Ammonium perfluorooctanoate may cause testosterone reduction by adversely affecting testis in relation to PPARα

Li, Y; Ramdhan, DH; Naito, H; Yamagishi, N; Ito, Y; Hayashi, Y; Yanagiba, Y; Okamura, A; Tamada, H; Gonzalez, FJ; Nakajima, T

HERO ID

1294081

Reference Type

Journal Article

Year

2011

Language

English

PMID

21712084

HERO ID 1294081
In Press No
Year 2011
Title Ammonium perfluorooctanoate may cause testosterone reduction by adversely affecting testis in relation to PPARα
Authors Li, Y; Ramdhan, DH; Naito, H; Yamagishi, N; Ito, Y; Hayashi, Y; Yanagiba, Y; Okamura, A; Tamada, H; Gonzalez, FJ; Nakajima, T
Journal Toxicology Letters
Volume 205
Issue 3
Page Numbers 265-272
Abstract Perfluorooctanoate, a peroxisome proliferator-activated receptor alpha (PPARα) agonist, has the potential to lower testosterone levels as a result of testicular toxicity. To elucidate the mechanism and impact of PPARα on this reproductive toxicity, ammonium perfluorooctanoate (APFO) at doses of 0, 1.0 (low) mg/kg/day, or 5.0 (high) mg/kg/day was orally given daily to 129/sv wild-type (mPPARα), Pparα-null and PPARα-humanized (hPPARα) mice for 6 weeks. Both low- and high-dose APFO significantly reduced plasma testosterone concentrations in mPPARα and hPPARα mice, respectively. These decreases may, in part, be associated with decreased expression of mitochondrial cytochrome P450 side-chain cleavage enzyme, steroidogenic acute regulatory protein or peripheral benzodiazepine receptor as well as microsomal cytochrome P450(17α) involved in the steroidogenesis. Additionally, both doses increased abnormalities in sperm morphology and vacuolated cells in the seminiferous tubules of both mouse lines. In contrast, APFO caused only a marginal effect either on the testosterone synthesis system or sperm and testis morphology in Pparα-null mice. These results suggest that APFO may disrupt testosterone biosynthesis by lowering the delivery of cholesterol into the mitochondria and decreasing the conversion of cholesterol to pregnenolone and androstandione in the testis of mPPARα and hPPARα mice, which may, in part, be related to APFO-induced mitochondrial damage.
Doi 10.1016/j.toxlet.2011.06.015
Pmid 21712084
Wosid WOS:000294578500006
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
Keyword Perfluorooctanoic acid; Peroxisome proliferator-activated receptor alpha; Reproductive toxicity; Testosterone