Bioanalysis of tetrahydrobiopterin with liquid chromatographic-mass spectrometric and its application for pharmacokinetics in apolipoprotein E knockout mice

Abstract Decreased level of endogenous tetrahydrobiopterin (BH4) has been associated with endothelial dysfunction, which is involved in vascular diseases. Despite its chemical instability due to auto-oxidation, exogenous supplementation of BH4 can reverse this dysfunction. Thus, a sensitive and simple liquid chromatographic-mass spectrometric (LC-MS) method was developed and validated for the measurement of BH4 in plasma after its oral or intravenous administration in apolipoprotein E (ApoE) knockout mice. Human plasma samples were prepared from protein precipitation, and chromatographic separation was performed on a C18 column with methanol-water mobile phases and a run time of 7 minutes with ion detection at m/z 242. The limit of quantitation was 10 ng/mL and inaccuracy and imprecision were ≤15%. In the presence of antioxidant dithioerythritol, recovery of BH4 was 80% and stable for 24 h post sample collection. Following oral or intravenous administration of BH4 in ApoE mice, the maximum concentrations detected were 102 and 483 ng/mL, respectively. Area under the curve values for oral BH4 were three time lower than those of intravenous BH4. The half-life of BH4 was 1.6 h, and it demonstrated low oral bioavailability (15%). Results of this study provide the basis for further studies of future clinical applications of BH4. Graphical Abstract

[1]  G. Ng,et al.  Endothelial dysfunction, endothelial nitric oxide bioavailability, tetrahydrobiopterin, and 5-methyltetrahydrofolate in cardiovascular disease. Where are we with therapy? , 2018, Microvascular research.

[2]  R. Farah,et al.  Tetrahydrobiopterin (BH4): Targeting endothelial nitric oxide synthase as a potential therapy for pulmonary hypertension , 2018, Cardiovascular therapeutics.

[3]  L. Valle-Mondragón,et al.  Association between bh4/bh2 ratio and Albuminuria in Hypertensive Type -2 Diabetic patients , 2017 .

[4]  J. Pollock,et al.  BH4 improves postprandial endothelial function after a high-fat meal in men and postmenopausal women , 2017, Menopause.

[5]  U. Förstermann,et al.  Roles of Vascular Oxidative Stress and Nitric Oxide in the Pathogenesis of Atherosclerosis , 2017, Circulation research.

[6]  U. Förstermann,et al.  Implication of eNOS Uncoupling in Cardiovascular Disease , 2017 .

[7]  A. Görlach,et al.  Folic Acid Promotes Recycling of Tetrahydrobiopterin and Protects Against Hypoxia-Induced Pulmonary Hypertension by Recoupling Endothelial Nitric Oxide Synthase. , 2015, Antioxidants & redox signaling.

[8]  Yingzi Zhao,et al.  Vascular nitric oxide: Beyond eNOS. , 2015, Journal of pharmacological sciences.

[9]  N. Mukhopadhyay,et al.  The Role of Nitric Oxide Synthase Uncoupling in Tumor Progression , 2015, Molecular Cancer Research.

[10]  B. Capaldo,et al.  Long-term follow-up of patients with phenylketonuria treated with tetrahydrobiopterin: a seven years experience , 2015, Orphanet Journal of Rare Diseases.

[11]  S. Shams,et al.  Tetrahydrobiopterin responsiveness in a series of 53 cases of phenylketonuria and hyperphenylalaninemia in Iran , 2015, Molecular genetics and metabolism reports.

[12]  J. Christodoulou,et al.  Phenylketonuria: a review of current and future treatments. , 2015, Translational pediatrics.

[13]  H. Kim,et al.  Quantification of Neurotransmitters in Mouse Brain Tissue by Using Liquid Chromatography Coupled Electrospray Tandem Mass Spectrometry , 2014, Journal of analytical methods in chemistry.

[14]  G. Douglas,et al.  Tetrahydrobiopterin in cardiovascular health and disease. , 2014, Antioxidants & redox signaling.

[15]  Y. Kihara,et al.  Oxidative stress and endothelial dysfunction: clinical evidence and therapeutic implications. , 2014, Trends in cardiovascular medicine.

[16]  A. Starr,et al.  The regulation of vascular tetrahydrobiopterin bioavailability. , 2013, Vascular pharmacology.

[17]  A. Svardal,et al.  Simultaneous quantification of tetrahydrobiopterin, dihydrobiopterin, and biopterin by liquid chromatography coupled electrospray tandem mass spectrometry. , 2012, Analytical biochemistry.

[18]  M. Crabtree,et al.  Recoupling the Cardiac Nitric Oxide Synthases: Tetrahydrobiopterin Synthesis and Recycling , 2012, Current Heart Failure Reports.

[19]  J. Francis,et al.  Systemic and Vascular Oxidation Limits the Efficacy of Oral Tetrahydrobiopterin Treatment in Patients With Coronary Artery Disease , 2012, Circulation.

[20]  M. Crabtree,et al.  Synthesis and recycling of tetrahydrobiopterin in endothelial function and vascular disease. , 2011, Nitric oxide : biology and chemistry.

[21]  B. Chien,et al.  Detection of tetrahydrobiopterin by LC-MS/MS in plasma from multiple species. , 2009, Bioanalysis.

[22]  D. Fekkes,et al.  Quantitation of total biopterin and tetrahydrobiopterin in plasma. , 2007, Clinical biochemistry.

[23]  N. Blau,et al.  Pharmacokinetics of orally administered tetrahydrobiopterin in patients with phenylalanine hydroxylase deficiency , 2006, Journal of Inherited Metabolic Disease.

[24]  E. Werner,et al.  High-performance liquid chromatographic methods for the quantification of tetrahydrobiopterin biosynthetic enzymes. , 1996, Journal of chromatography. B, Biomedical applications.

[25]  H. Kagamiyama,et al.  Autoradiographic distribution of [14C]tetrahydrobiopterin and its developmental change in mice. , 1993, The Journal of pharmacology and experimental therapeutics.

[26]  M. Heiner-Fokkema,et al.  BH4 treatment in BH4-responsive PKU patients: preliminary data on blood prolactin concentrations suggest increased cerebral dopamine concentrations. , 2015, Molecular genetics and metabolism.

[27]  D. Mould,et al.  Pharmacokinetics of Sapropterin in Patients with Phenylketonuria , 2008, Clinical pharmacokinetics.

[28]  N. Blau,et al.  Plasma tetrahydrobiopterin and its pharmacokinetic following oral administration. , 2004, Molecular genetics and metabolism.