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Reduced Endothelial NO-cGMP–Mediated Vascular Relaxation and Hypertension in IL-6–Infused Pregnant Rats
ABSTRACT—Placental ischemia during pregnancy is associated with increased plasma cytokines such as interleukin-6 (IL-6), which may contribute to increased vascular resistance and hypertension of pregnancy. We tested the hypothesis that an increase in plasma IL-6 during pregnancy is associated with i...
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Published in: | Hypertension (Dallas, Tex. 1979) Tex. 1979), 2004-02, Vol.43 (2, Part 2), p.434-444 |
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description | ABSTRACT—Placental ischemia during pregnancy is associated with increased plasma cytokines such as interleukin-6 (IL-6), which may contribute to increased vascular resistance and hypertension of pregnancy. We tested the hypothesis that an increase in plasma IL-6 during pregnancy is associated with impaired endothelium-dependent relaxation, enhanced vascular contraction, and hypertension. Systolic blood pressure was measured in virgin and pregnant Sprague-Dawley rats non-treated or infused with IL-6 (200 ng/kg per day for 5 days). Isometric contraction was measured in isolated aortic strips, and endothelial nitric oxide (NO) synthase (eNOS) was measured in aortic homogenate using Western blots. Blood pressure was greater in IL-6–infused (146±3) than in control pregnant rats (117±2 mm Hg). In endothelium-intact vascular strips, phenylephrine (Phe) caused greater increase in active stress in IL-6–infused (maximum10.6±0.6) than in control pregnant rats (maximum4.1±0.3×10 N/m). Acetylcholine (ACh)-induced relaxation of Phe contraction and vascular eNOS protein and nitrite/nitrate production were less in IL-6–infused than in control pregnant rats. N-nitro-l-arginine methyl ester (10 mol/L), inhibitor of NOS, or 1H-[1,2,4]oxadiazolo[4,3]-quinoxalin-1-one (10 mol/L), inhibitor of cGMP production in smooth muscle, inhibited ACh-induced relaxation and enhanced Phe-induced stress in control but not IL-6–infused pregnant rats. Endothelium removal enhanced Phe-induced stress in control but not in IL-6–infused pregnant rats. The blood pressure and vascular Phe-induced contraction, ACh relaxation, and eNOS protein were not different between control and IL-6–infused virgin rats. Thus, an endothelium-dependent NO-cGMP–mediated relaxation pathway is inhibited in systemic vessels of pregnant rats infused with IL-6. The results support a role for IL-6 as a possible mediator of the increased vascular resistance during hypertension of pregnancy. |
doi_str_mv | 10.1161/01.HYP.0000113044.46326.98 |
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We tested the hypothesis that an increase in plasma IL-6 during pregnancy is associated with impaired endothelium-dependent relaxation, enhanced vascular contraction, and hypertension. Systolic blood pressure was measured in virgin and pregnant Sprague-Dawley rats non-treated or infused with IL-6 (200 ng/kg per day for 5 days). Isometric contraction was measured in isolated aortic strips, and endothelial nitric oxide (NO) synthase (eNOS) was measured in aortic homogenate using Western blots. Blood pressure was greater in IL-6–infused (146±3) than in control pregnant rats (117±2 mm Hg). In endothelium-intact vascular strips, phenylephrine (Phe) caused greater increase in active stress in IL-6–infused (maximum10.6±0.6) than in control pregnant rats (maximum4.1±0.3×10 N/m). Acetylcholine (ACh)-induced relaxation of Phe contraction and vascular eNOS protein and nitrite/nitrate production were less in IL-6–infused than in control pregnant rats. N-nitro-l-arginine methyl ester (10 mol/L), inhibitor of NOS, or 1H-[1,2,4]oxadiazolo[4,3]-quinoxalin-1-one (10 mol/L), inhibitor of cGMP production in smooth muscle, inhibited ACh-induced relaxation and enhanced Phe-induced stress in control but not IL-6–infused pregnant rats. Endothelium removal enhanced Phe-induced stress in control but not in IL-6–infused pregnant rats. The blood pressure and vascular Phe-induced contraction, ACh relaxation, and eNOS protein were not different between control and IL-6–infused virgin rats. Thus, an endothelium-dependent NO-cGMP–mediated relaxation pathway is inhibited in systemic vessels of pregnant rats infused with IL-6. 