Regular swimming exercise prevented the acute and persistent mechanical muscle hyperalgesia by modulation of macrophages phenotypes and inflammatory cytokines via PPARγ receptors
•Regular swimming exercise controls persistent muscle hyperalgesia by involvement of PPARγ.•Macrophages and inflammatory cytokines are involved in persistent muscle hyperalgesia.•Macrophages phenotypes and cytokines expression are modulated by regular swimming exercise.•PPARγ induced by physical exe...
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Veröffentlicht in: | Brain, behavior, and immunity behavior, and immunity, 2021-07, Vol.95, p.462-476 |
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Sprache: | eng |
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Zusammenfassung: | •Regular swimming exercise controls persistent muscle hyperalgesia by involvement of PPARγ.•Macrophages and inflammatory cytokines are involved in persistent muscle hyperalgesia.•Macrophages phenotypes and cytokines expression are modulated by regular swimming exercise.•PPARγ induced by physical exercise modulates macrophages and cytokines related to chronic pain.
Physically active individuals are less likely to develop chronic pain, and physical exercise is an established strategy to control inflammatory diseases. Here, we hypothesized that 1) peripheral pro-inflammatory macrophages phenotype contribute to predisposition of the musculoskeletal to chronic pain, and that 2) activation of PPARγ receptors, modulation of macrophage phenotypes and cytokines through physical exercise would prevent persistent muscle pain. We tested these hypotheses using swimming exercise, pharmacological and immunochemical techniques in a rodent model of persistent muscle hyperalgesia. Swimming prevented the persistent mechanical muscle hyperalgesia most likely through activation of PPARγ receptors, as well as activation of PPARγ receptors by 15d-PGJ2 and depletion of muscle macrophages in sedentary animals. Acute and persistent muscle hyperalgesia were characterized by an increase in pro-inflammatory macrophages phenotype, and swimming and the 15d-PGJ2 prevented this increase and increased anti-inflammatory macrophages phenotype. Finally, IL-1β concentration in muscle increased in the acute phase, which was also prevented by PPARγ receptors activation through swimming. Besides, swimming increased muscle concentration of IL-10 in both acute and chronic phases, but only in the persistent phase through PPARγ receptors. Our findings suggest physical exercise activates PPARγ receptors and increases anti-inflammatory responses in the muscle tissue by modulating macrophages phenotypes and cytokines, thereby preventing the establishment of persistent muscle hyperalgesia. These results further highlight the potential of physical exercise to prevent chronic muscle pain. |
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ISSN: | 0889-1591 1090-2139 |
DOI: | 10.1016/j.bbi.2021.05.002 |