Sex differences in hepatic monooxygenases in winter flounder (Pseudopleuronectes americanus) and scup (Stenotomus chrysops) and regulation of P450 forms by estradiol.
Sex differences in hepatic monooxygenases in winter flounder (Pseudopleuronectes americanus) and scup (Stenotomus chrysops) and regulation of P450 forms by estradiol.
复制标题
冬鲽 (Pseudopleuronectes americanus) 和 scup (Stenotomus chrysops) 肝脏单加氧酶的性别差异以及雌二醇对 P450 形式的调节。
DOI:
10.1002/jez.1402590308
复制
发表时间:
1991
期刊:
影响因子:
--
通讯作者:
Stegeman,JJ
中科院分区:
文献类型:
--
作者:
Gray,ES;Woodin,BR;Stegeman,JJ
Details concerning the endogenous regulation of hepatic cytochrome P450 mono‐oxygenases in teleosts, and the features of this regulation common among fish species, are poorly known. Gonadally mature female winter flounder (Pseudopleuronectes americanus) have been reported to have severalfold lower levels of microsomal cytochromes P450 and b5and NADPH cytochrome c reductase than do males (Stegeman and Woodin ('84) Mar. Environ. Res., 14:422–425). These strong sex differences prompted more detailed study of P450 regulation in winter flounder liver, and a comparison with sex differences in another marine teleost, scup (Stenotomus chrysops). Ethoxyresorufin O‐deethylase (EROD) activity/nmol P450 was less in gonadally mature females than in males of both species. Immunoblot analysis with MAb 1‐12‐3 to P450E (the EROD catalyst) showed that the content of P450E counterpart was also much less in females of both species. Aminopyrine N‐demethylase (APND) and testosterone 6β‐hydroxylase (6β‐OHase) activities per nmol P450 were higher in gonadally mature female than in mature male flounder, differences not seen in scup. Polyclonal antibodies to scup P450A were shown to detect proteins in a number of teleosts. The levels of anti‐P450A cross‐reacting protein were greater in mature female than in male flounder, but as with 6β‐OHase activity, the content of this protein was not sexually differentiated in scup. Estradiol treatment of winter flounder depressed the rates of EROD, APND, 6β‐OHase, and estradiol 2‐OHase activities per mg protein, but APND and 6β‐OHase activities per nmol P450 were unchanged. Thus, E2promotes general decreases in some hepatic P450‐catalyzed activities, but in achieving sex differences there is also specific regulation of the P450E counterpart, and possibly of the 6β‐OHase (P450A?). Other factors, temporal or hormonal, can modify the effect of E2treatment, and may contribute to the specific regulation of P450 forms in naturally maturing fish, and to species differences in this regulation.