Literature DB >> 7284693

A test of the null equation for functional antagonism.

J Emmerson, D Mackay.   

Abstract

1 The quantitative model for functional antagonism and synergism has been tested by studying its ability to fit data obtained from the functional antagonism of (-)-isoprenaline by muscarinic agonists on guinea-pig isolated atria. 2 The general form of the null equation has been shown to fit the experimental curves satisfactorily. 3 Functional interaction between (-)-isoprenaline and muscarinic agonists on atria has been shown to be type I although there does seem to be a discrepancy between values of the functional affinity constants, KA1F and KA2F, estimated in two different ways. 4 The affinity constants, KA, of the muscarinic agonists for their receptors have been estimated by use of the selective irreversible antagonist propylbenzilylcholine mustard. The discrepancy between KAF (i.e. both KA1F and KA2F) and KA is small for pentyltrimethylammonium which is an agonist of low intrinsic efficacy. By contrast the discrepancy between KAF and KA is much greater for methylfurmethide and oxotremorine both of which have much higher intrinsic efficacies. These results are as predicted by the model. 5 It is suggested that the discrepancy between KA1F and KA2F may be due to the limited ability of the equation l/S omega = aI + bI/S alpha to describe quantitatively the relation between sequential stimuli. However, it is concluded that this complication need not interfere with the use of the model to study mechanisms and possible sites of functional interaction.

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Year:  1981        PMID: 7284693      PMCID: PMC2071831          DOI: 10.1111/j.1476-5381.1981.tb16782.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  4 in total

1.  The use of functional antagonism to determine whether beta-adrenoceptor agonists must have a lower efficacy than isoprenaline to be trachea-atria selective in vitro in guinea-pigs.

Authors:  S R O'Donnell; J C Wanstall
Journal:  Br J Pharmacol       Date:  1977-06       Impact factor: 8.739

2.  The model of functional interaction. I. Development and first check of a new model of functional synergism and antagonism.

Authors:  F G van den Brink
Journal:  Eur J Pharmacol       Date:  1973-06       Impact factor: 4.432

3.  The model of functional interaction. II. Experimental verification of a new model: the antagonism of beta-adrenoceptor stimulants and other agonists.

Authors:  F G van den Brink
Journal:  Eur J Pharmacol       Date:  1973-06       Impact factor: 4.432

4.  A general analysis of the receptor-drug interaction.

Authors:  D Mackay
Journal:  Br J Pharmacol Chemother       Date:  1966-01
  4 in total
  4 in total

1.  A comparison of effects measured with isotonic and isometric recording: II. Concentration-effect curves for physiological antagonists.

Authors:  R B Barlow; S M Bond; C Grant; D S McQueen; Z Yaqoob
Journal:  Br J Pharmacol       Date:  2001-08       Impact factor: 8.739

2.  Interactions between responses mediated by activation of adenosine A2 receptors and alpha 1-adrenoceptors in the rabbit isolated aorta.

Authors:  H L Wiener; G P Thalody; S Maayani
Journal:  Br J Pharmacol       Date:  1993-06       Impact factor: 8.739

3.  Extended concentration-response curves used to reflect full agonist efficacies and receptor occupancy-response coupling ranges.

Authors:  M J Lew
Journal:  Br J Pharmacol       Date:  1995-07       Impact factor: 8.739

4.  Experimental testing of Mackay's model for functional antagonism in the isolated costo-uterus of the rat.

Authors:  P J Henry; K M Lulich; J W Paterson
Journal:  Br J Pharmacol       Date:  1985-09       Impact factor: 8.739

  4 in total

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