Effects of amphetamine on steroidogenesis in MA-10 mouse Leydig tumor cells

Life Sci. 2003 Mar 14;72(17):1983-95. doi: 10.1016/s0024-3205(03)00011-0.

Abstract

Amphetamine influences plasma and testicular testosterone levels. However, there is no evidence that amphetamine can directly influence Leydig cell functions. In the present study, a MA-10 mouse Leydig tumor cell line was used to determine whether and how amphetamine affected Leydig cell steroidogenesis. MA-10 cells were treated with different concentrations of amphetamine without or with human chorionic gonadotropin (hCG) and/or enzyme precursors over different time durations. Steroid production, enzyme activities and StAR protein expression were determined. Amphetamine alone had no any effect on MA-10 cell steroidogenesis. However, amphetamine (10(-11)M and 10(-10)M) significantly enhanced hCG-treated progesterone production at 3 hr in MA-10 cells (p < 0.05). Furthermore, amphetamine significantly induced more progesterone production upon treatment with 22R-hydroxycholesterol (p < 0.05), a precursor of P450 side-chain cleavage enzyme (P450scc). However, amphetamine did not induce more progesterone production when treated with pregnenolone (p > 0.05), a precursor of 3beta-hydroxysteroid dehydrogenase. In addition, the expressions of StAR protein and P450scc enzyme were not significantly different between hCG alone and hCG plus amphetamine treatment in MA-10 cells (p > 0.05). These results suggested that amphetamine enhanced hCG-induced progesterone production in MA-10 cells by increasing P450scc activity without influencing StAR protein and P450scc enzyme expression or 3beta-HSD enzyme activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3-Hydroxysteroid Dehydrogenases / biosynthesis
  • Amphetamine / pharmacology*
  • Animals
  • Blotting, Western
  • Central Nervous System Stimulants / pharmacology*
  • Cholesterol Side-Chain Cleavage Enzyme / biosynthesis
  • Chorionic Gonadotropin / pharmacology
  • Leydig Cell Tumor / metabolism*
  • Male
  • Mice
  • Mitochondria / enzymology
  • Mitochondria / metabolism
  • Phosphoproteins / biosynthesis
  • Progesterone / biosynthesis
  • Radioimmunoassay
  • Steroids / biosynthesis*
  • Testicular Neoplasms / metabolism*
  • Tumor Cells, Cultured

Substances

  • Central Nervous System Stimulants
  • Chorionic Gonadotropin
  • Phosphoproteins
  • Steroids
  • steroidogenic acute regulatory protein
  • Progesterone
  • Amphetamine
  • 3-Hydroxysteroid Dehydrogenases
  • Cholesterol Side-Chain Cleavage Enzyme