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Kinetic studies of vitamin B6 metabolism in humans

Dissertation (MSc (Chemical Pathology))--University of Pretoria, 2001.

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Other Authors: Ubbink, Johan B.
Format: Thesis
Published: University of Pretoria 2013
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access_status_str Open Access
author2 Ubbink, Johan B.
author_browse Ubbink, Johan B.
author_facet Ubbink, Johan B.
collection Thesis
dc_rights_str_mv © 2001 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
description Dissertation (MSc (Chemical Pathology))--University of Pretoria, 2001.
format Thesis
id oai:repository.up.ac.za:2263/22786
institution University of Pretoria (South Africa)
last_indexed 2026-06-10T12:40:03.959Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2013
publishDateRange 2013
publishDateSort 2013
publisher University of Pretoria
publisherStr University of Pretoria
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source_str UPSpace — University of Pretoria Institutional Repository
spelling oai:repository.up.ac.za:2263/22786 Kinetic studies of vitamin B6 metabolism in humans Ubbink, Johan B. upetd@up.ac.za Van der Westhuizen, Christian Abraham Vitamin b6 Metabolism Chemical kinetics UCTD Dissertation (MSc (Chemical Pathology))--University of Pretoria, 2001. The primal aim of this thesis was to establish whether kinetic aspects of vitamin B6 metabolism predispose to earlier observed racial differences found in plasma pyridoxal-5'-phosphate (PLP). The active forms of vitamin B6 namely plasma PLP and pyridoxal (PL) as well as the three enzymes expressed in the erythrocyte involved in B6 metabolism, PL kinase, PLP phosphatase and pyridoxamine -5'- phosphate (pyridoxine -5'- phosphate) [PMP(PNP) ] oxidase were measured by high performance liquid chromatography. Phase one supported earlier experimental evidence and lower plasma PLP concentrations were found in blacks in a group of200 male volunteers recruited from the South African National Defence Force (SANDF). The respective enzyme activities involved in vitamin B6 metabolism, from the same test subjects, suggested similar PLP production from PMP and PL as well as PLP dephosphorylation which result in the release of PL into the circulating fluid. Since applied exclusion criteria eliminated the majority of biochemical, physiological, genetical - and disease related factors that influence vit B6 status, dietary factors and individual preferences regarding food intake, were most likely to be responsible for the significantly lower circulating plasma PLP encountered in blacks. Phase two compared pharmacokinetic parameters between 7 black - and 9 white test subjects recruited from the South African Police Services after a single 10 mg oral supplement ofpyridoxine hydrochloride. Statistical analysis of the parameters elimination half-life, elimination rate constant, clearance, volume of distribution, mean residence time, maximum peak concentration and time to maximum peak concentration failed to demonstrate any significant differences between the two groups. These results suggest consistent appearance rate, distribution and metabolism for the metabolites PLP and PL in the study population. A tendency in slower appearance rate, for both the metabolites PLP and PL, were observed in blacks and needs to be investigated further. The end product of vitamin B6 metabolism, 4-pyridoxic acid, which was expressed in terms of 24 hour urine volume, again failed to illustrate any significant differences between blacks and whites. These results suggested similar excretion properties in my population study. Furthermore, the pharmacokinetic parameters calculated for plasma PLP and PL respectively, were found to display one-compartment - and two-compartment pharmacokinetic model characteristics. This mono- and bi exponential elimination characteristics displayed by PLP and PL respectively could be of value in future research efforts in terms of sampling time. The distribution half-life can be determined by the calculation of two-compartment macro-rate constants. Fasting blood-samples should be collected when true baseline values are needed in the case of PL. Following vit B6 supplementation, one should allow at least 5 times the distribution half-life (5-6 hr in the case of PL) before blood-sampling in order to achieve true pharmacological response. Phase three of this study was conducted to illustrate the metabolic interplay ofthe enzymes PL kinase and PMP (PNP) oxidase involved in PLP production. The kinetic parameters, Michaelis- Menten constant and maximum velocity rate, at varying substrate concentrations, for the enzymes PL kinase and PMP (PNP) oxidase, were compared in 14 white - and 14 black male test subjects recruited from the SANDF. Both the average Michaelis-Menten constant and maximum velocity rate were higher in whites, but these differences were not statistically significant. The high individual variability for both parameters calculated, can possibly be ruled out if a crystalline enzyme form is used and should be investigated further. Chemical Pathology unrestricted 2013-09-06T13:45:42Z 2006-03-03 2013-09-06T13:45:42Z 2001-09-01 2001 2006-02-24 Dissertation Van der Westhuizen, CA 2001, Kinetic studies of vitamin B6 metabolism in humans, MSc dissertation, University of Pretoria, Pretoria, viewed yymmdd < http://hdl.handle.net/2263/22786 > H1208/ag http://hdl.handle.net/2263/22786 http://upetd.up.ac.za/thesis/available/etd-02242006-131417/ © 2001 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria. application/pdf University of Pretoria
spellingShingle Vitamin b6
Metabolism
Chemical kinetics
UCTD
Kinetic studies of vitamin B6 metabolism in humans
title Kinetic studies of vitamin B6 metabolism in humans
title_full Kinetic studies of vitamin B6 metabolism in humans
title_fullStr Kinetic studies of vitamin B6 metabolism in humans
title_full_unstemmed Kinetic studies of vitamin B6 metabolism in humans
title_short Kinetic studies of vitamin B6 metabolism in humans
title_sort kinetic studies of vitamin b6 metabolism in humans
topic Vitamin b6
Metabolism
Chemical kinetics
UCTD
url http://hdl.handle.net/2263/22786
http://upetd.up.ac.za/thesis/available/etd-02242006-131417/