Journal article

Measuring oxidative burden and predicting pharmacological response in coronary artery disease patients with a novel direct activator of haem-free/oxidised sGC

I Ahrens, J Habersberger, N Baumlin, H Qian, BK Smith, JP Stasch, C Bode, HHHW Schmidt, K Peter

Atherosclerosis | ELSEVIER IRELAND LTD | Published : 2011

Abstract

Objective: The soluble guanylate cyclase (sGC) activator Cinaciguat (BAY 58-2667) represents a novel class of drugs that selectively activate oxidised sGC. The extent of oxidised sGC depends on the patient's oxidative burden. We here describe two platelet-based assays that allow determining the extent of oxidised sGC and thus provide a basis for an individualised pharmacotherapy. Methods/Results: Platelets obtained from patients with (n= 12) and without (n= 12) coronary artery disease (CAD) were examined by flow cytometry (P-selectin expression), and Western blots (vasodilator associated phosphoprotein, VASP-phosphorylation). Results were compared to maximal oxidation of sGC achieved by the ..

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University of Melbourne Researchers

Grants

Awarded by Cardiac Society of Australia and New Zealand


Funding Acknowledgements

This work was supported by the Deutsche Forschungsgemeinschaft [DFG AH 185/1-1 to I.A.], by the National Health and Medical Research Council of Australia [K.P, J.H., N.B., B.K.S., H.H.H.W.S.] and by the Cardiac Society of Australia and New Zealand [J.H.].