The Impact of ATP-Sensitive K+ Channel Subtype Selectivity of Insulin Secretagogues for the Coronary Vasculature and the Myocardium

U Quast, D Stephan, S Bieger, U Russ - Diabetes, 2004 - Am Diabetes Assoc
Insulin secretagogues (sulfonylureas and glinides) increase insulin secretion by closing the
ATP-sensitive K + channel (K ATP channel) in the pancreatic β-cell membrane. K ATP …

Do the K+ channel openers relax smooth muscle by opening K+ channels?

U Quast - Trends in Pharmacological Sciences, 1993 - Elsevier
… 40); however, at 10 mM Ba2+ (a concentration that induces maximum vascular tone), the
vasorelaxant effect of cromakalim is abolished (Quast, U., unpublished observations). The …

[HTML][HTML] Whole body radiotherapy: A TBI-guideline

U Quast - Journal of medical physics, 2006 - journals.lww.com
Total Body Irradiation (TBI) is one main component in the interdisciplinary treatment of widely
disseminated malignancies predominantly of haematopoietic diseases. Combined with …

Direct reading measurement of absorbed dose with plastic scintillators—the general concept and applications to ophthalmic plaque dosimetry

…, C Wieczorek, H Kolanoski, U Quast - Medical …, 1996 - Wiley Online Library
We have developed dosemeters based on plastic scintillators for a variety of applications in
radiation therapy. The dosemeters consist basically of a tissue‐substituting scintillator probe, …

Total body irradiation—review of treatment techniquesin Europe

U Quast - Radiotherapy and Oncology, 1987 - Elsevier
In treatment of acute leukaemia and other disseminated diseases, high dose total body
irradiation (TBI)combined with intensive chemotherapy and bone marrow transplantation (BMT) …

Glibenclamide binding to sulphonylurea receptor subtypes: dependence on adenine nucleotides

…, C Löffler‐Walz, U Quast - British journal of …, 2002 - Wiley Online Library
… Figure 1B shows the effect of ATP in the presence of the ARS using 5 u ml −1 creatine …
This possibility was tested by scaling up the ARS 10 fold (creatine kinase 50 u ml −1 , creatine …

Potassium channel openers: pharmacological and clinical aspects

U Quast - Fundamental & clinical pharmacology, 1992 - Wiley Online Library
Opening of plasmalemmal K+ channels leads to cellular hyperpolarization which, in excitable
tissues possessing voltage‐dependent Ca 2+ channels, prevents the opening of such …

[HTML][HTML] Selectivity of repaglinide and glibenclamide for the pancreatic over the cardiovascular KATP channels

D Stephan, M Winkler, P Kühner, U Russ, U Quast - Diabetologia, 2006 - Springer
Aims/hypothesis Sulfonylureas and glinides close beta cell ATP-sensitive K + (K ATP ) channels
to increase insulin release; the concomitant closure of cardiovascular K ATP channels, …

In vitro and in vivo comparison of two K+ channel openers, diazoxide and cromakalim, and their inhibition by glibenclamide.

U Quast, NS Cook - Journal of Pharmacology and Experimental …, 1989 - ASPET
Diazoxide caused an increase in 86Rb+ efflux from the rat aorta and portal vein and inhibited
spontaneous activity of the latter at concentrations 100 times higher than the K+ channel …

Cellular pharmacology of potassium channel openers in vascular smooth muscle.

U Quast, JM Guillon, I Cavero - Cardiovascular research, 1994 - europepmc.org
Potassium channel opening is a physiological mechanism which excitable cells exploit to
maintain or restore their resting state. Thus drugs that open vascular potassium channels have …