Prolonged blood pressure reduction by orally active renin inhibitor RO 42-5892 in essential hypertension
OBJECTIVE--To investigate the effects of a novel specific renin inhibitor, RO 42-5892, with high affinity for human renin (Ki = 0.5 x 10(-9) mol/l), on plasma renin activity and angiotensin II concentration and on 24 hour ambulatory blood pressure in essential hypertension. DESIGN--Exploratory study...
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description | OBJECTIVE--To investigate the effects of a novel specific renin inhibitor, RO 42-5892, with high affinity for human renin (Ki = 0.5 x 10(-9) mol/l), on plasma renin activity and angiotensin II concentration and on 24 hour ambulatory blood pressure in essential hypertension. DESIGN--Exploratory study in which active treatment was preceded by placebo. SETTING--Inpatient unit of teaching hospital. PATIENTS--Nine men with uncomplicated essential hypertension who had a normal sodium intake. INTERVENTIONS--Two single intravenous doses of RO 42-5892 (100 and 1,000 micrograms/kg in 10 minutes) given to six patients and one single oral dose (600 mg) given to the three others as well as to three of the patients who also received the two intravenous doses. RESULTS--With both intravenous and oral doses renin activity fell in 10 minutes to undetectably low values, while angiotensin II concentration fell overall by 80-90% with intravenous dosing and by 30-40% after the oral dose. Angiotensin II concentration was back to baseline four hours after the low and six hours after the high intravenous dose and remained low for at least eight hours after the oral dose. Blood pressure fell rapidly both after low and high intravenous doses and after the oral dose and remained low for hours. With the high intravenous dose the daytime (0900-2230), night time (2300-0600), and next morning (0630-0830) systolic blood pressures were significantly (p less than 0.05) lowered by 12.5 (95% confidence interval 5.6 to 19.7), 12.2 (5.4 to 19.3), and 10.7 (3.2 to 18.5) mm Hg respectively, and daytime diastolic pressure was lowered by 9.3 (2.2 to 16.8) mmHg. With the oral dose daytime, night time, and next morning systolic blood pressures were lowered by 10.3 (5.5 to 15.4), 10.5 (4.2 to 17.2), and 9.7 (4.0 to 15.6) mm Hg, and daytime and night time diastolic pressures were lowered by 5.8 (0.9 to 11.0) and 6.0 (0.3-12) mm Hg respectively. CONCLUSIONS--The effect of the inhibitor on blood pressure was maintained over a longer period than its effect on angiotensin II. RO 42-5892 is orally active and has a prolonged antihypertensive effect in patients who did not have sodium depletion. This prolonged effect seems to be independent, at least in part, of the suppression of circulating angiotensin II. |
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fullrecord | <record><control><sourceid>jstor_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1663555</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>29708580</jstor_id><sourcerecordid>29708580</sourcerecordid><originalsourceid>FETCH-LOGICAL-b544t-a3f0fdbc139429eb755c50c8d4a7eaf64f612726698f5efcc6d6fedd732a70753</originalsourceid><addsrcrecordid>eNqFkUtvEzEUhUcIVKLSPRskSyA2aFK_HxukEgEFVbQqjwUby-PxNA4TO9gzFfn39ShRWtiwsnS_c4_P1amq5wjOESL8tFmv5gSiOReUzTFkj6oZolzWTBLyuJpBxVQtEZFPq5OcVxBCTIRUnB1VRxhDQiWfVcurFPsYblwLmj7GFmySy3lMDiTXjnbwMYBmC2Iyfb8FpgxuJxR8AD4sfeOHmMD1JaC4fKtwGYKy78LgTQ-W241Lgwu5uDyrnnSmz-5k_x5X3z-8_7Y4ry8uP35anF3UDaN0qA3pYNc2FhFFsXKNYMwyaGVLjXCm47TjCAvMuZIdc521vOWda1tBsBFQMHJcvd35bsZm7VpbopTsepP82qStjsbrv0nwS30TbzXinDA2GbzeG6T4e3R50Gufret7E1wcsxZKCcmJKsKX_whXcUyhHKeREJwSzPBkB3cqm2LOyXWHKAjqqUZdatSlRj3VqEuNZeXFwxMOC_vSCn-15yZb03fJBOvzQUYFogLTe5tVLiXduygBJZOw8HrHfR7cnwM36VeJQgTTX34s9OLzO3Z1_fOrnmK92emnwP894g5yP8z5</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1776432525</pqid></control><display><type>article</type><title>Prolonged blood pressure reduction by orally active renin inhibitor RO 42-5892 