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 |
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Zusammenfassung: | ► 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. |
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ISSN: | 1089-8603 1089-8611 |
DOI: | 10.1016/j.niox.2012.11.001 |