QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Full Text Full Text (PDF) Purchase Article View Shopping Cart Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Gieng, S. H. Articles by Rosales, F. J. Search for Related Content PubMed PubMed Citation Articles by Gieng, S. H. Articles by Rosales, F. J. Pubmed/NCBI databases Compound via MeSH Substance via MeSH Hazardous Substances DB VITAMIN A

---

Nutritional Immunology

Plasma ₁-Acid Glycoprotein Can Be Used to Adjust Inflammation-Induced Hyporetinolemia in Vitamin A-Sufficient, but Not Vitamin A-Deficient or -Supplemented Rats^1,2

Sin H. Gieng^* and Francisco J. Rosales^,3

^* Department of Nutritional Sciences, The Pennsylvania State University, University Park, PA 16802 and Mead Johnson Nutritionals, Evansville, IN 47721

³ To whom correspondence should be addressed: E-mail: francisco.rosales{at}bms.com.

We examined the association between ₁-acid glycoprotein (AGP), all-trans-retinol (retinol), and albumin concentrations in a longitudinal animal model of IL-6–induced inflammation. Vitamin A–sufficient (VAS) male Sprague-Dawley rats were administered recombinant human IL-6 [n = 4, 65 µg/(kg·d)] or PBS (n = 4) continuously for 7 d via osmotic minipumps. Plasma samples were obtained daily and concentrations of retinol, AGP, albumin, and total protein were measured. Compared with both baseline and controls, retinol and albumin decreased (P < 0.05), AGP increased (P < 0.05), and total protein concentrations were unaffected in IL-6–treated rats. In vitamin A–deficient (VAD) rats, AGP concentrations were significantly lower at all time points and increased only to one-third of that in VAS rats. The AGP cut-off value indicative of inflammation was 0.11 g/L (i.e., 95% upper limit of baseline concentrations). After 20.5 h, there was an inverse linear correlation between AGP concentrations and the relative change in retinol to baseline (y = –0.18x + 0.48, r = –0.84, P < 0.001). However, changes in AGP and albumin were not correlated (P = 0.94). The application of this function to retinol concentrations in rats from separate experiments showed that hyporetinolemia cannot be adjusted using plasma AGP in VAD or vitamin A–supplemented rats. In conclusion, correcting inflammation-induced hyporetinolemia using an acute-phase protein requires longitudinally derived data, knowledge of vitamin A status, and a common underlying mechanism of change.

KEY WORDS: • ₁-acid glycoprotein • correction factor • hyporetinolemia • inflammation • vitamin A