Literature DB >> 9740599

Transcription-modulating drugs: a new frontier in the treatment of essential hypertension.

T W Kurtz1, D G Gardner.   

Abstract

While the promises of gene therapy may be years away from realization, the therapeutic use of drugs that act by modifying gene transcription is a well-established practice in clinical medicine. Although transcription-modulating drugs are frequently used in many different specialties, the deliberate development and use of these agents in cardiovascular medicine has been comparatively limited. However, research advances in the area of gene transcription and in the molecular genetic regulation of blood pressure, insulin resistance, lipid metabolism, and cell growth are providing new opportunities for controlling the expression of genes that are relevant to the pathogenesis of cardiovascular disease and essential hypertension. These research advances are beginning to converge in the development of transcription-modulating drugs with the potential to attack genetically determined risk factors that often cluster in patients with essential hypertension. Ligand-activated transcription factors that serve as receptors for small lipophilic compounds such as the thiazolidinediones and retinoids represent examples of potential therapeutic targets with direct effects on the expression of genes relevant to the pathogenesis of essential hypertension and its complications. Mounting evidence suggesting that the superior cardiorenal protective properties of converting enzyme inhibitors are related in part to their ability to indirectly modify the expression of genes in the heart and vasculature provides provisional support for the clinical value of this therapeutic approach. Given the success of transcription-modulating drugs in the treatment of type II diabetes and many other clinical disorders, it is anticipated that these agents will be developed as tools for the prevention and treatment of hypertension and cardiovascular disease in the not too distant future.

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Year:  1998        PMID: 9740599     DOI: 10.1161/01.hyp.32.3.380

Source DB:  PubMed          Journal:  Hypertension        ISSN: 0194-911X            Impact factor:   10.190


  7 in total

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Authors:  Jia L Zhuo; Xiao C Li
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Authors:  J Plutzky
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Review 3.  Novel roles of intracrine angiotensin II and signalling mechanisms in kidney cells.

Authors:  Jia L Zhuo; Xiao C Li
Journal:  J Renin Angiotensin Aldosterone Syst       Date:  2007-03       Impact factor: 1.636

Review 4.  Nuclear factor-kappaB as a hormonal intracellular signaling molecule: focus on angiotensin II-induced cardiovascular and renal injury.

Authors:  Xiao C Li; Jia L Zhuo
Journal:  Curr Opin Nephrol Hypertens       Date:  2008-01       Impact factor: 2.894

5.  Intracellular ANG II directly induces in vitro transcription of TGF-beta1, MCP-1, and NHE-3 mRNAs in isolated rat renal cortical nuclei via activation of nuclear AT1a receptors.

Authors:  Xiao C Li; Jia L Zhuo
Journal:  Am J Physiol Cell Physiol       Date:  2008-02-06       Impact factor: 4.249

6.  Effects of AT1 receptor-mediated endocytosis of extracellular Ang II on activation of nuclear factor-kappa B in proximal tubule cells.

Authors:  Jia L Zhuo; Oscar A Carretero; Xiao C Li
Journal:  Ann N Y Acad Sci       Date:  2006-12       Impact factor: 5.691

Review 7.  Intratubular, Intracellular, and Mitochondrial Angiotensin II/AT1 (AT1a) Receptor/NHE3 Signaling Plays a Critical Role in Angiotensin II-Induced Hypertension and Kidney Injury.

Authors:  Xiao Chun Li; Chih-Hong Wang; Ana Paula Oliveira Leite; Jia Long Zhuo
Journal:  Front Physiol       Date:  2021-08-02       Impact factor: 4.566

  7 in total

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