Literature DB >> 17925483

Nutrition-induced ketosis alters metabolic and signaling gene networks in liver of periparturient dairy cows.

Juan J Loor1, Robin E Everts, Massimo Bionaz, Heather M Dann, Dawn E Morin, Rosane Oliveira, Sandra L Rodriguez-Zas, James K Drackley, Harris A Lewin.   

Abstract

Dairy cows are highly susceptible after parturition to developing liver lipidosis and ketosis, which are costly diseases to farmers. A bovine microarray platform consisting of 13,257-annotated oligonucleotides was used to study hepatic gene networks underlying nutrition-induced ketosis. On day 5 postpartum, 14 Holstein cows were randomly assigned to ketosis-induction (n = 7) or control (n = 7) groups. Cows in the ketosis-induction group were fed at 50% of day 4 intake until they developed signs of clinical ketosis, and cows in the control group were fed ad libitum throughout the treatment period. Liver was biopsied at 10-14 (ketosis) or 14 days postpartum (controls). Feed restriction increased blood concentrations of nonesterified fatty acids and beta-hydroxybutyrate, but decreased glucose. Liver triacylglycerol concentration also increased. A total of 2,415 genes were altered by ketosis (false discovery rate = 0.05). Ingenuity Pathway Analysis revealed downregulation of genes associated with oxidative phosphorylation, protein ubiquitination, and ubiquinone biosynthesis with ketosis. Other molecular adaptations included upregulation of genes and nuclear receptors associated with cytokine signaling, fatty acid uptake/transport, and fatty acid oxidation. Genes downregulated during ketosis included several associated with cholesterol metabolism, growth hormone signaling, proton transport, and fatty acid desaturation. Feed restriction and ketosis resulted in previously unrecognized alterations in gene network expression underlying key cellular functions and discrete metabolic events. These responses might help explain well-documented physiological adaptations to reduced feed intake in early postpartum cows and, thus, provide molecular targets that might be useful in prevention and treatment of liver lipidosis and ketosis.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17925483     DOI: 10.1152/physiolgenomics.00188.2007

Source DB:  PubMed          Journal:  Physiol Genomics        ISSN: 1094-8341            Impact factor:   3.107


  85 in total

1.  Endometrium as an early sensor of in vitro embryo manipulation technologies.

Authors:  Nadéra Mansouri-Attia; Olivier Sandra; Julie Aubert; Séverine Degrelle; Robin E Everts; Corinne Giraud-Delville; Yvan Heyman; Laurent Galio; Isabelle Hue; Xiangzhong Yang; X Cindy Tian; Harris A Lewin; Jean-Paul Renard
Journal:  Proc Natl Acad Sci U S A       Date:  2009-03-18       Impact factor: 11.205

2.  Buffalo liver transcriptome analysis suggests immune tolerance as its key adaptive mechanism during early postpartum negative energy balance.

Authors:  Sudhakar Singh; Naresh Golla; Davinder Sharma; Dheer Singh; Suneel Kumar Onteru
Journal:  Funct Integr Genomics       Date:  2019-05-09       Impact factor: 3.410

3.  Effect of dietary n-3 polyunsaturated fatty acids on transcription factor regulation in the bovine endometrium.

Authors:  Sinéad M Waters; Gerard S Coyne; David A Kenny; Dermot G Morris
Journal:  Mol Biol Rep       Date:  2014-01-22       Impact factor: 2.316

4.  Enhancing the role of veterinary vaccines reducing zoonotic diseases of humans: linking systems biology with vaccine development.

Authors:  L Garry Adams; Sangeeta Khare; Sara D Lawhon; Carlos A Rossetti; Harris A Lewin; Mary S Lipton; Joshua E Turse; Dennis C Wylie; Yu Bai; Kenneth L Drake
Journal:  Vaccine       Date:  2011-06-07       Impact factor: 3.641

Review 5.  Functional adaptations of the transcriptome to mastitis-causing pathogens: the mammary gland and beyond.

Authors:  Juan J Loor; Kasey M Moyes; Massimo Bionaz
Journal:  J Mammary Gland Biol Neoplasia       Date:  2011-10-04       Impact factor: 2.673

6.  Characterization of the prohormone complement in cattle using genomic libraries and cleavage prediction approaches.

Authors:  Bruce R Southey; Sandra L Rodriguez-Zas; Jonathan V Sweedler
Journal:  BMC Genomics       Date:  2009-05-16       Impact factor: 3.969

7.  Pleiotropic effects of negative energy balance in the postpartum dairy cow on splenic gene expression: repercussions for innate and adaptive immunity.

Authors:  D G Morris; S M Waters; S D McCarthy; J Patton; B Earley; R Fitzpatrick; J J Murphy; M G Diskin; D A Kenny; A Brass; D C Wathes
Journal:  Physiol Genomics       Date:  2009-06-30       Impact factor: 3.107

8.  Functional and gene network analyses of transcriptional signatures characterizing pre-weaned bovine mammary parenchyma or fat pad uncovered novel inter-tissue signaling networks during development.

Authors:  Paola Piantoni; Massimo Bionaz; Daniel E Graugnard; Kristy M Daniels; Robin E Everts; Sandra L Rodriguez-Zas; Harris A Lewin; Hurley L Hurley; Michael Akers; Juan J Loor
Journal:  BMC Genomics       Date:  2010-05-26       Impact factor: 3.969

9.  Systems biology analysis of gene expression during in vivo Mycobacterium avium paratuberculosis enteric colonization reveals role for immune tolerance.

Authors:  Sangeeta Khare; Sara D Lawhon; Kenneth L Drake; Jairo E S Nunes; Josely F Figueiredo; Carlos A Rossetti; Tamara Gull; Robin E Everts; Harris A Lewin; Cristi L Galindo; Harold R Garner; Leslie Garry Adams
Journal:  PLoS One       Date:  2012-08-17       Impact factor: 3.240

10.  Gene network and pathway analysis of bovine mammary tissue challenged with Streptococcus uberis reveals induction of cell proliferation and inhibition of PPARgamma signaling as potential mechanism for the negative relationships between immune response and lipid metabolism.

Authors:  Kasey M Moyes; James K Drackley; Dawn E Morin; Massimo Bionaz; Sandra L Rodriguez-Zas; Robin E Everts; Harris A Lewin; Juan J Loor
Journal:  BMC Genomics       Date:  2009-11-19       Impact factor: 3.969

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.