Literature DB >> 15956350

Expression of prolactin-releasing peptide and prolactin in the euryhaline mudskippers (Periophthalmus modestus): prolactin-releasing peptide as a primary regulator of prolactin.

T Sakamoto1, M Amano, S Hyodo, S Moriyama, A Takahashi, H Kawauchi, M Ando.   

Abstract

Prolactin (PRL)-releasing peptide (PrRP) is a strong candidate stimulator of pituitary PRL transcription and secretion in teleosts. However, the role in control of extrapituitary PRL expression is unclear even in mammals. To study the possible presence of PrRP-PRL axes not only in the brain-pituitary but also in peripheral organs, the expression patterns of PrRP, PRL and growth hormone (GH) were characterized in amphibious euryhaline mudskippers (Periophthalmus modestus). PrRP mRNA is abundantly expressed not only in the brain but also in the liver, gut and ovary, while less abundant expression was also detected in the skin and kidney. Corresponding to the distribution of PrRP mRNA, PRL mRNA was also detectable in these organs. During adaptation to different environments, the changes in mRNA levels of PrRP paralleled those in PRL in the brain-pituitary, liver and gut in an organ-specific manner. Brain PrRP mRNA and the pituitary PRL mRNA increased under freshwater and terrestrial conditions (P < 0.05); expression of PrRP and PRL in the gut of freshwater fish was higher (P < 0.05) than those in sea-water fish although there were no changes in fish kept out of water; no significant change was seen in the liver. Expressions of GH were not correlated with PrRP. In the gut, PrRP and PRL appear to be co-localized in the mucosal layer, especially in the mucous cells. Thus, PrRP may also be a local modulator of extrapituitary PRL expression and the PrRP-PRL axes in various organs may play an organ-specific role during environmental adaptation.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15956350     DOI: 10.1677/jme.1.01768

Source DB:  PubMed          Journal:  J Mol Endocrinol        ISSN: 0952-5041            Impact factor:   5.098


  7 in total

1.  Cell proliferation and apoptosis in the anterior intestine of an amphibious, euryhaline mudskipper (Periophthalmus modestus).

Authors:  H Takahashi; T Sakamoto; K Narita
Journal:  J Comp Physiol B       Date:  2006-02-16       Impact factor: 2.200

2.  High ambient ammonia promotes growth in a ureogenic goby, Mugilogobius abei.

Authors:  K Iwata; T Sakamoto; I Iwata; E Nishiguchi; M Kajimura
Journal:  J Comp Physiol B       Date:  2005-07-05       Impact factor: 2.200

Review 3.  Functions of two distinct "prolactin-releasing peptides" evolved from a common ancestral gene.

Authors:  Tetsuya Tachibana; Tatsuya Sakamoto
Journal:  Front Endocrinol (Lausanne)       Date:  2014-11-10       Impact factor: 5.555

Review 4.  The Amphibious Mudskipper: A Unique Model Bridging the Gap of Central Actions of Osmoregulatory Hormones Between Terrestrial and Aquatic Vertebrates.

Authors:  Yukitoshi Katayama; Tatsuya Sakamoto; Keiko Takanami; Yoshio Takei
Journal:  Front Physiol       Date:  2018-08-14       Impact factor: 4.566

5.  Neurohypophysial Hormones Regulate Amphibious Behaviour in the Mudskipper Goby.

Authors:  Tatsuya Sakamoto; Yudai Nishiyama; Aoi Ikeda; Hideya Takahashi; Susumu Hyodo; Nao Kagawa; Hirotaka Sakamoto
Journal:  PLoS One       Date:  2015-07-31       Impact factor: 3.240

Review 6.  Prolactin-Releasing Peptide: Physiological and Pharmacological Properties.

Authors:  Veronika Pražienková; Andrea Popelová; Jaroslav Kuneš; Lenka Maletínská
Journal:  Int J Mol Sci       Date:  2019-10-24       Impact factor: 5.923

Review 7.  Introducing the Amphibious Mudskipper Goby as a Unique Model to Evaluate Neuro/Endocrine Regulation of Behaviors Mediated by Buccal Sensation and Corticosteroids.

Authors:  Yukitoshi Katayama; Kazuhiro Saito; Tatsuya Sakamoto
Journal:  Int J Mol Sci       Date:  2020-09-14       Impact factor: 5.923

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.