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The Pharmaceutical Journal Vol 267 No 7172 p633-638
3 November 2001

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Interactions between nicorandil and sulphonylureas highlighted

Sulphonylureas can cause potentially harmful interactions with the potassium channel activator nicorandil (Ikorel), say researchers.

Dr Frank Reimann, department of clinical biochemistry, Addenbrooke's Hospital, Cambridge, and colleagues have demonstrated in an in vitro system that the activity of nicorandil is severely impaired by glimepiride and glibenclamide. However, its activity is unaffected by gliclazide, which is a more selective sulphonylurea, they say.

The researchers point out that nicorandil is increasingly used for the treatment of angina and, because the incidence of angina and type 2 diabetes comorbidity is high, polypharmacy with nicorandil and sulphonylureas is likely. Sulphonylureas stimulate insulin secretion by binding to sulphonylurea receptors in the ATP-sensitive potassium (KATP) channels in beta cells. Certain sulphonylureas block KATP channels in both pancreatic and cardiac beta cells. In contrast, gliclazide is highly specific to pancreatic beta cells and has little effect on cardiac KATP channels.

Dr Fiona Gribble, a co-author of the research, commented: "If you have patients who are being treated with the anti-anginal drug nicorandil then it is essential you use a drug that [is specific to pancreatic cells], such as gliclazide."

The study is published in Diabetes (2001;50:2253).

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