Characterization of high-salt and high-fat diets on cardiac and vascular function in mice
This study compared two established dietary formulations, high salt and high fat-high carbohydrate, separately or in combination on the induction cardiovascular dysfunction. One-month-old C57BL/6J mice were fed one of the following diets for 3 mo: (1) control diet consisting of a high fat-high sim-p...
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Veröffentlicht in: | Cardiovascular toxicology 2004, Vol.4 (1), p.37-46 |
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description | This study compared two established dietary formulations, high salt and high fat-high carbohydrate, separately or in combination on the induction cardiovascular dysfunction. One-month-old C57BL/6J mice were fed one of the following diets for 3 mo: (1) control diet consisting of a high fat-high sim-ple carbohydrate (HFHSC); (2) 8% NaCl diet (HS); or (3) HFHSC diet supplemented with 1% NaCl (HFHS). After 3 mo, the HFHSC mice demonstrated significantly increased end-diastolic volume and end-systolic volume, specifically increases of 35% and 78%, respectively (p < 0.01) and a reduction of ventricular stiffness by 27% (p = 0.015). The HS mice exhibited arterial hyper-tension with an increase of 33% in maximum end-systolic pressure (p =.024) and a decrease of 44% in arterial elastance (p = 0.020), corroborated by an increase in the heart weight to body weight ratios (p = 0.002) and vascular types I and III collagen (p = 0.03 and p = 0.0008, respectively). The HFHS group revealed a striking response of 230% to the alpha1-adrenergic challenge (p = 0.00034). These data suggest that the HFHSC diet causes dilated cardio-myopathy, whereas the HS diet produces arterial hypertension and the HFHS diet causes a vascular dysfunctional state that was highly responsive to alpha-adrenergic stimulation. |
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One-month-old C57BL/6J mice were fed one of the following diets for 3 mo: (1) control diet consisting of a high fat-high sim-ple carbohydrate (HFHSC); (2) 8% NaCl diet (HS); or (3) HFHSC diet supplemented with 1% NaCl (HFHS). After 3 mo, the HFHSC mice demonstrated significantly increased end-diastolic volume and end-systolic volume, specifically increases of 35% and 78%, respectively (p < 0.01) and a reduction of ventricular stiffness by 27% (p = 0.015). The HS mice exhibited arterial hyper-tension with an increase of 33% in maximum end-systolic pressure (p =.024) and a decrease of 44% in arterial elastance (p = 0.020), corroborated by an increase in the heart weight to body weight ratios (p = 0.002) and vascular types I and III collagen (p = 0.03 and p = 0.0008, respectively). The HFHS group revealed a striking response of 230% to the alpha1-adrenergic challenge (p = 0.00034). These data suggest that the HFHSC diet causes dilated cardio-myopathy, whereas the HS diet produces arterial hypertension and the HFHS diet causes a vascular dysfunctional state that was highly responsive to alpha-adrenergic stimulation.</description><identifier>ISSN: 1530-7905</identifier><identifier>EISSN: 1530-7905</identifier><identifier>EISSN: 1559-0259</identifier><identifier>DOI: 10.1385/CT:4:1:37</identifier><identifier>PMID: 15034204</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Animals ; Arteries - drug effects ; Collagen - biosynthesis ; Collagen - genetics ; Diet ; Dietary Carbohydrates - pharmacology ; Dietary Fats - pharmacology ; Heart - drug effects ; Heart Diseases - etiology ; Heart Diseases - physiopathology ; Heart failure ; Hemodynamics - drug effects ; Hypertension ; Mice ; Mice, Inbred C57BL ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - biosynthesis ; Sodium Chloride, Dietary - pharmacology ; Ventricular Function, Left - drug effects</subject><ispartof>Cardiovascular toxicology, 2004, Vol.4 (1), p.37-46</ispartof><rights>Humana Press Inc. 