The DOI matches its Crossref record; 44 of the 44 references it cites were found in a registry or an index.
Cyclic Guanosine Monophosphate Compartmentation in Rat Cardiac Myocytes
Open accessAbstract
Background— Cyclic guanosine monophosphate (cGMP) is the common second messenger for the cardiovascular effects of nitric oxide (NO) and natriuretic peptides, such as atrial or brain natriuretic peptide, which activate the soluble and particulate forms of guanylyl cyclase, respectively. However, natriuretic peptides and NO donors exert different effects on cardiac and vascular smooth muscle function. We therefore tested whether these differences are due to an intracellular compartmentation of cGMP and evaluated the role of phosphodiesterase (PDE) subtypes in this process. Methods and Results— Subsarcolemmal cGMP signals were monitored in adult rat cardiomyocytes by expression of the rat olfactory cyclic nucleotide–gated (CNG) channel α-subunit and recording of the associated cGMP-gated current ( I CNG ). Atrial natriuretic peptide (10 nmol/L) or brain natriuretic peptide (10 nmol/L) induced a clear activation of I CNG , whereas NO donors ( S -nitroso- N -acetyl-penicillamine, diethylamine NONOate, 3-morpholinosydnonimine, and spermine NO, all at 100 μmol/L) had little effect. The I CNG current was strongly potentiated by nonselective PDE inhibition with isobutyl methylxanthine (100 μmol/L) and by the PDE2 inhibitors erythro-9-(2-hydroxy-3-nonyl)adenine (10 μmol/L) and Bay 60-7550 (50 nmol/L). Surprisingly, sildenafil, a PDE5 inhibitor, produced a dose-dependent increase of I CNG activated by NO donors but had no effect (at 100 nmol/L) on the current elicited by atrial natriuretic peptide. Conclusions— These results indicate that in rat cardiomyocytes (1) the particulate cGMP pool is readily accessible at the plasma membrane, whereas the soluble pool is not; and (2) PDE5 controls the soluble but not the particulate pool, whereas the latter is under the exclusive control of PDE2. Differential spatiotemporal distributions of cGMP may therefore contribute to the specific effects of natriuretic peptides and NO donors on cardiac function.
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Cites
Cyclic Nucleotide-Gated Ion Channels
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Chronic inhibition of cyclic GMP phosphodiesterase 5A prevents and reverses cardiac hypertrophy
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The protein kinase A anchoring protein mAKAP coordinates two integrated cAMP effector pathways
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Cyclic GMP Phosphodiesterases and Regulation of Smooth Muscle Function
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mAKAP assembles a protein kinase A/PDE4 phosphodiesterase cAMP signaling module
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Ca2+ current is regulated by cyclic GMP-dependent protein kinase in mammalian cardiac myocytes.
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Self-citation
Cited by
Mammalian Cyclic Nucleotide Phosphodiesterases: Molecular Mechanisms and Physiological Functions
Francis, S. H., Blount, M. A., & Corbin, J. D. (2011) · Physiological Reviews · doi:10.1152/physrev.00030.2010 · Cited by 639
Phosphodiesterase 9A controls nitric-oxide-independent cGMP and hypertrophic heart disease
Lee, D. I., Zhu, G., Sasaki, T., Cho, G.-S., Hamdani, N., Holewinski, R., Jo, S.-H., Danner, T., Zhang, M., Rainer, P. P., et al. (2015) · Nature · doi:10.1038/nature14332 · Cited by 353
Immunohistochemical Localization of Phosphodiesterase 2A in Multiple Mammalian Species
Stephenson, D. T., Coskran, T. M., Wilhelms, M. B., Adamowicz, W. O., O'Donnell, M. M., Muravnick, K. B., Menniti, F. S., Kleiman, R. J., & Morton, D. (2009) · Journal of Histochemistry & Cytochemistry · doi:10.1369/jhc.2009.953471 · Cited by 289
Xu, X., Xiao, J.-C., Luo, L.-F., Wang, S., Zhang, J.-P., Huang, J.-J., Liu, M.-L., Liu, C.-G., Xu, K.-Q., Li, Y.-J., et al. (2008) · International Journal of Cardiology · doi:10.1016/j.ijcard.2007.08.041 · Cited by 53
Metadata
- Authors
- Castro, L. R. V., Verde, I., Cooper, D. M. F., & Fischmeister, R.
- Venue
- Circulation
- Published
- 2006-05-09
- Volume
- 113
- Issue
- 18
- Pages
- 2221-2228
- ISSN
- 0009-7322 (ISSN-L)
- 1524-4539
- OpenAlex
- W2064776178
- Cited by
- 274
- References
- 44
- FWCI
- 8.47
- Type
- journal article
- Language
- en
- Open access
- bronze
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