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Journal of Integrative Agriculture  2013, Vol. 12 Issue (6): 1049-1053    DOI: 10.1016/S1671-2927(00)8886
Animal Science · Veterinary Science Advanced Online Publication | Current Issue | Archive | Adv Search |
Dosage Effects of Fadrozole on Growth and Development of Sex-Reversed Genetic Female Chickens
 YANG Xiu-rong, JIANG He-sheng, ZHENG Jiang-xia, QU Lu-jiang, CHEN Si-rui, LI Jun-ying, XU Guiyun, YANG Ning
1 Department of Animal Genetics and Breeding, Guangxi University, Nanning 530004, P.R.China
2 Department of Animal Genetics and Breeding, National Engineering Laboratory for Animal Breeding, China Agricultural University,Beijing 100193, P.R.China
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摘要  Fadrozole, an aromatase inhibitor, can masculinize genetic female chickens and high-dose decreases the hatchability. Therefore, it is important to study the growth and development of sex-reversed females after hatch. Chick embryos from a population of CAU3 egg-type were treated with different concentrations of Fadrozole prior to the sexual differentiation at E3.0 (st18). At hatch, the phenotypic sex and genetic sex were identified by vent sexing and genetic diagnosis with CHD1, respectively. Body weight and shank length of sex reversal were tested at 8 and 20 wk, respectively. Testicular development, oviduct and ovarian degeneration were observed and serum concentration of estradiol and testosterone were tested with radioimmunoassay (RIA) at 30 wk. The results showed that body weight and shank length of sexreversed females were not significantly different between low-dose groups (0.1, 0.3, and 0.5 mg for F1, F2, and F3, respectively) and high-dose groups (1.0 and 1.3 mg for F4 and F5, respectively) (P>0.05). Left and right testes or ovotestes in F2, F3, F4, and F5 groups were heavier than that of in F1 group (P<0.05). While the gonad weight of treatment groups were less than that in male control (P<0.05), oviduct weight in F2, F3, F4, and F5 groups were significant differences compared with female control and F1 group (P<0.05). Egg number from onset of laying egg to 30 wk in F4 and F5 groups were less than in female control, F1 and F2 groups (P<0.05). Serum testosterone level in F5 group was significant higher compared with female control, F1, F2, F3, and F4 groups (P<0.05), but significant lower compared with male control (P<0.05). While concentration of serum estradiol in F5 group was significant lower compared with female control, F1, F2, and F4 groups (P<0.05). In conclusion, the concentration of Fadrozole do not affect postnatal growth of sex-reversed female chicken and the degree of sex-reversed females elevate with the increase of Fadrozole concentration at sex maturity.

Abstract  Fadrozole, an aromatase inhibitor, can masculinize genetic female chickens and high-dose decreases the hatchability. Therefore, it is important to study the growth and development of sex-reversed females after hatch. Chick embryos from a population of CAU3 egg-type were treated with different concentrations of Fadrozole prior to the sexual differentiation at E3.0 (st18). At hatch, the phenotypic sex and genetic sex were identified by vent sexing and genetic diagnosis with CHD1, respectively. Body weight and shank length of sex reversal were tested at 8 and 20 wk, respectively. Testicular development, oviduct and ovarian degeneration were observed and serum concentration of estradiol and testosterone were tested with radioimmunoassay (RIA) at 30 wk. The results showed that body weight and shank length of sexreversed females were not significantly different between low-dose groups (0.1, 0.3, and 0.5 mg for F1, F2, and F3, respectively) and high-dose groups (1.0 and 1.3 mg for F4 and F5, respectively) (P>0.05). Left and right testes or ovotestes in F2, F3, F4, and F5 groups were heavier than that of in F1 group (P<0.05). While the gonad weight of treatment groups were less than that in male control (P<0.05), oviduct weight in F2, F3, F4, and F5 groups were significant differences compared with female control and F1 group (P<0.05). Egg number from onset of laying egg to 30 wk in F4 and F5 groups were less than in female control, F1 and F2 groups (P<0.05). Serum testosterone level in F5 group was significant higher compared with female control, F1, F2, F3, and F4 groups (P<0.05), but significant lower compared with male control (P<0.05). While concentration of serum estradiol in F5 group was significant lower compared with female control, F1, F2, and F4 groups (P<0.05). In conclusion, the concentration of Fadrozole do not affect postnatal growth of sex-reversed female chicken and the degree of sex-reversed females elevate with the increase of Fadrozole concentration at sex maturity.
Keywords:  chicken       Fadrozole       growth and development       reproductive system       sex reversals  
Received: 28 February 2012   Accepted:
Fund: 

This work was supported in parts by the National High Technology R&D Program of China (2006AA10A121), the National Natural Science Foundation of China (30901017), and the China Postdoctoral Science Foundation (20100480837, 201104387).

