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Effects of Taurine on Aortic Rings Isolated from Fructose-fed Insulin Resistance Sprague–Dawley Rat are Changed
Purpose To observe and compare the effect of taurine on contractions of aortic rings isolated from normal (NC) and insulin resistance (IR) Sprague–Dawley rats, and to explore its underlying mechanism(s). Methods The IR animal model was made by feeding rats with high fructose diet for 8 weeks. Aortic...
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Published in: | Cardiovascular drugs and therapy 2008-12, Vol.22 (6), p.461-468 |
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creator | Xue, Wenxin Zhang, Mingsheng Li, Jie Wu, Dongmei Niu, Longgang Liang, Yueqin |
description | Purpose
To observe and compare the effect of taurine on contractions of aortic rings isolated from normal (NC) and insulin resistance (IR) Sprague–Dawley rats, and to explore its underlying mechanism(s).
Methods
The IR animal model was made by feeding rats with high fructose diet for 8 weeks. Aortic rings were isolated and suspended in a tissue bath, and tensions were recorded isometrically. The effects of taurine on provoked contractions of the rings were assessed in absence or presence of different potassium channel or NO-synthase inhibitors.
Results
Taurine (20–80 mM) concentration-dependently relaxed precontractions induced by KCl (30 mM) and phenylephrine (1 μM) in NC rings, but enhanced the precontractions in IR rings. Denudation of the endothelium and pretreatment with
N
G
-nitro-
l
-arginine methylester ester (0.1 mM) reversed the contraction enhancement of taurine to relaxation in IR rings. Tetraethylammonium (10 mM) nearly abolished taurine-induced relaxation of NC rings, and augmented taurine-induced contraction enhancement in IR rings. Iberiotoxin (100 nM) only augmented the contraction enhancement in IR rings. 4-Aminopyridine (1 mM), glibenclamide (10 μM) and indomethacin (10 μM) had no influence on the effect of taurine in both NC and IR rings.
Conclusion
Taurine enhances contractions in IR aortic rings but relaxes the contractions in normal rat aortic ring; the enhancement is endothelium-dependent and the relaxation is endothelium-independent. TEA-sensitive K
+
channel may be involved in these actions; BK
Ca
channel dysfunction and endothelium-derived substances may be related to the contraction enhancement induced by taurine in IR aorta. |
doi_str_mv | 10.1007/s10557-008-6124-9 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_213846566</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1593164971</sourcerecordid><originalsourceid>FETCH-LOGICAL-c399t-70f473445a1a78b798b07c625f8b2640d9e88d1941403cc996b092e0396c52193</originalsourceid><addsrcrecordid>eNp1kM9qGzEQh0VpaNy0D9BLEYUc1Y60-nsMbtIaAgUnPQutVnI3rFeOtEvIre-QN8yTRMamOfU0oPnmN6MPoU8UvlIA9a1QEEIRAE0kZZyYN2hBhWqIYpy-RQswDEjDQJ6i96XcQZ0xRr9Dp1RXXgNfoPvLGIOfCk4R37o592PAacQXKU-9x-t-3BS8KmlwU-hwzGmLr_Lsp1QCifVlNZZ56Ee8DqUvkxt9wDe77DZzeP779N09DOERr92EXQ54-ceNm9B9QCfRDSV8PNYz9Pvq8nb5k1z_-rFaXlwT3xgzEQWRq4Zz4ahTulVGt6C8ZCLqlkkOnQlad9RwyqHx3hjZ1u8GaIz0glHTnKEvh9xdTvdzKJO9S3Me60rLaKO5FFJWiB4gn1MpOUS7y_3W5UdLwe4d24NjWx3bvWO7D_58DJ7bbeheJ45SK3B-BFzxboi5eunLP46BASYEqxw7cKW2qpr8euH_t78AcGOTTg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>213846566</pqid></control><display><type>article</type><title>Effects of Taurine on Aortic Rings Isolated from Fructose-fed Insulin Resistance Sprague–Dawley Rat are Changed</title><source>Springer Nature</source><creator>Xue, Wenxin ; Zhang, Mingsheng ; Li, Jie ; Wu, Dongmei ; Niu, Longgang ; Liang, Yueqin</creator><creatorcontrib>Xue, Wenxin ; Zhang, Mingsheng ; Li, Jie ; Wu, Dongmei ; Niu, Longgang ; Liang, Yueqin</creatorcontrib><description>Purpose
To observe and compare the effect of taurine on contractions of aortic rings isolated from normal (NC) and insulin resistance (IR) Sprague–Dawley rats, and to explore its underlying mechanism(s).