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Etiology ; Cyclic GMP - metabolism ; Endothelium, Vascular - physiopathology ; Experimental diseases ; Female ; Hypertension - chemically induced ; Hypertension - metabolism ; Hypertension - physiopathology ; In Vitro Techniques ; Infusions, Intravenous ; Interleukin-6 - administration & dosage ; Interleukin-6 - blood ; Interleukin-6 - toxicity ; Medical sciences ; Nitric Oxide - metabolism ; Pregnancy ; Pregnancy Complications, Cardiovascular - chemically induced ; Pregnancy Complications, Cardiovascular - metabolism ; Pregnancy Complications, Cardiovascular - physiopathology ; Rats ; Rats, Sprague-Dawley ; Vasoconstriction ; Vasodilation</subject><ispartof>Hypertension (Dallas, Tex. 1979), 2004-02, Vol.43 (2, Part 2), p.434-444</ispartof><rights>2004 American Heart Association, Inc.</rights><rights>2004 INIST-CNRS</rights><rights>Copyright American Heart Association, Inc. Feb 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5104-a9daa3c59c9271773b8a9371140fdb81f8fca77b670c7ab9085332c72a1864af3</citedby><cites>FETCH-LOGICAL-c5104-a9daa3c59c9271773b8a9371140fdb81f8fca77b670c7ab9085332c72a1864af3</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=15587069$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14707155$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Orshal, Julia M</creatorcontrib><creatorcontrib>Khalil, Raouf A</creatorcontrib><title>Reduced Endothelial NO-cGMP–Mediated Vascular Relaxation and Hypertension in IL-6–Infused Pregnant Rats</title><title>Hypertension (Dallas, Tex. 1979)</title><addtitle>Hypertension</addtitle><description>ABSTRACT—Placental ischemia during pregnancy is associated with increased plasma cytokines such as interleukin-6 (IL-6), which may contribute to increased vascular resistance and hypertension of pregnancy. We tested the hypothesis that an increase in plasma IL-6 during pregnancy is associated with impaired endothelium-dependent relaxation, enhanced vascular contraction, and hypertension. Systolic blood pressure was measured in virgin and pregnant Sprague-Dawley rats non-treated or infused with IL-6 (200 ng/kg per day for 5 days). Isometric contraction was measured in isolated aortic strips, and endothelial nitric oxide (NO) synthase (eNOS) was measured in aortic homogenate using Western blots. Blood pressure was greater in IL-6–infused (146±3) than in control pregnant rats (117±2 mm Hg). In endothelium-intact vascular strips, phenylephrine (Phe) caused greater increase in active stress in IL-6–infused (maximum10.6±0.6) than in control pregnant rats (maximum4.1±0.3×10 N/m). Acetylcholine (ACh)-induced relaxation of Phe contraction and vascular eNOS protein and nitrite/nitrate production were less in IL-6–infused than in control pregnant rats. N-nitro-l-arginine methyl ester (10 mol/L), inhibitor of NOS, or 1H-[1,2,4]oxadiazolo[4,3]-quinoxalin-1-one (10 mol/L), inhibitor of cGMP production in smooth muscle, inhibited ACh-induced relaxation and enhanced Phe-induced stress in control but not IL-6–infused pregnant rats. Endothelium removal enhanced Phe-induced stress in control but not in IL-6–infused pregnant rats. The blood pressure and vascular Phe-induced contraction, ACh relaxation, and eNOS protein were not different between control and IL-6–infused virgin rats. Thus, an endothelium-dependent NO-cGMP–mediated relaxation pathway is inhibited in systemic vessels of pregnant rats infused with IL-6. The results support a role for IL-6 as a possible mediator of the increased vascular resistance during hypertension of pregnancy.