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Kinetics of Nitric Oxide Liberation by 3,4-Dihydro-1,2-Diazete 1,2-Dioxides and Their Vasodilatory Properties in Vitro and in Vivo
Derivatives of 3,4-dihydro-1,2-diazete 1,2-dioxides (DD) have been investigated as NO donors in vitro and in vivo. Using nitronylnitroxides as spin traps for NO, these compounds were shown to decompose in water solutions al physiological pH and temperature, producing two molecules of NO per one DD m...
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Published in: | Biochemical and biophysical research communications 1995-09, Vol.214 (3), p.1023-1032 |
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container_title | Biochemical and biophysical research communications |
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creator | Utepbergenov, D.I. Khramtsov, V.V. Vlassenko, L.P. Markel, A.L. Mazhukin, D.G. Tikhonov, A.Y. Volodarsky, L.B. |
description | Derivatives of 3,4-dihydro-1,2-diazete 1,2-dioxides (DD) have been investigated as NO donors
in vitro and
in vivo. Using nitronylnitroxides as spin traps for NO, these compounds were shown to decompose in water solutions al physiological pH and temperature, producing two molecules of NO per one DD molecule. Rate constants of DD decomposition were found to be in the range from 10
−8 to 6.5×10
−7 c(
−1) in water and between 3×10
−7 and 1.6×10
−5 c
−1 in dimethylsulfoxide.
In vitro experiments performed with perfused rat tail artery showed that some of DD derivatives are highly effective vasodilators in concentrations from 5 to 80 μM while standard NO donor 3-(4-morpholino)-sydnonimine, SIN-1, does not lead to arterial vasodilatation in these concentrations. Significant (up to 30%) decrease of systolic arterial blood pressure was observed in hereditary hypertensive rats (ISIAH-strain) when some of DD were injected intraperitoneally in doses 40-200 μ/kg b.w., while the same effect of trinitroglycerin, TNG, was found at much higher dose equal to 900 μg/kg b.w. |
doi_str_mv | 10.1006/bbrc.1995.2388 |
format | article |
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in vitro and
in vivo. Using nitronylnitroxides as spin traps for NO, these compounds were shown to decompose in water solutions al physiological pH and temperature, producing two molecules of NO per one DD molecule. Rate constants of DD decomposition were found to be in the range from 10
−8 to 6.5×10
−7 c(
−1) in water and between 3×10
−7 and 1.6×10
−5 c
−1 in dimethylsulfoxide.
In vitro experiments performed with perfused rat tail artery showed that some of DD derivatives are highly effective vasodilators in concentrations from 5 to 80 μM while standard NO donor 3-(4-morpholino)-sydnonimine, SIN-1, does not lead to arterial vasodilatation in these concentrations. Significant (up to 30%) decrease of systolic arterial blood pressure was observed in hereditary hypertensive rats (ISIAH-strain) when some of DD were injected intraperitoneally in doses 40-200 μ/kg b.w., while the same effect of trinitroglycerin, TNG, was found at much higher dose equal to 900 μg/kg b.w.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1006/bbrc.1995.2388</identifier><identifier>PMID: 7575505</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Arteries - drug effects ; Arteries - physiology ; Cyclic N-Oxides - chemical synthesis ; Cyclic N-Oxides - chemistry ; Cyclic N-Oxides - pharmacology ; Dose-Response Relationship, Drug ; Electron Spin Resonance Spectroscopy ; Indicators and Reagents ; Kinetics ; Magnetic Resonance Spectroscopy ; Molecular Conformation ; Molecular Structure ; Muscle, Smooth, Vascular - drug effects ; Muscle, Smooth, Vascular - physiology ; Nitric Oxide ; Nitroglycerin - pharmacology ; Rats ; Rats, Inbred SHR ; Structure-Activity Relationship ; Systole - drug effects ; Tail - blood supply ; Vasodilator Agents - chemistry ; Vasodilator Agents - pharmacology</subject><ispartof>Biochemical and biophysical research communications, 1995-09, Vol.214 (3), p.1023-1032</ispartof><rights>1995 Academic Press</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c339t-3a4027923a0d09fc4b62c93a73157102e4e012ab090adfc8e716e0117480c7823</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7575505$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Utepbergenov, D.I.</creatorcontrib><creatorcontrib>Khramtsov, V.V.</creatorcontrib><creatorcontrib>Vlassenko, L.P.</creatorcontrib><creatorcontrib>Markel, A.L.</creatorcontrib><creatorcontrib>Mazhukin, D.G.</creatorcontrib><creatorcontrib>Tikhonov, A.Y.</creatorcontrib><creatorcontrib>Volodarsky, L.B.</creatorcontrib><title>Kinetics of Nitric Oxide Liberation by 3,4-Dihydro-1,2-Diazete 1,2-Dioxides and Their Vasodilatory Properties in Vitro and in Vivo</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Derivatives of 3,4-dihydro-1,2-diazete 1,2-dioxides (DD) have been investigated as NO donors
in vitro and
in vivo. Using nitronylnitroxides as spin traps for NO, these compounds were shown to decompose in water solutions al physiological pH and temperature, producing two molecules of NO per one DD molecule. Rate constants of DD decomposition were found to be in the range from 10
−8 to 6.5×10
−7 c(
−1) in water and between 3×10
−7 and 1.6×10
−5 c
−1 in dimethylsulfoxide.
