Literature DB >> 15601925

Seasonal profiles of brain and pituitary gonadotropin-releasing hormone and plasma luteinizing hormone in relation to sex change of protandrous black porgy, Acanthopagrus schlegeli.

Jin-Lien Du1, Yan-Horn Lee, Wen-Shiun Yueh, Ching-Fong Chang.   

Abstract

Three molecular variants of GnRH in the brain (sbGnRH, sGnRH, and cGnRH-II) and two forms in the pituitary (sbGnRH and sGnRH) were detected in protandrous black porgy, Acanthopagrus schlegeli using chromatographic and immunological methods. In juvenile fish, brain sbGnRH, sGnRH, and cGnRH-II levels increased in May and reached their highest levels in July and August (the nonspawning season) and in January through March (the spawning season). In fish aged 1 yr and older, high levels of brain sbGnRH and sGnRH were detected in September, November, and February-March, but the levels of brain cGnRH-II remained constant. A gradual increase in pituitary sbGnRH was detected in juvenile fish from July to March. In fish aged 1+ yr, pituitary sbGnRH levels were high in September and March-May, but low in January-February. A close correlation between pituitary sbGnRH and plasma LH levels was found in juvenile fish and in those aged 1+ yr. In fish aged 2+ yr, significantly lower levels of plasma LH was detected during the nonspawning period in fish that changed sex compared with the fish that remained as males. Higher plasma LH levels were detected in the sex-changing fish from artificially sex-reversed female to male. FSH receptor and LH receptor transcripts were higher in bisexual testicular tissue than in ovarian tissue in 2+-yr-old fish. Direct effects of hCG on sex change were studied and the results show that exogenous hCG did not stimulate gonadal aromatase activity in 2+-yr-old fish. Therefore, it is suggested that high and basal levels of plasma LH during the nonspawning season correlate with the development of male and female gonad, respectively, in black porgy. This important role of the neuroendocrine system in sex change (for male direction) is proposed in hermaphroditic fish.

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Year:  2004        PMID: 15601925     DOI: 10.1095/biolreprod.104.033159

Source DB:  PubMed          Journal:  Biol Reprod        ISSN: 0006-3363            Impact factor:   4.285


  6 in total

Review 1.  The switch of secondary sex determination in protandrous black porgy, Acanthopagrus schlegeli.

Authors:  Guan-Chung Wu; Ching-Fong Chang
Journal:  Fish Physiol Biochem       Date:  2012-03-13       Impact factor: 2.794

2.  GnRH isoforms expression in relation to the gonadal cycle and to dominance rank in the gilthead seabream, Sparus aurata.

Authors:  José Reyes-Tomassini; Ten Tsao Wong; Yonathan Zohar
Journal:  Fish Physiol Biochem       Date:  2012-12-18       Impact factor: 2.794

3.  Seasonal relationship between gonadotropin, growth hormone, and estrogen receptor mRNA expression in the pituitary gland of largemouth bass.

Authors:  Christopher J Martyniuk; Kevin J Kroll; Wesley F Porak; Cheree Steward; Harry J Grier; Nancy D Denslow
Journal:  Gen Comp Endocrinol       Date:  2009-05-03       Impact factor: 2.822

Review 4.  Environmental Cues and Mechanisms Underpinning Sex Change in Fish.

Authors:  Laura Casas; Fran Saborido-Rey
Journal:  Sex Dev       Date:  2021-06-10       Impact factor: 1.824

5.  Sexual Fate Reprogramming in the Steroid-Induced Bi-Directional Sex Change in the Protogynous Orange-Spotted Grouper, Epinephelus coioides.

Authors:  Guan-Chung Wu; Wei-Guan Tey; Hau-Wen Li; Ching-Fong Chang
Journal:  PLoS One       Date:  2015-12-29       Impact factor: 3.240

6.  The Ovarian Transcriptome at the Early Stage of Testis Removal-Induced Male-To-Female Sex Change in the Protandrous Black Porgy Acanthopagrus schlegelii.

Authors:  Peng-Wei Tseng; Guan-Chung Wu; Wei-Lun Kuo; Yung-Che Tseng; Ching-Fong Chang
Journal:  Front Genet       Date:  2022-03-23       Impact factor: 4.599

  6 in total

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