</description><subject>Animals</subject><subject>Aorta - physiopathology</subject><subject>Arterial hypertension. Arterial hypotension</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Cardiology. Vascular system</subject><subject>Clinical manifestations. Epidemiology. Investigative techniques. Etiology</subject><subject>Cyclic GMP - metabolism</subject><subject>Endothelium, Vascular - physiopathology</subject><subject>Experimental diseases</subject><subject>Female</subject><subject>Hypertension - chemically induced</subject><subject>Hypertension - metabolism</subject><subject>Hypertension - physiopathology</subject><subject>In Vitro Techniques</subject><subject>Infusions, Intravenous</subject><subject>Interleukin-6 - administration & dosage</subject><subject>Interleukin-6 - blood</subject><subject>Interleukin-6 - toxicity</subject><subject>Medical sciences</subject><subject>Nitric Oxide - metabolism</subject><subject>Pregnancy</subject><subject>Pregnancy Complications, Cardiovascular - chemically induced</subject><subject>Pregnancy Complications, Cardiovascular - metabolism</subject><subject>Pregnancy Complications, Cardiovascular - physiopathology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Vasoconstriction</subject><subject>Vasodilation</subject><issn>0194-911X</issn><issn>1524-4563</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNpFkN9u0zAUhy0EYmXwCiiaxGWCj__ENndoGmuljlUVILiyTh2HZsucYicau-MdeEOeBG-tVN8c6Zzv55_0EXIGtAKo4T2Fav5jVdH8ADgVohI1Z3Vl9DMyA8lEKWTNn5MZBSNKA_D9hLxK6SbjQgj1kpyAUFSBlDNyu_bN5HxTXIRmGLe-77AvPl-X7vJq9e_P3yvfdDjm8zdMbuoxFmvf428cuyEUGJpi_rDzcfQhPS66UCyWZZ1zi9BOKcdW0f8MGMZijWN6TV602Cf_5jBPyddPF1_O5-Xy-nJx_nFZOglUlGgaRO6kcYYpUIpvNBquAARtm42GVrcOldrUijqFG0O15Jw5xRB0LbDlp-Rs_-8uDr8mn0Z7M0wx5ErLqGSaS0kz9GEPuTikFH1rd7G7w_hggdpHzZaCzZrtUbN90myNzuG3h4Zpc-ebY_TgNQPvDkD2hn0bMbguHTkptaK1yZzYc_dDP_qYbvvp3ke79diP26dqwWpdsjwpo0DLvGGC_wcpu5Zt</recordid><startdate>200402</startdate><enddate>200402</enddate><creator>Orshal, Julia M</creator><creator>Khalil, Raouf A</creator><general>American Heart Association, Inc</general><general>Lippincott</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>K9.</scope></search><sort><creationdate>200402</creationdate><title>Reduced Endothelial NO-cGMP–Mediated Vascular Relaxation and Hypertension in IL-6–Infused Pregnant Rats</title><author>Orshal, Julia M ; Khalil, Raouf A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5104-a9daa3c59c9271773b8a9371140fdb81f8fca77b670c7ab9085332c72a1864af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Aorta - physiopathology</topic><topic>Arterial hypertension. Arterial hypotension</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Cardiology. Vascular system</topic><topic>Clinical manifestations. Epidemiology. Investigative techniques. Etiology</topic><topic>Cyclic GMP - metabolism</topic><topic>Endothelium, Vascular - physiopathology</topic><topic>Experimental diseases</topic><topic>Female</topic><topic>Hypertension - chemically induced</topic><topic>Hypertension - metabolism</topic><topic>Hypertension - physiopathology</topic><topic>In Vitro Techniques</topic><topic>Infusions, Intravenous</topic><topic>Interleukin-6 - administration & dosage</topic><topic>Interleukin-6 - blood</topic><topic>Interleukin-6 - toxicity</topic><topic>Medical sciences</topic><topic>Nitric Oxide - metabolism</topic><topic>Pregnancy</topic><topic>Pregnancy Complications, Cardiovascular - chemically induced</topic><topic>Pregnancy Complications, Cardiovascular - metabolism</topic><topic>Pregnancy Complications, Cardiovascular - physiopathology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Vasoconstriction</topic><topic>Vasodilation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Orshal, Julia