Download e-book for iPad: Ciba Foundation Symposium 198 - P2 Purinoceptors: by CIBA Foundation Symposium

By CIBA Foundation Symposium

ISBN-10: 0470514906

ISBN-13: 9780470514900

ISBN-10: 0471961256

ISBN-13: 9780471961253

Many various pathological stipulations are at the moment less than research as healing goals of purines together with melanoma, cardiovascular stipulations, behavioural issues, irritation, immunoregulation, and neuroendocrine functionality. This booklet attracts jointly learn on all elements of P2 purinoceptors and discusses their use in several healing parts.

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Additional resources for Ciba Foundation Symposium 198 - P2 Purinoceptors: Localization, Function and Transduction Mechanisms

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J Physiol68:213-237 Dubyak G R 1991 Signal transduction by P2-purinergic receptors for extracellular ATP. Am J Respir Cell Mol Biol 4:295-300 Dunn PM, Blakeley AGH 1988 Suramin: a reversible P,-purinoceptor antagonist in the mouse vas deferens. Br J Pharmacol 93:243-245 Eccles J C 1964 The physiology of synapses. Springer-Verlag, Berlin Edwards FA, Gibb AJ, Colquhoun D 1992 ATP receptor-mediated synaptic currents in the central nervous system. Nature 359: 144-147 El-Moatassim C, Dornand J, Mani J C 1987 Extracellular ATP increases cytosolic free calcium in thymocytes and initiates the blastogenesis of the phorbol 12-myristate 13acetate-treated medullary population.

Figure 2 shows that there are two types of response to ATP and its analogues distinguishable in terms of mechanism and pharmacology. 450 . 150 01 0 I I 1 I I I 25 50 75 100 125 150 Bound (fmol/l06 cells) FIG. 1. Diadenosine tetraphosphate binding to adrenal preparations. Scatchard analysis of equilibrium of ['H]Ap,A binding to chromafin cells in culture. 0lpmol/mg protein) for the second binding site, respectively. (Inset A) Stacked representation of Ap,A structure. 7 Ci/mmol). Binding site densities were 11 fmol/mg tissue and 3 fmol/mg tissue for the adrenal gland medulla and cortex, respectively.

Burnurd: Because if Mg2+ or even Ca2+ ions are present, the ATPases will affect the result. Jacobson: Are you able to calculate the affinity from the kinetics? 4; the ki values for the other nucleotides are given in our chapter (Barnard et al 1996, this volume). I believe that degradation need not be a risk in the binding experiments on P2Y receptors, because we have done controls in which we have exposed these labelled compounds to the membranes in our divalent-cation-free medium and then run a chromatogram to find the percentage degraded.

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