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Pathway Description
Alprostadil Action Pathway
Homo sapiens
Drug Action Pathway
Alprostadil is a medication used for two distinct purposes. First, it is employed in the treatment of erectile dysfunction in men for whom oral treatment is either contraindicated or ineffective. It can be administered either through an intracavernosal injection or an intraurethral suppository. Alprostadil, a synthetic form of prostaglandin E1 (PGE1), acts as a potent vasodilator, promoting smooth muscle relaxation within the corpus cavernosum of the penis. This relaxation allows for increased blood flow into the penis, resulting in penile swelling, elongation, and rigidity, thus facilitating erections.
Second, alprostadil is used in neonatal patients with congenital heart defects that depend on a patent ductus arteriosus (DA) for survival until corrective or palliative surgery can be performed. In this context, alprostadil acts as a smooth muscle relaxant, preventing or reversing the functional closure of the DA that naturally occurs shortly after birth. By relaxing the DA smooth muscle, alprostadil ensures continued pulmonary or systemic blood flow in neonates with congenital heart defects. It's important to note that the use of alprostadil for these purposes should be under the supervision of healthcare professionals, as it involves specific dosages and administration methods tailored to the patient's condition.
References
Alprostadil Pathway References
Wishart DS, Feunang YD, Guo AC, Lo EJ, Marcu A, Grant JR, Sajed T, Johnson D, Li C, Sayeeda Z, Assempour N, Iynkkaran I, Liu Y, Maciejewski A, Gale N, Wilson A, Chin L, Cummings R, Le D, Pon A, Knox C, Wilson M: DrugBank 5.0: a major update to the DrugBank database for 2018. Nucleic Acids Res. 2018 Jan 4;46(D1):D1074-D1082. doi: 10.1093/nar/gkx1037.
Pubmed: 29126136
Hanchanale V, Eardley I: Alprostadil for the treatment of impotence. Expert Opin Pharmacother. 2014 Feb;15(3):421-8. doi: 10.1517/14656566.2014.873789. Epub 2013 Dec 26
Degoute CS: Controlled hypotension: a guide to drug choice. Drugs. 2007;67(7):1053-76
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