Anti-Inflammatory Effect of Caffeine on Muscle under Lipopolysaccharide-Induced Inflammation
Evidence has shown that caffeine administration reduces pro-inflammatory biomarkers, delaying fatigue and improving endurance performance. This study examined the effects of caffeine administration on the expression of inflammatory-, adenosine receptor- (the targets of caffeine), epigenetic-, and ox...
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Main Authors: | , , , , , , , |
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Format: | Book |
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MDPI AG,
2023-02-01T00:00:00Z.
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Summary: | Evidence has shown that caffeine administration reduces pro-inflammatory biomarkers, delaying fatigue and improving endurance performance. This study examined the effects of caffeine administration on the expression of inflammatory-, adenosine receptor- (the targets of caffeine), epigenetic-, and oxidative metabolism-linked genes in the <i>vastus lateralis</i> muscle of mice submitted to lipopolysaccharide (LPS)-induced inflammation. We showed that caffeine pre-treatment before LPS administration reduced the expression of <i>Il1b</i>, <i>Il6</i>, and <i>Tnfa</i>, and increased <i>Il10</i> and <i>Il13</i>. The negative modulation of the inflammatory response induced by caffeine involved the reduction of inflammasome components, <i>Asc</i> and <i>Casp1</i>, promoting an anti-inflammatory scenario. Caffeine treatment <i>per se</i> promoted the upregulation of adenosinergic receptors, <i>Adora1</i> and <i>Adora2A</i>, an effect that was counterbalanced by LPS. Moreover, there was observed a marked <i>Adora2A</i> promoter hypermethylation, which could represent a compensatory response towards the increased <i>Adora2A</i> expression. Though caffeine administration did not alter DNA methylation patterns, the expression of DNA demethylating enzymes, <i>Tet1</i> and <i>Tet2</i>, was increased in mice receiving Caffeine+LPS, when compared with the basal condition. Finally, caffeine administration attenuated the LPS-induced catabolic state, by rescuing basal levels of <i>Ampk</i> expression. Altogether, the anti-inflammatory effects of caffeine in the muscle can be mediated by modifications on the epigenetic landscape. |
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Item Description: | 10.3390/antiox12030554 2076-3921 |