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Diazoxide Disposition and Effect on Vascular Resistance and Compliance in Dogs

SUMMARY The disposition and systemic vascular effects of bolus intravenous doses of diazoxide (3.75,7.5, and 15.0 mg/kg) were studied in anesthetized open-chest dogs. Blood flow (0) and right atrial pressure (Pra) were independently controlled by a right heart bypass. The late phase disposition half...

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Published in:Hypertension (Dallas, Tex. 1979) Tex. 1979), 1981-03, Vol.3 (2), p.225-232
Main Author: OGILVIE, RICHARD I
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description SUMMARY The disposition and systemic vascular effects of bolus intravenous doses of diazoxide (3.75,7.5, and 15.0 mg/kg) were studied in anesthetized open-chest dogs. Blood flow (0) and right atrial pressure (Pra) were independently controlled by a right heart bypass. The late phase disposition halflife (beta t Vt) of diazoxide averaged 3.4 ± 0.5 hrs (x ± SEM) with an apparent volume of distribution at steady state of 1.3 ± 0.1 liter/kg. There was a dose-related reduction in arterial pressure (Po) with an excellent correlation between plasma diazoxide concentrations and the reduction in P. during the post drug-distribution phase. Diazoxide increased vascular capacitance (53 ± 16,91 ± 10, and 134 ± 21 ml after 3.75,7.5, and 15.0 mg/kg respectively) as determined by volume changes (V) in the bypass reservoir at a constant 0 &°d Pr. Transient changes in blood volume following an acute decrease in Pr. at constant 0 showed that blood was draining from two vascular compartments with different time constantsa fast time-constant compartment with a time constant of 0.052 minutes before and 0.048 minutes after diazoxide and a slow time-constant compartment with a time constant of 0.552 minutes before and 0.501 minutes after diazoxide. The major change in arterial resistance after all doses occurred in the slow time-constant compartment without a dear dose response. Arterial resistance in the fast time-constant compartment was unchanged after diazoxide 3.75 mg/kg but was reduced by an extent similar to that in the slow compartment after 15.0 rag/kg (-42% ± 9% vs −42% ± 4%). After diazoxide 3.75 mg/kg, venous compliance of both the slow and fast time-constant compartments was increased. Larger doses of diazoxide further increased compliance of the slow time-constant compartment but reduced compliance of the fast compartment. When the circulation was considered as a single compartment, diazoxide was 4 to 6 times more active on arterial resistance than on venous compliance. When the circulation was considered as consisting of two compartments in parallel, the major effect of low doses of diazoxide was on both arterial and venous portions of vessels with a slow time constant for flow, presumably including the splanchnic circulation. Larger doses of diazoxide were required to reduce arterial resistance of vessels with a fast time constant for flow.
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Blood flow (0) and right atrial pressure (Pra) were independently controlled by a right heart bypass. The late phase disposition halflife (beta t Vt) of diazoxide averaged 3.4 ± 0.5 hrs (x ± SEM) with an apparent volume of distribution at steady state of 1.3 ± 0.1 liter/kg. There was a dose-related reduction in arterial pressure (Po) with an excellent correlation between plasma diazoxide concentrations and the reduction in P. during the post drug-distribution phase. Diazoxide increased vascular capacitance (53 ± 16,91 ± 10, and 134 ± 21 ml after 3.75,7.5, and 15.0 mg/kg respectively) as determined by volume changes (V) in the bypass reservoir at a constant 0 &amp;°d Pr. Transient changes in blood volume following an acute decrease in Pr. at constant 0 showed that blood was draining from two vascular compartments with different time constantsa fast time-constant compartment with a time constant of 0.052 minutes before and 0.048 minutes after diazoxide and a slow time-constant compartment with a time constant of 0.552 minutes before and 0.501 minutes after diazoxide. The major change in arterial resistance after all doses occurred in the slow time-constant compartment without a dear dose response. Arterial resistance in the fast time-constant