Phosphodiesterase inhibitors, and

Alprostadil is approved as monotherapy for the management of ED. It is generally prescribed after failure of VEDs and phosphodiesterase inhibitors and for patients who cannot use these therapies. Of the available routes, the intracavern os al route is preferred over the intraurethral route because of better efficacy. [Pg.955]

A recent report from the U. K. deals with 1,4-bis(oxodihydropyridazin-yl)benzenes and congeners which are also potent phosphodiesterase inhibitors and inodilators [159], This investigation, together with computer-aided modelling studies on various phosphodiesterase III inhibitors [160], may well stimulate the rational design of additional pyridazine-derived inodilators. [Pg.151]

It is believed that theophylline can inhibit phosphodiesterase, which in turn can lead to elevated levels of cellular cyclic adenosine monophosphate, and subsequently, to the weakening of smooth musculature of the respiratory tract. However, theophylline is not a powerful phosphodiesterase inhibitor, and the necessary concentrations for this cannot be achieved in vivo. [Pg.315]

Compound 2 is a potent cyclic AMP phosphodiesterase inhibitor, and can be prepared in almost quantitative yield by treatment of 1 with 1.1 equivalents of sodium methoxide in refluxing methanol for 15-30 minutes. When either 1 or 2 is refluxed with excess of sodium methoxide in methanol, however, the quinoline derivative 3 is obtained in 92% yield. [Pg.118]

Otto-Bruc, A., Antonny, B., Vuong, T. M., Chardin, P., and Chabre, M. (1993). Interaction between the retinal cyclic GMP phosphodiesterase inhibitor and transducin. Kinetics and affinity studies. Biochemistry 32, 8636-8645. [Pg.60]

Gershengorn et al. [9] found in thyrotropic tumor cells in culture that cAMP analogues, phosphodiesterase inhibitors and cholera toxin caused an increase in TSH release that was additive to that of TRH, that there was no correlation between TSH release and cAMP levels and that there was no change in binding of cAMP to protein kinase, suggesting that cAMP is not the physiological mediator of TRH-in-duced TSH release. [Pg.114]

Herling and Bickel (1986) showed that gastric acid secretion in stomach-lumen perfused rats can be stimulated in vivo on the subreceptor level by IBMX (phosphodiesterase inhibitor) and forskolin (non-receptor activation of the adenylate cyclase). H+/K+-ATPase inhibitors and H2-antagonists show, according to their different modes of action, also a different inhibitory profile in this assay. [Pg.155]

Benzylisoquinolines (IQ,-CH2-Phe) Ethaverine and laudanosine (L-type Ca2+ channel blockers from opium) papaverine (cAMP phosphodiesterase inhibitor and smooth muscle relaxant derived from opium and Rauwolfia serpentina (Apocynaceae)) protopine (MD-Phe C9N Phe-MD) opium-derived smooth muscle relaxant) (+)-reticuline (opium-derived adrenergic receptor ligand and hair growth accelerant). [Pg.12]

Simple chromones (Phe ] y-pyran-4-one) include the glucoside biflorin (a cAMP phosphodiesterase inhibitor and free radical scavenger) and the 2-phenoxychromone capillarisin (an aldose reductase inhibitor) as well as a number of variously cytotoxic and antimicrobial compounds. [Pg.27]

Q10 Other bronchodilator agents include nebulized ipratropium. Ipratropium is a muscarinic receptor antagonist that helps to relax bronchial smooth muscle which has contracted via parasympathetic stimulation. The xanthines theophylline and aminophylline (theophylline ethylenediamine) are alternative bronchodilator agents. These agents may act as phosphodiesterase inhibitors and, although they have been used as bronchodilators for many years, adverse CNS, GI and cardiovascular effects may limit their usefulness. [Pg.208]

Cafleine, theobromine and theophylline, and related methylxanthine compounds, are mild stimulants and have everyday use, e.g. in tea. coffee, chocolate and some soft drinks. Methylxanthines work in part as PHOSPHODIESTERASE INHIBITORS and in part as antagonists at P,-purinoceptors (see ADENOSINE RECEPTOR ANTAGONISTS). [Pg.81]

The other major agents used in heart failure include diuretics, ACE inhibitors, (3,-selective sympa-thomimetics, (3-blockers, phosphodiesterase inhibitors, and vasodilators. [Pg.124]

Several newer approaches to antiplatelet drug development have been recently discovered (122). These include inhibitions of the vWf/GPIb interaction, the platelet/collagen interaction, and the thrombin-induced platelet activation. Other approaches to platelet inhibition include the use of serotonin antagonists (because serotonin induces platelet aggregation), nitric oxide-donating antiplatelet agents, phosphodiesterase inhibitors, and inducers of adenyl cyclase. [Pg.1243]

However, the bronchodilation which is easily demonstrated in the asthmatic is not evident in CB. Nevertheless, the bronchitic with airways obstruction will report improvement of exercise capability with effective theophylline therapy. Theophylline is a phosphodiesterase inhibitor and results in a decreased breakdown of cAMP. This action in the bronchial tree has not been shown to be of benefit in the pathophysiologic mechanisms of CB. Although the mechanism of action in CB is not clear, benefit may be related to central nervous system stimulation, cardiac action, its modest diuretic activity, or to actions not... [Pg.228]

Kerr NM, Danesh-Meyer HV (2009) Phosphodiesterase inhibitors and the eye. Clinical Experimental Ophthalmology 37 514-523. [Pg.212]

Kajana, S., Goshgarian, H.G., 2008. Administration of phosphodiesterase inhibitors and an adenosine A1 receptor antagonist induces phrenic nerve recovery in high cervical spinal cord injured rats. Exp. Neurol. 210 (2), 671—680. [Pg.539]

Huang, M., H. Shimizu, and J. W. Daly Accumulation of cyclic adenosine monophosphate in incubated slices of brain tissue. 2. Effect of depolarizing agents, membrane stabilizers, phosphodiesterase inhibitors and adenosine analogs. J. Med. Chem. 15, 462--466 (1972). [Pg.333]

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