Probiotics Supplementation Attenuates Inflammation and Oxidative Stress Induced by Chronic Sleep Restriction.
Yadong ZhengLuyan ZhangLaura BonfiliLuisa de VivoAnna Maria EleuteriMichele BellesiPublished in: Nutrients (2023)
Background: Insufficient sleep is a serious public health problem in modern society. It leads to increased risk of chronic diseases, and it has been frequently associated with cellular oxidative damage and widespread low-grade inflammation. Probiotics have been attracting increasing interest recently for their antioxidant and anti-inflammatory properties. Here, we tested the ability of probiotics to contrast oxidative stress and inflammation induced by sleep loss. Methods: We administered a multi-strain probiotic formulation (SLAB51) or water to normal sleeping mice and to mice exposed to 7 days of chronic sleep restriction (CSR). We quantified protein, lipid, and DNA oxidation as well as levels of gut-brain axis hormones and pro and anti-inflammatory cytokines in the brain and plasma. Furthermore, we carried out an evaluation of microglia morphology and density in the mouse cerebral cortex. Results: We found that CSR induced oxidative stress and inflammation and altered gut-brain axis hormones. SLAB51 oral administration boosted the antioxidant capacity of the brain, thus limiting the oxidative damage provoked by loss of sleep. Moreover, it positively regulated gut-brain axis hormones and reduced peripheral and brain inflammation induced by CSR. Conclusions: Probiotic supplementation can be a possible strategy to counteract oxidative stress and inflammation promoted by sleep loss.
Keyphrases
- oxidative stress
- resting state
- white matter
- physical activity
- sleep quality
- low grade
- functional connectivity
- public health
- cerebral ischemia
- anti inflammatory
- diabetic rats
- dna damage
- ischemia reperfusion injury
- high grade
- induced apoptosis
- signaling pathway
- spinal cord injury
- brain injury
- small molecule
- single molecule
- magnetic resonance imaging
- type diabetes
- endoplasmic reticulum stress
- fatty acid
- drug delivery
- neuropathic pain
- skeletal muscle
- inflammatory response
- adipose tissue