Aging and dietary modulation of elastase and interleukin-1β secretion
- J. G. Cannon(corresponding author),
- M. A. Fiatarone,
- M. Meydani,
- J. Gong,
- L. Scott,
- J. B. Blumberg
- Pennsylvania State University
Abstract
Aging is associated with diminished immune function that may stem from alterations in arachidonic acid metabolism and lipid peroxidation. This study sought to determine if dietary modification of fatty acids influenced neutrophil and monocyte secretion after an in vivo inflammatory stress in older human subjects. Volunteers participated in protocols that forced their quadriceps muscles to lengthen during tension development (eccentric stress). These protocols can cause inflammatory foci in the muscle as well as alterations in circulating leukocyte function. In this study, in vivo neutrophil degranulation was assessed by plasma elastase concentrations, and mononuclear cell function was assessed by interleukin-1β (IL-1β) secretion in vitro. In response to eccentric stress, older subjects (>60 yr old) taking a placebo had no apparent elastase response, whereas those taking fish oil supplements responded with a 142% increase in plasma elastase (P = 0.011), similar to responses of younger reference subjects (<33 yr old) taking no supplement. Overall, elastase responses correlated with individual plasma arachidonic acid-to-eicosapentaenoic acid ratios (r = -0.881, P = 0.004). Thus apparent age-related differences in elastase release were reconciled by individual differences in fatty acid nutriture. No significant temporal changes in urinary lipid peroxide excretion or IL-1β secretion were observed; however, age-associated differences were found.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages R208-R213Journal (Volume, Issue Number)
American Journal of Physiology - Regulatory Integrative and Comparative Physiology (Volume 268, Issue 1 37-1)Publication milestones
- Published - 1995
Publication status
ISSN
0363-6119Publication IDs
- Scopus: 0028812362
- PubMed: 7840322
