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1.
J Chromatogr A ; 1517: 79-85, 2017 Sep 29.
Article in English | MEDLINE | ID: mdl-28851527

ABSTRACT

A three column-switching high-performance liquid chromatography (HPLC) using an electrochemical detector (ECD) equipped with a diamond electrode was established to determine 3-hydroxypropylmercapturic acid (3-HPMA) in urine. An extracted urine sample was consecutively fractionated using a strong anion-exchange column (first column) and a C8 column (second column) via a switching valve before application on an Octa Decyl Silyl (ODS) column (third column), followed by ECD analysis. The% recovery of 3-HPMA standard throughout the three-column process and limit of detection (LOD) were 94±1% and 0.1pmol, respectively. A solid phase extraction step is required for the sensitive analysis of 3-HPMA in urine by column-switching HPLC-ECD despite a decreased% recovery (55%) of urine sample spiked with 100pmol of 3-HPMA. To test the utility of our column-switching HPLC-ECD method, 3-HPMA levels of 27 urine samples were determined, and the correlation between HPLC-ECD and LC-Electrospray ionization (ESI)-MS/MS method was examined. As a result, the median values of µmol 3-HPMA/g Creatinine (Cre) in urine obtained by column-switching HPLC-ECD and LC-MS/MS were 2.19±2.12µmol/g Cre and 2.13±3.38µmol/g Cre, respectively, and the calibration curve (y=1.5171x-1.007) exhibited good linearity within a defined range (r2=0.907). These results indicate that the combination of column-switching HPLC and ECD is a powerful tool for the specific, reliable detection of 3-HPMA in urine.


Subject(s)
Acetylcysteine/analogs & derivatives , Chromatography, High Pressure Liquid , Diamond , Electrochemistry , Electrodes , Urinalysis/methods , Acetylcysteine/urine , Calibration , Chromatography, Liquid/methods , Humans , Limit of Detection , Reproducibility of Results , Solid Phase Extraction , Tandem Mass Spectrometry
2.
Biochem Biophys Res Commun ; 473(2): 630-5, 2016 Apr 29.
Article in English | MEDLINE | ID: mdl-27037020

ABSTRACT

We previously reported that tissue damage during brain infarction was mainly caused by inactivation of proteins by acrolein. This time, it was tested why brain infarction increases in parallel with aging. A mouse model of photochemically induced thrombosis (PIT) was studied using 2, 6, and 12 month-old female C57BL/6 mice. The size of brain infarction in the mouse PIT model increased with aging. The volume of brain infarction in 12 month-old mice was approximately 2-fold larger than that in 2 month-old mice. The larger brain infarction in 12 month-old mice was due to an increase in acrolein based on an increase in the activity of spermine oxidase, together with a decrease in glutathione (GSH), a major acrolein-detoxifying compound in cells, based on the decrease in one of the subunits of glutathione biosynthesizing enzymes, γ-glutamylcysteine ligase modifier subunit, with aging. The results indicate that aggravation of brain infarction with aging was mainly due to the increase in acrolein production and the decrease in GSH in brain.


Subject(s)
Acrolein/metabolism , Aging , Brain Infarction/metabolism , Brain/pathology , Glutathione/metabolism , Animals , Brain/metabolism , Brain Infarction/pathology , Female , Mice , Mice, Inbred C57BL , Oxidoreductases Acting on CH-NH Group Donors/metabolism , Polyamine Oxidase
3.
Clin Chim Acta ; 441: 115-21, 2015 Feb 20.
Article in English | MEDLINE | ID: mdl-25542982

ABSTRACT

BACKGROUND: We previously reported that the level of urinary 3-hydroxypropyl mercapturic acid (3-HPMA)/creatinine (Cre) was reduced following stroke. The aim of this study was to determine whether the level of 3-HPMA/Cre in urine was reduced in subjects with dementia. METHODS: The level of 3-HPMA was measured by LC-MS/MS, and that of amino acid conjugated acrolein (AC-Acro) was by ELISA. The study included 128 elderly subjects divided into 74 non-demented (control), 22 mild cognitive impairment (MCI) and 32 Alzheimer's disease (AD) subjects. RESULTS: The urinary 3-HPMA/Cre and AC-Acro/Cre in MCI plus AD subjects were significantly lower than those in control subjects. In addition, urinary Cre in AD subjects was significantly higher than that in MCI subjects, and 3-HPMA/Cre and AC-Acro/Cre in AD subjects were significantly lower than that in MCI subjects. Among these three markers, the lower 3-HPMA/Cre ratio was most strongly correlated with the decline of MMSE (Mini-Mental State Examination) and the increase in CDRsob (Clinical Dementia Rating Scale Sum of Boxes Scores). Furthermore, reduction in 3-HPMA/Cre in urine was well correlated with increase in Aß40/42 in plasma in demented subjects. CONCLUSION: The results indicate that 3-HPMA/Cre in urine is the most reliable biochemical marker to distinguish AD subjects from MCI subjects among three markers.


Subject(s)
Acrolein/metabolism , Acrolein/urine , Alzheimer Disease/urine , Cognitive Dysfunction/urine , Creatinine/urine , Acetylcysteine/analogs & derivatives , Acetylcysteine/urine , Adult , Aged , Aged, 80 and over , Alzheimer Disease/metabolism , Cognitive Dysfunction/metabolism , Enzyme-Linked Immunosorbent Assay , Female , Humans , Male , Middle Aged
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