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Elevated 12-Lipoxygenase Activity in the Spontaneously Hypertensive Rat
We have previously demonstrated that administration of inhibitors of the lipoxygenase (LO) pathway of arachidonic acid metabolism lowers blood pressure in hypertensive rats. In addition, we have shown that LO inhibition attenuates pressor agonist-induced vascular reactivity in vitro and calcium mobi...
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Published in: | American journal of hypertension 1997-04, Vol.10 (4), p.371-378 |
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description | We have previously demonstrated that administration of inhibitors of the lipoxygenase (LO) pathway of arachidonic acid metabolism lowers blood pressure in hypertensive rats. In addition, we have shown that LO inhibition attenuates pressor agonist-induced vascular reactivity in vitro and calcium mobilization in cultured vascular smooth muscle cells (VSMC). To further elucidate the relationship between elevated LO activity and hypertension, 4, 8, and 12 week old hypertensive SHR were compared with age-matched Wistar-Kyoto (WKY) rats for plasma 12(S)-hydroxyeicosatetraenoic acid (12-HETE) concentration. 12-HETE levels were significantly elevated in the SHR compared to the WKY (SHR elevated by 154%, 159%, and 272% compared to WKY at 4, 8, and 12 weeks, respectively,
P < .01 for all ages). There were no differences in plasma potassium levels between SHR and WKY at any of the ages tested. Plasma aldosterone levels and plasma renin activity were in the normal range at the three ages. At 12 weeks of age, both serum (4.72 ± 0.23
v 2.18 ± 0.33
μg/mL,
P < .01), and aortic smooth muscle 12-HETE levels (0.94 ± 0.09
v 0.66 ± 0.08
μg/mg protein,
P < .05) were elevated in SHR compared with WKY. The 12 week old SHR were given a bolus of the LO inhibitor 5,8,11-eicosatriynoic acid (ETI, 7 mg/kg, intravenously) and blood pressure measured after 20 min. ETI reduced mean systolic blood pressure from 175.8 ± 4.2 to 141.6 ± 5.9 mm Hg (
P < .05). To investigate these effects of HETEs, cultured vascular smooth muscle cells were pretreated for 1 min with 12(S)HETE and then challenged with angiotensin II (AngII). The addition of 12(S)HETE increased AngII-induced intracellular calcium levels in normal cultured rat vascular smooth muscle cells by 78% compared to vehicle (
P < .05). Thus, LO products, which are high in SHR, may contribute to vascular tone through alterations in the intracellular calcium signal by potentiating calcium responses to pressors such as Ang II. |
doi_str_mv | 10.1016/S0895-7061(96)00488-8 |
format | article |
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P < .01 for all ages). There were no differences in plasma potassium levels between SHR and WKY at any of the ages tested. Plasma aldosterone levels and plasma renin activity were in the normal range at the three ages. At 12 weeks of age, both serum (4.72 ± 0.23
v 2.18 ± 0.33
μg/mL,
P < .01), and aortic smooth muscle 12-HETE levels (0.94 ± 0.09
v 0.66 ± 0.08
μg/mg protein,
P < .05) were elevated in SHR compared with WKY. The 12 week old SHR were given a bolus of the LO inhibitor 5,8,11-eicosatriynoic acid (ETI, 7 mg/kg, intravenously) and blood pressure measured after 20 min. ETI reduced mean systolic blood pressure from 175.8 ± 4.2 to 141.6 ± 5.9 mm Hg (
P < .05). To investigate these effects of HETEs, cultured vascular smooth muscle cells were pretreated for 1 min with 12(S)HETE and then challenged with angiotensin II (AngII). The addition of 12(S)HETE increased AngII-induced intracellular calcium levels in normal cultured rat vascular smooth muscle cells by 78% compared to vehicle (
