Strenuous resistive breathing induces proinflammatory cytokines and stimulates the HPA axis in humans

Citation
T. Vassilakopoulos et al., Strenuous resistive breathing induces proinflammatory cytokines and stimulates the HPA axis in humans, AM J P-REG, 277(4), 1999, pp. R1013-R1019
Citations number
47
Categorie Soggetti
Physiology
Journal title
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
ISSN journal
03636119 → ACNP
Volume
277
Issue
4
Year of publication
1999
Pages
R1013 - R1019
Database
ISI
SICI code
0363-6119(199910)277:4<R1013:SRBIPC>2.0.ZU;2-K
Abstract
Interleukin-1 beta (IL-1 beta) and interleukin-6 (IL-6), powerful stimulant s of the hypothalamic-pituitary-adrenal (HPA) axis, increase in response to whole body exercise. Strenuous inspiratory resistive breathing (IRB), a fo rm of clinically relevant "exercise" for the respiratory muscles, produces beta-endorphin through a largely unknown mechanism. We investigated (in 11 healthy humans) whether strenuous IRE produces proinflammatory cytokines an d beta-endorphin in parallel with stimulation of the HPA axis, assessed by concurrent measurement of ACTH. Subjects underwent either severe [at 75% of maximal inspiratory pressure (P-max)] or moderate (at 35% of P-m (max)) IR B. Plasma cytokines, beta-endorphin, and ACTH were measured at rest (point R), at the point at which the resistive load could not be sustained (point F), and at exhaustion [15 ruin later (point E)]. During severe IRE, IL-1 be ta increased from 0.83 +/- 0.12 pg/ml at point R to 1.88 +/- 0.53 and 4.06 +/- 1.27 pg/ml at points F and E, respectively (P < 0.01). IL-6 increased f rom 5.30 +/- 1.02 to 10.33 +/- 2.14 and 11.66 +/- 2.29 pg/ml at points F an d E, respectively (P = 0.02). ACTH and beta-endorphin fluctuated from 20.87 +/- 5.49 and 25.03 +/- 3.97 pg/ml at point R to 22.97 +/- 4.41 and 26.32 /- 3.93 pg/ml, respectively, at point F and increased to 46.96 +/- 8.55 and 40.32 +/- 5.94 pg/ml, respectively, at point E (P < 0.01, point E vs, poin t F). There was a positive correlation between the IL-6 at point F and the ACTH and beta-endorphin at point E (r = 0.88 and 0.94, respectively; P < 0. 01) as well as between the increase in IL-6 (between points R and F) and th e increases in ACTH and P-endorphin (between points F and E, r = 0.91 and 0 .92, respectively; P < 0.01). Moderate IRE did not produce any change. We c onclude that severe IRE produces proinflammatory cytokines and stimulates t he HPA axis in humans secondary to the production of cytokines (especially IL-6).