Annual changes in gonadal histology, gonadosomatic index (GSI), and plasma 11-ketotestosterone (11KT) levels were investigated in reared male common Japanese congers, Conger myriaster. Young fish, 20–30 cm in total length and around 20 g in body weight, caught in November 1996 (group 1) and in September 1999 (group 2) were reared for 3 years in seawater at temperatures ranging from 10 to 20 °C.
In most fish, only spermatogonia occupied the testes for 1 year and a few months after capture. Spermatocytes appeared in February, and both spermatids and spermatozoa appeared in March, in 1998 for group 1 and in 2001 for group 2. Spermiation was observed from May to September and reduction in testis was observed after October in both groups. GSI and plasma 11KT levels changed with progression of spermatogenesis. Although GSI was less than 1.0 and the plasma 11KT level less than 1.0 ng/ml, in the first year in most fish, both increased in the second year of rearing. GSI peaked in June 1998 (5.3±3.0; mean±standard deviation) in group 1 and May 2001 (2.3±1.3) in group 2, and bottomed in October (0.3±0.1) in both groups. Plasma 11KT levels peaked in March 1998 (5.8±1.9 ng/ml) in group 1 and May 2001 (4.4±2.4 ng/ml) in group 2, and bottomed in August in group 1 and September in group 2 (around 0.1 ng/ml in both groups). Spermatogenesis and changes in GSI and plasma 11KT levels were repeated the following year in both groups.
These observations indicate that males have an annual reproductive cycle under rearing conditions. It is possible that wild male common Japanese congers also have multiple spawning seasons in their lives. 相似文献
Vitellogenin (VTG) synthesis was induced by repeated injections of estradiol-17 in juvenile Atlantic halibut (Hippoglossus hippoglossus). VTG eluted as a large, phosphoprotein containing peak on DEAE-Sephacel chromatography of plasma from estradiol-17 treated juvenile and mature female, but not mature male halibut. A purification procedure for Atlantic halibut VTG was developed, where VTG was precipitated with MgCl2, EDTA and distilled water, and the precipitated protein submitted to anion exchange chromatography on DEAE-Sephacel. Precipitated VTG eluted as a broad, partly dissociated peak on DEAE-Sephacel, when chromatography was run at 4°C, but the protein appeared intact when analysed both by SDS PAGE and native PAGE. DEAE-Sephacel chromatography at room temperature resulted in an irregular elution pattern and a dissociated protein fraction, as analysed by SDS PAGE. Biochemical characterization of VTG showed that the molecular mass of the monomer was ca 160 kDa, as estimated by SDS-PAGE. The total lipid content was 19.8% w/w, with 64%, or 12.7% of the total weight, as phospholipid. Protein bound phosphorus constituted 0.62% w/w of halibut VTG. Plasma dilution curves from mature and maturing female halibut were parallel with a dilution curve from halibut egg yolk homogenate in an homologous RIA. Plasma from mature male, but not juvenile halibut crossreacted with the VTG antiserum. 相似文献