Resumen:
|
[EN] Wild female European eels were matured with CPE (carp pituitary extract) under three thermal regimes, two of
which were variable (T10–15 and T15–18, moving from 10 to 15 °C and from 15 to 18 °C, respectively) and ...[+]
[EN] Wild female European eels were matured with CPE (carp pituitary extract) under three thermal regimes, two of
which were variable (T10–15 and T15–18, moving from 10 to 15 °C and from 15 to 18 °C, respectively) and one
constant, at 18 °C (T18). Before and during hormonal treatment, the eels were sampled and biometric measurements
were taken. Immunoassays of sex steroids and vitellogenin were performed, as well as qPCR analyses of
gene expression (ovarian cyp19a1) and ovarian histology. Prior to the hormonal treatment, the silver eels
which had been maintained at 18 °C showed lower 11-KT and E2 plasma levels compared to those maintained
at 10 °C. In addition, in the early vitellogenic stage, the androgen and cyp19a1 levels were lower at 18 °C than
at 10 °C. Both these results and the positive correlations found between GSI and 11-KT (at the PV stage) and
between oocyte diameter and cyp19a1 levels (in the EV stage) suggest that early ovarian development is facilitated
at low temperatures. Vitellogenesis was induced by CPE in all the thermal groups, but progression to the
mid-vitellogenic stage was only observed after an accumulation of 900–1200 °D, at 15 or 18 °C, and progression
to the late vitellogenic stage was only observed after an accumulation higher than 1300 °D, at 18 °C. Although
temperature increased the rate of CPE-induced ovarian development, our results clearly indicate that this increase
is not linear, but exponential, with acceleration in the increase of GSI at 18 °C from the mid-vitellogenic
stage, or after an accumulation of 1300 °D. For the first time, a down-regulation of ovarian cyp19a1 caused by
high temperatures in CPE-treated eels was observed. These results demonstrate that temperature can modulate
eel ovarian development both before and after exogenous hormonal stimulations, and this knowledge could be
used to manipulate the timing of vitellogenesis progression under laboratory conditions
[-]
|
Agradecimientos:
|
This study was funded by the European Community's 7th Framework Programme under the Theme 2 "Food, Agriculture and Fisheries, and Biotechnology", grant agreement no.245257 (PRO-EEL). Ilaria Mazzeo and Victor Gallego had ...[+]
This study was funded by the European Community's 7th Framework Programme under the Theme 2 "Food, Agriculture and Fisheries, and Biotechnology", grant agreement no.245257 (PRO-EEL). Ilaria Mazzeo and Victor Gallego had predoctoral grants from Generalitat Valenciana and Spanish Ministry of Science and Innovation (MICINN), respectively. David S. Penaranda has a postdoc grant from UPV (CEI-01-10), mobility grants from UPV (PAID-00-11) and the Research Council of Norway (EJ/hsm IS-SIP, 2009) and also has been supported by a contract co-financed by MICINN and UPV (PTA2011-4948-I). F.-A. Weltzien received funding from the Norwegian University of Life Sciences.
[-]
|