4.1 Article

Acteoside reduces testosterone by inhibiting cAMP, p450scc, and StAR in rat Leydig cells

期刊

MOLECULAR & CELLULAR TOXICOLOGY
卷 11, 期 1, 页码 11-17

出版社

KOREAN SOCIETY TOXICOGENOMICS & TOXICOPROTEOMICS-KSTT
DOI: 10.1007/s13273-015-0002-x

关键词

Acteoside; cAMP; p450scc; StAR; Testosterone; Leydig cells

资金

  1. National Natural Science Foundation [J1103516, 2014HXFWBHQ-LSQ-001]

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The present study investigated the in vivo and in vitro effects of acteoside on testosterone production in Sprague-Dawley (SD) rats. The in vivo experiment revealed that acteoside reduced the testosterone level in serum significantly (P<0.05). The in vitro experiment also illustrated that acteoside significantly reduced testosterone production in SD rat Leydig cells in primary culture (P<0.05). Enzyme-linked immunosorbent assay results demonstrated that acteoside significantly reduced the cyclic adenosine 3',5'-monophosphate (cAMP) level (P<0.05), and Western blot analysis showed that acteoside significantly reduced cholesterol side-chain cleavage enzyme (p450scc) and steroidogenic acute regulatory (StAR) expression (P<0.05). Hoechst 33342 staining and Western blotting showed that acteoside did not induce apoptosis in Leydig cells. Together, these results suggest that the acteoside-induced reduction in testosterone production in rat may be at least partially due to down-regulation of cAMP, p450scc, and StAR, but not apoptosis.

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