Influence of maximal vasodilatation on glucose and sodium blood-tissue transport in canine heart
Vascular conductance ( G = flow pressure ) and permeability-surface products ( PS) of sodium and glucose were measured in the control state and during continuous infusion of vasodilating drugs in the isolated spontaneously beating canine heart perfused with blood at constant flow. PS was determined...
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Veröffentlicht in: | Microvascular research 1973-11, Vol.6 (3), p.347-359 |
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creator | Durán, Walter N. Alvarez, Osvaldo A. Yudilevich, David L. |
description | Vascular conductance (
G =
flow
pressure
) and permeability-surface products (
PS) of sodium and glucose were measured in the control state and during continuous infusion of vasodilating drugs in the isolated spontaneously beating canine heart perfused with blood at constant flow.
PS was determined by means of the first-circulation multiple tracers dilution method. Mean control
G was 0.77 ml × min
−1 × mm Hg
−1 × 100 g. The extent of vasodilatation was assessed by the ratio
G-
drug
G-
control
:papaverine, mean ratio 3.70 (2.59–4.73); dipyridamole, 3.50 (1.67–5.88); norepinephrine, 2.65 (1.18–4.23); nitroglycerin, 2.27 (1.66–3.25). The ratio for maximal vasodilatation was estimated to be 4–5.
PS-Na and
PS-glucose increased in a graded fashion with vasodilatation. With maximal vasodilatation the greatest increase observed in
PS-Na was twofold, in
PS-glucose 2.4-fold. The increase in
PS most likely results from a change in capillary surface area. These data demonstrate a large reserve of capillary transport capacity and a wide range of possible control of transcapillary diffusion in the coronary microcirculation. |
doi_str_mv | 10.1016/0026-2862(73)90083-6 |
format | Article |
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G =
flow
pressure
) and permeability-surface products (
PS) of sodium and glucose were measured in the control state and during continuous infusion of vasodilating drugs in the isolated spontaneously beating canine heart perfused with blood at constant flow.
PS was determined by means of the first-circulation multiple tracers dilution method. Mean control
G was 0.77 ml × min
−1 × mm Hg
−1 × 100 g. The extent of vasodilatation was assessed by the ratio
G-
drug
G-
control
:papaverine, mean ratio 3.70 (2.59–4.73); dipyridamole, 3.50 (1.67–5.88); norepinephrine, 2.65 (1.18–4.23); nitroglycerin, 2.27 (1.66–3.25). The ratio for maximal vasodilatation was estimated to be 4–5.
PS-Na and
PS-glucose increased in a graded fashion with vasodilatation. With maximal vasodilatation the greatest increase observed in
PS-Na was twofold, in
PS-glucose 2.4-fold. The increase in
PS most likely results from a change in capillary surface area. These data demonstrate a large reserve of capillary transport capacity and a wide range of possible control of transcapillary diffusion in the coronary microcirculation.</description><identifier>ISSN: 0026-2862</identifier><identifier>EISSN: 1095-9319</identifier><identifier>DOI: 10.1016/0026-2862(73)90083-6</identifier><identifier>PMID: 4203475</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Biological Transport, Active ; Blood Pressure - drug effects ; Capillary Permeability - drug effects ; Chromium Radioisotopes ; Coronary Vessels - drug effects ; Diffusion ; Dipyridamole - pharmacology ; Dogs ; Glucose - metabolism ; Hematocrit ; Microcirculation ; Myocardium - metabolism ; Nitroglycerin - pharmacology ; Norepinephrine - pharmacology ; Papaverine - pharmacology ; Perfusion ; Radioisotopes ; Sodium - metabolism ; Sodium Isotopes ; Tritium ; Vascular Resistance - drug effects ; Vasodilator Agents - pharmacology</subject><ispartof>Microvascular research, 1973-11, Vol.6 (3), p.347-359</ispartof><rights>1973</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-3edef0d7c5eac7bd6431c22c82d05ccdb3fe9051cfdf60a7f813d6fe944bb6813</citedby><cites>FETCH-LOGICAL-c357t-3edef0d7c5eac7bd6431c22c82d05ccdb3fe9051cfdf60a7f813d6fe944bb6813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0026-2862(73)90083-6$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/4203475$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Durán, Walter N.</creatorcontrib><creatorcontrib>Alvarez, Osvaldo A.</creatorcontrib><creatorcontrib>Yudilevich, David L.</creatorcontrib><title>Influence of maximal vasodilatation on glucose and sodium blood-tissue transport in canine heart</title><title>Microvascular research</title><addtitle>Microvasc Res</addtitle><description>Vascular conductance (
G =
flow
pressure
) and permeability-surface products (
PS) of sodium and glucose were measured in the control state and during continuous infusion of vasodilating drugs in the isolated spontaneously beating canine heart perfused with blood at constant flow.
