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Expressional Changes of Connexin Isoform Genes in the Rat Caput Epididymis Exposed to Flutamide or Estradiol Benzoate at the Early Postnatal Age.

作者信息

Lee Ki-Ho

机构信息

Department of Biochemistry and Molecular Biology, College of Medicine, Eulji University, Daejeon 301-746, Korea.

出版信息

Dev Reprod. 2017 Sep;21(3):317-325. doi: 10.12717/DR.2017.21.3.317. Epub 2017 Sep 30.

DOI:10.12717/DR.2017.21.3.317
PMID:29082347
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5651698/
Abstract

Direct communication between neighboring cells through connexin ()-based gap junction is a crucial biolo-gical manner to regulate functions of a tissue consisting of multi-cell types. The present research evaluated expressional changes of isoforms in the caput epididymis of adult rat exposed to estradiol benzoate (EB) or flutamide (Flu) at the early postnatal age. A single subcutaneous administration of EB at a low-dose [0.015 µg /kg body weight (BW)] or a high-dose (1.5 µg/kg BW) or Flu at a low-dose (500 µg/kg BW) or a high-dose (5 mg/kg BW) was performed to an animal at 1 week of age. Quantitative real-time PCR analysis was employed to determine expressional changes of isoforms. The transcript levels of s30.3 and 37 were decreased by a low-dose EB treatment, while decreases of s31, 31.1, 32, 40, and 45 transcript levels were observed with a low-dose EB treatment. The treatment of a high-dose EB resulted in expressional reduction of s30.3, 31, 31.1, 37, 40, 43, and 45. The Flu treatment at a low dose caused increases of s26, 37, and 40 transcript levels but decreases of s31.1, 43, and 45 transcript levels. Increases of s30.3, 31, 37, and 40 mRNA amounts were induced by a high-dose Flu treatment. However, exposure to a high-dose Flu produced expressional decreases of s31.1, 32, and 43 in the adult caput epididymis. These observations suggest that exposure to EB or Flu at the neonatal period could lead to aberrant expression of isoforms in the adult caput epididymis.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e3/5651698/815c62c4786a/dr-21-3-317-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e3/5651698/17c6d3ab7c2e/dr-21-3-317-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e3/5651698/238e006b43cf/dr-21-3-317-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e3/5651698/831e5b554416/dr-21-3-317-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e3/5651698/815c62c4786a/dr-21-3-317-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e3/5651698/17c6d3ab7c2e/dr-21-3-317-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e3/5651698/238e006b43cf/dr-21-3-317-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e3/5651698/831e5b554416/dr-21-3-317-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e3/5651698/815c62c4786a/dr-21-3-317-g4.jpg

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本文引用的文献

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Dev Reprod. 2016 Sep;20(3):237-245. doi: 10.12717/DR.2016.20.3.237.
2
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Dev Reprod. 2015 Jun;19(2):69-77. doi: 10.12717/DR.2015.19.2.069.
3
Postnatal exposure to flutamide affects CDH1 and CTNNB1 gene expression in adult pig epididymis and prostate and alters metabolism of testosterone.
产后暴露于氟他胺会影响成年猪附睾和前列腺中 CDH1 和 CTNNB1 基因的表达,并改变睾酮的代谢。
Andrology. 2014 Mar;2(2):186-97. doi: 10.1111/j.2047-2927.2013.00172.x. Epub 2013 Dec 18.
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Gap junctions.缝隙连接。
Cold Spring Harb Perspect Biol. 2009 Jul;1(1):a002576. doi: 10.1101/cshperspect.a002576.
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Gap junctions: basic structure and function.间隙连接:基本结构与功能
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