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Distribution of phosphodiesterase type 5 (PDE5) in the lateral wall of the guinea pig urinary bladder
Objective To study PDE5 localisation by visualising the product of phosphodiesterase type 5 (PDE5) inhibition, namely cGMP, to determine the site of action of inhibitors in the urinary bladder. Materials and Methods Bladders of nine male guinea pigs were dissected and treated in wells containing 2 m...
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Published in: | BJU international 2013-07, Vol.112 (2), p.246-257 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Objective
To study PDE5 localisation by visualising the product of phosphodiesterase type 5 (PDE5) inhibition, namely cGMP, to determine the site of action of inhibitors in the urinary bladder.
Materials and Methods
Bladders of nine male guinea pigs were dissected and treated in wells containing 2 mL Krebs' solution and 1 μM of the specific PDE5 inhibitor vardenafil at 36 °C for 30 min.
After stimulating tissues with 100 μM of the nitric oxide (NO) donor diethylamine‐NONOate for 10 min, the tissues were snap‐frozen and 9–10 μm sections were cut.
Sections were examined for cGMP immunoreactivity and also stained for vimentin, a marker for interstitial cells and the neuromarkers protein gene product 9.5 (PGP9.5), synaptic vesicle protein 2 (SV2), neurofilament (NF) and calcitonin gene‐related peptide (CGRP), using the two‐step indirect immunohistochemistry technique.
Results
After PDE5 inhibition, cGMP was found to be present in the urothelium, suburothelial interstitial cells and endothelium of blood vessels.
cGMP was not expressed in nerves positive for CGRP, NF and SV2, and was expressed only in very few efferent nerves positive for PGP9.5.
Conclusion
Our data show that the possible sites of action of PDE5 inhibition in the bladder are the urothelium, suburothelial interstitial cells and blood vessels, rather than the bladder nerve fibres. |
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ISSN: | 1464-4096 1464-410X |
DOI: | 10.1111/bju.12031 |