compartment was unchanged after diazoxide 3.75 mg/kg but was reduced by an extent similar to that in the slow compartment after 15.0 rag/kg (-42% ± 9% vs −42% ± 4%). After diazoxide 3.75 mg/kg, venous compliance of both the slow and fast time-constant compartments was increased. Larger doses of diazoxide further increased compliance of the slow time-constant compartment but reduced compliance of the fast compartment. When the circulation was considered as a single compartment, diazoxide was 4 to 6 times more active on arterial resistance than on venous compliance. When the circulation was considered as consisting of two compartments in parallel, the major effect of low doses of diazoxide was on both arterial and venous portions of vessels with a slow time constant for flow, presumably including the splanchnic circulation. 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Blood flow (0) and right atrial pressure (Pra) were independently controlled by a right heart bypass. The late phase disposition halflife (beta t Vt) of diazoxide averaged 3.4 ± 0.5 hrs (x ± SEM) with an apparent volume of distribution at steady state of 1.3 ± 0.1 liter/kg. There was a dose-related reduction in arterial pressure (Po) with an excellent correlation between plasma diazoxide concentrations and the reduction in P. during the post drug-distribution phase. Diazoxide increased vascular capacitance (53 ± 16,91 ± 10, and 134 ± 21 ml after 3.75,7.5, and 15.0 mg/kg respectively) as determined by volume changes (V) in the bypass reservoir at a constant 0 &amp;°d Pr. Transient changes in blood volume following an acute decrease in Pr. at constant 0 showed that blood was draining from two vascular compartments with different time constantsa fast time-constant compartment with a time constant of 0.052 minutes before and 0.048 minutes after diazoxide and a slow time-constant compartment with a time constant of 0.552 minutes before and 0.501 minutes after diazoxide. The major change in arterial resistance after all doses occurred in the slow time-constant compartment without a dear dose response. Arterial resistance in the fast time-constant compartment was unchanged after diazoxide 3.75 mg/kg but was reduced by an extent similar to that in the slow compartment after 15.0 rag/kg (-42% ± 9% vs −42% ± 4%). After diazoxide 3.75 mg/kg, venous compliance of both the slow and fast time-constant compartments was increased. Larger doses of diazoxide further increased compliance of the slow time-constant compartment but reduced compliance of the fast compartment. When the circulation was considered as a single compartment, diazoxide was 4 to 6 times more active on arterial resistance than on venous compliance. When the circulation was considered as consisting of two compartments in parallel, the major effect of low doses of diazoxide was on both arterial and venous portions of vessels with a slow time constant for flow, presumably including the splanchnic circulation. Larger doses of diazoxide were required to reduce arterial resistance of vessels with a fast time constant for flow.</description><subject>Animals</subject><subject>Blood Circulation - drug effects</subject><subject>Blood Pressure - drug effects</subject><subject>Blood Volume - drug effects</subject><subject>Diazoxide - blood</subject><subject>Diazoxide - pharmacology</subject><subject>Dogs - physiology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Elasticity</subject><subject>Vascular Resistance - drug effects</subject><subject>Veins - drug effects</subject><subject>Venous Pressure - drug effects</subject><issn>0194-911X</issn><issn>1524-4563</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><recordid>eNo9kM1LAzEQxYMotVav3oQ9eds1k2S_jtJWKxQVUdFTSLOzNrq7qZtdqv71xrY4MAyP9-YdfoScAo0AErigEM1e7yMesYixeI8MIWYiFHHC98mQQi7CHODlkBw5904pCCHSARmkDBKepkNyOzHqx36ZAoOJcSvrTGdsE6imCKZliboLvHpWTveVaoMHdMZ1qtG4SYxtvarMRpommNg3d0wOSlU5PNndEXm6mj6OZ-H87vpmfDkPNU9jFpYLRrOsyHiu-UIVuRYCtU5LYEzlyOI4Ayg0g0xninNBGeSlUiIBhSgYcD4i59veVWs_e3SdrI3TWFWqQds7mcYJhRSED0bboG6tcy2WctWaWrXfEqj8AygpSA9QcsmkB-gfznbN_aLG4j--I-Z9sfXXtuqwdR9Vv8ZWLlFV3VJSP4IlWQh5BpR7FfoFxn8B-cp6hg</recordid><startdate>198103</startdate><enddate>198103</enddate><creator>OGILVIE, RICHARD I</creator><general>American Heart Association, Inc</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>198103</creationdate><title>Diazoxide