In vitro experiments performed with perfused rat tail artery showed that some of DD derivatives are highly effective vasodilators in concentrations from 5 to 80 μM while standard NO donor 3-(4-morpholino)-sydnonimine, SIN-1, does not lead to arterial vasodilatation in these concentrations. Significant (up to 30%) decrease of systolic arterial blood pressure was observed in hereditary hypertensive rats (ISIAH-strain) when some of DD were injected intraperitoneally in doses 40-200 μ/kg b.w., while the same effect of trinitroglycerin, TNG, was found at much higher dose equal to 900 μg/kg b.w.</description><subject>Animals</subject><subject>Arteries - drug effects</subject><subject>Arteries - physiology</subject><subject>Cyclic N-Oxides - chemical synthesis</subject><subject>Cyclic N-Oxides - chemistry</subject><subject>Cyclic N-Oxides - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Electron Spin Resonance Spectroscopy</subject><subject>Indicators and Reagents</subject><subject>Kinetics</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Molecular Conformation</subject><subject>Molecular Structure</subject><subject>Muscle, Smooth, Vascular - drug effects</subject><subject>Muscle, Smooth, Vascular - physiology</subject><subject>Nitric Oxide</subject><subject>Nitroglycerin - pharmacology</subject><subject>Rats</subject><subject>Rats, Inbred SHR</subject><subject>Structure-Activity Relationship</subject><subject>Systole - drug effects</subject><subject>Tail - blood supply</subject><subject>Vasodilator Agents - chemistry</subject><subject>Vasodilator Agents - pharmacology</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><recordid>eNp1kE1vEzEQhi0EKqFw5YbkE6duGNu78fqIWr5ERDmUipvltWfVQck62E5FOPLL8TYRN04ee555rXkYeylgKQBWb4Yh-aUwpltK1feP2EKAgUYKaB-zBVSikUZ8f8qe5fwDQIh2Zc7Yme5010G3YH8-04SFfOZx5F-oJPL8-hcF5GsaMLlCceLDgauLtrmiu0NIsREXstbuNxbkxzrOE5m7KfCbO6TEb12OgTauxHTgX1PcYSpUCZr4bf0kPqAPl_v4nD0Z3Sbji9N5zr69f3dz-bFZX3_4dPl23XilTGmUa0FqI5WDAGb07bCS3iinlei0AIktgpBuqOu7MPoetVjVF6HbHrzupTpnr4-5uxR_7jEXu6XscbNxE8Z9trpKEb1uK7g8gj7FnBOOdpdo69LBCrCzdDtLt7N0O0uvA69Oyfthi-EffrJc-_2xj3W9e8JksyecPAZK6IsNkf4X_RdF4Y8K</recordid><startdate>19950925</startdate><enddate>19950925</enddate><creator>Utepbergenov, D.I.</creator><creator>Khramtsov, V.V.</creator><creator>Vlassenko, L.P.</creator><creator>Markel, A.L.</creator><creator>Mazhukin, D.G.</creator><creator>Tikhonov, A.Y.</creator><creator>Volodarsky, L.B.</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>19950925</creationdate><title>Kinetics of Nitric Oxide Liberation by 3,4-Dihydro-1,2-Diazete 1,2-Dioxides and Their Vasodilatory Properties in Vitro and in Vivo</title><author>Utepbergenov, D.I. ; Khramtsov, V.V. ; Vlassenko, L.P. ; Markel, A.L. ; Mazhukin, D.G. ; Tikhonov, A.Y. ; Volodarsky, L.B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c339t-3a4027923a0d09fc4b62c93a73157102e4e012ab090adfc8e716e0117480c7823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Arteries - drug effects</topic><topic>Arteries - physiology</topic><topic>Cyclic N-Oxides - chemical synthesis</topic><topic>Cyclic N-Oxides - chemistry</topic><topic>Cyclic N-Oxides - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Electron Spin Resonance Spectroscopy</topic><topic>Indicators and Reagents</topic><topic>Kinetics</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Molecular Conformation</topic><topic>Molecular Structure</topic><topic>Muscle, Smooth, Vascular - drug effects</topic><topic>Muscle, Smooth, Vascular - physiology</topic><topic>Nitric Oxide</topic><topic>Nitroglycerin - pharmacology</topic><topic>Rats</topic><topic>Rats, Inbred SHR</topic><topic>Structure-Activity Relationship</topic><topic>Systole - drug effects</topic><topic>Tail - blood supply</topic><topic>Vasodilator Agents - chemistry</topic><topic>Vasodilator Agents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Utepbergenov, D.I.