Synergistic Effects of High Blood Cholesterol and Hypertension on Leukocyte and Platelet Recruitment in the Cerebral Microcirculation
Hypertension or hypercholesterolemia can induce a proinflammatory and prothrombogenic phenotype in the microcirculation of the brain; however, less is known about how the combination of these risk factors affects the vasculature. We recently reported that a moderate (60%) increase in plasma choleste...
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Veröffentlicht in: | Hypertension (Dallas, Tex. 1979) Tex. 1979), 2014-04, Vol.63 (4), p.747-752 |
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description | Hypertension or hypercholesterolemia can induce a proinflammatory and prothrombogenic phenotype in the microcirculation of the brain; however, less is known about how the combination of these risk factors affects the vasculature. We recently reported that a moderate (60%) increase in plasma cholesterol blunts the recruitment of leukocytes and platelets in the cerebral microvessels elicited by hypertension. In this study, we examined whether larger increments in blood cholesterol (4-fold) exerts a similar modulating influence on the vasculature in the presence of hypertension. Apolipoprotein E–knockout mice with deoxycorticosterone acetate salt–induced hypertension were placed on a high-cholesterol diet and exhibited exaggerated leukocyte and platelet adhesion responses in cerebral microvessels. Intermittent feeding (every fourth day) with high-cholesterol diet yielded similar phenotypic changes in the vasculature. Once the mice were placed on high-cholesterol diet, 4 days on normal diet (ND) were needed to revert to a normal vascular phenotype. Angiotensin II type 1 receptors and reactive oxygen species seem to contribute to the vascular responses induced by hypercholesterolemia and hypertension. Our findings indicate that the combination of hypertension and large increases in plasma cholesterol concentration results in a severe, but reversible, inflammatory and thrombogenic phenotype in the cerebral microvasculature. |
doi_str_mv | 10.1161/HYPERTENSIONAHA.113.02627 |
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We recently reported that a moderate (60%) increase in plasma cholesterol blunts the recruitment of leukocytes and platelets in the cerebral microvessels elicited by hypertension. In this study, we examined whether larger increments in blood cholesterol (4-fold) exerts a similar modulating influence on the vasculature in the presence of hypertension. Apolipoprotein E–knockout mice with deoxycorticosterone acetate salt–induced hypertension were placed on a high-cholesterol diet and exhibited exaggerated leukocyte and platelet adhesion responses in cerebral microvessels. Intermittent feeding (every fourth day) with high-cholesterol diet yielded similar phenotypic changes in the vasculature. Once the mice were placed on high-cholesterol diet, 4 days on normal diet (ND) were needed to revert to a normal vascular phenotype. Angiotensin II type 1 receptors and reactive oxygen species seem to contribute to the vascular responses induced by hypercholesterolemia and hypertension. Our findings indicate that the combination of hypertension and large increases in plasma cholesterol concentration results in a severe, but reversible, inflammatory and thrombogenic phenotype in the cerebral microvasculature.</description><identifier>ISSN: 0194-911X</identifier><identifier>EISSN: 1524-4563</identifier><identifier>DOI: 10.1161/HYPERTENSIONAHA.113.02627</identifier><identifier>PMID: 24379186</identifier><identifier>CODEN: HPRTDN</identifier><language>eng</language><publisher>Hagerstown, MD: American Heart Association, Inc</publisher><subject>Animals ; Apolipoproteins E - deficiency ; Apolipoproteins E - genetics ; Apolipoproteins E - physiology ; Arterial hypertension. Arterial hypotension ; Biological and medical sciences ; Blood and lymphatic vessels ; Blood Platelets - pathology ; Blood Platelets - physiology ; Cardiology. Vascular system ; Cell Adhesion - physiology ; Cell Movement - physiology ; Cerebrovascular Circulation - physiology ; Cholesterol, Dietary - adverse effects ; Comorbidity ; Desoxycorticosterone Acetate - adverse effects ; Disease Models, Animal ; Disorders of blood lipids. Hyperlipoproteinemia ; Hypercholesterolemia - complications ; Hypercholesterolemia - epidemiology ; Hypercholesterolemia - etiology ; Hypertension - chemically induced ; Hypertension - complications ; Hypertension - epidemiology ; Leukocytes - pathology ; Leukocytes - physiology ; Male ; Medical sciences ; Metabolic diseases ; Mice ; Mice, Knockout ; Phenotype ; Reactive Oxygen Species - metabolism ; Receptor, Angiotensin, Type 1 - physiology</subject><ispartof>Hypertension (Dallas, Tex. 1979), 2014-04, Vol.63 (4), p.747-752</ispartof><rights>2014 American Heart