Sucralose Targets the Insulin Signaling Pathway in the SH-SY5Y Neuroblastoma Cell Line.
Marina ČovićMilorad ZjalicLovro MihajlovićMarianna PapJasenka WagnerDario MandićŽeljko DebeljakMarija HefferPublished in: Metabolites (2023)
Sucralose is widely used as a non-nutritive sweetener (NNS). However, in order to justify its use as a non-nutritive food additive, sucralose would have to be metabolically neutral. The aim of this study was to examine whether sucralose altered the insulin signaling pathway in an in vitro cell model of Parkinson's disease (PD)-the dopaminergic differentiated cell line SH-SY5Y. Cells were exposed to sucralose alone and in combination with either insulin or levodopa. Activation of the insulin signaling pathway was assessed by quantifying protein kinase B (AKT) and glycogen synthase kinase 3 (GSK3), as well as the phosphorylated forms of insulin-like growth factor 1 receptor (IGF1-R). Metabolic effects were assayed using MALDI-TOF MS analysis. In the cell viability test, 2 mM sucralose had a negative effect, and levodopa in all combinations had a positive effect. Sucralose treatment alone suppressed GSK3 and IGF1-R phosphorylation in a dose-dependent manner. This treatment also altered the metabolism of fatty acids and amino acids, especially when combined with insulin and levodopa. Suppression of the insulin signaling pathway and sucralose-induced changes in the metabolic profile could underlie a diet-acquired insulin resistance, previously associated with neurodegeneration, or may be an altered response to insulin or levodopa medical therapy.
Keyphrases
- signaling pathway
- type diabetes
- pi k akt
- induced apoptosis
- glycemic control
- protein kinase
- insulin resistance
- cell cycle arrest
- parkinson disease
- epithelial mesenchymal transition
- deep brain stimulation
- cell proliferation
- adipose tissue
- physical activity
- fatty acid
- weight loss
- metabolic syndrome
- high fat diet
- amino acid
- cell therapy
- tyrosine kinase
- oxidative stress
- single cell
- stem cells
- skeletal muscle
- cell death
- climate change
- combination therapy
- smoking cessation