Methods
The IR animal model was made by feeding rats with high fructose diet for 8 weeks. Aortic rings were isolated and suspended in a tissue bath, and tensions were recorded isometrically. The effects of taurine on provoked contractions of the rings were assessed in absence or presence of different potassium channel or NO-synthase inhibitors.
Results
Taurine (20–80 mM) concentration-dependently relaxed precontractions induced by KCl (30 mM) and phenylephrine (1 μM) in NC rings, but enhanced the precontractions in IR rings. Denudation of the endothelium and pretreatment with
N
G
-nitro-
l
-arginine methylester ester (0.1 mM) reversed the contraction enhancement of taurine to relaxation in IR rings. Tetraethylammonium (10 mM) nearly abolished taurine-induced relaxation of NC rings, and augmented taurine-induced contraction enhancement in IR rings. Iberiotoxin (100 nM) only augmented the contraction enhancement in IR rings. 4-Aminopyridine (1 mM), glibenclamide (10 μM) and indomethacin (10 μM) had no influence on the effect of taurine in both NC and IR rings.
Conclusion
Taurine enhances contractions in IR aortic rings but relaxes the contractions in normal rat aortic ring; the enhancement is endothelium-dependent and the relaxation is endothelium-independent. TEA-sensitive K
+
channel may be involved in these actions; BK
Ca
channel dysfunction and endothelium-derived substances may be related to the contraction enhancement induced by taurine in IR aorta.</description><identifier>ISSN: 0920-3206</identifier><identifier>EISSN: 1573-7241</identifier><identifier>DOI: 10.1007/s10557-008-6124-9</identifier><identifier>PMID: 18612804</identifier><identifier>CODEN: CDTHET</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject><![CDATA[4-Aminopyridine - pharmacology ; Acetylcholine - pharmacology ; Administration, Oral ; Animals ; Aorta - drug effects ; Aorta - pathology ; Biological and medical sciences ; Blood Glucose - drug effects ; Blood Pressure ; Cardiology ; Cardiovascular system ; Cyclooxygenase Inhibitors - administration & dosage ; Disease Models, Animal ; Dose-Response Relationship, Drug ; Drug Synergism ; Endothelium, Vascular - injuries ; Endothelium-Dependent Relaxing Factors - pharmacology ; Fructose - administration & dosage ; Fructose - adverse effects ; Glyburide - pharmacology ; In Vitro Techniques ; Indomethacin - administration & dosage ; Insulin - blood ; Insulin Resistance ; Male ; Medical sciences ; Medicine ; Medicine & Public Health ; NG-Nitroarginine Methyl Ester - pharmacology ; Nitric Oxide - blood ; Nitric Oxide Donors - pharmacology ; Nitroprusside - pharmacology ; Peptides - pharmacology ; Pharmacology. Drug treatments ; Phenylephrine - antagonists & inhibitors ; Phenylephrine - pharmacology ; Potassium Channel Blockers - classification ; Potassium Channel Blockers - pharmacology ; Potassium Chloride - antagonists & inhibitors ; Potassium Chloride - pharmacology ; Rats ; Rats, Sprague-Dawley ; Taurine - antagonists & inhibitors ; Taurine - pharmacology ; Tetraethylammonium - pharmacology ; Vasoconstriction - drug effects ; Vasodilation - drug effects]]></subject><ispartof>Cardiovascular drugs and therapy, 2008-12, Vol.22 (6), p.461-468</ispartof><rights>Springer Science+Business Media, LLC 2008</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c399t-70f473445a1a78b798b07c625f8b2640d9e88d1941403cc996b092e0396c52193</citedby><cites>FETCH-LOGICAL-c399t-70f473445a1a78b798b07c625f8b2640d9e88d1941403cc996b092e0396c52193</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=20902552$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18612804$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xue, Wenxin</creatorcontrib><creatorcontrib>Zhang, Mingsheng</creatorcontrib><creatorcontrib>Li, Jie</creatorcontrib><creatorcontrib>Wu, Dongmei</creatorcontrib><creatorcontrib>Niu, Longgang</creatorcontrib><creatorcontrib>Liang, Yueqin</creatorcontrib><title>Effects of Taurine on Aortic Rings Isolated from Fructose-fed Insulin Resistance Sprague–Dawley Rat are Changed</title><title>Cardiovascular drugs and therapy</title><addtitle>Cardiovasc Drugs Ther</addtitle><addtitle>Cardiovasc Drugs Ther</addtitle><description>Purpose
To observe and compare the effect of taurine on contractions of aortic rings isolated from normal (NC) and insulin resistance (IR) Sprague–Dawley rats, and to explore its underlying mechanism(s).
