The role of plasma and vascular tetrahydrobiopterin in vascular disease states

<p>The endothelial nitric oxide synthase (eNOS) co-factor tetrahydrobiopterin (BH4) has been shown to play a pivotal role in maintaining endothelial function in experimental vascular disease models. In BH4-deficient states, eNOS becomes enzymatically ‘uncoupled’, generating reactive oxygen spe...

Szczegółowa specyfikacja

Opis bibliograficzny
1. autor: Cunnington, C
Kolejni autorzy: Channon, K
Format: Praca dyplomowa
Język:English
Wydane: 2011
Hasła przedmiotowe:
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author Cunnington, C
author2 Channon, K
author_facet Channon, K
Cunnington, C
author_sort Cunnington, C
collection OXFORD
description <p>The endothelial nitric oxide synthase (eNOS) co-factor tetrahydrobiopterin (BH4) has been shown to play a pivotal role in maintaining endothelial function in experimental vascular disease models. In BH4-deficient states, eNOS becomes enzymatically ‘uncoupled’, generating reactive oxygen species instead of nitric oxide, thus promoting endothelial dysfunction. In humans with coronary artery disease (CAD), higher vascular BH4 levels have been shown to be associated with improved endothelial function, and genetic variation in endogenous BH4 synthesis has implicated a causal role. Accordingly, BH4 has been proposed as a potential therapeutic target in vascular disease states. The work in this thesis aims to further elucidate the roles of exogenous and endogenous BH4 in humans.</p><p>In a randomised, placebo-controlled clinical trial of oral BH4 therapy in patients with CAD, exogenous BH4 had no effect on endothelial function or vascular oxidative stress. Subsequent pharmacokinetic and pharmacodynamic analysis revealed that oral BH4 significantly augmented BH4 levels in plasma and in venous tissue (but not in arterial tissue), but also increased levels of the oxidation product dihydrobiopterin (BH2), which lacks eNOS cofactor activity. Thus, there was a null effect on overall biopterin redox status.</p><p>To further understand the mechanics of exogenous BH4 oxidation, ex vivo studies of human blood and vascular tissue demonstrated that exogenous BH4 is very rapidly oxidised to BH2; co-administration with an antioxidant had only a modest effect on preventing BH4 oxidation in blood, with no beneficial effect on biopterin redox state in the vasculature.</p><p>Finally, using a “Mendelian randomisation” approach, I studied the effects of a haplotype of GCH1 (the gene encoding the rate limiting enzyme in BH4 synthesis) on endogenous BH4 bioavailability and vascular function in healthy individuals. In patients with CAD, this haplotype has been associated with decreased BH4 bioavailability and eNOS uncoupling, however in healthy individuals the haplotype exerted no significant effect, likely due to reduced inflammatory stimulation of GCH1.</p>
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spelling oxford-uuid:33df2f8a-f16b-4271-988a-4500ed89d35e2024-12-07T12:40:58ZThe role of plasma and vascular tetrahydrobiopterin in vascular disease statesThesishttp://purl.org/coar/resource_type/c_db06uuid:33df2f8a-f16b-4271-988a-4500ed89d35eCardiovascular diseaseEnglishOxford University Research Archive - Valet2011Cunnington, CChannon, K<p>The endothelial nitric oxide synthase (eNOS) co-factor tetrahydrobiopterin (BH4) has been shown to play a pivotal role in maintaining endothelial function in experimental vascular disease models. In BH4-deficient states, eNOS becomes enzymatically ‘uncoupled’, generating reactive oxygen species instead of nitric oxide, thus promoting endothelial dysfunction. In humans with coronary artery disease (CAD), higher vascular BH4 levels have been shown to be associated with improved endothelial function, and genetic variation in endogenous BH4 synthesis has implicated a causal role. Accordingly, BH4 has been proposed as a potential therapeutic target in vascular disease states. The work in this thesis aims to further elucidate the roles of exogenous and endogenous BH4 in humans.</p><p>In a randomised, placebo-controlled clinical trial of oral BH4 therapy in patients with CAD, exogenous BH4 had no effect on endothelial function or vascular oxidative stress. Subsequent pharmacokinetic and pharmacodynamic analysis revealed that oral BH4 significantly augmented BH4 levels in plasma and in venous tissue (but not in arterial tissue), but also increased levels of the oxidation product dihydrobiopterin (BH2), which lacks eNOS cofactor activity. Thus, there was a null effect on overall biopterin redox status.</p><p>To further understand the mechanics of exogenous BH4 oxidation, ex vivo studies of human blood and vascular tissue demonstrated that exogenous BH4 is very rapidly oxidised to BH2; co-administration with an antioxidant had only a modest effect on preventing BH4 oxidation in blood, with no beneficial effect on biopterin redox state in the vasculature.</p><p>Finally, using a “Mendelian randomisation” approach, I studied the effects of a haplotype of GCH1 (the gene encoding the rate limiting enzyme in BH4 synthesis) on endogenous BH4 bioavailability and vascular function in healthy individuals. In patients with CAD, this haplotype has been associated with decreased BH4 bioavailability and eNOS uncoupling, however in healthy individuals the haplotype exerted no significant effect, likely due to reduced inflammatory stimulation of GCH1.</p>
spellingShingle Cardiovascular disease
Cunnington, C
The role of plasma and vascular tetrahydrobiopterin in vascular disease states
title The role of plasma and vascular tetrahydrobiopterin in vascular disease states
title_full The role of plasma and vascular tetrahydrobiopterin in vascular disease states
title_fullStr The role of plasma and vascular tetrahydrobiopterin in vascular disease states
title_full_unstemmed The role of plasma and vascular tetrahydrobiopterin in vascular disease states
title_short The role of plasma and vascular tetrahydrobiopterin in vascular disease states
title_sort role of plasma and vascular tetrahydrobiopterin in vascular disease states
topic Cardiovascular disease
work_keys_str_mv AT cunningtonc theroleofplasmaandvasculartetrahydrobiopterininvasculardiseasestates
AT cunningtonc roleofplasmaandvasculartetrahydrobiopterininvasculardiseasestates