Antihypertensive Activity of SCH 31846, a Non-Sulfhydryl Angiotensin-Converting Enzyme Inhibitor

SUMMARYThe antihypertensive, hemodynamic, and autonomic actions of SCH 31846, a new, potent and long-acting non-sulfhydryl angiotensin-converting enzyme (ACE) inhibitor, were evaluated in several experimental preparations. Oral administration of 0.3–3 mg/kg caused dose-related decreases in blood pre...

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Veröffentlicht in:Journal of cardiovascular pharmacology 1983-07, Vol.5 (4), p.655-667
Hauptverfasser: Baum, Thomas, Sybertz, Edmund J, Watkins, Robert W, Ahn, Ho Sam, Nelson, Steven, Eynon, Emma, Vliet, Gary Vander, Pula, Kathryn K, Sabin, Crawford, Desiderio, Denise M, Becker, Frederick T, Vemulapalli, Subbarao
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container_end_page 667
container_issue 4
container_start_page 655
container_title Journal of cardiovascular pharmacology
container_volume 5
creator Baum, Thomas
Sybertz, Edmund J
Watkins, Robert W
Ahn, Ho Sam
Nelson, Steven
Eynon, Emma
Vliet, Gary Vander
Pula, Kathryn K
Sabin, Crawford
Desiderio, Denise M
Becker, Frederick T
Vemulapalli, Subbarao
description SUMMARYThe antihypertensive, hemodynamic, and autonomic actions of SCH 31846, a new, potent and long-acting non-sulfhydryl angiotensin-converting enzyme (ACE) inhibitor, were evaluated in several experimental preparations. Oral administration of 0.3–3 mg/kg caused dose-related decreases in blood pressure in spontaneously hypertensive rats (SHRs). Pretreatment with a diuretic augmented the maximum hypotensive response attainable. Single doses (3 mg/kg) of SCH 31846 reduced pressure for over 24 h. Five-day treatment lowered pressure progressively. Single oral doses of 3.2 and 10 mg/kg reduced blood pressure of conscious normotensive dogs. Diuretic pretreatment also enhanced the response. The antihypertensive action of SCH 31846 in SHRs was eliminated by nephrectomy, but not attenuated by indomethacin, indicating its dependency on renal renin but not on prostaglandin synthesis. Other studies using SHRs pointed to an absence of a central effect. SCH 31846 (1 mg/kg i.v.) decreased blood pressure and peripheral resistance of anesthetized dogs but did not alter cardiac output. Autonomic interactions were examined in normal and diuretic-pretreated SHRs and anesthetized dogs. SCH 31846 affected the response to sympathetic nerve stimulation and cardiovascular reflexes only minimally. It is concluded that SCH 31846 is a potent and long-lasting antihypertensive agent, the action of which is mediated, in all probability, by ACE inhibition.
doi_str_mv 10.1097/00005344-198307000-00022
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Oral administration of 0.3–3 mg/kg caused dose-related decreases in blood pressure in spontaneously hypertensive rats (SHRs). Pretreatment with a diuretic augmented the maximum hypotensive response attainable. Single doses (3 mg/kg) of SCH 31846 reduced pressure for over 24 h. Five-day treatment lowered pressure progressively. Single oral doses of 3.2 and 10 mg/kg reduced blood pressure of conscious normotensive dogs. Diuretic pretreatment also enhanced the response. The antihypertensive action of SCH 31846 in SHRs was eliminated by nephrectomy, but not attenuated by indomethacin, indicating its dependency on renal renin but not on prostaglandin synthesis. Other studies using SHRs pointed to an absence of a central effect. SCH 31846 (1 mg/kg i.v.) decreased blood pressure and peripheral resistance of anesthetized dogs but did not alter cardiac output. Autonomic interactions were examined in normal and diuretic-pretreated SHRs and anesthetized dogs. SCH 31846 affected the response to sympathetic nerve stimulation and cardiovascular reflexes only minimally. 