in essential hypertension</title><source>Jstor Complete Legacy</source><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>van den Meiracker, A H ; Admiraal, P J ; Man in 't Veld, A J ; Derkx, F H ; Ritsema van Eck, H J ; Mulder, P ; van Brummelen, P ; Schalekamp, M A</creator><creatorcontrib>van den Meiracker, A H ; Admiraal, P J ; Man in 't Veld, A J ; Derkx, F H ; Ritsema van Eck, H J ; Mulder, P ; van Brummelen, P ; Schalekamp, M A</creatorcontrib><description>OBJECTIVE--To investigate the effects of a novel specific renin inhibitor, RO 42-5892, with high affinity for human renin (Ki = 0.5 x 10(-9) mol/l), on plasma renin activity and angiotensin II concentration and on 24 hour ambulatory blood pressure in essential hypertension. DESIGN--Exploratory study in which active treatment was preceded by placebo. SETTING--Inpatient unit of teaching hospital. PATIENTS--Nine men with uncomplicated essential hypertension who had a normal sodium intake. INTERVENTIONS--Two single intravenous doses of RO 42-5892 (100 and 1,000 micrograms/kg in 10 minutes) given to six patients and one single oral dose (600 mg) given to the three others as well as to three of the patients who also received the two intravenous doses. RESULTS--With both intravenous and oral doses renin activity fell in 10 minutes to undetectably low values, while angiotensin II concentration fell overall by 80-90% with intravenous dosing and by 30-40% after the oral dose. Angiotensin II concentration was back to baseline four hours after the low and six hours after the high intravenous dose and remained low for at least eight hours after the oral dose. Blood pressure fell rapidly both after low and high intravenous doses and after the oral dose and remained low for hours. With the high intravenous dose the daytime (0900-2230), night time (2300-0600), and next morning (0630-0830) systolic blood pressures were significantly (p less than 0.05) lowered by 12.5 (95% confidence interval 5.6 to 19.7), 12.2 (5.4 to 19.3), and 10.7 (3.2 to 18.5) mm Hg respectively, and daytime diastolic pressure was lowered by 9.3 (2.2 to 16.8) mmHg. With the oral dose daytime, night time, and next morning systolic blood pressures were lowered by 10.3 (5.5 to 15.4), 10.5 (4.2 to 17.2), and 9.7 (4.0 to 15.6) mm Hg, and daytime and night time diastolic pressures were lowered by 5.8 (0.9 to 11.0) and 6.0 (0.3-12) mm Hg respectively. CONCLUSIONS--The effect of the inhibitor on blood pressure was maintained over a longer period than its effect on angiotensin II. RO 42-5892 is orally active and has a prolonged antihypertensive effect in patients who did not have sodium depletion. This prolonged effect seems to be independent, at least in part, of the suppression of circulating angiotensin II.</description><identifier>ISSN: 0959-8138</identifier><identifier>ISSN: 0959-8146</identifier><identifier>EISSN: 1468-5833</identifier><identifier>EISSN: 1756-1833</identifier><identifier>DOI: 10.1136/bmj.301.6745.205</identifier><identifier>PMID: 2203486</identifier><language>eng</language><publisher>London: British Medical Journal Publishing Group</publisher><subject>Administration, Oral ; Adult ; Angiotensin II - blood ; Antihypertensive Agents - administration & dosage ; Antihypertensive Agents - therapeutic use ; Antihypertensives ; Biological and medical sciences ; Blood ; Blood plasma ; Blood pressure ; Blood Pressure - drug effects ; Cardiology. Vascular system ; Dosage ; Drug Evaluation ; Enzymes ; Heart rate ; Humans ; Hypertension ; Hypertension - blood ; Hypertension - drug therapy ; Imidazoles ; Injections, Intravenous ; Male ; Medical sciences ; Middle Aged ; Placebos ; Renin - antagonists & inhibitors ; Renin - blood ; Renin - therapeutic use ; Sodium ; Time Factors</subject><ispartof>BMJ, 1990-07, Vol.301 (6745), p.205-210</ispartof><rights>Copyright 1990 British Medical Journal</rights><rights>1993 INIST-CNRS</rights><rights>Copyright BMJ Publishing Group LTD Jul 