Endothelin A-receptor blockade in experimental diabetes improves glucose balance and gastrointestinal function

Author:

BALSIGER Bruno1,RICKENBACHER Andreas1,BODEN Penelope Jane2,BIECKER Erwin1,TSUI Janice3,DASHWOOD Michael3,REICHEN Jürg1,SHAW Sidney George2

Affiliation:

1. Clinical Pharmacology, University of Bern, Murtenstrasse 35, 3010 Bern, Switzerland

2. Department of Clinical Research, University of Bern, Murtenstrasse 35, 3010 Bern, Switzerland

3. The Royal Free and University College Medical School, University College London, Royal Free Campus, Pond Street, London NW3 2QG, U.K.

Abstract

Secondary complications of diabetes mellitus often involve gastrointestinal dysfunction. In the experimental Goto Kakizaki rat, a model of Type II diabetes, hyperglycaemia and reduced glucose clearance is associated with elevated plasma endothelin (ET)-1 levels and selective decreases in nitric oxide synthase in circular muscle, longitudinal muscle and neuronal elements of the gastrointestinal tract. Functionally, this is accompanied by decreased nitrergic relaxatory responses of jejunal longitudinal muscle to tetrodotoxin-sensitive electrical field stimulation. Long-term treatment with a selective ET A-type receptor antagonist, markedly reduced hyperglycaemia and restored plasma glucose clearance rates towards normal. This was associated with a restoration of NG-nitro-L-arginine methyl ester-sensitive relaxatory responses of jejunal longitudinal muscle to electrical field stimulation. The results indicate that beneficial effects of ETA receptor blockade on gastrointestinal function may result from an improvement in insulin sensitivity with concomitant reduction of the severity of hyperglycaemia. ETA receptor blockade may represent a new therapeutic principle for improving glucose tolerance in Type II diabetes and could be beneficial in alleviating or preventing hyperglycaemia-related secondary complications in this condition.

Publisher

Portland Press Ltd.

Subject

General Medicine

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