Methods
The IR animal model was made by feeding rats with high fructose diet for 8 weeks. Aortic rings were isolated and suspended in a tissue bath, and tensions were recorded isometrically. The effects of taurine on provoked contractions of the rings were assessed in absence or presence of different potassium channel or NO-synthase inhibitors.
Results
Taurine (20–80 mM) concentration-dependently relaxed precontractions induced by KCl (30 mM) and phenylephrine (1 μM) in NC rings, but enhanced the precontractions in IR rings. Denudation of the endothelium and pretreatment with
N
G
-nitro-
l
-arginine methylester ester (0.1 mM) reversed the contraction enhancement of taurine to relaxation in IR rings. Tetraethylammonium (10 mM) nearly abolished taurine-induced relaxation of NC rings, and augmented taurine-induced contraction enhancement in IR rings. Iberiotoxin (100 nM) only augmented the contraction enhancement in IR rings. 4-Aminopyridine (1 mM), glibenclamide (10 μM) and indomethacin (10 μM) had no influence on the effect of taurine in both NC and IR rings.
Conclusion
Taurine enhances contractions in IR aortic rings but relaxes the contractions in normal rat aortic ring; the enhancement is endothelium-dependent and the relaxation is endothelium-independent. TEA-sensitive K
+
channel may be involved in these actions; BK
Ca
channel dysfunction and endothelium-derived substances may be related to the contraction enhancement induced by taurine in IR aorta.</description><subject>4-Aminopyridine - pharmacology</subject><subject>Acetylcholine - pharmacology</subject><subject>Administration, Oral</subject><subject>Animals</subject><subject>Aorta - drug effects</subject><subject>Aorta - pathology</subject><subject>Biological and medical sciences</subject><subject>Blood Glucose - drug effects</subject><subject>Blood Pressure</subject><subject>Cardiology</subject><subject>Cardiovascular system</subject><subject>Cyclooxygenase Inhibitors - administration & dosage</subject><subject>Disease Models, Animal</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Synergism</subject><subject>Endothelium, Vascular - injuries</subject><subject>Endothelium-Dependent Relaxing Factors - pharmacology</subject><subject>Fructose - administration & dosage</subject><subject>Fructose - adverse effects</subject><subject>Glyburide - pharmacology</subject><subject>In Vitro Techniques</subject><subject>Indomethacin - administration & dosage</subject><subject>Insulin - blood</subject><subject>Insulin Resistance</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>NG-Nitroarginine Methyl Ester - pharmacology</subject><subject>Nitric Oxide - blood</subject><subject>Nitric Oxide Donors - pharmacology</subject><subject>Nitroprusside - pharmacology</subject><subject>Peptides - pharmacology</subject><subject>Pharmacology. Drug treatments</subject><subject>Phenylephrine - antagonists & inhibitors</subject><subject>Phenylephrine - pharmacology</subject><subject>Potassium Channel Blockers - classification</subject><subject>Potassium Channel Blockers - pharmacology</subject><subject>Potassium Chloride - antagonists & inhibitors</subject><subject>Potassium Chloride - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Taurine - antagonists & inhibitors</subject><subject>Taurine - pharmacology</subject><subject>Tetraethylammonium - pharmacology</subject><subject>Vasoconstriction - drug effects</subject><subject>Vasodilation - drug effects</subject><issn>0920-3206</issn><issn>1573-7241</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp1kM9qGzEQh0VpaNy0D9BLEYUc1Y60-nsMbtIaAgUnPQutVnI3rFeOtEvIre-QN8yTRMamOfU0oPnmN6MPoU8UvlIA9a1QEEIRAE0kZZyYN2hBhWqIYpy-RQswDEjDQJ6i96XcQZ0xRr9Dp1RXXgNfoPvLGIOfCk4R37o592PAacQXKU-9x-t-3BS8KmlwU-hwzGmLr_Lsp1QCifVlNZZ56Ee8DqUvkxt9wDe77DZzeP779N09DOERr92EXQ54-ceNm9B9QCfRDSV8PNYz9Pvq8nb5k1z_-rFaXlwT3xgzEQWRq4Zz4ahTulVGt6C8ZCLqlkkOnQlad9RwyqHx3hjZ1u8GaIz0glHTnKEvh9xdTvdzKJO9S3Me60rLaKO5FFJWiB4gn1MpOUS7y_3W5UdLwe4d24NjWx3bvWO7D_58DJ7bbeheJ45SK3B-BFzxboi5eunLP46BASYEqxw7cKW2qpr8euH_t78AcGOTTg</recordid><startdate>20081201</startdate><enddate>20081201</enddate><creator>Xue, Wenxin</creator><creator>Zhang, Mingsheng</creator><creator>Li, Jie</creator><creator>Wu, Dongmei</creator><creator>Niu, Longgang</creator><creator>Liang, Yueqin</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7Z</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20081201</creationdate><title>Effects