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Diethyldithiocarbamate potentiates the effects of protamine sulphate in the isolated rat uterus. Redox report : communications in free radical research [Redox Rep] Journal article

 
Orescanin-Dusić Z, Milovanović S, Blagojević D, Nikolić-Kokić A, Radojicić R, Spasojević I, Spasić M 
Diethyldithiocarbamate potentiates the effects of protamine sulphate in the isolated rat uterus. [Journal Article, Research Support, Non-U.S. Gov't]
Redox Rep 2009; 14(2):48-54.


Protamine sulphate causes potassium ion channel-mediated relaxation of spontaneous and calcium ion-induced contractions of the isolated rat uterus. Diethyldithiocarbamate (DDC) potentiated the effect of protamine sulphate. A mechanism for DDC's action was postulated on the basis of its interactions with divalent iron ions and Cu,Zn-SOD. DDC chelates divalent iron ions creating DDC-iron (Fe-DDC) complexes. Fe-DDC forms stable NO-Fe-DDC(2) complexes by NO scavenging and de-nitrosylation processes, which in combination with DDC (5 mM) provoke inhibition of Cu,Zn-SOD resulting in specific oxidative conditions culminating in potassium ion channel opening, membrane hyperpolarisation, inhibition of calcium ion influx and subsequent muscle relaxation. As Fe-DDC and NO-Fe-DDC(2) complexes exclude divalent iron ions from participating in the hydroxyl radical generating Fenton reaction, DDC can also prevent iron-related pathophysiological manifestations. Such permissive roles of DDC open the possibility for application of its pharmacological form (disulfiram) to a wider spectrum of pathophysiological conditions related to smooth muscles.



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