Literature DB >> 21472224

Gene expression in the adrenal glands of three spontaneously hypertensive rat substrains.

Mohammad S Ashenagar1, Masaki Tabuchi, Kosho Kinoshita, Kana Ooshima, Atsuko Niwa, Yuko Watanabe, Momoko Yoshida, Kazunori Shimada, Teruo Yasunaga, Hiromichi Yamanishi, Hideaki Higashino.   

Abstract

We examined gene expression profiles in rat adrenal glands using genome-wide microarray technology. Gene expression levels were determined in four rat strains, including one normotensive strain [Wistar-Kyoto (WKY)] and three substrains derived from WKY rats: spontaneously hypertensive rats (SHR), stroke-prone SHR (SHRSP) and malignant SHRSP (M-SHRSP). This study represents the first attempt at using microarrays to compare gene expression profiles in SHR, SHRSP and M-SHRSP adrenal glands, employing WKY as controls. Expression measurements were made in these four rat strains at 6 and 9 weeks of age; 6 weeks of age covers the pre-hypertensive period in SHR and SHRSP, and 9 weeks of age is the period of rapidly rising blood pressure (BP). Since the aim of this study was to identify candidate genes involved in the genesis of hypertension in the SHR substrains, we identified genes that were consistently different in their expression, isolating 87 up-regulated genes showing a more than 4-fold increase and 128 down-regulated genes showing a less than 1/4-fold decrease in at least two different experiments. We classified all these up- or down-regulated genes by their expression profiles, and searched for candidate genes. At 6 weeks of age, several BP-regulating genes including sparc/osteonectin (Spock2), kynureninase (Kynu), regulator of G-protein signaling 2 (Rgs2) and gap junction protein α1 (Gja1) were identified as up-regulated, and urotensin 2 (Uts2), cytoplasmic epoxide hydrolase 2 (Ephx2), apelin (Apln), insulin-like growth factor 1 receptor (Igf1r) and angiotensin II receptor-associated protein (Agtrap) were identified as down-regulated. The Kynu and Ephx2 genes have previously been reported by other groups to be responsible for hypertension in SHR; however, our present approach identified at least seven new candidate genes.

Entities:  

Year:  2010        PMID: 21472224     DOI: 10.3892/mmr_00000242

Source DB:  PubMed          Journal:  Mol Med Rep        ISSN: 1791-2997            Impact factor:   2.952


  4 in total

1.  Whole rat DNA array survey for candidate genes related to hypertension in kidneys from three spontaneously hypertensive rat substrains at two stages of age and with hypotensive induction caused by hydralazine hydrochloride.

Authors:  Kosho Kinoshita; Mohammad Said Ashenagar; Masaki Tabuchi; Hideaki Higashino
Journal:  Exp Ther Med       Date:  2011-01-14       Impact factor: 2.447

2.  Gene Expression and MicroRNA Expression Analysis in Small Arteries of Spontaneously Hypertensive Rats. Evidence for ER Stress.

Authors:  Teresa Palao; Karl Swärd; Aldo Jongejan; Perry D Moerland; Judith de Vos; Angela van Weert; Silvia M Arribas; Gergely Groma; Ed vanBavel; Erik N T P Bakker
Journal:  PLoS One       Date:  2015-09-10       Impact factor: 3.240

3.  A new approach to identifying hypertension-associated genes in the mesenteric artery of spontaneously hypertensive rats and stroke-prone spontaneously hypertensive rats.

Authors:  Takashi Ikawa; Yuko Watanabe; Daisuke Okuzaki; Naohisa Goto; Nobutaka Okamura; Kyosuke Yamanishi; Toshihide Higashino; Hiromichi Yamanishi; Haruki Okamura; Hideaki Higashino
Journal:  J Hypertens       Date:  2019-08       Impact factor: 4.844

4.  Dissecting the genetic components of a quantitative trait locus for blood pressure and renal pathology on rat chromosome 3.

Authors:  H H Caline Koh-Tan; Mohammed Dashti; Ting Wang; Wendy Beattie; John Mcclure; Barbara Young; Anna F Dominiczak; Martin W McBride; Delyth Graham
Journal:  J Hypertens       Date:  2017-02       Impact factor: 4.844

  4 in total

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