28, 1990</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b544t-a3f0fdbc139429eb755c50c8d4a7eaf64f612726698f5efcc6d6fedd732a70753</citedby><cites>FETCH-LOGICAL-b544t-a3f0fdbc139429eb755c50c8d4a7eaf64f612726698f5efcc6d6fedd732a70753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/29708580$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/29708580$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,776,780,799,881,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4714724$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2203486$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van den Meiracker, A H</creatorcontrib><creatorcontrib>Admiraal, P J</creatorcontrib><creatorcontrib>Man in 't Veld, A J</creatorcontrib><creatorcontrib>Derkx, F H</creatorcontrib><creatorcontrib>Ritsema van Eck, H J</creatorcontrib><creatorcontrib>Mulder, P</creatorcontrib><creatorcontrib>van Brummelen, P</creatorcontrib><creatorcontrib>Schalekamp, M A</creatorcontrib><title>Prolonged blood pressure reduction by orally active renin inhibitor RO 42-5892 in essential hypertension</title><title>BMJ</title><addtitle>BMJ</addtitle><description>OBJECTIVE--To investigate the effects of a novel specific renin inhibitor, RO 42-5892, with high affinity for human renin (Ki = 0.5 x 10(-9) mol/l), on plasma renin activity and angiotensin II concentration and on 24 hour ambulatory blood pressure in essential hypertension. DESIGN--Exploratory study in which active treatment was preceded by placebo. SETTING--Inpatient unit of teaching hospital. PATIENTS--Nine men with uncomplicated essential hypertension who had a normal sodium intake. INTERVENTIONS--Two single intravenous doses of RO 42-5892 (100 and 1,000 micrograms/kg in 10 minutes) given to six patients and one single oral dose (600 mg) given to the three others as well as to three of the patients who also received the two intravenous doses. RESULTS--With both intravenous and oral doses renin activity fell in 10 minutes to undetectably low values, while angiotensin II concentration fell overall by 80-90% with intravenous dosing and by 30-40% after the oral dose. Angiotensin II concentration was back to baseline four hours after the low and six hours after the high intravenous dose and remained low for at least eight hours after the oral dose. Blood pressure fell rapidly both after low and high intravenous doses and after the oral dose and remained low for hours. With the high intravenous dose the daytime (0900-2230), night time (2300-0600), and next morning (0630-0830) systolic blood pressures were significantly (p less than 0.05) lowered by 12.5 (95% confidence interval 5.6 to 19.7), 12.2 (5.4 to 19.3), and 10.7 (3.2 to 18.5) mm Hg respectively, and daytime diastolic pressure was lowered by 9.3 (2.2 to 16.8) mmHg. With the oral dose daytime, night time, and next morning systolic blood pressures were lowered by 10.3 (5.5 to 15.4), 10.5 (4.2 to 17.2), and 9.7 (4.0 to 15.6) mm Hg, and daytime and night time diastolic pressures were lowered by 5.8 (0.9 to 11.0) and 6.0 (0.3-12) mm Hg respectively. CONCLUSIONS--The effect of the inhibitor on blood pressure was maintained over a longer period than its effect on angiotensin II. RO 42-5892 is orally active and has a prolonged antihypertensive effect in patients who did not have sodium depletion. This prolonged effect seems to be independent, at least in part, of the suppression of circulating angiotensin II.