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c254t-6b51ecdf602340464f50f291372c64529cdd70054335bb51aff349780568f9a03</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15034204$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Qianli</creatorcontrib><creatorcontrib>Larson, Douglas F</creatorcontrib><creatorcontrib>Slayback, Denise</creatorcontrib><creatorcontrib>Lundeen, Tamara F</creatorcontrib><creatorcontrib>Baxter, Jeffrey H</creatorcontrib><creatorcontrib>Watson, Ronald R</creatorcontrib><title>Characterization of high-salt and high-fat diets on cardiac and vascular function in mice</title><title>Cardiovascular toxicology</title><addtitle>Cardiovasc Toxicol</addtitle><description>This study compared two established dietary formulations, high salt and high fat-high carbohydrate, separately or in combination on the induction cardiovascular dysfunction. One-month-old C57BL/6J mice were fed one of the following diets for 3 mo: (1) control diet consisting of a high fat-high sim-ple carbohydrate (HFHSC); (2) 8% NaCl diet (HS); or (3) HFHSC diet supplemented with 1% NaCl (HFHS). After 3 mo, the HFHSC mice demonstrated significantly increased end-diastolic volume and end-systolic volume, specifically increases of 35% and 78%, respectively (p < 0.01) and a reduction of ventricular stiffness by 27% (p = 0.015). The HS mice exhibited arterial hyper-tension with an increase of 33% in maximum end-systolic pressure (p =.024) and a decrease of 44% in arterial elastance (p = 0.020), corroborated by an increase in the heart weight to body weight ratios (p = 0.002) and vascular types I and III collagen (p = 0.03 and p = 0.0008, respectively). The HFHS group revealed a striking response of 230% to the alpha1-adrenergic challenge (p = 0.00034). These data suggest that the HFHSC diet causes dilated cardio-myopathy, whereas the HS diet produces arterial hypertension and the HFHS diet causes a vascular dysfunctional state that was highly responsive to alpha-adrenergic stimulation.</description><subject>Animals</subject><subject>Arteries - drug effects</subject><subject>Collagen - biosynthesis</subject><subject>Collagen - genetics</subject><subject>Diet</subject><subject>Dietary Carbohydrates - pharmacology</subject><subject>Dietary Fats - pharmacology</subject><subject>Heart - drug effects</subject><subject>Heart Diseases - etiology</subject><subject>Heart Diseases - physiopathology</subject><subject>Heart failure</subject><subject>Hemodynamics - drug effects</subject><subject>Hypertension</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - biosynthesis</subject><subject>Sodium Chloride, Dietary - pharmacology</subject><subject>Ventricular Function, Left - drug effects</subject><issn>1530-7905</issn><issn>1530-7905</issn><issn>1559-0259</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqF0UlLxDAUB_AgijMuB7-AFA-Ch-rL3s5NihsMeBkPnkImTZwMXcakFfTT21lA8eIpCfnxf7z3EDrDcI1pxm-K2YRN8ITKPTTGnEIqc-D7v-4jdBTjEoAQIvghGmEOlBFgY_RaLHTQprPBf-nOt03SumTh3xZp1FWX6KbcvpzuktLbLiYDMTqUXpvN74eOpq90SFzfmE2Ab5LaG3uCDpyuoj3dncfo5f5uVjym0-eHp-J2mhrCWZeKOcfWlE4AoQyYYI6DIzmmkhjBOMlNWUoAzijl88Fq5yjLZQZcZC7XQI_R5TZ3Fdr33sZO1T4aW1W6sW0flcSSAc3wvxDLjK3LDvDiD1y2fWiGJlQmcyHyYeYDutoiE9oYg3VqFXytw6fCoNZbUcVMMYUVlYM93wX289qWP3K3BvoNQbWFEA</recordid><startdate>2004</startdate><enddate>2004</enddate><creator>Yu, Qianli</creator><creator>Larson, Douglas F</creator><creator>Slayback, Denise</creator><creator>Lundeen, Tamara F</creator><creator>Baxter, Jeffrey H</creator><creator>Watson, Ronald R</creator><general>Springer Nature B.V</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>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</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>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7U7</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>2004</creationdate><title>Characterization of high-salt and high-fat diets on cardiac and vascular function in mice</title><author>Yu, Qianli ; Larson, Douglas F ; Slayback, Denise ; Lundeen, Tamara F ; Baxter, Jeffrey H ; Watson, Ronald