P < .05). Thus, LO products, which are high in SHR, may contribute to vascular tone through alterations in the intracellular calcium signal by potentiating calcium responses to pressors such as Ang II.</description><identifier>ISSN: 0895-7061</identifier><identifier>EISSN: 1879-1905</identifier><identifier>EISSN: 1941-7225</identifier><identifier>DOI: 10.1016/S0895-7061(96)00488-8</identifier><identifier>PMID: 9128202</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>12-Hydroxy-5,8,10,14-eicosatetraenoic Acid - blood ; Aging ; Animals ; Arachidonate 12-Lipoxygenase - analysis ; arachidonic acid pathway ; Arterial hypertension. Arterial hypotension ; Biological and medical sciences ; Blood and lymphatic vessels ; calcium ; Calcium - metabolism ; Cardiology. Vascular system ; Cells, Cultured ; Experimental diseases ; Hypertension - metabolism ; Hypertension - physiopathology ; Lipoxygenase ; Male ; Medical sciences ; Muscle, Smooth, Vascular - metabolism ; Muscle, Smooth, Vascular - physiopathology ; Rats ; Rats, Inbred SHR ; Rats, Inbred WKY ; spontaneously hypertensive rat</subject><ispartof>American journal of hypertension, 1997-04, Vol.10 (4), p.371-378</ispartof><rights>1997 Elsevier Science Inc.</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c528t-bcdb81baf230f6550f07c453ba40f2789feea7952651edb902c6d34aae3c8cab3</citedby></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=2663657$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9128202$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sasaki, Masato</creatorcontrib><creatorcontrib>Hori, Mark T</creatorcontrib><creatorcontrib>Hino, Toru</creatorcontrib><creatorcontrib>Golub, Michael S</creatorcontrib><creatorcontrib>Tuck, Michael L</creatorcontrib><title>Elevated 12-Lipoxygenase Activity in the Spontaneously Hypertensive Rat</title><title>American journal of hypertension</title><addtitle>AJH</addtitle><description>We have previously demonstrated that administration of inhibitors of the lipoxygenase (LO) pathway of arachidonic acid metabolism lowers blood pressure in hypertensive rats. In addition, we have shown that LO inhibition attenuates pressor agonist-induced vascular reactivity in vitro and calcium mobilization in cultured vascular smooth muscle cells (VSMC). To further elucidate the relationship between elevated LO activity and hypertension, 4, 8, and 12 week old hypertensive SHR were compared with age-matched Wistar-Kyoto (WKY) rats for plasma 12(S)-hydroxyeicosatetraenoic acid (12-HETE) concentration. 12-HETE levels were significantly elevated in the SHR compared to the WKY (SHR elevated by 154%, 159%, and 272% compared to WKY at 4, 8, and 12 weeks, respectively,
P < .01 for all ages). There were no differences in plasma potassium levels between SHR and WKY at any of the ages tested. Plasma aldosterone levels and plasma renin activity were in the normal range at the three ages. At 12 weeks of age, both serum (4.72 ± 0.23
v 2.18 ± 0.33
μg/mL,
P < .01), and aortic smooth muscle 12-HETE levels (0.94 ± 0.09
v 0.66 ± 0.08
μg/mg protein,
P < .05) were elevated in SHR compared with WKY. The 12 week old SHR were given a bolus of the LO inhibitor 5,8,11-eicosatriynoic acid (ETI, 7 mg/kg, intravenously) and blood pressure measured after 20 min. ETI reduced mean systolic blood pressure from 175.8 ± 4.2 to 141.6 ± 5.9 mm Hg (
P < .05). To investigate these effects of HETEs, cultured vascular smooth muscle cells were pretreated for 1 min with 12(S)HETE and then challenged with angiotensin II (AngII). The addition of 12(S)HETE increased AngII-induced intracellular calcium levels in normal cultured rat vascular smooth muscle cells by 78% compared to vehicle (
