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H Carswell

Publications and source records attributed to H Carswell.

23 records · Page 2Linked to original sources

Beta-adrenoceptor heterogeneity in guinea-pig airways: comparison of functional and receptor labelling studies.

The distribution of beta-adrenoceptor subtypes in guinea-pig airways has been studied by radioligand binding assays and analysis of mechanical responses. Binding studies with the ligands [3H]-dihydroalprenolol and [125I]-cyanopindolol, revealed that beta-adrenoceptors were unevenly distributed throughout the airways with the highest density located in the parenchyma and the lowest density in the trachea. The relative proportion of beta 1:beta 2-adrenoceptor binding sites was assessed by computer-assisted analysis of the inhibition curves generated by selective agents. It was virtually identical in each region and in the order of 15:85%. beta-Adrenoceptor agonists caused concentration-dependent relaxations of both tracheal spirals and parenchymal lung strips. This response appeared to be mediated by both beta 1- and beta 2-adrenoceptors in tracheal spirals as the pA2 value for the beta 1-selective antagonist, atenolol, varied depending upon which agonist was used, and, in the presence of the beta 2-adrenoceptor antagonist ICI 118,551, noradrenaline and isoprenaline produced biphasic concentration-effect curves. In parenchymal lung strips only the one subtype was involved as antagonist pA2 values were not dependent on the agonist used and the properties were consistent with those expected for a beta 2-adrenoceptor.

Animals↗

Distribution and characteristics of histamine H1-receptors in guinea-pig airways identified by [3H]mepyramine.

The distribution and characteristics of histamine H1-receptors in various regions of guinea-pig airways have been studied using the antagonist [3H]mepyramine. A similar density of specific [3H]mepyramine sites was found in trachea, bronchi and parenchyma and these sites possessed pharmacological properties expected of a histamine H1-receptor. In addition, there was a large component of [3H]mepyramine binding that did not show stereoselectivity towards the isomers of chlorpheniramine and as such cannot be considered to represent binding to an H1-receptor. This non-specific component accounted for approximately 80% of total [3H]mepyramine binding when assays were performed in Tris-HCl buffer but was considerably reduced by the presence of sodium ions in the incubation buffer. The present results do not confirm previous reports on the heterogeneity of histamine H1-receptors in guinea-pig lung and suggest that this may, in part, be due to difficulties in accurately assessing true receptor specific binding.

Aminopyridines↗