Association, Inc</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5077-f2e1809dc81fcd8380671f1b159375f24ca9f82672553063cec57f5f60aa22203</citedby><cites>FETCH-LOGICAL-c5077-f2e1809dc81fcd8380671f1b159375f24ca9f82672553063cec57f5f60aa22203</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3674,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28387904$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24379186$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rodrigues, Stephen F</creatorcontrib><creatorcontrib>Almeida-Paula, Lidiana D</creatorcontrib><creatorcontrib>Granger, Daniel N</creatorcontrib><title>Synergistic Effects of High Blood Cholesterol and Hypertension on Leukocyte and Platelet Recruitment in the Cerebral Microcirculation</title><title>Hypertension (Dallas, Tex. 1979)</title><addtitle>Hypertension</addtitle><description>Hypertension or hypercholesterolemia can induce a proinflammatory and prothrombogenic phenotype in the microcirculation of the brain; however, less is known about how the combination of these risk factors affects the vasculature. We recently reported that a moderate (60%) increase in plasma cholesterol blunts the recruitment of leukocytes and platelets in the cerebral microvessels elicited by hypertension. In this study, we examined whether larger increments in blood cholesterol (4-fold) exerts a similar modulating influence on the vasculature in the presence of hypertension. Apolipoprotein E–knockout mice with deoxycorticosterone acetate salt–induced hypertension were placed on a high-cholesterol diet and exhibited exaggerated leukocyte and platelet adhesion responses in cerebral microvessels. Intermittent feeding (every fourth day) with high-cholesterol diet yielded similar phenotypic changes in the vasculature. Once the mice were placed on high-cholesterol diet, 4 days on normal diet (ND) were needed to revert to a normal vascular phenotype. Angiotensin II type 1 receptors and reactive oxygen species seem to contribute to the vascular responses induced by hypercholesterolemia and hypertension. Our findings indicate that the combination of hypertension and large increases in plasma cholesterol concentration results in a severe, but reversible, inflammatory and thrombogenic phenotype in the cerebral microvasculature.</description><subject>Animals</subject><subject>Apolipoproteins E - deficiency</subject><subject>Apolipoproteins E - genetics</subject><subject>Apolipoproteins E - physiology</subject><subject>Arterial hypertension. Arterial hypotension</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Blood Platelets - pathology</subject><subject>Blood Platelets - physiology</subject><subject>Cardiology. Vascular system</subject><subject>Cell Adhesion - physiology</subject><subject>Cell Movement - physiology</subject><subject>Cerebrovascular Circulation - physiology</subject><subject>Cholesterol, Dietary - adverse effects</subject><subject>Comorbidity</subject><subject>Desoxycorticosterone Acetate - adverse effects</subject><subject>Disease Models, Animal</subject><subject>Disorders of blood lipids. Hyperlipoproteinemia</subject><subject>Hypercholesterolemia - complications</subject><subject>Hypercholesterolemia - epidemiology</subject><subject>Hypercholesterolemia - etiology</subject><subject>Hypertension - chemically induced</subject><subject>Hypertension - complications</subject><subject>Hypertension - epidemiology</subject><subject>Leukocytes - pathology</subject><subject>Leukocytes - physiology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Phenotype</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Receptor, Angiotensin, Type 1 - physiology</subject><issn>0194-911X</issn><issn>1524-4563</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkd1uEzEQhS0EoiHwCshccLnFP2vv7gVIaRTYSqGt2iLB1cpxxllTZx3ZXqo8AO-NaUr5uUKyZGnmOzNndBB6RckxpZK-ab9cLC6vF2dXp-dns3aWi_yYMMmqR2hCBSuLUkj-GE0IbcqiofTzEXoW41dCaFmW1VN0xEpeNbSWE_T9aj9A2NiYrMYLY0CniL3Brd30-MR5v8bz3juICYJ3WA1r3O53EBIM0foB57eE8cbrfYK77oVTCRwkfAk6jDZtYUjYDjj1gOcQYBWUwx-tDl7boMdM5zHP0ROjXIQX9_8UfXq_uJ63xfL8w-l8tiy0IFVVGAa0Js1a19Todc1rIitq6IqKhlfCsFKrxtRMVkwITiTXoEVlhJFEKcYY4VP07jB3N662sNbZW7bT7YLdqrDvvLLd353B9t3Gf-t4I6XIW6aoOQzI_mMMYB60lHQ_s-n-ySYXeXeXTda-_HP5g_JXGBl4fQ-oqJUzQQ3axt9cPrhqSJm5twfu1rscS7xx4y2ErgflUv8fRn4A_pmw0A</recordid><startdate>201404</startdate><enddate>201404</enddate><creator>Rodrigues, Stephen F</creator><creator>Almeida-Paula, Lidiana D</creator><creator>Granger, Daniel N</creator><general>American Heart Association, Inc</general><general>Lippincott Williams & Wilkins</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>5PM</scope></search><sort><creationdate>201404</creationdate><title>Synergistic Effects of High Blood Cholesterol and Hypertension on Leukocyte and Platelet Recruitment in the Cerebral Microcirculation</title><author>Rodrigues, Stephen F ; Almeida-Paula, Lidiana D ; Granger, Daniel N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5077-f2e1809dc81fcd8380671f1b159375f24ca9f82672553063cec57f5f60aa22203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Apolipoproteins E - deficiency</topic><topic>Apolipoproteins E - genetics</topic><topic>Apolipoproteins