Dinitrosyl iron complexes with glutathione as NO and NO+ donors

► Binuclear dinitrosyl iron complexes with glutathione are stable in strong acid solutions. ► Binuclear dinitrosyl iron complexes with glutathione can release both NO and NO+. ► Mononitrosyl iron complexes with non-thiol-ligands release only NO molecules. It has been found that heating of solutions...

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Veröffentlicht in:Nitric oxide 2013-02, Vol.29, p.4-16
Hauptverfasser: Borodulin, Rostislav R., Kubrina, Lyudmila N., Mikoyan, Vasak D., Poltorakov, Alexander P., Shvydkiy, Vyacheslav О., Burbaev, Dosymzhan Sh, Serezhenkov, Vladimir A., Yakhontova, Elena R., Vanin, Anatoly F.
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container_start_page 4
container_title Nitric oxide
container_volume 29
creator Borodulin, Rostislav R.
Kubrina, Lyudmila N.
Mikoyan, Vasak D.
Poltorakov, Alexander P.
Shvydkiy, Vyacheslav О.
Burbaev, Dosymzhan Sh
Serezhenkov, Vladimir A.
Yakhontova, Elena R.
Vanin, Anatoly F.
description ► Binuclear dinitrosyl iron complexes with glutathione are stable in strong acid solutions. ► Binuclear dinitrosyl iron complexes with glutathione can release both NO and NO+. ► Mononitrosyl iron complexes with non-thiol-ligands release only NO molecules. It has been found that heating of solutions of the binuclear form of dinitrosyl iron complexes (B-DNIC) with glutathione in a degassed Thunberg apparatus (рН 1.0, 70°С, 6h) results in their decomposition with a concomitant release of four gaseous NO molecules per one B-DNIC. Further injection of air into the Thunberg apparatus initiates fast oxidation of NO to NO2 and formation of two GS-NO molecules per one B-DNIC. Under similar conditions, the decomposition of B-DNIC solutions in the Thunberg apparatus in the presence of air is complete within 30–40min and is accompanied by formation of four GS-NO molecules per one B-DNIC. It is suggested that the latter events are determined by oxidation of B-DNIC iron and concominant release of four nitrosonium ions (NO+) from each complex. Binding of NO+ to thiol groups of glutathione provokes GS-NO synthesis. At neutral рН, decomposition of B-DNIC is initiated by strong iron chelators, viz., о-phenanthroline and N-methyl-d-glucamine dithiocarbamate (MGD). In the former case, the reaction occurs under anaerobic conditions (degassed Thunberg apparatus) and is accompanied by a release of four NO molecules from B-DNIC. Under identical conditions, MGD-induced decomposition of B-DNIC gives two EPR-active mononuclear mononitrosyl iron complexes with MGD (MNIC–MGD) able to incorporate two iron molecules and two NO molecules from each B-DNIC. The other two NO molecules released from B-DNIC (most probably, in the form of nitrosonium ions) bind to thiol groups of MGD to give corresponding S-nitrosothiols. Acidification of test solutions to рН 1.0 initiates hydrolysis of MGD and, as a consequence, decomposition of MNIC–MGD and the S-nitrosated form of MGD; the gaseous phase contains four NO molecules (as calculated per each B-DNIC). The data obtained testify to the ability of B-DNIC with glutathione (and, probably, of B-DNIC with other thiol-containing ligands) to release both NO molecules and nitrosonium ions upon their decomposition. As far as nitrosyl iron complexes with non-thiol-containing ligands predominantly represented by the mononuclear mononitrosyl iron form (MNIC) are concerned, their decomposition yields exclusively NO molecules.
