The influence of affinity, efficacy, and slope factor on the estimates obtained by the receptorial responsiveness method (RRM): a computer simulation study

Author:

Grenczer Maria12345,Pinter Akos12345,Zsuga Judit12345,Kemeny-Beke Adam12345,Juhasz Bela12345,Szodoray Peter12345,Tosaki Arpad12345,Gesztelyi Rudolf12345

Affiliation:

1. Department of Pharmacology, Faculty of Pharmacy, University of Debrecen, P.O. Box 8, H-4012 Debrecen, Hungary.

2. Institute of Mathematics, Faculty of Science and Technology, University of Debrecen, P.O. Box 33, H-4010 Debrecen, Hungary.

3. Department of Neurology, Faculty of Medicine, University of Debrecen, P.O. Box 31, H-4012 Debrecen, Hungary.

4. Department of Ophthalmology, Faculty of Medicine, University of Debrecen, P.O. Box 30, H-4012 Debrecen, Hungary.

5. Institute of Immunology, Rikshospitalet, University of Oslo, Sognsvannsveien 20, 0027 Oslo, Norway.

Abstract

The receptorial responsiveness method (RRM) was proposed to characterize changes in the concentration of degradable agonists in the microenvironment of their receptors. The characterization is done by providing concentrations of a stable agonist for the same receptor that is equieffective with the change in concentration to be characterized. RRM is based on the analysis of concentration–effect (E/c) curves reflecting the simultaneous action of the degradable and the stable agonist. In the present study, we investigated whether dissimilar affinity and (or) efficacy of the coacting agonists as well as the steepness of the E/c curves influence the reliability of RRM. E/c curves were simulated based on the operational model and then analyzed with RRM. We found that dissimilarity in affinity of the coacting agonists did not affect the accuracy of RRM estimates. In contrast, accuracy of the estimation depended on the magnitude of the concentration to be assessed, the operational slope factor, and the operational efficacy ratio of the coacting agonists. However, our results suggest that proper choice of a stable agonist for a degradable one can help to ensure reliable results, since information about the change in concentration of a degradable agonist is otherwise difficult to obtain.

Publisher

Canadian Science Publishing

Subject

Physiology (medical),Pharmacology,General Medicine,Physiology

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