Effects of protein malnutrition on IL-6-mediated signaling in the liver and the systemic acute-phase response in rats
American Journal of Physiology - Regulatory Integrative and Comparative Physiology, ISSN: 0363-6119, Vol: 287, Issue: 4 56-4, Page: R801-8
2004
- 72Citations
- 37Captures
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Metrics Details
- Citations72
- Citation Indexes72
- 72
- CrossRef53
- Captures37
- Readers37
- 37
Article Description
This study examines the effects of malnutrition on IL-6 signaling pathways of rats fed 2% vs. 20% casein diets for 14 days. Effects of malnutrition on the abundance and IL-6-stimulated phosphorylation of signaling proteins in the JAK-STAT and MAP kinase pathways were examined in the liver. Changes of the acute-phase response as reflected by serum α-acid glycoprotein (AG), TNF-α (TNF), and IL-1β (IL-1) were compared in the two dietary groups at 0, 4, 8,16, and 24 h after IL-6 administration. Under basal conditions, the abundance of the IL-6 receptor, gp130, JAK1, STAT1, and STAT3 proteins and levels of phosphorylation of ERK1/2 and p38 were significantly increased in the liver in the 2% casein group compared with the 20% casein group. With IL-6 stimulation, the increased phosphorylation per unit of protein of these signaling proteins was not different in the liver between the two groups. Before IL-6 stimulation, serum levels of TNF, IL-1, IL-6, and AG were significantly higher in the 2% casein group than in the 20% casein group. After bolus injection of IL-6, changes in IL-1 and AG were similar in the two dietary groups, although a slight decline in AG level was noted after 8 h of IL-6 administration in the 2% protein group. These data demonstrate that protein malnutrition produces changes in inflammation-related proteins characteristic of a low-grade systemic inflammatory response and, thus, can serve as an inflammatory stimulus. The capacity for response to IL-6 is preserved, suggesting adaptive preservation of acute-phase responsiveness during malnutrition.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=4644279972&origin=inward; http://dx.doi.org/10.1152/ajpregu.00715.2003; http://www.ncbi.nlm.nih.gov/pubmed/15371280; https://www.physiology.org/doi/10.1152/ajpregu.00715.2003; http://www.physiology.org/doi/10.1152/ajpregu.00715.2003; https://www.physiology.org/action/captchaChallenge?redirectUrl=https%3A%2F%2Fwww.physiology.org%2Fdoi%2Ffull%2F10.1152%2Fajpregu.00715.2003
American Physiological Society
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