8. Ulusal Veteriner Biyokimya ve Klinik Biyokimya Kongresi (8.Vetbiyokimya-2016), Bursa, Türkiye, 22 - 24 Eylül 2016, cilt.1, sa.1, ss.164-165
Objective:
This study was planned in order to
effect of thymoquinone (TQ) known pro inflammatory and antioxidant proporties
the potential oxidative DNA damage and reveals the effects of antioxidant system
in high glucose added kidney cell line.
Material and Methods: BHK-21 cellswere cultured with the
regular passages. MTT cell viability was determined of IC50 for TQ and glucose.
Cells were seed into plates.Control, glucose (285mM), TQ (10uM), and its cross
groups were prepared. Cells were used for analysis after hours 24 incubation.
In these examples; 8-OHdG, TAS, TOS were analyzed by ELISA.
Results: The 8-OHdG levels in TQ+glucose (p≤0.05)
group were higher than control and other groups. TQ group’s levels (p≤0.05) decreased
according to glucose group. TAS levels of TQ group (p≤0.05) were higher than
other groups, but, this was not statistically significant. TOS (p≤0.05)
increased in all groups compared to the control. However, no significant difference
was found between study groups. While OSI value increased in all groups (p≤0.05)
compared to controls, only in the group given TQ group (p≤0.05) were lower than
glucose and glucose+TQ.
Conclusions: Consequently, the TQ treatment on the high
glucose added BHK-21 cell line were obtained that high oxidative DNA damage and
TOS and unchanged TAS levels. The high glucose added groups had higher OSI index
than TQ and control groups.
Keywords:
glucose, cell culture, thymoquinone, DNA damage, TAS/TOS