Literature DB >> 10872446

The molecular basis of hypertension.

D L Garbers1, S K Dubois.   

Abstract

More than 50 million Americans display blood pressures outside the safe physiological range. Unfortunately for most individuals, the molecular basis of hypertension is unknown, in part because pathological elevations of blood pressure are the result of abnormal expression of multiple genes. This review identifies a number of important blood pressure regulatory genes including their loci in the human, mouse, and rat genome. Phenotypes of gene deletions and overexpression in mice are summarized. More detailed discussion of selected gene products follows, beginning with proteins involved in ion transport, specifically the epithelial sodium channel and sodium proton exchangers. Next, proteins involved in vasodilation/natriuresis are discussed with emphasis on natriuretic peptides, guanylin/uroguanylin, and nitric oxide. The renin angiotensin aldosterone system has an important role antagonizing the vasodilatory cyclic GMP system.

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Year:  1999        PMID: 10872446     DOI: 10.1146/annurev.biochem.68.1.127

Source DB:  PubMed          Journal:  Annu Rev Biochem        ISSN: 0066-4154            Impact factor:   23.643


  14 in total

1.  The region of rat chromosome 10 (the ngfr gene locus) is associated with blood pressure increase in response to emotional stress.

Authors:  O E Redina; N E Lapteva; S L Khanina; N A Machanova; G M Dymshits; A L Markel
Journal:  Dokl Biochem Biophys       Date:  2001 Sep-Oct       Impact factor: 0.788

Review 2.  Global analysis of gene expression in mammalian kidney.

Authors:  Olga Soutourina; Lydie Cheval; Alain Doucet
Journal:  Pflugers Arch       Date:  2004-12-21       Impact factor: 3.657

3.  Alterations in the regulation of androgen-sensitive Cyp 4a monooxygenases cause hypertension.

Authors:  V R Holla; F Adas; J D Imig; X Zhao; E Price; N Olsen; W J Kovacs; M A Magnuson; D S Keeney; M D Breyer; J R Falck; M R Waterman; J H Capdevila
Journal:  Proc Natl Acad Sci U S A       Date:  2001-04-24       Impact factor: 11.205

4.  Increased renal proximal convoluted tubule transport contributes to hypertension in Cyp4a14 knockout mice.

Authors:  Raymond Quigley; Sumana Chakravarty; Xueying Zhao; John D Imig; Jorge H Capdevila
Journal:  Nephron Physiol       Date:  2009-08-28

5.  Conditional and targeted overexpression of vascular chymase causes hypertension in transgenic mice.

Authors:  H Ju; R Gros; X You; S Tsang; M Husain; M Rabinovitch
Journal:  Proc Natl Acad Sci U S A       Date:  2001-06-19       Impact factor: 11.205

6.  Vascular endothelium is critically involved in the hypotensive and hypovolemic actions of atrial natriuretic peptide.

Authors:  Karim Sabrane; Markus N Kruse; Larissa Fabritz; Bernd Zetsche; Danuta Mitko; Boris V Skryabin; Melanie Zwiener; Hideo A Baba; Masashi Yanagisawa; Michaela Kuhn
Journal:  J Clin Invest       Date:  2005-06       Impact factor: 14.808

7.  A genetic model provides evidence that the receptor for atrial natriuretic peptide (guanylyl cyclase-A) inhibits cardiac ventricular myocyte hypertrophy.

Authors:  I Kishimoto; K Rossi; D L Garbers
Journal:  Proc Natl Acad Sci U S A       Date:  2001-02-13       Impact factor: 11.205

8.  Cloning of a novel human NHEDC1 (Na+/H+ exchanger like domain containing 1) gene expressed specifically in testis.

Authors:  Guangming Ye; Cong Chen; Dingding Han; Xiabin Xiong; Yahui Kong; Bo Wan; Long Yu
Journal:  Mol Biol Rep       Date:  2006-09       Impact factor: 2.316

9.  Protein kinase G-I deficiency induces pulmonary hypertension through Rho A/Rho kinase activation.

Authors:  Yidan D Zhao; Lei Cai; Muhammad K Mirza; Xiaojia Huang; Dave L Geenen; Franz Hofmann; Jason X-J Yuan; You-Yang Zhao
Journal:  Am J Pathol       Date:  2012-06       Impact factor: 4.307

10.  Anti-oxidants correct disturbance of redox enzymes in the hearts of rat fetuses with congenital diaphragmatic hernia.

Authors:  Rosa Aras-López; L Almeida; V Andreu-Fernández; J Tovar; L Martínez
Journal:  Pediatr Surg Int       Date:  2017-10-27       Impact factor: 1.827

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