doi_str_mv 10.1016/j.niox.2012.11.001
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It has been found that heating of solutions of the binuclear form of dinitrosyl iron complexes (B-DNIC) with glutathione in a degassed Thunberg apparatus (рН 1.0, 70°С, 6h) results in their decomposition with a concomitant release of four gaseous NO molecules per one B-DNIC. Further injection of air into the Thunberg apparatus initiates fast oxidation of NO to NO2 and formation of two GS-NO molecules per one B-DNIC. Under similar conditions, the decomposition of B-DNIC solutions in the Thunberg apparatus in the presence of air is complete within 30–40min and is accompanied by formation of four GS-NO molecules per one B-DNIC. It is suggested that the latter events are determined by oxidation of B-DNIC iron and concominant release of four nitrosonium ions (NO+) from each complex. Binding of NO+ to thiol groups of glutathione provokes GS-NO synthesis. At neutral рН, decomposition of B-DNIC is initiated by strong iron chelators, viz., о-phenanthroline and N-methyl-d-glucamine dithiocarbamate (MGD). In the former case, the reaction occurs under anaerobic conditions (degassed Thunberg apparatus) and is accompanied by a release of four NO molecules from B-DNIC. Under identical conditions, MGD-induced decomposition of B-DNIC gives two EPR-active mononuclear mononitrosyl iron complexes with MGD (MNIC–MGD) able to incorporate two iron molecules and two NO molecules from each B-DNIC. The other two NO molecules released from B-DNIC (most probably, in the form of nitrosonium ions) bind to thiol groups of MGD to give corresponding S-nitrosothiols. Acidification of test solutions to рН 1.0 initiates hydrolysis of MGD and, as a consequence, decomposition of MNIC–MGD and the S-nitrosated form of MGD; the gaseous phase contains four NO molecules (as calculated per each B-DNIC). The data obtained testify to the ability of B-DNIC with glutathione (and, probably, of B-DNIC with other thiol-containing ligands) to release both NO molecules and nitrosonium ions upon their decomposition. As far as nitrosyl iron complexes with non-thiol-containing ligands predominantly represented by the mononuclear mononitrosyl iron form (MNIC) are concerned, their decomposition yields exclusively NO molecules.</description><identifier>ISSN: 1089-8603</identifier><identifier>EISSN: 1089-8611</identifier><identifier>DOI: 10.1016/j.niox.2012.11.001</identifier><identifier>PMID: 23219858</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Dinitrosyl iron complexes ; Glutathione - chemistry ; Iron - chemistry ; Molecular Structure ; Nitric oxide ; Nitric Oxide - chemistry ; Nitric Oxide Donors - chemistry ; Nitrogen Oxides - chemistry ; Nitrosonium ion ; Oxidation-Reduction ; S-nitrosation</subject><ispartof>Nitric oxide, 2013-02, Vol.29, p.4-16</ispartof><rights>2012 Elsevier Inc.</rights><rights>Copyright © 2012 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-33996454f77b9c0d65929f308a87445cc6836d9ac51028d5a770313e50e405a73</citedby><cites>FETCH-LOGICAL-c356t-33996454f77b9c0d65929f308a87445cc6836d9ac51028d5a770313e50e405a73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.niox.2012.11.001$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23219858$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Borodulin, Rostislav R.</creatorcontrib><creatorcontrib>Kubrina, Lyudmila N.</creatorcontrib><creatorcontrib>Mikoyan, Vasak D.</creatorcontrib><creatorcontrib>Poltorakov, Alexander P.</creatorcontrib><creatorcontrib>Shvydkiy, Vyacheslav О.</creatorcontrib><creatorcontrib>Burbaev, Dosymzhan Sh</creatorcontrib><creatorcontrib>Serezhenkov, Vladimir A.</creatorcontrib><creatorcontrib>Yakhontova, Elena R.</creatorcontrib><creatorcontrib>Vanin, Anatoly F.