Corresponding Authors:  Correspondence YANG Ning, Tel: +86-10-62731351, Fax: +86-10-62732741, E-mail: nyang@cau.edu.cn   
About author:  YANG Xiu-rong, E-mail: yangxiurong09@gmail.com

Cite this article: 

YANG Xiu-rong, JIANG He-sheng, ZHENG Jiang-xia, QU Lu-jiang, CHEN Si-rui, LI Jun-ying, XU Guiyun, YANG Ning. 2013. Dosage Effects of Fadrozole on Growth and Development of Sex-Reversed Genetic Female Chickens. Journal of Integrative Agriculture, 12(6): 1049-1053.

[1]Abinawanto, Shimada K, Yoshida K, Saito N. 1996. Effectsof aromatase inhibitor on sex differentiation and levelsof P450 (17 alpha) and P450 arom messenger ribonucleicacid of gonads in chicken embryos. General andComparative Endocrinology, 102, 241-246

[2]Abinawanto, Zhang C, Saito N, Matsuda Y, Shimada K.1998. Identification of sperm-bearing female-specificchromosome in the sex-reversed chicken. Journal ofExperimental Zoology, 280, 65-72

[3]Akazome Y, Mori T. 1999. Evidence of sex reversal in thegonads of chicken embryos after oestrogen treatmentas detected by expression of lutropin receptor. Journalof Reproduction and Fertility, 115, 9-14

[4]Bruggeman V, van As P, Decuypere E. 2002. Developmentalendocrinology of the reproductive axis in the chickenembryo. Comparative Biochemistry and Physiology(Part A: Molecular & Integrative Physiology), 131, 839-846

[5]Burke W H, Henry M H. 1999. Gonadal development andgrowth of chickens and turkeys hatched from eggsinjected with an aromatase inhibitor. Poultry Science,78, 1019-1033

[6]Elbrecht A, Smith R G. 1992. Aromatase enzyme activityand sex determination in chickens. Science, 255, 467-470

[7]Fridolfsson A K, Cheng H, Copeland N G, Jenkins N A, LiuH C, Raudsepp T, Woodage T, Chowdhary B, HalversonJ, Ellegren H. 1998. Evolution of the avian sexchromosomes from an ancestral pair of autosomes.Proceedings of the National Academy of Sciences ofthe United States of America, 95, 8147-8152

[8]Hamburger V, and Hamilton H L. 1951. A series of normalstages in the development of the chick embryo. Journalof Morphology, 88, 49-92

[9]Hu R, Geng X, Ma J, Chen Y, Li Z, Ding X. 2003. A simpleand universal method for molecular sexing of birds.Journal of Experimental Biology, 36, 401-404

[10]Hudson Q J, Smith C A, Sinclair A H. 2005. Aromataseinhibition reduces expression of FOXL2 in theembryonic chicken ovary. Developmental Dynamics,233, 1052-1055

[11]Scheib D. 1983. Effects and role of estrogens in aviangonadal differentiation. Differentiation, 23, S87-S92.Smith C A, Katz M, Sinclair A H. 2003. DMRT1 is upregulatedin the gonads during female-to-male sex reversal in ZWchicken embryos. Biology of Reproduction, 68, 560-570

[12]Vaillant S, Dorizzi M, Pieau C, Richard-Mercier N. 2001. Sexreversal and aromatase in chicken. Journal ofExperimental Zoology, 290, 727-740

[13]Vaillant S, Guemene D, Dorizzi M, Pieau C, Richard-MercierN, Brillard J P. 2003. Degree of sex reversal as related toplasma steroid levels in genetic female chickens (Gallusdomesticus) treated with Fadrozole. MolecularReproduction and Development, 65, 420-428

[14]Wartenberg H, Lenz E, Schweikert H U. 1992. Sexualdifferentiation and the germ cell in sex reversed gonadsafter aromatase inhibition in the chicken embryo.Andrologia, 24, 1-6

[15]Yang X, Zheng J, Na R, Li J, Yang N. 2008. Degree of sexdifferentiation of genetic female chickens treated withdifferent dose of aromatase inhibitor. SexualDevelopment, 2, 309-315

[16]Yang X, Zheng J, Xu G, Qu L, Chen S, Li J, Yang N. 2011.Methylation status of cMHM and expression of sexspecificgenes in adult sex-reversed female chickens.Sexual Development, 5, 147-154
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