</description><subject>Administration, Oral</subject><subject>Adult</subject><subject>Angiotensin II - blood</subject><subject>Antihypertensive Agents - administration & dosage</subject><subject>Antihypertensive Agents - therapeutic use</subject><subject>Antihypertensives</subject><subject>Biological and medical sciences</subject><subject>Blood</subject><subject>Blood plasma</subject><subject>Blood pressure</subject><subject>Blood Pressure - drug effects</subject><subject>Cardiology. Vascular system</subject><subject>Dosage</subject><subject>Drug Evaluation</subject><subject>Enzymes</subject><subject>Heart rate</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Hypertension - blood</subject><subject>Hypertension - drug therapy</subject><subject>Imidazoles</subject><subject>Injections, Intravenous</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Placebos</subject><subject>Renin - antagonists & inhibitors</subject><subject>Renin - blood</subject><subject>Renin - therapeutic use</subject><subject>Sodium</subject><subject>Time Factors</subject><issn>0959-8138</issn><issn>0959-8146</issn><issn>1468-5833</issn><issn>1756-1833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkUtvEzEUhUcIVKLSPRskSyA2aFK_HxukEgEFVbQqjwUby-PxNA4TO9gzFfn39ShRWtiwsnS_c4_P1amq5wjOESL8tFmv5gSiOReUzTFkj6oZolzWTBLyuJpBxVQtEZFPq5OcVxBCTIRUnB1VRxhDQiWfVcurFPsYblwLmj7GFmySy3lMDiTXjnbwMYBmC2Iyfb8FpgxuJxR8AD4sfeOHmMD1JaC4fKtwGYKy78LgTQ-W241Lgwu5uDyrnnSmz-5k_x5X3z-8_7Y4ry8uP35anF3UDaN0qA3pYNc2FhFFsXKNYMwyaGVLjXCm47TjCAvMuZIdc521vOWda1tBsBFQMHJcvd35bsZm7VpbopTsepP82qStjsbrv0nwS30TbzXinDA2GbzeG6T4e3R50Gufret7E1wcsxZKCcmJKsKX_whXcUyhHKeREJwSzPBkB3cqm2LOyXWHKAjqqUZdatSlRj3VqEuNZeXFwxMOC_vSCn-15yZb03fJBOvzQUYFogLTe5tVLiXduygBJZOw8HrHfR7cnwM36VeJQgTTX34s9OLzO3Z1_fOrnmK92emnwP894g5yP8z5</recordid><startdate>19900728</startdate><enddate>19900728</enddate><creator>van den Meiracker, A H</creator><creator>Admiraal, P J</creator><creator>Man in 't Veld, A J</creator><creator>Derkx, F H</creator><creator>Ritsema van Eck, H J</creator><creator>Mulder, P</creator><creator>van Brummelen, P</creator><creator>Schalekamp, M A</creator><general>British Medical Journal Publishing Group</general><general>British Medical Association</general><general>BMJ Publishing Group LTD</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ASE</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FPQ</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K6X</scope><scope>K9.</scope><scope>LK8</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19900728</creationdate><title>Prolonged blood pressure reduction by orally active renin inhibitor RO 42-5892 in essential hypertension</title><author>van den Meiracker, A H ; Admiraal, P J ; Man in 't Veld, A J ; Derkx, F H ; Ritsema van Eck, H J ; Mulder, P ; van Brummelen, P ; Schalekamp, M A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b544t-a3f0fdbc139429eb755c50c8d4a7eaf64f612726698f5efcc6d6fedd732a70753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Administration, Oral</topic><topic>Adult</topic><topic>Angiotensin II - blood</topic><topic>Antihypertensive Agents - administration & dosage</topic><topic>Antihypertensive Agents - therapeutic use</topic><topic>Antihypertensives</topic><topic>Biological and medical sciences</topic><topic>Blood</topic><topic>Blood plasma</topic><topic>Blood pressure</topic><topic>Blood Pressure - drug effects</topic><topic>Cardiology. Vascular system</topic><topic>Dosage</topic><topic>Drug Evaluation</topic><topic>Enzymes</topic><topic>Heart rate</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Hypertension - blood</topic><topic>Hypertension - drug therapy</topic><topic>Imidazoles</topic><topic>Injections, Intravenous</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Placebos</topic><topic>Renin - antagonists & inhibitors</topic><topic>Renin - blood</topic><topic>Renin - therapeutic use</topic><topic>Sodium</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van den Meiracker, A H</creatorcontrib><creatorcontrib>Admiraal, P J</creatorcontrib><creatorcontrib>Man in 't Veld, A J</creatorcontrib><creatorcontrib>Derkx, F H</creatorcontrib><creatorcontrib>Ritsema van Eck, H J</creatorcontrib><creatorcontrib>Mulder, P</creatorcontrib><creatorcontrib>van Brummelen, P</creatorcontrib><creatorcontrib>Schalekamp, M A</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>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Index</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>British