非那雄胺
5α还原酶抑制剂
机制(生物学)
阿尔法(金融)
化学
药理学
医学
内科学
哲学
临床心理学
认识论
结构效度
癌症
心理测量学
前列腺
作者
Shraddha T. Nemane,Omprakash G. Bhusnure,Sachin B. Gholve,Pooja R. Mitakari,Pawan N. Karwa
标识
DOI:10.22270/jddt.v9i3-s.3013
摘要
This review gives the information about the Finasteride i.e. 5alpha-reductase inhibitor. Primarily finasteride isused to treat BPH i.e benign prostatic hyperplasia and male androgenetic alopecia. Five-alpha reductase inhibitors (5α-RIs) could stimulate male sexual dysfunction due to their effects on testosterone and DHT i.e. dihydrotestosterone. Some studies account insignificant or acceptable adverse effects, which decrease after a changeable period of time so that they do not require terminating finasteride administration. The 5alpha-reductase inhibitor finasteride blocks the conversion of TT to DHT i.e. testosterone to dihydrotestosterone (DHT), the androgen responsible for androgenetic alopecia i.e. male pattern hair loss. This paper presents a possible explanation of the Finasteride drug. Keywords: Finasteride, 5alpha-reductase inhibitor, BPH, DHT, alopecia.
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