Postprandial Cysteine/Cystine Redox Potential in Human Plasma Varies with Meal Content of Sulfur Amino Acids, ,

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Abstract

Few data are available on plasma redox responses to sulfur amino acid (SAA) loads. In this study, we had 2 aims: to determine whether the SAA content of a meal affected postprandial plasma cysteine (Cys), cystine (CySS), or redox potential (EhCySS) in humans and whether SAA intake level (adequate or inadequate) in the days preceding the meal challenge affected these postprandial levels. Eight healthy individuals aged 18–36 y were equilibrated for 3 d to adequate SAA, fed chemically defined meals without SAA for 5 d (inadequate SAA) and then fed isoenergetic, isonitrogenous meals with adequate SAA for 5 d. On the first and last days with the chemically defined meals, a morning meal containing 60% of the daily food intake was given, and plasma Cys, CySS, and EhCySS were determined over an 8-h postprandial time course. Following equilibration to adequate intake, provision of the meal with SAA resulted in increased plasma Cys and CySS concentrations and more reduced plasma EhCySS compared with the postprandial values following the same meal without SAA. Equilibration to inadequate SAA intake for the days preceding the meal challenge did not affect this response. The magnitude of the difference in postprandial plasma EhCySS (10 mV) due to meal content of SAA was comparable to those which alter physiologic signaling and/or are associated with disease risk. Consequently, the SAA content of meals could affect physiologic signaling and associated disease mechanisms in the postprandial period by changes in Cys, CySS, or EhCySS.

Abbreviations used:

AUC
area under the curve
CDO
cysteine dioxygenase
CL
metabolic clearance
CySS
cystine
EhCySS
redox potential of cysteine/cystine couple
GCRC
General Clinical Research Center
kelim
elimination rate constant
SAA
sulfur amino acid
t1/2
elimination half-life
VD
apparent volume of distribution

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1

Supported by NIH grants ES012929 and ES011195 (D.P.J.), DK55850, and K24 RR023356 (T.R.Z.) and Emory General Clinical Research Center grant M01 RR00039/UL1 RR025008.

2

Author disclosures: Y. Park, T. R. Ziegler, N. Gletsu-Miller, Y. Liang, T. Yu, C. J. Accardi, and D. P. Jones, no conflicts of interest.

3

Supplemental Figure 1 is available with the online posting of this paper at jn.nutrition.org.