Palmitate Compromises C6 Astrocytic Cell Viability and Mitochondrial Function.
Luisa O SchmittAntonella BlancoSheila V LimaGianni ManciniNatália Ferreira MendesAlexandra LatiniJoana Margarida GasparPublished in: Metabolites (2024)
Consumption of high-fat diets (HFD) is associated with brain alterations, including changes in feeding behavior, cognitive decline, and dementia. Astrocytes play a role in HFD-induced neuroinflammation and brain dysfunction; however, this process is not entirely understood. We hypothesized that exposure to saturated fatty acids can compromise astrocyte viability and mitochondrial function. The C6 (astrocytes) cell line was treated with palmitate or stearate (200 µM and 400 µM) for 6 h. Cell viability, morphology, inflammatory markers, and oxidative stress were evaluated. To assess mitochondrial function, various parameters were measured (membrane potential, mass, respiration, and complex activities). We observed that 6 h of treatment with 400 µM palmitate decreased cell viability, and treatment with 200 µM palmitate changed the astrocyte morphology. Palmitate increased inflammatory markers (TNF-α and IL6) but did not induce oxidative stress. Palmitate significantly decreased the mitochondrial membrane potential and mitochondrial mass. Complex I activity also decreased in palmitate-treated cells; however, no changes were observed in mitochondrial respiration. In conclusion, palmitate, a saturated fatty acid, induces inflammation and impairs mitochondrial function, leading to reduced astrocytic cell viability and changes in cellular morphology. Our study provides valuable insights into the potential mechanisms underlying the relationship between saturated fatty acids, astrocytes, and mitochondrial function in obesity-related brain dysfunction.
Keyphrases
- oxidative stress
- fatty acid
- induced apoptosis
- diabetic rats
- cognitive decline
- mild cognitive impairment
- dna damage
- ischemia reperfusion injury
- resting state
- weight loss
- rheumatoid arthritis
- high fat diet
- insulin resistance
- cerebral ischemia
- metabolic syndrome
- multiple sclerosis
- cell proliferation
- physical activity
- heat shock
- functional connectivity
- inflammatory response
- adipose tissue
- body mass index
- climate change
- subarachnoid hemorrhage
- heat shock protein
- weight gain
- lps induced