Resveratrol Mitigates Metabolism in Human Microglia Cells.
Luise SchlotteroseMariya S PravdivtsevaFrowin EllermannOlav JansenJan-Bernd HövenerFrank D SönnichsenFrançois CossaisRalph LuciusKirsten HattermannPublished in: Antioxidants (Basel, Switzerland) (2023)
The recognition of the role of microglia cells in neurodegenerative diseases has steadily increased over the past few years. There is growing evidence that the uncontrolled and persisting activation of microglial cells is involved in the progression of diseases such as Alzheimer's or Parkinson's disease. The inflammatory activation of microglia cells is often accompanied by a switch in metabolism to higher glucose consumption and aerobic glycolysis. In this study, we investigate the changes induced by the natural antioxidant resveratrol in a human microglia cell line. Resveratrol is renowned for its neuroprotective properties, but little is known about its direct effect on human microglia cells. By analyzing a variety of inflammatory, neuroprotective, and metabolic aspects, resveratrol was observed to reduce inflammasome activity, increase the release of insulin-like growth factor 1, decrease glucose uptake, lower mitochondrial activity, and attenuate cellular metabolism in a 1 H NMR-based analysis of whole-cell extracts. To this end, studies were mainly performed by analyzing the effect of exogenous stressors such as lipopolysaccharide or interferon gamma on the metabolic profile of microglial cells. Therefore, this study focuses on changes in metabolism without any exogenous stressors, demonstrating how resveratrol might provide protection from persisting neuroinflammation.
Keyphrases
- induced apoptosis
- cell cycle arrest
- oxidative stress
- endothelial cells
- endoplasmic reticulum stress
- cell death
- signaling pathway
- stem cells
- metabolic syndrome
- type diabetes
- lipopolysaccharide induced
- blood pressure
- magnetic resonance
- pi k akt
- skeletal muscle
- induced pluripotent stem cells
- radiation therapy
- dendritic cells
- lps induced
- adipose tissue
- cell proliferation
- blood glucose
- weight loss
- case control