Literature DB >> 16946131

Tetrahydrobiopterin and cardiovascular disease.

An L Moens1, David A Kass.   

Abstract

Tetrahydrobiopterin (BH4) is an essential cofactor for the aromatic amino acid hydroxylases, which are essential in the formation of neurotransmitters, and for nitric oxide synthase. It is presently used clinically to treat some forms of phenylketonuria (PKU) that can be ameliorated by BH4 supplementation. Recent evidence supports potential cardiovascular benefits from BH4 replacement for the treatment of hypertension, ischemia-reperfusion injury, and cardiac hypertrophy with chamber remodeling. Such disorders exhibit BH4 depletion because of its oxidation and/or reduced synthesis, which can result in functional uncoupling of nitric oxide synthase (NOS). Uncoupled NOS generates more oxygen free radicals and less nitric oxide, shifting the nitroso-redox balance and having adverse consequences on the cardiovascular system. While previously difficult to use as a treatment because of chemical instability and cost, newer methods to synthesize stable BH4 suggest its novel potential as a therapeutic agent. This review discusses the biochemistry, physiology, and evolving therapeutic potential of BH4 for cardiovascular disease.

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Year:  2006        PMID: 16946131     DOI: 10.1161/01.ATV.0000243924.00970.cb

Source DB:  PubMed          Journal:  Arterioscler Thromb Vasc Biol        ISSN: 1079-5642            Impact factor:   8.311


  72 in total

1.  Nitric oxide synthase 3 contributes to ventilator-induced lung injury.

Authors:  Katerina Vaporidi; Roland C Francis; Kenneth D Bloch; Warren M Zapol
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2.  Local tetrahydrobiopterin administration augments reflex cutaneous vasodilation through nitric oxide-dependent mechanisms in aged human skin.

Authors:  Anna E Stanhewicz; Rebecca S Bruning; Caroline J Smith; W Larry Kenney; Lacy A Holowatz
Journal:  J Appl Physiol (1985)       Date:  2011-12-08

Review 3.  Endothelium-derived vasoactive factors and hypertension: possible roles in pathogenesis and as treatment targets.

Authors:  Michel Félétou; Ralf Köhler; Paul M Vanhoutte
Journal:  Curr Hypertens Rep       Date:  2010-08       Impact factor: 5.369

4.  Polymorphisms of genes in nitric oxide-forming pathway associated with ischemic stroke in Chinese Han population.

Authors:  Jiang-tao Yan; Lan Zhang; Yu-jun Xu; Xiao-jing Wang; Cong-yi Wang; Dao-wen Wang
Journal:  Acta Pharmacol Sin       Date:  2011-10-03       Impact factor: 6.150

Review 5.  Oxidative stress in diabetic nephropathy.

Authors:  N Kashihara; Y Haruna; V K Kondeti; Y S Kanwar
Journal:  Curr Med Chem       Date:  2010       Impact factor: 4.530

Review 6.  Mechanisms of I/R-Induced Endothelium-Dependent Vasodilator Dysfunction.

Authors:  Ronald J Korthuis
Journal:  Adv Pharmacol       Date:  2017-12-08

7.  GTP cyclohydrolase 1 gene 3'-UTR C+243T variant predicts worsening outcome in patients with first-onset ischemic stroke.

Authors:  Ling Tang; Lan Zhang; Hu Ding; Wei Tu; Jiangtao Yan
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2010-12-22

8.  Sexual dimorphism, the aging kidney, and involvement of nitric oxide deficiency.

Authors:  Chris Baylis
Journal:  Semin Nephrol       Date:  2009-11       Impact factor: 5.299

Review 9.  Cellular signaling and NO production.

Authors:  Thomas Michel; Paul M Vanhoutte
Journal:  Pflugers Arch       Date:  2010-01-16       Impact factor: 3.657

10.  Hypertension, cardiac hypertrophy, and impaired vascular relaxation induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin are associated with increased superoxide.

Authors:  Phillip G Kopf; Janice K Huwe; Mary K Walker
Journal:  Cardiovasc Toxicol       Date:  2008-10-11       Impact factor: 3.231

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