</creatorcontrib><title>Dinitrosyl iron complexes with glutathione as NO and NO+ donors</title><title>Nitric oxide</title><addtitle>Nitric Oxide</addtitle><description>► Binuclear dinitrosyl iron complexes with glutathione are stable in strong acid solutions. ► Binuclear dinitrosyl iron complexes with glutathione can release both NO and NO+. ► Mononitrosyl iron complexes with non-thiol-ligands release only NO molecules. It has been found that heating of solutions of the binuclear form of dinitrosyl iron complexes (B-DNIC) with glutathione in a degassed Thunberg apparatus (рН 1.0, 70°С, 6h) results in their decomposition with a concomitant release of four gaseous NO molecules per one B-DNIC. Further injection of air into the Thunberg apparatus initiates fast oxidation of NO to NO2 and formation of two GS-NO molecules per one B-DNIC. Under similar conditions, the decomposition of B-DNIC solutions in the Thunberg apparatus in the presence of air is complete within 30–40min and is accompanied by formation of four GS-NO molecules per one B-DNIC. It is suggested that the latter events are determined by oxidation of B-DNIC iron and concominant release of four nitrosonium ions (NO+) from each complex. Binding of NO+ to thiol groups of glutathione provokes GS-NO synthesis. At neutral рН, decomposition of B-DNIC is initiated by strong iron chelators, viz., о-phenanthroline and N-methyl-d-glucamine dithiocarbamate (MGD). In the former case, the reaction occurs under anaerobic conditions (degassed Thunberg apparatus) and is accompanied by a release of four NO molecules from B-DNIC. Under identical conditions, MGD-induced decomposition of B-DNIC gives two EPR-active mononuclear mononitrosyl iron complexes with MGD (MNIC–MGD) able to incorporate two iron molecules and two NO molecules from each B-DNIC. The other two NO molecules released from B-DNIC (most probably, in the form of nitrosonium ions) bind to thiol groups of MGD to give corresponding S-nitrosothiols. Acidification of test solutions to рН 1.0 initiates hydrolysis of MGD and, as a consequence, decomposition of MNIC–MGD and the S-nitrosated form of MGD; the gaseous phase contains four NO molecules (as calculated per each B-DNIC). The data obtained testify to the ability of B-DNIC with glutathione (and, probably, of B-DNIC with other thiol-containing ligands) to release both NO molecules and nitrosonium ions upon their decomposition. As far as nitrosyl iron complexes with non-thiol-containing ligands predominantly represented by the mononuclear mononitrosyl iron form (MNIC) are concerned, their decomposition yields exclusively NO molecules.</description><subject>Dinitrosyl iron complexes</subject><subject>Glutathione - chemistry</subject><subject>Iron - chemistry</subject><subject>Molecular Structure</subject><subject>Nitric oxide</subject><subject>Nitric Oxide - chemistry</subject><subject>Nitric Oxide Donors - chemistry</subject><subject>Nitrogen Oxides - chemistry</subject><subject>Nitrosonium ion</subject><subject>Oxidation-Reduction</subject><subject>S-nitrosation</subject><issn>1089-8603</issn><issn>1089-8611</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kF9LwzAUxYMobk6_gA_SR0Fa703aNAVBZP6F4V70OWRp6jK6Ziatbt_ejk0ffTr3wjkHzo-Qc4QEAfn1ImmsWycUkCaICQAekCGCKGLBEQ__bmADchLCAgBSJvgxGVBGsRCZGJLbe9vY1ruwqSPrXRNpt1zVZm1C9G3befRRd61q59Y1JlIhep1Gqil7uYpK1zgfTslRpepgzvY6Iu-PD2_j53gyfXoZ301izTLexowVBU-ztMrzWaGh5FlBi4qBUCJP00xrLhgvC6UzBCrKTOU5MGQmA5NC_7ERudz1rrz77Exo5dIGbepaNcZ1QSIVOROUp9hb6c6q-1nBm0quvF0qv5EIcgtOLuQWnNyCk4iyB9eHLvb93Wxpyr_IL6necLMzmH7llzVeBm1No01pvdGtLJ39r_8H0g18ng</recordid><startdate>20130228</startdate><enddate>20130228</enddate><creator>Borodulin, Rostislav R.</creator><creator>Kubrina, Lyudmila N.</creator><creator>Mikoyan, Vasak D.</creator><creator>Poltorakov, Alexander P.</creator><creator>Shvydkiy, Vyacheslav О.</creator><creator>Burbaev, Dosymzhan Sh</creator><creator>Serezhenkov, Vladimir A.</creator><creator>Yakhontova, Elena R.</creator><creator>Vanin, Anatoly F.</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>20130228</creationdate><title>Dinitrosyl iron complexes with glutathione as NO and NO+ donors</title><author>Borodulin, Rostislav R. ; Kubrina, Lyudmila N. ; Mikoyan, Vasak D. ; Poltorakov, Alexander P. ; Shvydkiy, Vyacheslav О. ; Burbaev, Dosymzhan Sh ; Serezhenkov, Vladimir A. ; Yakhontova, Elena R. ; Vanin, Anatoly F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-33996454f77b9c0d65929f308a87445cc6836d9ac51028d5a770313e50e405a73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Dinitrosyl iron complexes</topic><topic>Glutathione - chemistry</topic><topic>Iron - chemistry</topic><topic>Molecular Structure</topic><topic>Nitric oxide</topic><topic>Nitric Oxide - chemistry</topic><topic>Nitric Oxide Donors - chemistry</topic><topic>Nitrogen Oxides - chemistry</topic><topic>Nitrosonium ion</topic><topic>Oxidation-Reduction</topic><topic>S-nitrosation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Borodulin, Rostislav R.