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The Selectivity and Potency of the New PDE5 Inhibitor TPN729MA
- Source :
- The Journal of Sexual Medicine. 10:2790-2797
- Publication Year :
- 2013
- Publisher :
- Oxford University Press (OUP), 2013.
-
Abstract
- Introduction TPN729MA is a newly developed phosphodiesterase type 5 inhibitor (PDE5i) for the treatment of erectile dysfunction, which offers potential for greater selectivity and longer duration of action than PDE5i in current clinical use. Aim We investigated the in vitro inhibitory potency and selectivity of TPN729MA on PDE isozymes, and its efficacy in animal models. Methods The inhibition of 11 human recombinant PDEs by TPN729MA, sildenafil, and tadalafil were determined using radioimmunoassay. The effect of TPN729MA and sildenafil on intracavernous pressure (ICP), blood pressure (BP), and ICP/BP ratio were determined in a rat model of erection induced by electric stimulation and in a dog model of erection induced by sodium nitroprusside injection. Main Outcome Measures The main outcome measures were IC 50 of TPN729MA, sildenafil, and tadalafil for PDE1-PDE11; maximum ICP; BP and ICP/BP ratio. Results The IC 50 of TPN729MA, sildenafil, and tadalafil for PDE5 was 2.28, 5.22, and 2.35 nM, respectively. TPN729MA showed 248, 366, 20, and 2671-fold selectivity against PDE1, PDE4, PDE6, and PDE11, respectively. TPN729MA showed excellent selectivity against PDE2, 3, 7, 8, 9, and 10 (>10,000-fold). In the rat model of erection, TPN729MA (5.0 and 2.5 mg/kg), but not sildenafil, significantly increased the maximum ICP compared with vehicle. Significantly increased ICP/BP was observed in the TPN729MA (5.0 mg/kg) group at all time points, in the TPN729MA (2.5 mg/kg) group at 75, 90, 105, and 120 minutes time points, and in sildenafil group at 75 and 90 minutes time points compared with vehicle. In the dog model of erection, TPN729MA and sildenafil significantly increased ICP and ICP/BP but showed no significant effect on BP compared with vehicle. Conclusions TPN729MA is a potent PDE5i with a balanced selectivity profile. TPN729MA shows excellent in vitro and in vivo potency, and a longer effect on erectile function than sildenafil in animal model. Wang Z, Zhu D, Yang X, Li J, Jiang X, Tian G, Terrett NK, Jin J, Wu H, He Q, Yang B, and Shen J. The selectivity and potency of the new PDE5 Inhibitor TPN729MA. J Sex Med 2013;10:2790–2797.
- Subjects :
- Male
Nitroprusside
medicine.medical_specialty
Sildenafil
Urology
Endocrinology, Diabetes and Metabolism
Blood Pressure
Pharmacology
Piperazines
Sildenafil Citrate
Tadalafil
Rats, Sprague-Dawley
Inhibitory Concentration 50
chemistry.chemical_compound
Dogs
Endocrinology
Erectile Dysfunction
In vivo
Internal medicine
medicine
Animals
Humans
Potency
Sulfones
Cyclic guanosine monophosphate
Phosphodiesterase 5 Inhibitors
medicine.disease
Rats
Isoenzymes
Psychiatry and Mental health
Erectile dysfunction
Reproductive Medicine
chemistry
Purines
cGMP-specific phosphodiesterase type 5
Sodium nitroprusside
Carbolines
medicine.drug
Subjects
Details
- ISSN :
- 17436095
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- The Journal of Sexual Medicine
- Accession number :
- edsair.doi.dedup.....cc0d6949c501e878009d89d66ed9878c