PS was determined by means of the first-circulation multiple tracers dilution method. Mean control
G was 0.77 ml × min
−1 × mm Hg
−1 × 100 g. The extent of vasodilatation was assessed by the ratio
G-
drug
G-
control
:papaverine, mean ratio 3.70 (2.59–4.73); dipyridamole, 3.50 (1.67–5.88); norepinephrine, 2.65 (1.18–4.23); nitroglycerin, 2.27 (1.66–3.25). The ratio for maximal vasodilatation was estimated to be 4–5.
PS-Na and
PS-glucose increased in a graded fashion with vasodilatation. With maximal vasodilatation the greatest increase observed in
PS-Na was twofold, in
PS-glucose 2.4-fold. The increase in
PS most likely results from a change in capillary surface area. These data demonstrate a large reserve of capillary transport capacity and a wide range of possible control of transcapillary diffusion in the coronary microcirculation.</description><subject>Animals</subject><subject>Biological Transport, Active</subject><subject>Blood Pressure - drug effects</subject><subject>Capillary Permeability - drug effects</subject><subject>Chromium Radioisotopes</subject><subject>Coronary Vessels - drug effects</subject><subject>Diffusion</subject><subject>Dipyridamole - pharmacology</subject><subject>Dogs</subject><subject>Glucose - metabolism</subject><subject>Hematocrit</subject><subject>Microcirculation</subject><subject>Myocardium - metabolism</subject><subject>Nitroglycerin - pharmacology</subject><subject>Norepinephrine - pharmacology</subject><subject>Papaverine - pharmacology</subject><subject>Perfusion</subject><subject>Radioisotopes</subject><subject>Sodium - metabolism</subject><subject>Sodium Isotopes</subject><subject>Tritium</subject><subject>Vascular Resistance - drug effects</subject><subject>Vasodilator Agents - pharmacology</subject><issn>0026-2862</issn><issn>1095-9319</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1973</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLxTAQhYMoen38A4WsRBfVPNq03QgivkBwo-uYJhONtMk1SUX_va334lIIDJlzZobzIXRIyRklVJwTwkTBGsFOan7aEtLwQmygBSVtVbSctpto8WfZQbspvRNCadWybbRdMsLLulqgl3tv-xG8BhwsHtSXG1SPP1UKxvUqq-yCx9N77UcdEmDlDZ61ccBdH4IpsktpBJyj8mkZYsbOY62884DfQMW8j7as6hMcrOseer65frq6Kx4eb--vLh8Kzas6FxwMWGJqXYHSdWdEyalmTDfMkEpr03ELLamotsYKomrbUG7E1CvLrhPTZw8dr_YuY_gYIWU5uKSh75WHMCbZMDoFbsVkLFdGHUNKEaxcxil0_JaUyBmsnKnJmZqsufwFK-exo_X-sRvA_A2tSU76xUqHKeSngyiTdjNX4yLoLE1w_x_4Aeo6idM</recordid><startdate>197311</startdate><enddate>197311</enddate><creator>Durán, Walter N.</creator><creator>Alvarez, Osvaldo A.</creator><creator>Yudilevich, David L.</creator><general>Elsevier 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>197311</creationdate><title>Influence of maximal vasodilatation on glucose and sodium blood-tissue transport in canine heart</title><author>Durán, Walter N. ; Alvarez, Osvaldo A. ; Yudilevich, David L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-3edef0d7c5eac7bd6431c22c82d05ccdb3fe9051cfdf60a7f813d6fe944bb6813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1973</creationdate><topic>Animals</topic><topic>Biological Transport, Active</topic><topic>Blood Pressure - drug effects</topic><topic>Capillary Permeability - drug effects</topic><topic>Chromium Radioisotopes</topic><topic>Coronary Vessels - drug effects</topic><topic>Diffusion</topic><topic>Dipyridamole - pharmacology</topic><topic>Dogs</topic><topic>Glucose - metabolism</topic><topic>Hematocrit</topic><topic>Microcirculation</topic><topic>Myocardium - metabolism</topic><topic>Nitroglycerin - pharmacology</topic><topic>Norepinephrine - pharmacology</topic><topic>Papaverine - pharmacology</topic><topic>Perfusion</topic><topic>Radioisotopes</topic><topic>Sodium - metabolism</topic><topic>Sodium Isotopes</topic><topic>Tritium</topic><topic>Vascular Resistance - drug effects</topic><topic>Vasodilator Agents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Durán, Walter N.</creatorcontrib><creatorcontrib>Alvarez, Osvaldo A.</creatorcontrib><creatorcontrib>Yudilevich, David L.</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>Microvascular research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Durán, Walter N.</au><au>Alvarez, Osvaldo A.</au><au>Yudilevich, David L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of maximal vasodilatation on glucose and sodium blood-tissue transport in canine heart</atitle><jtitle>Microvascular research</jtitle><addtitle>Microvasc Res</addtitle><date>1973-11</date><risdate>1973</risdate><volume>6</volume><issue>3</issue><spage>347</spage><epage>359</epage><pages>347-359</pages><issn>0026-2862</issn><eissn>1095-9319</eissn><abstract>Vascular conductance (
G =
flow
pressure
) and permeability-surface products (
PS) of sodium and glucose were measured in the control state and during continuous infusion of vasodilating drugs in the isolated spontaneously beating canine heart perfused with blood at constant flow.
PS was determined by means of the first-circulation multiple tracers dilution method. Mean control
G was 0.77 ml × min
−1 × mm Hg
−1 × 100 g. The extent of vasodilatation was assessed by the ratio
G-
drug
G-
control
:papaverine, mean ratio 3.70 (2.59–4.73); dipyridamole, 3.50 (1.67–5.88); norepinephrine, 2.65 (1.18–4.23); nitroglycerin, 2.27 (1.66–3.25). The ratio for maximal vasodilatation was estimated to be 4–5.
PS-Na and
PS-glucose increased in a graded fashion with vasodilatation. With maximal vasodilatation the greatest increase observed in
PS-Na was twofold, in
PS-glucose 2.4-fold. The increase in
PS most likely results from a change in capillary surface area. These data demonstrate a large reserve of capillary transport capacity and a wide range of possible control of transcapillary diffusion in the coronary microcirculation.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>4203475</pmid><doi>10.1016/0026-2862(73)90083-6</doi><tpages>13</tpages></addata></record> |
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source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Animals Biological Transport, Active Blood Pressure - drug effects Capillary Permeability - drug effects Chromium Radioisotopes Coronary Vessels - drug effects Diffusion Dipyridamole - pharmacology Dogs Glucose - metabolism Hematocrit Microcirculation Myocardium - metabolism Nitroglycerin - pharmacology Norepinephrine - pharmacology Papaverine - pharmacology Perfusion Radioisotopes Sodium - metabolism Sodium Isotopes Tritium Vascular Resistance - drug effects Vasodilator Agents - pharmacology |
title | Influence of maximal vasodilatation on glucose and sodium blood-tissue transport in canine heart |
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