Interleukin-6 and tumor necrosis factor-alpha production after acute psychological stress, exercise, and infused isoproterenol: Differential effects and pathways

Citation
Mu. Goebel et al., Interleukin-6 and tumor necrosis factor-alpha production after acute psychological stress, exercise, and infused isoproterenol: Differential effects and pathways, PSYCHOS MED, 62(4), 2000, pp. 591-598
Citations number
65
Categorie Soggetti
Psychiatry,"Clinical Psycology & Psychiatry","Neurosciences & Behavoir
Journal title
PSYCHOSOMATIC MEDICINE
ISSN journal
00333174 → ACNP
Volume
62
Issue
4
Year of publication
2000
Pages
591 - 598
Database
ISI
SICI code
0033-3174(200007/08)62:4<591:IATNFP>2.0.ZU;2-Y
Abstract
Objective: The aim of the study was to assess the effects of three differen t methods of acute activation of the sympathetic nervous system on lipopoly saccharide-induced in vitro production of interleukin-6 (IL-6) and tumor ne crosis factor-alpha (TNF-alpha). Methods: Thirty-two healthy volunteers per formed speech and exercise tasks and underwent a 30-minute infusion of isop roterenol. Results: As expected, acute activation of the sympathetic nervou s system led to leukocytosis, including increases in lymphocyte, monocyte, and granulocyte populations (p values < .05). Lipopolysaccharide-induced IL -6 production was increased after both the speaking and exercise tasks (p v alues < .001), whereas TNF-alpha production was elevated only after exercis e (p < .05). In contrast, infusion of isoproterenol inhibited TNF-alpha pro duction (p < .001) and caused no change in IL-6 production. Conclusions: In response to the challenges, IL-6 and TNF-alpha production showed different profiles. Purely beta-agonist stimulation led to downregulation of TNF-alp ha production, providing evidence of the antiinflammatory effect of in vivo beta-receptor activation. The enhanced production of both cytokines after exercise, and of IL-6 after the speech task, can be best explained by a sim ultaneous upregulation of proinflammatory and inflammation-responding media tors. These effects may have an important role in controlling the immune re sponse to acute psychological and physical stress.