General administration of cyclohexenonic long-chain fatty alcohol ameliorates hyperreactivity of STZ-induced diabetic rat aorta
Diabetic neuropathy, a major complication of diabetes mellitus, is associated with the development of vascular dysfunction and autonomic neuropathy. We studied the effects of cyclohexenonic long-chain fatty alcohol (FA) on streptozotocin-diabetic hyperreactivity in the rat aorta smooth muscle. The r...
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creator | Kinoshita, Yukako Saito, Motoaki Satoh, Itaru Shomori, Kohei Suzuki, Hiroto Yamada, Masashi Kono, Tomoharu Satoh, Keisuke |
description | Diabetic neuropathy, a major complication of diabetes mellitus, is associated with the development of vascular dysfunction and autonomic neuropathy. We studied the effects of cyclohexenonic long-chain fatty alcohol (FA) on streptozotocin-diabetic hyperreactivity in the rat aorta smooth muscle. The rats were divided randomly into four groups and were maintained for 4 weeks: age-matched control rats, diabetic rats without treatment with FA, and diabetic rats treated with FA (2 and 8 mg/kg, i.p. everyday). The serum glucose and insulin levels were determined, and the contractile responses of the aorta induced by a thromboxane A
2 agonist, U46619 and KCl were investigated. Treatment with FA did not alter rats' diabetic status, i.e., body weight, thickness of the aorta, serum glucose levels, and serum insulin levels, but significantly improved the diabetic-induced hyperreactivity of the rat aorta in a dose-dependent manner. Removal of endothelium did not change contractile force between groups. In histological examinations, thinning of smooth muscle bundle in the wall of aorta was observed in the diabetic rat, which was not significantly improved by treatment with FA. Our data indicate that FA can prevent hyperreactivity in the diabetic aorta. |
doi_str_mv | 10.1016/j.lfs.2005.07.043 |
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2 agonist, U46619 and KCl were investigated. Treatment with FA did not alter rats' diabetic status, i.e., body weight, thickness of the aorta, serum glucose levels, and serum insulin levels, but significantly improved the diabetic-induced hyperreactivity of the rat aorta in a dose-dependent manner. Removal of endothelium did not change contractile force between groups. In histological examinations, thinning of smooth muscle bundle in the wall of aorta was observed in the diabetic rat, which was not significantly improved by treatment with FA. Our data indicate that FA can prevent hyperreactivity in the diabetic aorta.</description><identifier>ISSN: 0024-3205</identifier><identifier>EISSN: 1879-0631</identifier><identifier>DOI: 10.1016/j.lfs.2005.07.043</identifier><identifier>PMID: 16310809</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Acetylcholine - pharmacology ; Animals ; Aorta ; Aorta - drug effects ; Aorta - pathology ; Aorta - physiology ; Aorta - physiopathology ; Blood Glucose - metabolism ; Cyclohexanones - pharmacology ; Cyclohexenonic long-chain fatty alcohol ; Diabetes ; Diabetes Mellitus, Experimental - blood ; Diabetes Mellitus, Experimental - pathology ; Diabetes Mellitus, Experimental - physiopathology ; Fatty Alcohols - pharmacology ; In Vitro Techniques ; Male ; Malondialdehyde - metabolism ; Muscle, Smooth, Vascular - drug effects ; Muscle, Smooth, Vascular - pathology ; Muscle, Smooth, Vascular - physiopathology ; Rat ; Rats ; Rats, Sprague-Dawley ; Reference Values ; Thromboxane A 2 ; Vasoconstriction - drug effects ; Vasodilation - drug effects</subject><ispartof>Life sciences (1973), 2006-02, Vol.78 (13), p.1508-1514</ispartof><rights>2005 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-abfdcaddd04a4e79679be5f131522be3949237b2f888bba6281e7b00deed99ec3</citedby><cites>FETCH-LOGICAL-c417t-abfdcaddd04a4e79679be5f131522be3949237b2f888bba6281e7b00deed99ec3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0024320505009367$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16310809$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kinoshita, Yukako</creatorcontrib><creatorcontrib>Saito, Motoaki</creatorcontrib><creatorcontrib>Satoh, Itaru</creatorcontrib><creatorcontrib>Shomori, Kohei</creatorcontrib><creatorcontrib>Suzuki, Hiroto</creatorcontrib><creatorcontrib>Yamada, Masashi</creatorcontrib><creatorcontrib>Kono, Tomoharu</creatorcontrib><creatorcontrib>Satoh, Keisuke</creatorcontrib><title>General