Polychlorinated biphenyl (PCB)-based transformer fluids belong to a class of environmentally persistent mixtures with known toxic effects. Here, we studied the acute effects of
Askarel (which contains
Aroclor 1260) and two substitute transformer fluids (the
silicone oil-based DC561 and the
mineral oil-based ENOL C) on rat testicular steroidogenesis. Single intraperitoneal (ip; 10 mg/kg
body weight) or bilateral intratesticular (itt; 25 microg/testis)
injections of
Askarel markedly decreased serum
androgen levels 24 hr after administration. In acute testicular cultures from these animals,
chorionic gonadotropin-stimulated
progesterone and
androgen productions were severely attenuated. When itt was injected or added in vitro,
Askarel inhibited 3ss-hydroxysteroid
dehydrogenase (3ssHSD), stimulated
17[alpha]-hydroxylase/
lyase (P450c17), and did not affect 17ss-hydroxysteroid
dehydrogenase in testicular postmitochondrial fractions. The ip-injected
Askarel did not affect 3ssHSD, but inhibited P450c17, suggesting that a more intensive metabolism of peripherally injected
Askarel reduces the circulating levels of active ingredients below the threshold needed for inhibition of 3ssHSD and generates a derivative that inhibits P450c17. In contrast to
Askarel, itt-injection (25 microg/testis) of DC561 and ENOL C did not affect in vivo and in vitro steroidogenesis. These findings show the acute effects of
Askarel, but not
silicone and
mineral oils, on testicular steroidogenesis.