کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2532811 | 1559033 | 2011 | 8 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Pharmacological characterization of zinc and copper interaction with the human alpha1A-adrenoceptor Pharmacological characterization of zinc and copper interaction with the human alpha1A-adrenoceptor](/preview/png/2532811.png)
Metal ions have a major role in human health, and interact with many classes of receptors including the G-protein coupled receptors. In the peripheral system, zinc mainly accumulates in the soft prostate organ and, with copper, influences prostate disease progression, from normal to hypertrophic or cancerous states. The development of these pathologies may be influenced by the α1A-adrenoceptor, the principal regulator of prostate tonicity. There is currently no information on possible interactions between metals and the α1A-adrenoceptor. We therefore studied the effects of several mono- and divalent ions on this receptor subtype using binding and functional experiments performed on expressed cloned human α1A-adrenoceptor. Regardless of the counter anion used, Zn2+ and Cu2+ interact with α1A-adrenoceptor with apparent affinities in the low micromolar range. In addition, using specific binding experiments, we established that these ions acted as negative allosteric ligands on prazosin/α1A-adrenoceptor interaction, but in a different manner from the allosteric modulator 5-(N-ethyl-N-isopropyl)-amiloride, suggesting distinct mode of interaction. In addition, the presence of Cu2+ weakly decreased epinephrine affinity, whereas the addition of Zn2+ shifted to the left the epinephrine binding curve, revealing a positive allosteric effect but only on half of the binding site. Finally, cell-based functional experiments demonstrated that Zn2+ and Cu2+ antagonized epinephrine activation in an insurmountable manner, by reducing agonist efficacy without any shift in the epinephrine activation curves. This study shows the interactions between metal ions and the α1A-adrenoceptor with affinities compatible with physiological concentrations and suggests that zinc and copper may have a biological role in prostate function.
Journal: European Journal of Pharmacology - Volume 655, Issues 1–3, 25 March 2011, Pages 1–8