administration of cyclohexenonic long-chain fatty alcohol ameliorates hyperreactivity of STZ-induced diabetic rat aorta</title><title>Life sciences (1973)</title><addtitle>Life Sci</addtitle><description>Diabetic neuropathy, a major complication of diabetes mellitus, is associated with the development of vascular dysfunction and autonomic neuropathy. We studied the effects of cyclohexenonic long-chain fatty alcohol (FA) on streptozotocin-diabetic hyperreactivity in the rat aorta smooth muscle. The rats were divided randomly into four groups and were maintained for 4 weeks: age-matched control rats, diabetic rats without treatment with FA, and diabetic rats treated with FA (2 and 8 mg/kg, i.p. everyday). The serum glucose and insulin levels were determined, and the contractile responses of the aorta induced by a thromboxane A
2 agonist, U46619 and KCl were investigated. Treatment with FA did not alter rats' diabetic status, i.e., body weight, thickness of the aorta, serum glucose levels, and serum insulin levels, but significantly improved the diabetic-induced hyperreactivity of the rat aorta in a dose-dependent manner. Removal of endothelium did not change contractile force between groups. In histological examinations, thinning of smooth muscle bundle in the wall of aorta was observed in the diabetic rat, which was not significantly improved by treatment with FA. Our data indicate that FA can prevent hyperreactivity in the diabetic aorta.</description><subject>Acetylcholine - pharmacology</subject><subject>Animals</subject><subject>Aorta</subject><subject>Aorta - drug effects</subject><subject>Aorta - pathology</subject><subject>Aorta - physiology</subject><subject>Aorta - physiopathology</subject><subject>Blood Glucose - metabolism</subject><subject>Cyclohexanones - pharmacology</subject><subject>Cyclohexenonic long-chain fatty alcohol</subject><subject>Diabetes</subject><subject>Diabetes Mellitus, Experimental - blood</subject><subject>Diabetes Mellitus, Experimental - pathology</subject><subject>Diabetes Mellitus, Experimental - physiopathology</subject><subject>Fatty Alcohols - pharmacology</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Malondialdehyde - metabolism</subject><subject>Muscle, Smooth, Vascular - drug effects</subject><subject>Muscle, Smooth, Vascular - pathology</subject><subject>Muscle, Smooth, Vascular - physiopathology</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reference Values</subject><subject>Thromboxane A 2</subject><subject>Vasoconstriction - drug effects</subject><subject>Vasodilation - drug effects</subject><issn>0024-3205</issn><issn>1879-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kL1uFDEURi0EIkvCA9AgV3QzXI9nxjOiQhEEpEgpEpo0ln_usF557MX2RmzFq-NoV6KjcnHPdyQfQt4xaBmw8eOu9UtuO4ChBdFCz1-QDZvE3MDI2UuyAej6hncwXJA3Oe-ggoPgr8kFq3eYYN6QPzcYMClPlV1dcLkkVVwMNC7UHI2PW_yNIQZnqI_hZ2O2ygW6qFKOVHkTt7EuV_Qu1h1muj3uMSVUprgnV5mquX94bFywB4OWWqc0liqrNFUxFXVFXi3KZ3x7fi_Jj69fHq6_Nbd3N9-vP982pmeiNEov1ihrLfSqRzGPYtY4LIyzoes08rmfOy50t0zTpLUau4mh0AAW0c4zGn5JPpy8-xR_HTAXubps0HsVMB6yHMU48hqlguwEmhRzTrjIfXKrSkfJQD5XlztZq8vn6hKErNXr5v1ZftAr2n-Lc-YKfDoBWL_45DDJbByGmsQlNEXa6P6j_wvob5Z-</recordid><startdate>20060223</startdate><enddate>20060223</enddate><creator>Kinoshita, Yukako</creator><creator>Saito, Motoaki</creator><creator>Satoh, Itaru</creator><creator>Shomori, Kohei</creator><creator>Suzuki, Hiroto</creator><creator>Yamada, Masashi</creator><creator>Kono, Tomoharu</creator><creator>Satoh, Keisuke</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>20060223</creationdate><title>General administration of cyclohexenonic long-chain fatty alcohol ameliorates hyperreactivity of STZ-induced diabetic rat aorta</title><author>Kinoshita, Yukako ; Saito, Motoaki ; Satoh, Itaru ; Shomori, Kohei ; Suzuki, Hiroto ; Yamada, Masashi ; Kono, Tomoharu ; Satoh, Keisuke</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-abfdcaddd04a4e79679be5f131522be3949237b2f888bba6281e7b00deed99ec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Acetylcholine - pharmacology</topic><topic>Animals</topic><topic>Aorta</topic><topic>Aorta - drug effects</topic><topic>Aorta - pathology</topic><topic>Aorta - physiology</topic><topic>Aorta - physiopathology</topic><topic>Blood Glucose - metabolism</topic><topic>Cyclohexanones - pharmacology</topic><topic>Cyclohexenonic long-chain fatty alcohol</topic><topic>Diabetes</topic><topic>Diabetes Mellitus, Experimental - blood</topic><topic>Diabetes Mellitus, Experimental - pathology</topic><topic>Diabetes Mellitus, Experimental - physiopathology</topic><topic>Fatty Alcohols - pharmacology</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Malondialdehyde - metabolism</topic><topic>Muscle, Smooth, Vascular - drug effects</topic><topic>Muscle, Smooth, Vascular - pathology</topic><topic>Muscle, Smooth, Vascular - physiopathology</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reference Values</topic><topic>Thromboxane A 2</topic><topic>Vasoconstriction - drug effects</topic><topic>Vasodilation - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kinoshita, Yukako</creatorcontrib><creatorcontrib>Saito, Motoaki</creatorcontrib><creatorcontrib>Satoh, Itaru</creatorcontrib><creatorcontrib>Shomori, Kohei</creatorcontrib><creatorcontrib>Suzuki, Hiroto</creatorcontrib><creatorcontrib>Yamada, Masashi</creatorcontrib><creatorcontrib>Kono, Tomoharu</creatorcontrib><creatorcontrib>Satoh, Keisuke</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Life sciences (1973)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kinoshita, Yukako</au><au>Saito, Motoaki</au><au>Satoh, Itaru</au><au>Shomori, Kohei</au><au>Suzuki, Hiroto</au><au>Yamada, Masashi</au><au>Kono, Tomoharu</au><au>Satoh, Keisuke</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>General administration of cyclohexenonic long-chain fatty alcohol ameliorates hyperreactivity of STZ-induced diabetic rat aorta</atitle><jtitle>Life sciences (1973)</jtitle><addtitle>Life Sci</addtitle><date>2006-02-23</date><risdate>2006</risdate><volume>78</volume><issue>13</issue><spage>1508</spage><epage>1514</epage><pages>1508-1514</pages><issn>0024-3205</issn><eissn>1879-0631</eissn><abstract>Diabetic neuropathy, a major complication of diabetes mellitus, is associated with the development of vascular dysfunction and autonomic neuropathy. We studied the effects of cyclohexenonic long-chain fatty alcohol (FA) on streptozotocin-diabetic hyperreactivity in the rat aorta smooth muscle. The rats were divided randomly into four groups and were maintained for 4 weeks: age-matched control rats, diabetic rats without treatment with FA, and diabetic rats treated with FA (2 and 8 mg/kg, i.p. everyday). The serum glucose and insulin levels were determined, and the contractile responses of the aorta induced by a thromboxane A
2 agonist, U46619 and KCl were investigated. Treatment with FA did not alter rats' diabetic status, i.e., body weight, thickness of the aorta, serum glucose levels, and serum insulin levels, but significantly improved the diabetic-induced hyperreactivity of the rat aorta in a dose-dependent manner. Removal of endothelium did not change contractile force between groups. In histological examinations, thinning of smooth muscle bundle in the wall of aorta was observed in the diabetic rat, which was not significantly improved by treatment with FA. Our data indicate that FA can prevent hyperreactivity in the diabetic aorta.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>16310809</pmid><doi>10.1016/j.lfs.2005.07.043</doi><tpages>7</tpages></addata></record> |
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subjects | Acetylcholine - pharmacology Animals Aorta Aorta - drug effects Aorta - pathology Aorta - physiology Aorta - physiopathology Blood Glucose - metabolism Cyclohexanones - pharmacology Cyclohexenonic long-chain fatty alcohol Diabetes Diabetes Mellitus, Experimental - blood Diabetes Mellitus, Experimental - pathology Diabetes Mellitus, Experimental - physiopathology Fatty Alcohols - pharmacology In Vitro Techniques Male Malondialdehyde - metabolism Muscle, Smooth, Vascular - drug effects Muscle, Smooth, Vascular - pathology Muscle, Smooth, Vascular - physiopathology Rat Rats Rats, Sprague-Dawley Reference Values Thromboxane A 2 Vasoconstriction - drug effects Vasodilation - drug effects |
title | General administration of cyclohexenonic long-chain fatty alcohol ameliorates hyperreactivity of STZ-induced diabetic rat aorta |
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