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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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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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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