of Taurine on Aortic Rings Isolated from Fructose-fed Insulin Resistance Sprague–Dawley Rat are Changed</title><author>Xue, Wenxin ; Zhang, Mingsheng ; Li, Jie ; Wu, Dongmei ; Niu, Longgang ; Liang, Yueqin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-70f473445a1a78b798b07c625f8b2640d9e88d1941403cc996b092e0396c52193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>4-Aminopyridine - pharmacology</topic><topic>Acetylcholine - pharmacology</topic><topic>Administration, Oral</topic><topic>Animals</topic><topic>Aorta - drug effects</topic><topic>Aorta - pathology</topic><topic>Biological and medical sciences</topic><topic>Blood Glucose - drug effects</topic><topic>Blood Pressure</topic><topic>Cardiology</topic><topic>Cardiovascular system</topic><topic>Cyclooxygenase Inhibitors - administration & dosage</topic><topic>Disease Models, Animal</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Synergism</topic><topic>Endothelium, Vascular - injuries</topic><topic>Endothelium-Dependent Relaxing Factors - pharmacology</topic><topic>Fructose - administration & dosage</topic><topic>Fructose - adverse effects</topic><topic>Glyburide - pharmacology</topic><topic>In Vitro Techniques</topic><topic>Indomethacin - administration & dosage</topic><topic>Insulin - blood</topic><topic>Insulin Resistance</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>NG-Nitroarginine Methyl Ester - pharmacology</topic><topic>Nitric Oxide - blood</topic><topic>Nitric Oxide Donors - pharmacology</topic><topic>Nitroprusside - pharmacology</topic><topic>Peptides - pharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Phenylephrine - antagonists & inhibitors</topic><topic>Phenylephrine - pharmacology</topic><topic>Potassium Channel Blockers - classification</topic><topic>Potassium Channel Blockers - pharmacology</topic><topic>Potassium Chloride - antagonists & inhibitors</topic><topic>Potassium Chloride - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Taurine - antagonists & inhibitors</topic><topic>Taurine - pharmacology</topic><topic>Tetraethylammonium - pharmacology</topic><topic>Vasoconstriction - drug effects</topic><topic>Vasodilation - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xue, Wenxin</creatorcontrib><creatorcontrib>Zhang, Mingsheng</creatorcontrib><creatorcontrib>Li, Jie</creatorcontrib><creatorcontrib>Wu, Dongmei</creatorcontrib><creatorcontrib>Niu, Longgang</creatorcontrib><creatorcontrib>Liang, Yueqin</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>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Engineering Research Database</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>PML(ProQuest Medical Library)</collection><collection>Biochemistry Abstracts 1</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><jtitle>Cardiovascular drugs and therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xue, Wenxin</au><au>Zhang, Mingsheng</au><au>Li, Jie</au><au>Wu, Dongmei</au><au>Niu, Longgang</au><au>Liang, Yueqin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Taurine on Aortic Rings Isolated from Fructose-fed Insulin Resistance Sprague–Dawley Rat are Changed</atitle><jtitle>Cardiovascular drugs and therapy</jtitle><stitle>Cardiovasc Drugs Ther</stitle><addtitle>Cardiovasc Drugs Ther</addtitle><date>2008-12-01</date><risdate>2008</risdate><volume>22</volume><issue>6</issue><spage>461</spage><epage>468</epage><pages>461-468</pages><issn>0920-3206</issn><eissn>1573-7241</eissn><coden>CDTHET</coden><abstract>Purpose
To observe and compare the effect of taurine on contractions of aortic rings isolated from normal (NC) and insulin resistance (IR) Sprague–Dawley rats, and to explore its underlying mechanism(s).