P < .05). Thus, LO products, which are high in SHR, may contribute to vascular tone through alterations in the intracellular calcium signal by potentiating calcium responses to pressors such as Ang II.</description><subject>12-Hydroxy-5,8,10,14-eicosatetraenoic Acid - blood</subject><subject>Aging</subject><subject>Animals</subject><subject>Arachidonate 12-Lipoxygenase - analysis</subject><subject>arachidonic acid pathway</subject><subject>Arterial hypertension. Arterial hypotension</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>calcium</subject><subject>Calcium - metabolism</subject><subject>Cardiology. Vascular system</subject><subject>Cells, Cultured</subject><subject>Experimental diseases</subject><subject>Hypertension - metabolism</subject><subject>Hypertension - physiopathology</subject><subject>Lipoxygenase</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Muscle, Smooth, Vascular - metabolism</subject><subject>Muscle, Smooth, Vascular - physiopathology</subject><subject>Rats</subject><subject>Rats, Inbred SHR</subject><subject>Rats, Inbred WKY</subject><subject>spontaneously hypertensive rat</subject><issn>0895-7061</issn><issn>1879-1905</issn><issn>1941-7225</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqFkEtP20AURkcViAbKT0DyAlVlYTqPzGuFEKIJUhBSKRJiMxqPr8tQxzYzkwj_e0wcpUtWd_Gd-zoInRB8TjARP--x0jyXWJAfWpxhPFUqV1_QhCipc6Ix30OTHfIVHcb4ggdKCHKADjShimI6QbPrGtY2QZkRmi981771f6GxEbJLl_zapz7zTZaeIbvv2ibZBtpVrPts3ncQEjTRryH7bdM3tF_ZOsLxth6hh1_Xf67m-eJudnN1ucgdpyrlhSsLRQpbUYYrwTmusHRTzgo7xRWVSlcAVmpOBSdQFhpTJ0o2tRaYU84W7Ah9H-d2oX1dQUxm6aODuh4vM8MIpjUTA8hH0IU2xgCV6YJf2tAbgs2HQLMRaD7sGC3MRqBRQ9_JdsGqWEK569oaG_LTbW6js3UVbON83GFUCCa4HLBsxBqbVgF2uX15JlpLKfiA5CPiY4K3_0T4Z4Rkkpv545N5nN0-yQUWm8suRh4Gv2sPwUTnoXFQ-gAumbL1n_z2DkVhp2Q</recordid><startdate>19970401</startdate><enddate>19970401</enddate><creator>Sasaki, Masato</creator><creator>Hori, Mark T</creator><creator>Hino, Toru</creator><creator>Golub, Michael S</creator><creator>Tuck, Michael L</creator><general>Elsevier Inc</general><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>7X8</scope></search><sort><creationdate>19970401</creationdate><title>Elevated 12-Lipoxygenase Activity in the Spontaneously Hypertensive Rat</title><author>Sasaki, Masato ; Hori, Mark T ; Hino, Toru ; Golub, Michael S ; Tuck, Michael L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c528t-bcdb81baf230f6550f07c453ba40f2789feea7952651edb902c6d34aae3c8cab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>12-Hydroxy-5,8,10,14-eicosatetraenoic Acid - blood</topic><topic>Aging</topic><topic>Animals</topic><topic>Arachidonate 12-Lipoxygenase - analysis</topic><topic>arachidonic acid pathway</topic><topic>Arterial hypertension. Arterial hypotension</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>calcium</topic><topic>Calcium - metabolism</topic><topic>Cardiology. Vascular system</topic><topic>Cells, Cultured</topic><topic>Experimental diseases</topic><topic>Hypertension - metabolism</topic><topic>Hypertension - physiopathology</topic><topic>Lipoxygenase</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Muscle, Smooth, Vascular - metabolism</topic><topic>Muscle, Smooth, Vascular - physiopathology</topic><topic>Rats</topic><topic>Rats, Inbred SHR</topic><topic>Rats, Inbred WKY</topic><topic>spontaneously hypertensive rat</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sasaki, Masato</creatorcontrib><creatorcontrib>Hori, Mark