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Oral administration of 0.3–3 mg/kg caused dose-related decreases in blood pressure in spontaneously hypertensive rats (SHRs). Pretreatment with a diuretic augmented the maximum hypotensive response attainable. Single doses (3 mg/kg) of SCH 31846 reduced pressure for over 24 h. Five-day treatment lowered pressure progressively. Single oral doses of 3.2 and 10 mg/kg reduced blood pressure of conscious normotensive dogs. Diuretic pretreatment also enhanced the response. The antihypertensive action of SCH 31846 in SHRs was eliminated by nephrectomy, but not attenuated by indomethacin, indicating its dependency on renal renin but not on prostaglandin synthesis. Other studies using SHRs pointed to an absence of a central effect. SCH 31846 (1 mg/kg i.v.) decreased blood pressure and peripheral resistance of anesthetized dogs but did not alter cardiac output. Autonomic interactions were examined in normal and diuretic-pretreated SHRs and anesthetized dogs. SCH 31846 affected the response to sympathetic nerve stimulation and cardiovascular reflexes only minimally. It is concluded that SCH 31846 is a potent and long-lasting antihypertensive agent, the action of which is mediated, in all probability, by ACE inhibition.</description><subject>Angiotensin-Converting Enzyme Inhibitors</subject><subject>Animals</subject><subject>Antihypertensive Agents</subject><subject>Blood Pressure - drug effects</subject><subject>Captopril - pharmacology</subject><subject>Dogs</subject><subject>Female</subject><subject>Hemodynamics - drug effects</subject><subject>Hydrochlorothiazide - pharmacology</subject><subject>Hypertension - physiopathology</subject><subject>Indoles - pharmacology</subject><subject>Indomethacin - pharmacology</subject><subject>Injections, Intraventricular</subject><subject>Male</subject><subject>Nephrectomy</subject><subject>Propanolamines - pharmacology</subject><subject>Rats</subject><subject>Reflex - drug effects</subject><subject>Renin - blood</subject><issn>0160-2446</issn><issn>1533-4023</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1983</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1PHDEMhiPUChban4CUE6cGnDjJzBxXKyhIiB4o5zAfGSbtbLIkM4uGX9-BXbjVkmVb9mtLjwmhHM45FNkFzKZQSsaLHCGbKza7EAdkwRUikyDwC1kA18CElPqIHKf0B4BLlelDcqh5gajVgjwu_eC6aWPjYH1yW0uX9eC2bphoaOn96poiz6X-QUt6Fzy7H_u2m5o49XTpn1x4F3m2Cn47b3D-iV7612lt6Y3vXOWGEL-Rr23ZJ_t9H0_Iw9Xl79U1u_3182a1vGW1BCVYLRQqrssKdMYxh0pVkFdNg6Wq9JzWvC1BFTznmRDIi7rSsmmzVkAhUQqJJ-Rst3cTw_No02DWLtW270tvw5hMDhpRiGwezHeDdQwpRduaTXTrMk6Gg3mDaz7gmk-45h3uLD3d3xirtW0-hXuac1_u-i-hH2xMf_vxxUbT2bIfOvO_n-E_NBKCmw</recordid><startdate>198307</startdate><enddate>198307</enddate><creator>Baum, Thomas</creator><creator>Sybertz, Edmund J</creator><creator>Watkins, Robert W</creator><creator>Ahn, Ho Sam</creator><creator>Nelson, Steven</creator><creator>Eynon, Emma</creator><creator>Vliet, Gary Vander</creator><creator>Pula, Kathryn K</creator><creator>Sabin, Crawford</creator><creator>Desiderio, Denise M</creator><creator>Becker, Frederick T</creator><creator>Vemulapalli, Subbarao</creator><general>Lippincott-Raven Publishers</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>7X8</scope></search><sort><creationdate>198307</creationdate><title>Antihypertensive Activity of SCH 31846, a Non-Sulfhydryl Angiotensin-Converting Enzyme Inhibitor</title><author>Baum, Thomas ; Sybertz, Edmund J ; Watkins, Robert W ; Ahn, Ho Sam ; Nelson, Steven ; Eynon, Emma ; Vliet, Gary Vander ; Pula, Kathryn K ; Sabin, Crawford ; Desiderio, Denise M ; Becker, Frederick T ; Vemulapalli, Subbarao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4052-c253516ab0671380b5b08bdd3a5b6b08c1fa059181722319cb64df7f209434243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1983</creationdate><topic>Angiotensin-Converting Enzyme Inhibitors</topic><topic>Animals</topic><topic>Antihypertensive Agents</topic><topic>Blood Pressure - drug effects</topic><topic>Captopril - pharmacology</topic><topic>Dogs</topic><topic>Female</topic><topic>Hemodynamics - drug effects</topic><topic>Hydrochlorothiazide - pharmacology</topic><topic>Hypertension - physiopathology</topic><topic>Indoles - pharmacology</topic><topic>Indomethacin - pharmacology</topic><topic>Injections, Intraventricular</topic><topic>Male</topic><topic>Nephrectomy</topic><topic>Propanolamines - pharmacology</topic><topic>Rats</topic><topic>Reflex - drug effects</topic><topic>Renin - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baum, Thomas</creatorcontrib><creatorcontrib>Sybertz, Edmund J</creatorcontrib><creatorcontrib>Watkins, Robert W</creatorcontrib><creatorcontrib>Ahn, Ho Sam</creatorcontrib><creatorcontrib>Nelson, Steven</creatorcontrib><creatorcontrib>Eynon, Emma</creatorcontrib><creatorcontrib>Vliet, Gary Vander</creatorcontrib><creatorcontrib>Pula, Kathryn K</creatorcontrib><creatorcontrib>Sabin, Crawford</creatorcontrib><creatorcontrib>Desiderio, Denise M</creatorcontrib><creatorcontrib>Becker, Frederick T</creatorcontrib><creatorcontrib>Vemulapalli, Subbarao</creatorcontrib><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>Journal of cardiovascular pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baum, Thomas</au><au>Sybertz, Edmund J</au><au>Watkins, Robert W</au><au>Ahn, Ho Sam</au><au>Nelson, Steven</au><au>Eynon, Emma</au><au>Vliet, Gary Vander</au><au>Pula, Kathryn K</au><au>Sabin, Crawford</au><au>Desiderio, Denise M</au><au>Becker, Frederick T</au><au>Vemulapalli, Subbarao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antihypertensive Activity of SCH 31846, a Non-Sulfhydryl Angiotensin-Converting Enzyme Inhibitor</atitle><jtitle>Journal of cardiovascular pharmacology</jtitle><addtitle>J Cardiovasc Pharmacol</addtitle><date>1983-07</date><risdate>1983</risdate><volume>5</volume><issue>4</issue><spage>655</spage><epage>667</epage><pages>655-667</pages><issn>0160-2446</issn><eissn>1533-4023</eissn><abstract>SUMMARYThe antihypertensive, hemodynamic, and autonomic actions of SCH 31846, a new, potent and long-acting non-sulfhydryl angiotensin-converting enzyme (ACE) inhibitor, were evaluated in several experimental preparations. Oral administration of 0.3–3 mg/kg caused dose-related decreases in blood pressure in spontaneously hypertensive rats (SHRs). Pretreatment with a diuretic augmented the maximum hypotensive response attainable. Single doses (3 mg/kg) of SCH 31846 reduced pressure for over 24 h. Five-day treatment lowered pressure progressively. Single oral doses of 3.2 and 10 mg/kg reduced blood pressure of conscious normotensive dogs. Diuretic pretreatment also enhanced the response. The antihypertensive action of SCH 31846 in SHRs was eliminated by nephrectomy, but not attenuated by indomethacin, indicating its dependency on renal renin but not on prostaglandin synthesis. Other studies using SHRs pointed to an absence of a central effect. SCH 31846 (1 mg/kg i.v.) decreased blood pressure and peripheral resistance of anesthetized dogs but did not alter cardiac output. Autonomic interactions were examined in normal and diuretic-pretreated SHRs and anesthetized dogs. 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source MEDLINE; Journals@Ovid LWW Legacy Archive; Journals@Ovid Complete; EZB-FREE-00999 freely available EZB journals
subjects Angiotensin-Converting Enzyme Inhibitors
Animals
Antihypertensive Agents
Blood Pressure - drug effects
Captopril - pharmacology
Dogs
Female
Hemodynamics - drug effects
Hydrochlorothiazide - pharmacology
Hypertension - physiopathology
Indoles - pharmacology
Indomethacin - pharmacology
Injections, Intraventricular
Male
Nephrectomy
Propanolamines - pharmacology
Rats
Reflex - drug effects
Renin - blood
title Antihypertensive Activity of SCH 31846, a Non-Sulfhydryl Angiotensin-Converting Enzyme Inhibitor
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