These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Inhibition of human and rat testicular steroidogenic enzyme activities by bisphenol A.
    Author: Ye L, Zhao B, Hu G, Chu Y, Ge RS.
    Journal: Toxicol Lett; 2011 Nov 30; 207(2):137-42. PubMed ID: 21925253.
    Abstract:
    Bisphenol A (BPA) is a potential endocrine disruptor. It has been shown that it reduces serum testosterone level in rodents after exposure. However, the mechanism is unclear. The object of the present study is to investigate the effects of BPA on human and rat steroidogenic enzymes including P450 17α-hydroxylase/17,20-lyase (CYP17A1), 3β-hydroxysteroid dehydrogenase (3β-HSD) and 17β-hydroxysteroid dehydrogenase 3 (17β-HSD3). Human and rat testis microsomes were exposed to various concentrations of BPA (10(-8)-10(-4)M). BPA inhibited human and rat 3β-HSD, CYP17A1 and 17β-HSD3 activities. The half maximal inhibitory concentrations (IC(50)s) of BPA for human and rat testis 3β-HSD were 7.92±1.03 and 26.49±3.03 μM (200 μM pregnenolone), respectively. The IC(50)s for human and rat CYP17A1 (1 μM progesterone) were 18.99±3.75 and 64.67±4.04 μM, respectively. BPA was a weak HSD17B3 inhibitor with IC(50)s of about 100 μM (200 nM androstenedione). BPA also concentration-dependently inhibited testosterone production by rat Leydig cells. In conclusion, BPA is an inhibitor for 3β-HSD, CYP17A1 and 17β-HSD3. Human 3β-HSD and CYP17A1 are more sensitive to BPA than rat 3β-HSD and CYP17A1.
    [Abstract] [Full Text] [Related] [New Search]