</creatorcontrib><creatorcontrib>Khramtsov, V.V.</creatorcontrib><creatorcontrib>Vlassenko, L.P.</creatorcontrib><creatorcontrib>Markel, A.L.</creatorcontrib><creatorcontrib>Mazhukin, D.G.</creatorcontrib><creatorcontrib>Tikhonov, A.Y.</creatorcontrib><creatorcontrib>Volodarsky, L.B.</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>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Utepbergenov, D.I.</au><au>Khramtsov, V.V.</au><au>Vlassenko, L.P.</au><au>Markel, A.L.</au><au>Mazhukin, D.G.</au><au>Tikhonov, A.Y.</au><au>Volodarsky, L.B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Kinetics of Nitric Oxide Liberation by 3,4-Dihydro-1,2-Diazete 1,2-Dioxides and Their Vasodilatory Properties in Vitro and in Vivo</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>1995-09-25</date><risdate>1995</risdate><volume>214</volume><issue>3</issue><spage>1023</spage><epage>1032</epage><pages>1023-1032</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Derivatives of 3,4-dihydro-1,2-diazete 1,2-dioxides (DD) have been investigated as NO donors
in vitro and
in vivo. Using nitronylnitroxides as spin traps for NO, these compounds were shown to decompose in water solutions al physiological pH and temperature, producing two molecules of NO per one DD molecule. Rate constants of DD decomposition were found to be in the range from 10
−8 to 6.5×10
−7 c(
−1) in water and between 3×10
−7 and 1.6×10
−5 c
−1 in dimethylsulfoxide.
In vitro experiments performed with perfused rat tail artery showed that some of DD derivatives are highly effective vasodilators in concentrations from 5 to 80 μM while standard NO donor 3-(4-morpholino)-sydnonimine, SIN-1, does not lead to arterial vasodilatation in these concentrations. Significant (up to 30%) decrease of systolic arterial blood pressure was observed in hereditary hypertensive rats (ISIAH-strain) when some of DD were injected intraperitoneally in doses 40-200 μ/kg b.w., while the same effect of trinitroglycerin, TNG, was found at much higher dose equal to 900 μg/kg b.w.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>7575505</pmid><doi>10.1006/bbrc.1995.2388</doi><tpages>10</tpages></addata></record> |
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source | ScienceDirect Journals |
subjects | Animals Arteries - drug effects Arteries - physiology Cyclic N-Oxides - chemical synthesis Cyclic N-Oxides - chemistry Cyclic N-Oxides - pharmacology Dose-Response Relationship, Drug Electron Spin Resonance Spectroscopy Indicators and Reagents Kinetics Magnetic Resonance Spectroscopy Molecular Conformation Molecular Structure Muscle, Smooth, Vascular - drug effects Muscle, Smooth, Vascular - physiology Nitric Oxide Nitroglycerin - pharmacology Rats Rats, Inbred SHR Structure-Activity Relationship Systole - drug effects Tail - blood supply Vasodilator Agents - chemistry Vasodilator Agents - pharmacology |
title | Kinetics of Nitric Oxide Liberation by 3,4-Dihydro-1,2-Diazete 1,2-Dioxides and Their Vasodilatory Properties in Vitro and in Vivo |
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