tadalafil 20mg
Drug is used to treat erection.
It is a reversible selective inhibitor of specific phosphodiesterase type 5 (PDE-5) cGMP. When sexual stimulation causes local release of nitric oxide, inhibition of PDE-5 tadalafilom leads to increased levels of cGMP in the cavernous body of penis. The result is relaxation of smooth muscles of arteries and blood flow to the tissues of the penis that causes an erection. Tadalafil has no effect in absence of sexual stimulation.
Studies in vitro have shown that tadalafil is a selective inhibitor of PDE-5. PDE-5 - an enzyme found in smooth muscles of cavernous bodies in the vascular smooth muscles of internal organs, skeletal muscle, platelets, kidney, lung cerebellum.
Effects of cialis for PDE-5 is more active than other phosphodiesterase. This selectivity against PDE-5 compared with FDE3 is important, because FDE3 is an enzyme involved in the reduction of cardiac muscle. In addition, cialis is approximately 700 times more active against PDE-5 than in respect FDE6 found in the retina. cialis also 10 000 times more active than PDE-5, compared with its effect on FDE7-FDE10.
cialis improves erection and the possibility of successful sexual intercourse.
The drug acts within 36 h. The effect is manifested as little as 16 minutes after taking the drug in the presence of sexual stimulation.
cialis in healthy individuals causes no significant change in systolic and diastolic blood pressure compared with placebo in the supine position (mean maximum decrease of cialis Table. 20 mg. cialis is no significant change in heart rate.
cialis does not cause changes color recognition (blue / green), which explains its low affinity for FDE6. In addition, no marked effect of cialis on visual acuity, electroretinogram, intraocular pressure and pupil size.
When using cialis in a daily dose of 10 mg found no clinically significant effect of the drug on the number and concentration of sperm motility and sperm morphology.

