Literature DB >> 23063409

Lactogenic hormones stimulate expression of lipogenic genes but not glucose transporters in bovine mammary gland.

Y Shao1, E H Wall, T B McFadden, Y Misra, X Qian, R Blauwiekel, D Kerr, F-Q Zhao.   

Abstract

During the onset of lactation, there is a dramatic increase in the expression of glucose transporters (GLUT) and a group of enzymes involved in milk fat synthesis in the bovine mammary gland. The objective of this study was to investigate whether the lactogenic hormones mediate both of these increases. Bovine mammary explants were cultured for 48, 72, or 96 h with the following hormone treatments: no hormone (control), IGF-I, insulin (Ins), Ins + hydrocortisone + ovine prolactin (InsHPrl), or Ins + hydrocortisone + prolactin + 17β-estradiol (InsHPrlE). The relative expression of β-casein, α-lactalbumin, sterol regulatory element binding factor 1 (SREBF1), fatty acid synthase (FASN), acetyl-CoA carboxylase α (ACACA), stearyol-CoA desaturase (SCD), GLUT1, GLUT8, and GLUT12 were measured by real-time PCR. Exposure to the lactogenic hormone combinations InsHPrl and InsHPrlE for 96 h stimulated expression of β-casein and α-lactalbumin mRNA by several hundred-fold and also increased the expression of SREBF1, FASN, ACACA, and SCD genes in mammary explants (P < 0.01). However, those hormone combinations had no effect on GLUT1 or GLUT8 expression and inhibited GLUT12 expression by 50% after 72 h of treatment (P < 0.05). In separate experiments, the expression of GLUTs in the mouse mammary epithelial cell line HC11 or in bovine primary mammary epithelial cells was not increased by lactogenic hormone treatments. Moreover, treatment of dairy cows with bovine prolactin had no effect on GLUT expression in the mammary gland. In conclusion, lactogenic hormones clearly stimulate expression of milk protein and lipogenic genes, but they do not appear to mediate the marked up-regulation of GLUT expression in the mammary gland during the onset of lactation.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 23063409     DOI: 10.1016/j.domaniend.2012.09.001

Source DB:  PubMed          Journal:  Domest Anim Endocrinol        ISSN: 0739-7240            Impact factor:   2.290


  7 in total

Review 1.  Morphological, hormonal, and molecular changes in different maternal tissues during lactation and post-lactation.

Authors:  Gustavo Canul-Medina; Cristina Fernandez-Mejia
Journal:  J Physiol Sci       Date:  2019-09-28       Impact factor: 2.781

Review 2.  Biology of glucose transport in the mammary gland.

Authors:  Feng-Qi Zhao
Journal:  J Mammary Gland Biol Neoplasia       Date:  2013-11-13       Impact factor: 2.673

3.  Emerging evidence of the physiological role of hypoxia in mammary development and lactation.

Authors:  Yong Shao; Feng-Qi Zhao
Journal:  J Anim Sci Biotechnol       Date:  2014-01-21

4.  Supplemental Smartamine M in higher-energy diets during the prepartal period improves hepatic biomarkers of health and oxidative status in Holstein cows.

Authors:  Mario Vailati-Riboni; Johan S Osorio; Erminio Trevisi; Daniel Luchini; Juan J Loor
Journal:  J Anim Sci Biotechnol       Date:  2017-02-06

5.  GLUT1 and lactose synthetase are critical genes for lactose synthesis in lactating sows.

Authors:  Yinzhi Zhang; Shihai Zhang; Wutai Guan; Fang Chen; Lin Cheng; Yantao Lv; Jun Chen
Journal:  Nutr Metab (Lond)       Date:  2018-06-13       Impact factor: 4.169

6.  Prolactin-induced Subcellular Targeting of GLUT1 Glucose Transporter in Living Mammary Epithelial Cells.

Authors:  Arieh Riskin; Yehudit Mond
Journal:  Rambam Maimonides Med J       Date:  2015-10-26

7.  Polyherbal formula (ASILACT®) induces Milk production in lactating rats through Upregulation of α-Lactalbumin and aquaporin expression.

Authors:  Fara Silvia Yuliani; Setyo Purwono; Ahmad Hamim Sadewa; Ema Damayanti; Didik Setyo Heriyanto
Journal:  BMC Complement Med Ther       Date:  2020-11-26
  7 in total

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