Literature DB >> 18832082

Microarray analysis of the transcriptome of the subfornical organ in the rat: regulation by fluid and food deprivation.

Charles Hindmarch1, Mark Fry, Song T Yao, Pauline M Smith, David Murphy, Alastair V Ferguson.   

Abstract

We have employed microarray technology using Affymetrix 230 2.0 genome chips to initially catalog the transcriptome of the subfornical organ (SFO) under control conditions and to also evaluate the changes (common and differential) in gene expression induced by the challenges of fluid and food deprivation. We have identified a total of 17,293 genes tagged as present in one of our three experimental conditions, transcripts, which were then used as the basis for further filtering and statistical analysis. In total, the expression of 46 genes was changed in the SFO following dehydration compared with control animals (22 upregulated and 24 downregulated), with the largest change being the greater than fivefold increase in brain-derived neurotrophic factor (BDNF) expression, while significant changes in the expression of the calcium-sensing (upregulated) and apelin (downregulated) receptors were also reported. In contrast, food deprivation caused greater than twofold changes in a total of 687 transcripts (222 upregulated and 465 downregulated), including significant reductions in vasopressin, oxytocin, promelanin concentrating hormone, cocaine amphetamine-related transcript (CART), and the endothelin type B receptor, as well as increases in the expression of the GABA(B) receptor. Of these regulated transcripts, we identified 37 that are commonly regulated by fasting and dehydration, nine that were uniquely regulated by dehydration, and 650 that are uniquely regulated by fasting. We also found five transcripts that were differentially regulated by fasting and dehydration including BDNF and CART. In these studies we have for the first time described the transcriptome of the rat SFO and have in addition identified genes, the expression of which is significantly modified by either water or food deprivation.

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Year:  2008        PMID: 18832082     DOI: 10.1152/ajpregu.90560.2008

Source DB:  PubMed          Journal:  Am J Physiol Regul Integr Comp Physiol        ISSN: 0363-6119            Impact factor:   3.619


  18 in total

Review 1.  Significance of SGK1 in the regulation of neuronal function.

Authors:  Florian Lang; Nathalie Strutz-Seebohm; Guiscard Seebohm; Undine E Lang
Journal:  J Physiol       Date:  2010-06-07       Impact factor: 5.182

Review 2.  Physiological roles for the subfornical organ: a dynamic transcriptome shaped by autonomic state.

Authors:  Charles Colin Thomas Hindmarch; Alastair V Ferguson
Journal:  J Physiol       Date:  2015-10-13       Impact factor: 5.182

3.  ENaC-expressing neurons in the sensory circumventricular organs become c-Fos activated following systemic sodium changes.

Authors:  Rebecca L Miller; Michelle H Wang; Paul A Gray; Lawrence B Salkoff; Arthur D Loewy
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2013-09-18       Impact factor: 3.619

4.  Mapping Molecular Datasets Back to the Brain Regions They are Extracted from: Remembering the Native Countries of Hypothalamic Expatriates and Refugees.

Authors:  Arshad M Khan; Alice H Grant; Anais Martinez; Gully A P C Burns; Brendan S Thatcher; Vishwanath T Anekonda; Benjamin W Thompson; Zachary S Roberts; Daniel H Moralejo; James E Blevins
Journal:  Adv Neurobiol       Date:  2018

5.  Apelin acts in the subfornical organ to influence neuronal excitability and cardiovascular function.

Authors:  Li Dai; Pauline M Smith; Markus Kuksis; Alastair V Ferguson
Journal:  J Physiol       Date:  2013-04-29       Impact factor: 5.182

6.  5-HT neurons of the area postrema become c-Fos-activated after increases in plasma sodium levels and transmit interoceptive information to the nucleus accumbens.

Authors:  Rebecca L Miller; Arthur D Loewy
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2014-03-05       Impact factor: 3.619

7.  ENaC γ-expressing astrocytes in the circumventricular organs, white matter, and ventral medullary surface: sites for Na+ regulation by glial cells.

Authors:  Rebecca L Miller; Arthur D Loewy
Journal:  J Chem Neuroanat       Date:  2013-10-18       Impact factor: 3.052

8.  Osmoregulation requires brain expression of the renal Na-K-2Cl cotransporter NKCC2.

Authors:  Agnieszka Konopacka; Jing Qiu; Song T Yao; Michael P Greenwood; Mingkwan Greenwood; Thomas Lancaster; Wataru Inoue; Andre de Souza Mecawi; Fernanda M V Vechiato; Juliana B M de Lima; Ricardo Coletti; See Ziau Hoe; Andrew Martin; Justina Lee; Marina Joseph; Charles Hindmarch; Julian Paton; Jose Antunes-Rodrigues; Jaideep Bains; David Murphy
Journal:  J Neurosci       Date:  2015-04-01       Impact factor: 6.167

9.  A comparison of physiological and transcriptome responses to water deprivation and salt loading in the rat supraoptic nucleus.

Authors:  Michael P Greenwood; Andre S Mecawi; See Ziau Hoe; Mohd Rais Mustafa; Kory R Johnson; Ghada A Al-Mahmoud; Lucila L K Elias; Julian F R Paton; Jose Antunes-Rodrigues; Harold Gainer; David Murphy; Charles C T Hindmarch
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2015-01-28       Impact factor: 3.619

Review 10.  G protein-coupled receptors in the hypothalamic paraventricular and supraoptic nuclei--serpentine gateways to neuroendocrine homeostasis.

Authors:  Georgina G J Hazell; Charles C Hindmarch; George R Pope; James A Roper; Stafford L Lightman; David Murphy; Anne-Marie O'Carroll; Stephen J Lolait
Journal:  Front Neuroendocrinol       Date:  2011-07-23       Impact factor: 8.606

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