[3H]Sildenafil Binding to Phosphodiesterase-5 Is Specific, Kinetically Heterogeneous, and Stimulated by cGMP
| Autor: | James L. Weeks, Karl P. Kuhn, Layla F. Saidi, Jackie D. Corbin, Mitsi A. Blount, Yew Seng Jonathan Ho, Alfreda Beasley, James H. Hurley, Sharron H. Francis, Jun Kotera |
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| Rok vydání: | 2003 |
| Předmět: |
Male
Insecta Phosphodiesterase Inhibitors Sildenafil Stereochemistry Allosteric regulation Transfection Tritium Piperazines Sildenafil Citrate Radioligand Assay chemistry.chemical_compound 3' 5'-Cyclic-GMP Phosphodiesterases Animals Humans Drug Interactions Nucleotide Sulfones Binding site Purine metabolism Cyclic GMP Lung Cells Cultured Cyclic Nucleotide Phosphodiesterases Type 5 Pharmacology chemistry.chemical_classification Binding Sites CGMP binding Phosphoric Diester Hydrolases Binding protein respiratory tract diseases chemistry Purines cGMP-specific phosphodiesterase type 5 Molecular Medicine |
| Zdroj: | Molecular Pharmacology. 63:1364-1372 |
| ISSN: | 1521-0111 0026-895X |
| DOI: | 10.1124/mol.63.6.1364 |
| Popis: | Sildenafil (Viagra) potentiates penile erection by acting as a nonhydrolyzable analog of cGMP and competing with this nucleotide for catalysis by phosphodiesterase-5 (PDE5), but the characteristics of direct binding of radiolabeled sildenafil to PDE5 have not been determined. [3H]Sildenafil binding to PDE5 was retained when filtered through nitrocellulose or glass-fiber membranes. Binding was inhibited by excess sildenafil, 2-(2-methylpyridin-4-yl)methyl-4-(3,4,5-trimethoxyphenyl)-8-(pyrimidin-2-yl)methoxy-1,2-dihydro-1-oxo-2,7-naphthyridine-3-carboxylic acid methyl ester hydrochloride (T-0156), 3-isobutyl-1-methylxanthine, EDTA, or cGMP, but not by cAMP or 5'-GMP. PDE5 was the only [3H]sildenafil binding protein detected in human lung extract. Using purified recombinant PDE5, [3H]sildenafil exchange dissociation yielded two components with t1/2 values of 1 and 14 min and corresponding calculated KD values of 12 and 0.83 nM, respectively. This implied the existence of two conformers of the PDE5 catalytic site. [3H]Sildenafil binding isotherm of PDE5 indicated KD was 8.3 to 13.3 nM, and low cGMP decreased the KD to 4.8 nM but only slightly increased Bmax to a maximum of 0.61 mol/mol-subunit. Results suggest that these effects occur via cGMP binding to the allosteric cGMP binding sites of PDE5. Results imply that by inhibiting PDE5 and thereby increasing cGMP, sildenafil accentuates its own binding affinity for PDE5, which further elevates cGMP. The data also indicate that after physiological elevation, cGMP may directly stimulate the catalytic site by binding to the allosteric cGMP-binding sites of PDE5, thus causing negative feedback on this pathway. |
| Databáze: | OpenAIRE |
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