T</creatorcontrib><creatorcontrib>Hino, Toru</creatorcontrib><creatorcontrib>Golub, Michael S</creatorcontrib><creatorcontrib>Tuck, Michael L</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>MEDLINE - Academic</collection><jtitle>American journal of hypertension</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sasaki, Masato</au><au>Hori, Mark T</au><au>Hino, Toru</au><au>Golub, Michael S</au><au>Tuck, Michael L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Elevated 12-Lipoxygenase Activity in the Spontaneously Hypertensive Rat</atitle><jtitle>American journal of hypertension</jtitle><addtitle>AJH</addtitle><date>1997-04-01</date><risdate>1997</risdate><volume>10</volume><issue>4</issue><spage>371</spage><epage>378</epage><pages>371-378</pages><issn>0895-7061</issn><eissn>1879-1905</eissn><eissn>1941-7225</eissn><abstract>We have previously demonstrated that administration of inhibitors of the lipoxygenase (LO) pathway of arachidonic acid metabolism lowers blood pressure in hypertensive rats. In addition, we have shown that LO inhibition attenuates pressor agonist-induced vascular reactivity in vitro and calcium mobilization in cultured vascular smooth muscle cells (VSMC). To further elucidate the relationship between elevated LO activity and hypertension, 4, 8, and 12 week old hypertensive SHR were compared with age-matched Wistar-Kyoto (WKY) rats for plasma 12(S)-hydroxyeicosatetraenoic acid (12-HETE) concentration. 12-HETE levels were significantly elevated in the SHR compared to the WKY (SHR elevated by 154%, 159%, and 272% compared to WKY at 4, 8, and 12 weeks, respectively,
P < .01 for all ages). There were no differences in plasma potassium levels between SHR and WKY at any of the ages tested. Plasma aldosterone levels and plasma renin activity were in the normal range at the three ages. At 12 weeks of age, both serum (4.72 ± 0.23
v 2.18 ± 0.33
μg/mL,
P < .01), and aortic smooth muscle 12-HETE levels (0.94 ± 0.09
v 0.66 ± 0.08
μg/mg protein,
P < .05) were elevated in SHR compared with WKY. The 12 week old SHR were given a bolus of the LO inhibitor 5,8,11-eicosatriynoic acid (ETI, 7 mg/kg, intravenously) and blood pressure measured after 20 min. ETI reduced mean systolic blood pressure from 175.8 ± 4.2 to 141.6 ± 5.9 mm Hg (
P < .05). To investigate these effects of HETEs, cultured vascular smooth muscle cells were pretreated for 1 min with 12(S)HETE and then challenged with angiotensin II (AngII). The addition of 12(S)HETE increased AngII-induced intracellular calcium levels in normal cultured rat vascular smooth muscle cells by 78% compared to vehicle (
P < .05). Thus, LO products, which are high in SHR, may contribute to vascular tone through alterations in the intracellular calcium signal by potentiating calcium responses to pressors such as Ang II.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>9128202</pmid><doi>10.1016/S0895-7061(96)00488-8</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid - blood Aging Animals Arachidonate 12-Lipoxygenase - analysis arachidonic acid pathway Arterial hypertension. Arterial hypotension Biological and medical sciences Blood and lymphatic vessels calcium Calcium - metabolism Cardiology. Vascular system Cells, Cultured Experimental diseases Hypertension - metabolism Hypertension - physiopathology Lipoxygenase Male Medical sciences Muscle, Smooth, Vascular - metabolism Muscle, Smooth, Vascular - physiopathology Rats Rats, Inbred SHR Rats, Inbred WKY spontaneously hypertensive rat |
title | Elevated 12-Lipoxygenase Activity in the Spontaneously Hypertensive Rat |
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