Disposition and Effect on Vascular Resistance and Compliance in Dogs</title><author>OGILVIE, RICHARD I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3752-fb2088d839c3bad9c44ecc7f122a9e255811dc218c8a3340219faa461aee42133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1981</creationdate><topic>Animals</topic><topic>Blood Circulation - drug effects</topic><topic>Blood Pressure - drug effects</topic><topic>Blood Volume - drug effects</topic><topic>Diazoxide - blood</topic><topic>Diazoxide - pharmacology</topic><topic>Dogs - physiology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Elasticity</topic><topic>Vascular Resistance - drug effects</topic><topic>Veins - drug effects</topic><topic>Venous Pressure - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>OGILVIE, RICHARD I</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>Hypertension (Dallas, Tex. 1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>OGILVIE, RICHARD I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diazoxide Disposition and Effect on Vascular Resistance and Compliance in Dogs</atitle><jtitle>Hypertension (Dallas, Tex. 1979)</jtitle><addtitle>Hypertension</addtitle><date>1981-03</date><risdate>1981</risdate><volume>3</volume><issue>2</issue><spage>225</spage><epage>232</epage><pages>225-232</pages><issn>0194-911X</issn><eissn>1524-4563</eissn><abstract>SUMMARY The disposition and systemic vascular effects of bolus intravenous doses of diazoxide (3.75,7.5, and 15.0 mg/kg) were studied in anesthetized open-chest dogs. Blood flow (0) and right atrial pressure (Pra) were independently controlled by a right heart bypass. The late phase disposition halflife (beta t Vt) of diazoxide averaged 3.4 ± 0.5 hrs (x ± SEM) with an apparent volume of distribution at steady state of 1.3 ± 0.1 liter/kg. There was a dose-related reduction in arterial pressure (Po) with an excellent correlation between plasma diazoxide concentrations and the reduction in P. during the post drug-distribution phase. Diazoxide increased vascular capacitance (53 ± 16,91 ± 10, and 134 ± 21 ml after 3.75,7.5, and 15.0 mg/kg respectively) as determined by volume changes (V) in the bypass reservoir at a constant 0 &amp;°d Pr. Transient changes in blood volume following an acute decrease in Pr. at constant 0 showed that blood was draining from two vascular compartments with different time constantsa fast time-constant compartment with a time constant of 0.052 minutes before and 0.048 minutes after diazoxide and a slow time-constant compartment with a time constant of 0.552 minutes before and 0.501 minutes after diazoxide. The major change in arterial resistance after all doses occurred in the slow time-constant compartment without a dear dose response. Arterial resistance in the fast time-constant compartment was unchanged after diazoxide 3.75 mg/kg but was reduced by an extent similar to that in the slow compartment after 15.0 rag/kg (-42% ± 9% vs −42% ± 4%). After diazoxide 3.75 mg/kg, venous compliance of both the slow and fast time-constant compartments was increased. Larger doses of diazoxide further increased compliance of the slow time-constant compartment but reduced compliance of the fast compartment. When the circulation was considered as a single compartment, diazoxide was 4 to 6 times more active on arterial resistance than on venous compliance. When the circulation was considered as consisting of two compartments in parallel, the major effect of low doses of diazoxide was on both arterial and venous portions of vessels with a slow time constant for flow, presumably including the splanchnic circulation. Larger doses of diazoxide were required to reduce arterial resistance of vessels with a fast time constant for flow.</abstract><cop>United States</cop><pub>American Heart Association, Inc</pub><pmid>7216377</pmid><doi>10.1161/01.HYP.3.2.225</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Blood Circulation - drug effects
Blood Pressure - drug effects
Blood Volume - drug effects
Diazoxide - blood
Diazoxide - pharmacology
Dogs - physiology
Dose-Response Relationship, Drug
Elasticity
Vascular Resistance - drug effects
Veins - drug effects
Venous Pressure - drug effects
title Diazoxide Disposition and Effect on Vascular Resistance and Compliance in Dogs
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