Methods
The IR animal model was made by feeding rats with high fructose diet for 8 weeks. Aortic rings were isolated and suspended in a tissue bath, and tensions were recorded isometrically. The effects of taurine on provoked contractions of the rings were assessed in absence or presence of different potassium channel or NO-synthase inhibitors.
Results
Taurine (20–80 mM) concentration-dependently relaxed precontractions induced by KCl (30 mM) and phenylephrine (1 μM) in NC rings, but enhanced the precontractions in IR rings. Denudation of the endothelium and pretreatment with
N
G
-nitro-
l
-arginine methylester ester (0.1 mM) reversed the contraction enhancement of taurine to relaxation in IR rings. Tetraethylammonium (10 mM) nearly abolished taurine-induced relaxation of NC rings, and augmented taurine-induced contraction enhancement in IR rings. Iberiotoxin (100 nM) only augmented the contraction enhancement in IR rings. 4-Aminopyridine (1 mM), glibenclamide (10 μM) and indomethacin (10 μM) had no influence on the effect of taurine in both NC and IR rings.
Conclusion
Taurine enhances contractions in IR aortic rings but relaxes the contractions in normal rat aortic ring; the enhancement is endothelium-dependent and the relaxation is endothelium-independent. TEA-sensitive K
+
channel may be involved in these actions; BK
Ca
channel dysfunction and endothelium-derived substances may be related to the contraction enhancement induced by taurine in IR aorta.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>18612804</pmid><doi>10.1007/s10557-008-6124-9</doi><tpages>8</tpages></addata></record> |
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source | Springer Nature |
subjects | 4-Aminopyridine - pharmacology Acetylcholine - pharmacology Administration, Oral Animals Aorta - drug effects Aorta - pathology Biological and medical sciences Blood Glucose - drug effects Blood Pressure Cardiology Cardiovascular system Cyclooxygenase Inhibitors - administration & dosage Disease Models, Animal Dose-Response Relationship, Drug Drug Synergism Endothelium, Vascular - injuries Endothelium-Dependent Relaxing Factors - pharmacology Fructose - administration & dosage Fructose - adverse effects Glyburide - pharmacology In Vitro Techniques Indomethacin - administration & dosage Insulin - blood Insulin Resistance Male Medical sciences Medicine Medicine & Public Health NG-Nitroarginine Methyl Ester - pharmacology Nitric Oxide - blood Nitric Oxide Donors - pharmacology Nitroprusside - pharmacology Peptides - pharmacology Pharmacology. Drug treatments Phenylephrine - antagonists & inhibitors Phenylephrine - pharmacology Potassium Channel Blockers - classification Potassium Channel Blockers - pharmacology Potassium Chloride - antagonists & inhibitors Potassium Chloride - pharmacology Rats Rats, Sprague-Dawley Taurine - antagonists & inhibitors Taurine - pharmacology Tetraethylammonium - pharmacology Vasoconstriction - drug effects Vasodilation - drug effects |
title | Effects of Taurine on Aortic Rings Isolated from Fructose-fed Insulin Resistance Sprague–Dawley Rat are Changed |
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