Results Expression of Kv1.2, Kv1.5, and Kv2.1 was higher in MAs but was not different in aortas of SHRs as compared to WKYs. In the TA, expression of Kv1.2 and Kv1.5 was higher while that of Kv2.1 was lower in SHR compared to WKY. In the MA, the larger expression of an 80 kDa species of Kv1.2 in SHRs was associated with a lower expression of a 60 kDa species. Kv2.1 gene expression was larger in MAs from SHRs but not different in TAs. Kv currents associated with Kv1.X and Kv2.1 channels were both larger in MA myocytes from SHRs but less than expected based upon differences in Kv α-subunit protein expression. Conclusions For the MA, Kv protein expression and current components between WKYs and SHRs were qualitatively consistent, but differences in gene and protein expression were not closely correlated. The higher expression of Kv subunits in small mesenteric arteries (SMAs) of SHR would tend to maintain normal myogenic activity and vasoconstrictor reserve, and could be viewed as a form of homeostatic remodeling.</description><subject>Animals</subject><subject>Antibody Specificity</subject><subject>Arterial hypertension. Arterial hypotension</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Cardiology. Vascular system</subject><subject>CHO Cells</subject><subject>Cricetinae</subject><subject>Cricetulus</subject><subject>Experimental diseases</subject><subject>Gene Expression - physiology</subject><subject>Humans</subject><subject>Hypertension - genetics</subject><subject>Hypertension - physiopathology</subject><subject>Kidney - cytology</subject><subject>Kv1.2 Potassium Channel - genetics</subject><subject>Kv1.2 Potassium Channel - immunology</subject><subject>Kv1.2 Potassium Channel - physiology</subject><subject>Kv1.5 Potassium Channel - genetics</subject><subject>Kv1.5 Potassium Channel - immunology</subject><subject>Kv1.5 Potassium Channel - physiology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mesenteric Arteries - physiology</subject><subject>Monocytes - physiology</subject><subject>Patch-Clamp Techniques</subject><subject>Potassium Channels, Voltage-Gated - genetics</subject><subject>Potassium Channels, Voltage-Gated - immunology</subject><subject>Potassium Channels, Voltage-Gated - physiology</subject><subject>Rats</subject><subject>Rats, Inbred SHR</subject><subject>Rats, Inbred WKY</subject><subject>Shab Potassium Channels - genetics</subject><subject>Shab Potassium Channels - immunology</subject><subject>Shab Potassium Channels - physiology</subject><subject>Tail - blood supply</subject><subject>Thoracic Arteries - physiology</subject><issn>0895-7061</issn><issn>1941-7225</issn><issn>1879-1905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqF0ctuEzEUgGELgWgorNgjS6hsqgm2x7dZVqFtIJGQKDdlY3lmjumEiT3YE9TseAfekCfBVaJWYsPKm0_Hx78Rek7JlJJSv7br6ykjRE05f4AmtOK0UIyJh2hCdCUKRSQ9Qk9SWhNCuJT0MTqimiquNZsg-Bz60X4DfGlHaPHiFM-urffQ4_ObIUJKXfC48_gsjhA7SDg4_KVLo41_fv1e7MIYsPUtvhqCH62HsE39Ds93A2TvU_cT8Ac7pqfokbN9gmeH8xh9ujj_OJsXy_eXb2dny6Lhgo5FVZfEKcKZUFYJpyrtKGhR123NZOsoZVDXglBBWWlr2siWA3AtndBOcqnKY_RqP3eI4ccW0mg2XWqg7_erGUWYVhUhGb78B67DNvq8m6GEcSVKJmVWp3vVxJBSBGeG2G1s3GVkbtub3N7ctjecZ_3iMHNbb6C9t4fYGZwcgE2N7V20vunSnWOEaq4rev-KsB3-c2Oxh_lD4OaO2vjd5BhKmPnXlVlcvZldLFfvzKr8C5Z2qCI</recordid><startdate>20080201</startdate><enddate>20080201</enddate><creator>Cox, Robert H.</creator><creator>Fromme, Samantha J.</creator><creator>Folander, Kimberly L.</creator><creator>Swanson, Richard J.</creator><general>Oxford University Press</general><general>Elsevier Science</general><scope>BSCLL</scope><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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20080201</creationdate><title>Voltage Gated K+ Channel Expression in Arteries of Wistar–Kyoto and Spontaneously Hypertensive Rats</title><author>Cox, Robert H. ; Fromme, Samantha J. ; Folander, Kimberly L. ; Swanson, Richard J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-9b30f704257a75f798f1e85bbdb26df112ebb5015123ab1c6d4ee486f58f64673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Antibody Specificity</topic><topic>Arterial hypertension. Arterial hypotension</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Cardiology. Vascular system</topic><topic>CHO Cells</topic><topic>Cricetinae</topic><topic>Cricetulus</topic><topic>Experimental diseases</topic><topic>Gene Expression - physiology</topic><topic>Humans</topic><topic>Hypertension - genetics</topic><topic>Hypertension - physiopathology</topic><topic>Kidney - cytology</topic><topic>Kv1.2 Potassium Channel - genetics</topic><topic>Kv1.2 Potassium Channel - immunology</topic><topic>Kv1.2 Potassium Channel - physiology</topic><topic>Kv1.5 Potassium Channel - genetics</topic><topic>Kv1.5 Potassium Channel - immunology</topic><topic>Kv1.5 Potassium Channel - physiology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mesenteric Arteries - physiology</topic><topic>Monocytes - physiology</topic><topic>Patch-Clamp Techniques</topic><topic>Potassium Channels, Voltage-Gated - genetics</topic><topic>Potassium Channels, Voltage-Gated - immunology</topic><topic>Potassium Channels, Voltage-Gated - physiology</topic><topic>Rats</topic><topic>Rats, Inbred SHR</topic><topic>Rats, Inbred WKY</topic><topic>Shab Potassium Channels - genetics</topic><topic>Shab Potassium Channels - immunology</topic><topic>Shab Potassium Channels - physiology</topic><topic>Tail - blood supply</topic><topic>Thoracic Arteries - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cox, Robert H.</creatorcontrib><creatorcontrib>Fromme, Samantha J.</creatorcontrib><creatorcontrib>Folander, Kimberly L.</creatorcontrib><creatorcontrib>Swanson, Richard J.</creatorcontrib><collection>Istex</collection><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>Health & 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>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical 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>MEDLINE - Academic</collection><jtitle>American journal of hypertension</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cox, Robert H.</au><au>Fromme, Samantha J.</au><au>Folander, Kimberly L.</au><au>Swanson, Richard J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Voltage Gated K+ Channel Expression in Arteries of Wistar–Kyoto and Spontaneously Hypertensive Rats</atitle><jtitle>American journal of hypertension</jtitle><addtitle>AJH</addtitle><date>2008-02-01</date><risdate>2008</risdate><volume>21</volume><issue>2</issue><spage>213</spage><epage>218</epage><pages>213-218</pages><issn>0895-7061</issn><eissn>1941-7225</eissn><eissn>1879-1905</eissn><coden>AJHYE6</coden><abstract>Background We have previously demonstrated differences in the gene expression of voltage-gated K v1.X channel α-subunits in arteries from Wistar–Kyoto rats (WKYs) and spontaneously hypertensive rats (SHRs). The purpose of this study was to test the hypothesis that these differences are also present at the protein level. Methods Proteins were isolated from the aorta, mesenteric (MAs) and tail arteries (TAs) of 12- to 15-week-old male WKY and SHR, and analyzed by immunoblotting. Kv currents were recorded from MA myocytes by patch clamp methods. Results Expression of Kv1.2, Kv1.5, and Kv2.1 was higher in MAs but was not different in aortas of SHRs as compared to WKYs. In the TA, expression of Kv1.2 and Kv1.5 was higher while that of Kv2.1 was lower in SHR compared to WKY. In the MA, the larger expression of an 80 kDa species of Kv1.2 in SHRs was associated with a lower expression of a 60 kDa species. Kv2.1 gene expression was larger in MAs from SHRs but not different in TAs. Kv currents associated with Kv1.X and Kv2.1 channels were both larger in MA myocytes from SHRs but less than expected based upon differences in Kv α-subunit protein expression. Conclusions For the MA, Kv protein expression and current components between WKYs and SHRs were qualitatively consistent, but differences in gene and protein expression were not closely correlated. The higher expression of Kv subunits in small mesenteric arteries (SMAs) of SHR would tend to maintain normal myogenic activity and vasoconstrictor reserve, and could be viewed as a form of homeostatic remodeling.</abstract><cop>New York, NY</cop><pub>Oxford University Press</pub><pmid>18174882</pmid><doi>10.1038/ajh.2007.44</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antibody Specificity Arterial hypertension. Arterial hypotension Biological and medical sciences Blood and lymphatic vessels Cardiology. Vascular system CHO Cells Cricetinae Cricetulus Experimental diseases Gene Expression - physiology Humans Hypertension - genetics Hypertension - physiopathology Kidney - cytology Kv1.2 Potassium Channel - genetics Kv1.2 Potassium Channel - immunology Kv1.2 Potassium Channel - physiology Kv1.5 Potassium Channel - genetics Kv1.5 Potassium Channel - immunology Kv1.5 Potassium Channel - physiology Male Medical sciences Mesenteric Arteries - physiology Monocytes - physiology Patch-Clamp Techniques Potassium Channels, Voltage-Gated - genetics Potassium Channels, Voltage-Gated - immunology Potassium Channels, Voltage-Gated - physiology Rats Rats, Inbred SHR Rats, Inbred WKY Shab Potassium Channels - genetics Shab Potassium Channels - immunology Shab Potassium Channels - physiology Tail - blood supply Thoracic Arteries - physiology |
title | Voltage Gated K+ Channel Expression in Arteries of Wistar–Kyoto and Spontaneously Hypertensive Rats |
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