Cargando…

Tolerability and pharmacokinetics of oxaloacetate 100 mg capsules in Alzheimer's subjects

Bioenergetics and bioenergetic-related functions are altered in Alzheimer's disease (AD) subjects. These alterations represent therapeutic targets and provide an underlying rationale for modifying brain bioenergetics in AD-affected persons. Preclinical studies in cultured cells and mice found t...

Descripción completa

Detalles Bibliográficos
Autores principales: Swerdlow, Russell H., Bothwell, Rebecca, Hutfles, Lewis, Burns, Jeffrey M., Reed, Gregory A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816034/
https://www.ncbi.nlm.nih.gov/pubmed/27051598
http://dx.doi.org/10.1016/j.bbacli.2016.03.005
_version_ 1782424656181985280
author Swerdlow, Russell H.
Bothwell, Rebecca
Hutfles, Lewis
Burns, Jeffrey M.
Reed, Gregory A.
author_facet Swerdlow, Russell H.
Bothwell, Rebecca
Hutfles, Lewis
Burns, Jeffrey M.
Reed, Gregory A.
author_sort Swerdlow, Russell H.
collection PubMed
description Bioenergetics and bioenergetic-related functions are altered in Alzheimer's disease (AD) subjects. These alterations represent therapeutic targets and provide an underlying rationale for modifying brain bioenergetics in AD-affected persons. Preclinical studies in cultured cells and mice found that administering oxaloacetate (OAA), a Krebs cycle and gluconeogenesis intermediate, enhanced bioenergetic fluxes and upregulated some brain bioenergetic infrastructure-related parameters. We therefore conducted a study to provide initial data on the tolerability and pharmacokinetics of OAA in AD subjects. Six AD subjects received OAA 100 mg capsules twice a day for one month. The intervention was well-tolerated. Blood level measurements following ingestion of a 100 mg OAA capsule showed modest increases in OAA concentrations, but pharmacokinetic analyses were complicated by relatively high amounts of endogenous OAA. We conclude that OAA 100 mg capsules twice per day for one month are safe in AD subjects but do not result in a consistent and clear increase in the OAA blood level, thus necessitating future clinical studies to evaluate higher doses.
format Online
Article
Text
id pubmed-4816034
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-48160342016-04-05 Tolerability and pharmacokinetics of oxaloacetate 100 mg capsules in Alzheimer's subjects Swerdlow, Russell H. Bothwell, Rebecca Hutfles, Lewis Burns, Jeffrey M. Reed, Gregory A. BBA Clin Regular Article Bioenergetics and bioenergetic-related functions are altered in Alzheimer's disease (AD) subjects. These alterations represent therapeutic targets and provide an underlying rationale for modifying brain bioenergetics in AD-affected persons. Preclinical studies in cultured cells and mice found that administering oxaloacetate (OAA), a Krebs cycle and gluconeogenesis intermediate, enhanced bioenergetic fluxes and upregulated some brain bioenergetic infrastructure-related parameters. We therefore conducted a study to provide initial data on the tolerability and pharmacokinetics of OAA in AD subjects. Six AD subjects received OAA 100 mg capsules twice a day for one month. The intervention was well-tolerated. Blood level measurements following ingestion of a 100 mg OAA capsule showed modest increases in OAA concentrations, but pharmacokinetic analyses were complicated by relatively high amounts of endogenous OAA. We conclude that OAA 100 mg capsules twice per day for one month are safe in AD subjects but do not result in a consistent and clear increase in the OAA blood level, thus necessitating future clinical studies to evaluate higher doses. Elsevier 2016-03-10 /pmc/articles/PMC4816034/ /pubmed/27051598 http://dx.doi.org/10.1016/j.bbacli.2016.03.005 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Swerdlow, Russell H.
Bothwell, Rebecca
Hutfles, Lewis
Burns, Jeffrey M.
Reed, Gregory A.
Tolerability and pharmacokinetics of oxaloacetate 100 mg capsules in Alzheimer's subjects
title Tolerability and pharmacokinetics of oxaloacetate 100 mg capsules in Alzheimer's subjects
title_full Tolerability and pharmacokinetics of oxaloacetate 100 mg capsules in Alzheimer's subjects
title_fullStr Tolerability and pharmacokinetics of oxaloacetate 100 mg capsules in Alzheimer's subjects
title_full_unstemmed Tolerability and pharmacokinetics of oxaloacetate 100 mg capsules in Alzheimer's subjects
title_short Tolerability and pharmacokinetics of oxaloacetate 100 mg capsules in Alzheimer's subjects
title_sort tolerability and pharmacokinetics of oxaloacetate 100 mg capsules in alzheimer's subjects
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816034/
https://www.ncbi.nlm.nih.gov/pubmed/27051598
http://dx.doi.org/10.1016/j.bbacli.2016.03.005
work_keys_str_mv AT swerdlowrussellh tolerabilityandpharmacokineticsofoxaloacetate100mgcapsulesinalzheimerssubjects
AT bothwellrebecca tolerabilityandpharmacokineticsofoxaloacetate100mgcapsulesinalzheimerssubjects
AT hutfleslewis tolerabilityandpharmacokineticsofoxaloacetate100mgcapsulesinalzheimerssubjects
AT burnsjeffreym tolerabilityandpharmacokineticsofoxaloacetate100mgcapsulesinalzheimerssubjects
AT reedgregorya tolerabilityandpharmacokineticsofoxaloacetate100mgcapsulesinalzheimerssubjects