R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c254t-6b51ecdf602340464f50f291372c64529cdd70054335bb51aff349780568f9a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Arteries - drug effects</topic><topic>Collagen - biosynthesis</topic><topic>Collagen - genetics</topic><topic>Diet</topic><topic>Dietary Carbohydrates - pharmacology</topic><topic>Dietary Fats - pharmacology</topic><topic>Heart - drug effects</topic><topic>Heart Diseases - etiology</topic><topic>Heart Diseases - physiopathology</topic><topic>Heart failure</topic><topic>Hemodynamics - drug effects</topic><topic>Hypertension</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - biosynthesis</topic><topic>Sodium Chloride, Dietary - pharmacology</topic><topic>Ventricular Function, Left - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, Qianli</creatorcontrib><creatorcontrib>Larson, Douglas F</creatorcontrib><creatorcontrib>Slayback, Denise</creatorcontrib><creatorcontrib>Lundeen, Tamara F</creatorcontrib><creatorcontrib>Baxter, Jeffrey H</creatorcontrib><creatorcontrib>Watson, Ronald R</creatorcontrib><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>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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>AIDS and Cancer Research Abstracts</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>ProQuest Central China</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Cardiovascular toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Qianli</au><au>Larson, Douglas F</au><au>Slayback, Denise</au><au>Lundeen, Tamara F</au><au>Baxter, Jeffrey H</au><au>Watson, Ronald R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of high-salt and high-fat diets on cardiac and vascular function in mice</atitle><jtitle>Cardiovascular toxicology</jtitle><addtitle>Cardiovasc Toxicol</addtitle><date>2004</date><risdate>2004</risdate><volume>4</volume><issue>1</issue><spage>37</spage><epage>46</epage><pages>37-46</pages><issn>1530-7905</issn><eissn>1530-7905</eissn><eissn>1559-0259</eissn><abstract>This study compared two established dietary formulations, high salt and high fat-high carbohydrate, separately or in combination on the induction cardiovascular dysfunction. One-month-old C57BL/6J mice were fed one of the following diets for 3 mo: (1) control diet consisting of a high fat-high sim-ple carbohydrate (HFHSC); (2) 8% NaCl diet (HS); or (3) HFHSC diet supplemented with 1% NaCl (HFHS). After 3 mo, the HFHSC mice demonstrated significantly increased end-diastolic volume and end-systolic volume, specifically increases of 35% and 78%, respectively (p < 0.01) and a reduction of ventricular stiffness by 27% (p = 0.015). The HS mice exhibited arterial hyper-tension with an increase of 33% in maximum end-systolic pressure (p =.024) and a decrease of 44% in arterial elastance (p = 0.020), corroborated by an increase in the heart weight to body weight ratios (p = 0.002) and vascular types I and III collagen (p = 0.03 and p = 0.0008, respectively). The HFHS group revealed a striking response of 230% to the alpha1-adrenergic challenge (p = 0.00034). These data suggest that the HFHSC diet causes dilated cardio-myopathy, whereas the HS diet produces arterial hypertension and the HFHS diet causes a vascular dysfunctional state that was highly responsive to alpha-adrenergic stimulation.</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>15034204</pmid><doi>10.1385/CT:4:1:37</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Arteries - drug effects Collagen - biosynthesis Collagen - genetics Diet Dietary Carbohydrates - pharmacology Dietary Fats - pharmacology Heart - drug effects Heart Diseases - etiology Heart Diseases - physiopathology Heart failure Hemodynamics - drug effects Hypertension Mice Mice, Inbred C57BL Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - biosynthesis Sodium Chloride, Dietary - pharmacology Ventricular Function, Left - drug effects |
title | Characterization of high-salt and high-fat diets on cardiac and vascular function in mice |
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