The Investigation of the Induction of Diketocarotenoids Senescence in SHSY5Y Cells

Introduction: Recently, studies of diketocarotenoids such as astaxanthin (Ax) and canthaxanthin (Cx) with powerful antioxidant have focused on numerous biological mechanisms such as singlet oxygen quenching, radical scavenging, antidiabetic, anticarcinogenesis, antiinflammatory, antiobesity and antimelanogenesis activities. There is evidence demonstrating that diketocarotenoid confers neuroprotective effects in experimental models of chronic neurodegenerative disorders and neurological diseases. This study used Ax and Cx to detect its role on senescence of SHSY5Y Cells. Methods: In this study, the sample included the cell control group (SHSY5Y cell line) that did not receive Ax and Cx, , and the experimental group that received Ax and Cx (20 mM). Ax and Cx were treated with SHSY5Y cell line at 48 hours. To measure the expression of BAX, Bcl2 and PPARγ different groups were compared by real‑time PCR analysis. The cell senescence effects of Ax and Cx, a βgalactosidase (SAβgal) senescence assay was evaluated. The results were analyzed by the oneway analysis of variance (ANOVA) using Prism version 6.0 software. Results: The results showed that treatment with Ax and Cx (20 mM) for 48h induced apoptosis and senescence. The BAX and Bcl2 gene expression analysis revealed a significant impact of Ax and Cx in apoptosis induction (P lt;0.05). The measuring of cell senescence also indicated that Ax and Cx exhibited a senescence inductive activity as determined by an increase in βgalactosidase activity and PPARγ gene expression (P lt;0.05). Conclusion: It appears that Ax and Cx have therapeutic properties in SHSY5Y cells and can cause the proliferation of these cells to cease. The results suggest that Ax and Cx treatment may be beneficial for therapy of neuroblastoma and neurodegenerative disorders.