Alkaline Phosphatase Relieves Colitis in Obese Mice Subjected to Forced Exercise via Its Anti-Inflammatory and Intestinal Microbiota-Shaping Properties.
Dagmara WojcikZbigniew SliwowskiSlawomir KwiecienGrzegorz GinterMarcin SurmiakMagdalena Hubalewska-MazgajAnna ChmuraAdrianna WojcikTomasz KosciolekAleksandra DanielakAneta TargoszMalgorzata StrzalkaUrszula SzczyrkAgata Ptak-BelowskaMarcin MagierowskiJan BilskiTomasz BrzozowskiPublished in: International journal of molecular sciences (2024)
Intestinal alkaline phosphatase (IAP) is an enzyme that plays a protective role in the gut. This study investigated the effect of IAP treatment on experimental colitis in mice subjected to forced exercise on a high-fat diet. C57BL/6 mice with TNBS colitis were fed a high-fat diet and subjected to forced treadmill exercise with or without IAP treatment. Disease activity, oxidative stress, inflammatory cytokines, and gut microbiota were assessed. Forced exercise exacerbated colitis in obese mice, as evidenced by increased disease activity index (DAI), oxidative stress markers, and proinflammatory adipokines and cytokines. IAP treatment significantly reduced these effects and promoted the expression of barrier proteins in the colonic mucosa. Additionally, IAP treatment altered the gut microbiota composition, favoring beneficial Verrucomicrobiota and reducing pathogenic Clostridia and Odoribacter. IAP treatment ameliorates the worsening effect of forced exercise on murine colitis by attenuating oxidative stress, downregulating proinflammatory biomarkers, and modulating the gut microbiota. IAP warrants further investigation as a potential therapeutic strategy for ulcerative colitis.
Keyphrases
- high fat diet
- oxidative stress
- disease activity
- ulcerative colitis
- rheumatoid arthritis
- systemic lupus erythematosus
- high intensity
- insulin resistance
- adipose tissue
- physical activity
- dna damage
- combination therapy
- type diabetes
- ischemia reperfusion injury
- metabolic syndrome
- anti inflammatory
- skeletal muscle
- induced apoptosis
- mouse model
- heat shock
- single molecule
- diabetic rats
- heat stress
- high fat diet induced
- heat shock protein