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2018
DOI: 10.1016/j.ejphar.2018.06.018
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Effect of co-administration of two different phosphodiesterase inhibitors and a β3-adrenoceptor agonist in an experimental model of detrusor overactivity

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Cited by 3 publications
(2 citation statements)
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“…In L-NAME treated mice, rolipram induced more relaxation than the other drugs, enhancing relaxation response to BRL 37344 at almost all concentrations, but no synergistic effect with tadalafil was observed. The relaxant effect of BRL 37344 was enhanced by rolipram but not by tadalafil, suggesting that PDE-4 inhibition, especially when associated with β3-AR, could represent a potential treatment for DO 31 . Thus, other studies using the rolipram and BRL 37344 combination may contribute to the treatment of DO.…”
Section: Discussionmentioning
confidence: 97%
“…In L-NAME treated mice, rolipram induced more relaxation than the other drugs, enhancing relaxation response to BRL 37344 at almost all concentrations, but no synergistic effect with tadalafil was observed. The relaxant effect of BRL 37344 was enhanced by rolipram but not by tadalafil, suggesting that PDE-4 inhibition, especially when associated with β3-AR, could represent a potential treatment for DO 31 . Thus, other studies using the rolipram and BRL 37344 combination may contribute to the treatment of DO.…”
Section: Discussionmentioning
confidence: 97%
“…S-type APPDs are synthetic intermediates for the synthesis of cardiac propranolol, which is a drug for the treatment of cardiovascular diseases. 1,2 They can also be used to synthesize phosphodiesterase inhibitors 3,4 for the treatment of heart disease. Furthermore, R-type APPDs are precursors for a synthetic insect growth regulator.…”
Section: Introductionmentioning
confidence: 99%