E - physiology</topic><topic>Arterial hypertension. Arterial hypotension</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Blood Platelets - pathology</topic><topic>Blood Platelets - physiology</topic><topic>Cardiology. Vascular system</topic><topic>Cell Adhesion - physiology</topic><topic>Cell Movement - physiology</topic><topic>Cerebrovascular Circulation - physiology</topic><topic>Cholesterol, Dietary - adverse effects</topic><topic>Comorbidity</topic><topic>Desoxycorticosterone Acetate - adverse effects</topic><topic>Disease Models, Animal</topic><topic>Disorders of blood lipids. Hyperlipoproteinemia</topic><topic>Hypercholesterolemia - complications</topic><topic>Hypercholesterolemia - epidemiology</topic><topic>Hypercholesterolemia - etiology</topic><topic>Hypertension - chemically induced</topic><topic>Hypertension - complications</topic><topic>Hypertension - epidemiology</topic><topic>Leukocytes - pathology</topic><topic>Leukocytes - physiology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Phenotype</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Receptor, Angiotensin, Type 1 - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rodrigues, Stephen F</creatorcontrib><creatorcontrib>Almeida-Paula, Lidiana D</creatorcontrib><creatorcontrib>Granger, Daniel N</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>PubMed Central (Full Participant titles)</collection><jtitle>Hypertension (Dallas, Tex. 1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rodrigues, Stephen F</au><au>Almeida-Paula, Lidiana D</au><au>Granger, Daniel N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synergistic Effects of High Blood Cholesterol and Hypertension on Leukocyte and Platelet Recruitment in the Cerebral Microcirculation</atitle><jtitle>Hypertension (Dallas, Tex. 1979)</jtitle><addtitle>Hypertension</addtitle><date>2014-04</date><risdate>2014</risdate><volume>63</volume><issue>4</issue><spage>747</spage><epage>752</epage><pages>747-752</pages><issn>0194-911X</issn><eissn>1524-4563</eissn><coden>HPRTDN</coden><abstract>Hypertension or hypercholesterolemia can induce a proinflammatory and prothrombogenic phenotype in the microcirculation of the brain; however, less is known about how the combination of these risk factors affects the vasculature. We recently reported that a moderate (60%) increase in plasma cholesterol blunts the recruitment of leukocytes and platelets in the cerebral microvessels elicited by hypertension. In this study, we examined whether larger increments in blood cholesterol (4-fold) exerts a similar modulating influence on the vasculature in the presence of hypertension. Apolipoprotein E–knockout mice with deoxycorticosterone acetate salt–induced hypertension were placed on a high-cholesterol diet and exhibited exaggerated leukocyte and platelet adhesion responses in cerebral microvessels. Intermittent feeding (every fourth day) with high-cholesterol diet yielded similar phenotypic changes in the vasculature. Once the mice were placed on high-cholesterol diet, 4 days on normal diet (ND) were needed to revert to a normal vascular phenotype. Angiotensin II type 1 receptors and reactive oxygen species seem to contribute to the vascular responses induced by hypercholesterolemia and hypertension. Our findings indicate that the combination of hypertension and large increases in plasma cholesterol concentration results in a severe, but reversible, inflammatory and thrombogenic phenotype in the cerebral microvasculature.</abstract><cop>Hagerstown, MD</cop><pub>American Heart Association, Inc</pub><pmid>24379186</pmid><doi>10.1161/HYPERTENSIONAHA.113.02627</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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source | Journals@Ovid Ovid Autoload; MEDLINE; American Heart Association Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Animals Apolipoproteins E - deficiency Apolipoproteins E - genetics Apolipoproteins E - physiology Arterial hypertension. Arterial hypotension Biological and medical sciences Blood and lymphatic vessels Blood Platelets - pathology Blood Platelets - physiology Cardiology. Vascular system Cell Adhesion - physiology Cell Movement - physiology Cerebrovascular Circulation - physiology Cholesterol, Dietary - adverse effects Comorbidity Desoxycorticosterone Acetate - adverse effects Disease Models, Animal Disorders of blood lipids. Hyperlipoproteinemia Hypercholesterolemia - complications Hypercholesterolemia - epidemiology Hypercholesterolemia - etiology Hypertension - chemically induced Hypertension - complications Hypertension - epidemiology Leukocytes - pathology Leukocytes - physiology Male Medical sciences Metabolic diseases Mice Mice, Knockout Phenotype Reactive Oxygen Species - metabolism Receptor, Angiotensin, Type 1 - physiology |
title | Synergistic Effects of High Blood Cholesterol and Hypertension on Leukocyte and Platelet Recruitment in the Cerebral Microcirculation |
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