Cargando…

Development of a Method and Validation for the Quantitation of FruArg in Mice Plasma and Brain Tissue Using UPLC–MS/MS

[Image: see text] Aged garlic extract (AGE) is a popular nutritional supplement and is believed to promote health benefits by exhibiting antioxidant and anti-inflammatory activities and hypolipidemic and antiplatelet effects. We have previously identified N-α-(1-deoxy-d-fructos-1-yl)-l-arginine (Fru...

Descripción completa

Detalles Bibliográficos
Autores principales: Johnson, Mitch C., Song, Hailong, Cui, Jiankun, Mossine, Valeri V., Gu, Zezong, Greenlief, C. Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5088453/
https://www.ncbi.nlm.nih.gov/pubmed/27819064
http://dx.doi.org/10.1021/acsomega.6b00220
_version_ 1782464099050848256
author Johnson, Mitch C.
Song, Hailong
Cui, Jiankun
Mossine, Valeri V.
Gu, Zezong
Greenlief, C. Michael
author_facet Johnson, Mitch C.
Song, Hailong
Cui, Jiankun
Mossine, Valeri V.
Gu, Zezong
Greenlief, C. Michael
author_sort Johnson, Mitch C.
collection PubMed
description [Image: see text] Aged garlic extract (AGE) is a popular nutritional supplement and is believed to promote health benefits by exhibiting antioxidant and anti-inflammatory activities and hypolipidemic and antiplatelet effects. We have previously identified N-α-(1-deoxy-d-fructos-1-yl)-l-arginine (FruArg) as a major contributor to the bioactivity of AGE in BV-2 microglial cells whereby it exerted a significant ability to attenuate lipopolysaccharide-induced neuroinflammatory responses and to regulate the Nrf2-mediated antioxidant response. Here, we report on a sensitive ultraperformance liquid chromatography–tandem mass spectrometry (UPLC–MS/MS) protocol that was validated for the quantitation of FruArg in mouse plasma and brain tissue samples. Solid-phase extraction was used to separate FruArg from proteins and phospholipids present in the biological fluids. Results indicated that FruArg was readily absorbed into the blood circulation of mice after intraperitoneal injections. FruArg was reliably detected in the subregions of the brain tissue postinjection, indicating that it penetrates the blood–brain barrier in subnanomolar concentrations that are sufficient for its biological activity.
format Online
Article
Text
id pubmed-5088453
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-50884532016-11-02 Development of a Method and Validation for the Quantitation of FruArg in Mice Plasma and Brain Tissue Using UPLC–MS/MS Johnson, Mitch C. Song, Hailong Cui, Jiankun Mossine, Valeri V. Gu, Zezong Greenlief, C. Michael ACS Omega [Image: see text] Aged garlic extract (AGE) is a popular nutritional supplement and is believed to promote health benefits by exhibiting antioxidant and anti-inflammatory activities and hypolipidemic and antiplatelet effects. We have previously identified N-α-(1-deoxy-d-fructos-1-yl)-l-arginine (FruArg) as a major contributor to the bioactivity of AGE in BV-2 microglial cells whereby it exerted a significant ability to attenuate lipopolysaccharide-induced neuroinflammatory responses and to regulate the Nrf2-mediated antioxidant response. Here, we report on a sensitive ultraperformance liquid chromatography–tandem mass spectrometry (UPLC–MS/MS) protocol that was validated for the quantitation of FruArg in mouse plasma and brain tissue samples. Solid-phase extraction was used to separate FruArg from proteins and phospholipids present in the biological fluids. Results indicated that FruArg was readily absorbed into the blood circulation of mice after intraperitoneal injections. FruArg was reliably detected in the subregions of the brain tissue postinjection, indicating that it penetrates the blood–brain barrier in subnanomolar concentrations that are sufficient for its biological activity. American Chemical Society 2016-10-25 /pmc/articles/PMC5088453/ /pubmed/27819064 http://dx.doi.org/10.1021/acsomega.6b00220 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Johnson, Mitch C.
Song, Hailong
Cui, Jiankun
Mossine, Valeri V.
Gu, Zezong
Greenlief, C. Michael
Development of a Method and Validation for the Quantitation of FruArg in Mice Plasma and Brain Tissue Using UPLC–MS/MS
title Development of a Method and Validation for the Quantitation of FruArg in Mice Plasma and Brain Tissue Using UPLC–MS/MS
title_full Development of a Method and Validation for the Quantitation of FruArg in Mice Plasma and Brain Tissue Using UPLC–MS/MS
title_fullStr Development of a Method and Validation for the Quantitation of FruArg in Mice Plasma and Brain Tissue Using UPLC–MS/MS
title_full_unstemmed Development of a Method and Validation for the Quantitation of FruArg in Mice Plasma and Brain Tissue Using UPLC–MS/MS
title_short Development of a Method and Validation for the Quantitation of FruArg in Mice Plasma and Brain Tissue Using UPLC–MS/MS
title_sort development of a method and validation for the quantitation of fruarg in mice plasma and brain tissue using uplc–ms/ms
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5088453/
https://www.ncbi.nlm.nih.gov/pubmed/27819064
http://dx.doi.org/10.1021/acsomega.6b00220
work_keys_str_mv AT johnsonmitchc developmentofamethodandvalidationforthequantitationoffruarginmiceplasmaandbraintissueusinguplcmsms
AT songhailong developmentofamethodandvalidationforthequantitationoffruarginmiceplasmaandbraintissueusinguplcmsms
AT cuijiankun developmentofamethodandvalidationforthequantitationoffruarginmiceplasmaandbraintissueusinguplcmsms
AT mossinevaleriv developmentofamethodandvalidationforthequantitationoffruarginmiceplasmaandbraintissueusinguplcmsms
AT guzezong developmentofamethodandvalidationforthequantitationoffruarginmiceplasmaandbraintissueusinguplcmsms
AT greenliefcmichael developmentofamethodandvalidationforthequantitationoffruarginmiceplasmaandbraintissueusinguplcmsms