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Isidori, A.M., Buvat, J., Corona, G., Goldstein, I., Jannini, E.A., Lenzy, A., Porst, H., Salonia, A., Traish, A.M. and Maggi, M. (2013) A Critical Analysis of the Role of Testosterone in Erectile Function: From Pathophysiology to Treatment—A Systemic Review. European Urology, 65, 99-112.
https://doi.org/10.1016/j.eururo.2013.08.048

has been cited by the following article:

  • TITLE: The Analysis of Primer Gene of Phosphodiesterase Type 5 (PDE5) on Erectyle Dysfungction

    AUTHORS: Theopilus W. Watuguly, Indranila K. Samsuria, Pudji Astuti, Tri Rini Nuringtyas, Nastiti Wijayanti, Syahran Wael

    KEYWORDS: Erectile Disfunction, PDE5, Primer, PCR

    JOURNAL NAME: Open Journal of Applied Sciences, Vol.8 No.9, September 28, 2018

    ABSTRACT: Backround: Erectile dysfunction (ED) is the inability of male reproductive organs within sexual intercourse caused by neurogenic and hormonal disorders. There are some causes of ED such as hypertension, stress, neurological disorders, stroke, diabetes, atherosclerosis, lifestyle, alcohol, smoking, and age-related hormonal decline can cause infertility. The natural treatment of sexual dysfunction through aphrodisiac activity of the plant is to increase sexual hormones, spermatogenesis activity and through PDE5 inhibitors such as sildenafil, verdenafil, and tadalafil which can inhibit the hydrolysis of second messenger cGMP of penis smooth muscle cells. Primer Design for amplification of several PDE5 gene nucleotide sequences obtained from NCBI gen banks and tested directly through explosions at NCBI and also using MEGA 6, primer 3 plus, and fast PCR software. The natural treatment of sexual dysfunction through aphrodisiac activity from plants to increase sexual hormone, spermatogenesis activity and inhibitor PDE5 such as sildenafil, vardenafil, and tadalafil can inhibit hydrolysis second messenger of cells cGMP smooth penis muscles. Method: Primer design stages for several sequences are data supply, multiple sequence alignment, sequence trimming, primer design (fastPCR input), in silico PCR analysis, and primer evaluation (Primer Test, OligoCalc and BLAST). Results: Primer of PDE5 that is choosen is with reverse sequence 5-TGCATTGACCATGTCTCTCGTT-3, forward 5-CGCCGATCTGGGCTGAACTA-3 able to amplify template DNA at temperature 67.2°C, 65.8°C, 63.7°C, however, the DNA band fragment looks not very clear, while it is more clearly seen at Tm temperature 61.2°C, 59.1°C, 57.8°C and 57°C. Conclusion: PDE5 primers can be amplified well at temperature 61.2°C, 59.1°C, 57.8°C and 57°C. PDE5 primer succeeded in amplifying DNA with a product length of 402 bp.