Nursing Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMJ</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van den Meiracker, A H</au><au>Admiraal, P J</au><au>Man in 't Veld, A J</au><au>Derkx, F H</au><au>Ritsema van Eck, H J</au><au>Mulder, P</au><au>van Brummelen, P</au><au>Schalekamp, M A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prolonged blood pressure reduction by orally active renin inhibitor RO 42-5892 in essential hypertension</atitle><jtitle>BMJ</jtitle><addtitle>BMJ</addtitle><date>1990-07-28</date><risdate>1990</risdate><volume>301</volume><issue>6745</issue><spage>205</spage><epage>210</epage><pages>205-210</pages><issn>0959-8138</issn><issn>0959-8146</issn><eissn>1468-5833</eissn><eissn>1756-1833</eissn><abstract>OBJECTIVE--To investigate the effects of a novel specific renin inhibitor, RO 42-5892, with high affinity for human renin (Ki = 0.5 x 10(-9) mol/l), on plasma renin activity and angiotensin II concentration and on 24 hour ambulatory blood pressure in essential hypertension. DESIGN--Exploratory study in which active treatment was preceded by placebo. SETTING--Inpatient unit of teaching hospital. PATIENTS--Nine men with uncomplicated essential hypertension who had a normal sodium intake. INTERVENTIONS--Two single intravenous doses of RO 42-5892 (100 and 1,000 micrograms/kg in 10 minutes) given to six patients and one single oral dose (600 mg) given to the three others as well as to three of the patients who also received the two intravenous doses. RESULTS--With both intravenous and oral doses renin activity fell in 10 minutes to undetectably low values, while angiotensin II concentration fell overall by 80-90% with intravenous dosing and by 30-40% after the oral dose. Angiotensin II concentration was back to baseline four hours after the low and six hours after the high intravenous dose and remained low for at least eight hours after the oral dose. Blood pressure fell rapidly both after low and high intravenous doses and after the oral dose and remained low for hours. With the high intravenous dose the daytime (0900-2230), night time (2300-0600), and next morning (0630-0830) systolic blood pressures were significantly (p less than 0.05) lowered by 12.5 (95% confidence interval 5.6 to 19.7), 12.2 (5.4 to 19.3), and 10.7 (3.2 to 18.5) mm Hg respectively, and daytime diastolic pressure was lowered by 9.3 (2.2 to 16.8) mmHg. With the oral dose daytime, night time, and next morning systolic blood pressures were lowered by 10.3 (5.5 to 15.4), 10.5 (4.2 to 17.2), and 9.7 (4.0 to 15.6) mm Hg, and daytime and night time diastolic pressures were lowered by 5.8 (0.9 to 11.0) and 6.0 (0.3-12) mm Hg respectively. CONCLUSIONS--The effect of the inhibitor on blood pressure was maintained over a longer period than its effect on angiotensin II. RO 42-5892 is orally active and has a prolonged antihypertensive effect in patients who did not have sodium depletion. This prolonged effect seems to be independent, at least in part, of the suppression of circulating angiotensin II.</abstract><cop>London</cop><pub>British Medical Journal Publishing Group</pub><pmid>2203486</pmid><doi>10.1136/bmj.301.6745.205</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Oral Adult Angiotensin II - blood Antihypertensive Agents - administration & dosage Antihypertensive Agents - therapeutic use Antihypertensives Biological and medical sciences Blood Blood plasma Blood pressure Blood Pressure - drug effects Cardiology. Vascular system Dosage Drug Evaluation Enzymes Heart rate Humans Hypertension Hypertension - blood Hypertension - drug therapy Imidazoles Injections, Intravenous Male Medical sciences Middle Aged Placebos Renin - antagonists & inhibitors Renin - blood Renin - therapeutic use Sodium Time Factors |
title | Prolonged blood pressure reduction by orally active renin inhibitor RO 42-5892 in essential hypertension |
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