</creatorcontrib><creatorcontrib>Kubrina, Lyudmila N.</creatorcontrib><creatorcontrib>Mikoyan, Vasak D.</creatorcontrib><creatorcontrib>Poltorakov, Alexander P.</creatorcontrib><creatorcontrib>Shvydkiy, Vyacheslav О.</creatorcontrib><creatorcontrib>Burbaev, Dosymzhan Sh</creatorcontrib><creatorcontrib>Serezhenkov, Vladimir A.</creatorcontrib><creatorcontrib>Yakhontova, Elena R.</creatorcontrib><creatorcontrib>Vanin, Anatoly F.</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>Nitric oxide</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Borodulin, Rostislav R.</au><au>Kubrina, Lyudmila N.</au><au>Mikoyan, Vasak D.</au><au>Poltorakov, Alexander P.</au><au>Shvydkiy, Vyacheslav О.</au><au>Burbaev, Dosymzhan Sh</au><au>Serezhenkov, Vladimir A.</au><au>Yakhontova, Elena R.</au><au>Vanin, Anatoly F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dinitrosyl iron complexes with glutathione as NO and NO+ donors</atitle><jtitle>Nitric oxide</jtitle><addtitle>Nitric Oxide</addtitle><date>2013-02-28</date><risdate>2013</risdate><volume>29</volume><spage>4</spage><epage>16</epage><pages>4-16</pages><issn>1089-8603</issn><eissn>1089-8611</eissn><abstract>► Binuclear dinitrosyl iron complexes with glutathione are stable in strong acid solutions. ► Binuclear dinitrosyl iron complexes with glutathione can release both NO and NO+. ► Mononitrosyl iron complexes with non-thiol-ligands release only NO molecules. It has been found that heating of solutions of the binuclear form of dinitrosyl iron complexes (B-DNIC) with glutathione in a degassed Thunberg apparatus (рН 1.0, 70°С, 6h) results in their decomposition with a concomitant release of four gaseous NO molecules per one B-DNIC. Further injection of air into the Thunberg apparatus initiates fast oxidation of NO to NO2 and formation of two GS-NO molecules per one B-DNIC. Under similar conditions, the decomposition of B-DNIC solutions in the Thunberg apparatus in the presence of air is complete within 30–40min and is accompanied by formation of four GS-NO molecules per one B-DNIC. It is suggested that the latter events are determined by oxidation of B-DNIC iron and concominant release of four nitrosonium ions (NO+) from each complex. Binding of NO+ to thiol groups of glutathione provokes GS-NO synthesis. At neutral рН, decomposition of B-DNIC is initiated by strong iron chelators, viz., о-phenanthroline and N-methyl-d-glucamine dithiocarbamate (MGD). In the former case, the reaction occurs under anaerobic conditions (degassed Thunberg apparatus) and is accompanied by a release of four NO molecules from B-DNIC. Under identical conditions, MGD-induced decomposition of B-DNIC gives two EPR-active mononuclear mononitrosyl iron complexes with MGD (MNIC–MGD) able to incorporate two iron molecules and two NO molecules from each B-DNIC. The other two NO molecules released from B-DNIC (most probably, in the form of nitrosonium ions) bind to thiol groups of MGD to give corresponding S-nitrosothiols. Acidification of test solutions to рН 1.0 initiates hydrolysis of MGD and, as a consequence, decomposition of MNIC–MGD and the S-nitrosated form of MGD; the gaseous phase contains four NO molecules (as calculated per each B-DNIC). The data obtained testify to the ability of B-DNIC with glutathione (and, probably, of B-DNIC with other thiol-containing ligands) to release both NO molecules and nitrosonium ions upon their decomposition. As far as nitrosyl iron complexes with non-thiol-containing ligands predominantly represented by the mononuclear mononitrosyl iron form (MNIC) are concerned, their decomposition yields exclusively NO molecules.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23219858</pmid><doi>10.1016/j.niox.2012.11.001</doi><tpages>13</tpages></addata></record>
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Dinitrosyl iron complexes
Glutathione - chemistry
Iron - chemistry
Molecular Structure
Nitric oxide
Nitric Oxide - chemistry
Nitric Oxide Donors - chemistry
Nitrogen Oxides - chemistry
Nitrosonium ion
Oxidation-Reduction
S-nitrosation
title Dinitrosyl iron complexes with glutathione as NO and NO+ donors
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