In vitro Evaluation of the Effects of Lycopene on Caspase System and Oxidative DNA Damage in High‑Glucose Condition
1, 2★, 2, 3, 4★ Corresponding author
- 1Health Science High School, Muş Alparslan University, Mus, Turkey.
- 2Department of Biochemistry, Veterinary Medical Faculty, Van Yuzuncu Yil University, Turkey.
- 3Ozalp Vocational High School, Van Yuzuncu Yil University, Turkey.
- 4Department of Medical Biology, Faculty of Medicine, Van Yuzuncu Yil University, Van, Turkey.
CORRESPONDENCE
Semiha Dede
Department of Biochemistry, Veterinary Medical Faculty, Van Yuzuncu Yil University, Turkey.
Received: 19-09-2018; Revised: 09-11-2018.
Volume 15, Issue 62S · pp. S30–S33 · 2019 · DOI: 10.4103/pm.pm_488_18
ABSTRACT
Background: The present study was planned to investigate the effects of lycopene, on the caspase‑dependent apoptosis in high‑dose glucose (HG)‑treated PC12 cell line. PC12 cells were cultured in vitro.Materials and Methods: HG was prepared as G (250 mM), and lycopene was prepared as L1 (10 μM), L2 (20 μM), and L3 (40 μM). After 6 h of incubation, the cells were exposed to trypsin, and the samples were obtained with freeze/ thaw method. Caspase 3, 8, 9; 8‑hydroxy‑2‑deoxyguanosine (8‑OHdG); and M30 were determined (enzyme‑linked immunosorbent assay).Results: 8‑OHdG increased in L3 (P ≤ 0.001), whereas L1 caused a decrease in HG group (P ≤ 0.001). Caspase‑3 decreased significantly in L1, L2, and L3G compared to control (P ≤ 0.001) group. Caspase‑8 increased significantly in L1, L1G, L2G, and all L3 glucose groups (P ≤ 0.001). There was no difference for Caspase‑9. M30 was not affected by L and HG, which decreased significantly (P ≤ 0.001).Conclusion: As a result, it was determined that, when PC12 cell line was treated with HG, lycopene application had effects on caspase enzymes and DNA damage.
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Bazyel, B., Dede, S., Cetin, S., Yuksek, V., & Taşpinar, M. (2019). In vitro Evaluation of the Effects of Lycopene on Caspase System and Oxidative DNA Damage in High‑Glucose Condition. Pharmacognosy Magazine, 15(62S), S30–S33. https://doi.org/10.4103/pm.pm_488_18
