Aromatase inhibitor and 17?-methyltestosterone cause sex-reversal from genetical females to phenotypic males and suppression of P450 aromatase gene expression in Japanese flounder (Paralichthys olivaceus)

Author(s):  
Takeshi Kitano ◽  
Kazufumi Takamune ◽  
Yoshitaka Nagahama ◽  
Shin-Ichi Abe
2014 ◽  
Vol 117 (1) ◽  
pp. 66-72 ◽  
Author(s):  
B.N.V. Lakshminarayana ◽  
V. Praveen Chakravarthi ◽  
K.V. Brahmaiah ◽  
V.H. Rao

2013 ◽  
Vol 25 (1) ◽  
pp. 234
Author(s):  
E. K. N. Arashiro ◽  
S. Wohlres-Viana ◽  
M. P. Palhao ◽  
L. S. A. Camargo ◽  
M. Henry ◽  
...  

It is well documented that the size of the dominant follicle at deviation is smaller in Bos indicus compared with in Bos taurus breeds. The physiological mechanisms underlying this difference, however, are unknown. The aim of the present study was to evaluate the dynamic of oestradiol production during follicle development close to the expected moment of deviation in Bos taurus and Bos indicus dairy heifers. Intrafollicular concentration of oestradiol (E2) and P450 aromatase gene expression in granulosa cells (GC) were evaluated in Gir (n = 10) and Holstein (n = 10) heifers. Follicular waves were synchronized with an intravaginal progesterone device (1 g, Sincrogest, Ourofino Agropecuária, São Paulo, Brazil) and benzoate oestradiol (2 mg im, Sincrodiol, Ourofino Agropecuária). Ultrasonography evaluations (MyLab30 Vet Gold, Esaote, Genova, Italy, with a 7.5-MHz transducer) were performed every 24 h to detect the emergence of the new follicular waves. The largest follicle of each wave was individually aspirated by ovum pickup before, at the expected diameter, or after deviation in both Gir (4.6 ± 0.2, 6.3 ± 0.2, and 8.5 ± 0.6 mm, respectively) and Holstein heifers (6.0 ± 0.5, 8.6 ± 0.4, and 10.2 ± 0.2 mm, respectively), as previously described (Arashiro et al. 2012 Reprod. Fertil. Dev. 24, 175). Follicular fluid (FF) samples were centrifuged and the supernatant stored at –20°C until E2 and progesterone (P4) determination by RIA. The pellet of GCs was washed twice with PBS, kept in RNAlater, and frozen at –20°C until RNA extraction and reverse transcription. Relative transcript quantification was performed by real-time PCR. The β-actin gene was used as control. Samples of FF with E2:P4 ratio <1 or presenting contamination by theca cells (detected by the expression of 17α-hydroxylase) were not used for statistical analyses. Concentration of E2 in FF was evaluated between breeds and among follicle size classes by ANOVA and differences among means compared by Student t-test or Tukey’s test, respectively. Within breeds, relative gene expression was accessed by pair-wise fixed reallocation randomization test (software REST®). Results are shown as mean ± SEM. In both breeds, concentration of E2 in FF progressively increased with follicular diameter (P < 0.05). Intrafollicular concentration of E2 (ng mL–1) was greater (P < 0.05) in Holstein than in Gir before (58.5 ± 11.7 v. 8.8 ± 2.0), at expected (226.0 ± 49.9 v. 78.9 ± 21.0), and after follicle deviation (579.1 ± 45.0 v. 185.0 ± 34.9). Interestingly, however, follicles with similar diameters (~6 or 8 mm) showed similar (P > 0.05) E2 concentrations between Holstein and Gir. Moreover, in both breeds, the relative expression of P450 aromatase gene in GC first increased (3.9 ± 2.4 and 67.5 ± 52.8 for Holstein and Gir, respectively; P < 0.05) at the same stage of follicular development (8 mm). The present results suggest that the smaller size of follicles at deviation in Bos indicus is not related to an earlier increase in intrafollicular E2 production. CNPq, CAPES, and Fapemig (CVZ APQ 02863/09).


2007 ◽  
Vol 107 (3-5) ◽  
pp. 149-155 ◽  
Author(s):  
Junshin Iwabuchi ◽  
Syun Wako ◽  
Tatsuya Tanaka ◽  
Azusa Ishikawa ◽  
Yuki Yoshida ◽  
...  

2009 ◽  
Vol 54 (No. 12) ◽  
pp. 566-574 ◽  
Author(s):  
E. Chronowska ◽  
M. Tománek ◽  
T. Kott

The objective of the present work was to study the effect of a nonsteroidal aromatase inhibitor (fadrozole) on proliferation, estradiol production, aromatase expression and telomerase activity (TA) in pig granulosa cells (GC) from small (1–2 mm) and large (5–7 mm) follicles. The cells were treated with fadrozole for 48 h and 72 h in basal and FSH-stimulated conditions. Fadrozole caused a decrease (<i>P</i> < 0.05) of 3H-thymidine incorporation in granulosa cells derived from small (1–2 mm) and large follicles (5–7 mm). The proliferative potential of small-follicle GC was significantly higher (<i>P</i> < 0.01) under all culture conditions. Estradiol production was suppressed (<i>P</i> < 0.01) in both granulosa cell populations cultured in the presence of fadrozole for 48 and 72 h. Fadrozole caused a decrease (<i>P</i> < 0.05) of aromatase gene expression in small-follicle granulosa cell incubated for 72 h and in large-follicle GC after 48 h of culture. Large-follicle GC were characterized by a higher (<i>P</i> < 0.01) level of estradiol production and aromatase gene expression. Telomerase activity decreased (<i>P</i> < 0.05) in large-follicle granulosa cells incubated in the presence of an aromatase inhibitor for 72 h. The TA level in large-follicle granulosa cells was higher (<i>P</i> < 0.01) in comparison to small-follicle GC in all culture conditions after 72 h of incubation. The results of the present study suggest the important role of telomerase in the process of follicular growth and development.


2013 ◽  
Vol 34 (5) ◽  
pp. 480-488 ◽  
Author(s):  
William J. Trickler ◽  
Xiaoqing Guo ◽  
Elvis Cuevas ◽  
Syed F. Ali ◽  
Merle G. Paule ◽  
...  

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