Resveratrol Alleviates the Early Challenges of Implant-Based Drug Delivery in a Human Glial Cell Model.
Luise SchlotteroseFrançois CossaisRalph LuciusKirsten HattermannPublished in: International journal of molecular sciences (2024)
Brain diseases are oftentimes life-threatening and difficult to treat. The local administration of drug substances using brain implants can increase on-site concentrations and decrease systemic side effects. However, the biocompatibility of potential brain implant materials needs to be evaluated carefully as implants can trigger foreign body reactions, particularly by increasing the microglia and astrocyte reactivity. To date, these tests have been frequently conducted in very simple in vitro models, in particular not respecting the key players in glial cell reactions and the challenges of surgical implantation characterized by the disruption of oxygen and nutrient supply. Thus, we established an in vitro model in which we treated human glial cell lines with reduced oxygen and glucose levels. The model displayed cytokine and reactive oxygen species release from reactive microglia and an increase in a marker of reactive astrocytes, galectin-3. Moreover, the treatment caused changes in the cell survival and triggered the production of hypoxia-inducible factor 1α. In this comprehensive platform, we demonstrated the protective effect of the natural polyphenol resveratrol as a model substance, which might be included in brain implants to ease the undesired glial cell response. Overall, a glial-cell-based in vitro model of the initial challenges of local brain disease treatment may prove useful for investigating new therapy options.
Keyphrases
- neuropathic pain
- resting state
- white matter
- single cell
- cell therapy
- drug delivery
- endothelial cells
- soft tissue
- functional connectivity
- reactive oxygen species
- cerebral ischemia
- inflammatory response
- multiple sclerosis
- type diabetes
- spinal cord injury
- metabolic syndrome
- adipose tissue
- mesenchymal stem cells
- emergency department
- bone marrow
- climate change
- skeletal muscle
- insulin resistance
- replacement therapy
- drug induced
- adverse drug
- newly diagnosed
- tissue engineering
- human health