M</creatorcontrib><creatorcontrib>Khalil, Raouf A</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 Health & Medical Complete (Alumni)</collection><jtitle>Hypertension (Dallas, Tex. 1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Orshal, Julia M</au><au>Khalil, Raouf A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reduced Endothelial NO-cGMP–Mediated Vascular Relaxation and Hypertension in IL-6–Infused Pregnant Rats</atitle><jtitle>Hypertension (Dallas, Tex. 1979)</jtitle><addtitle>Hypertension</addtitle><date>2004-02</date><risdate>2004</risdate><volume>43</volume><issue>2, Part 2</issue><spage>434</spage><epage>444</epage><pages>434-444</pages><issn>0194-911X</issn><eissn>1524-4563</eissn><coden>HPRTDN</coden><abstract>ABSTRACT—Placental ischemia during pregnancy is associated with increased plasma cytokines such as interleukin-6 (IL-6), which may contribute to increased vascular resistance and hypertension of pregnancy. We tested the hypothesis that an increase in plasma IL-6 during pregnancy is associated with impaired endothelium-dependent relaxation, enhanced vascular contraction, and hypertension. Systolic blood pressure was measured in virgin and pregnant Sprague-Dawley rats non-treated or infused with IL-6 (200 ng/kg per day for 5 days). Isometric contraction was measured in isolated aortic strips, and endothelial nitric oxide (NO) synthase (eNOS) was measured in aortic homogenate using Western blots. Blood pressure was greater in IL-6–infused (146±3) than in control pregnant rats (117±2 mm Hg). In endothelium-intact vascular strips, phenylephrine (Phe) caused greater increase in active stress in IL-6–infused (maximum10.6±0.6) than in control pregnant rats (maximum4.1±0.3×10 N/m). Acetylcholine (ACh)-induced relaxation of Phe contraction and vascular eNOS protein and nitrite/nitrate production were less in IL-6–infused than in control pregnant rats. N-nitro-l-arginine methyl ester (10 mol/L), inhibitor of NOS, or 1H-[1,2,4]oxadiazolo[4,3]-quinoxalin-1-one (10 mol/L), inhibitor of cGMP production in smooth muscle, inhibited ACh-induced relaxation and enhanced Phe-induced stress in control but not IL-6–infused pregnant rats. Endothelium removal enhanced Phe-induced stress in control but not in IL-6–infused pregnant rats. The blood pressure and vascular Phe-induced contraction, ACh relaxation, and eNOS protein were not different between control and IL-6–infused virgin rats. Thus, an endothelium-dependent NO-cGMP–mediated relaxation pathway is inhibited in systemic vessels of pregnant rats infused with IL-6. The results support a role for IL-6 as a possible mediator of the increased vascular resistance during hypertension of pregnancy.</abstract><cop>Philadelphia, PA</cop><cop>Hagerstown, MD</cop><pub>American Heart Association, Inc</pub><pmid>14707155</pmid><doi>10.1161/01.HYP.0000113044.46326.98</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Aorta - physiopathology Arterial hypertension. Arterial hypotension Biological and medical sciences Blood and lymphatic vessels Cardiology. Vascular system Clinical manifestations. Epidemiology. Investigative techniques. Etiology Cyclic GMP - metabolism Endothelium, Vascular - physiopathology Experimental diseases Female Hypertension - chemically induced Hypertension - metabolism Hypertension - physiopathology In Vitro Techniques Infusions, Intravenous Interleukin-6 - administration & dosage Interleukin-6 - blood Interleukin-6 - toxicity Medical sciences Nitric Oxide - metabolism Pregnancy Pregnancy Complications, Cardiovascular - chemically induced Pregnancy Complications, Cardiovascular - metabolism Pregnancy Complications, Cardiovascular - physiopathology Rats Rats, Sprague-Dawley Vasoconstriction Vasodilation |
title | Reduced Endothelial NO-cGMP–Mediated Vascular Relaxation and Hypertension in IL-6–Infused Pregnant Rats |
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