04.02 (Agilent Technology, USA) and the following operating conditions: HP-5 column (30 m find more x 0.32 mm x 0.25 μm film thickness, cross-linked 5% PH ME siloxane);

injector in split-less mode operated at 250 °C; oven temperature (column) at 100 °C for 1 min, then changed to 250 °C with 25 °C/min ramp rate, then changed to 280 °C with 5 °C/min ramp rate, held at 280 °C for 5 min, and post run at 290 °C for 5 min. Oxygen free nitrogen as make-up gas and helium as carrier gas were from TIG, Bangkok. The limit of detection for α-cypermethrin was 0.1 μg/kg tissue. Pooled liver samples spiked with α-cypermethrin (80 μg/kg) and analysed along the study samples gave intra-batch (n = 8) and inter-batch (n = 10) coefficients of variation of 8.5% and 13.7%, respectively. All statistical analyses were performed using SPSS software (SPSS Inc., Chicago, IL; Version 11.5) and Selleckchem Protease Inhibitor Library GraphPad Prism 5 for Mac OS X (version 5.0c; GraphPad Software, Inc., La Jolla, CA, USA). All data are given as mean with standard deviation. Differences between groups were assessed by means of one-way ANOVA with Bonferroni’s multiple comparisons test and considered significant at P <0.05. The toxic and pro-oxidative

effects of the pesticide α-cypermethrin have been investigated in rats [3], [9], [11], [12], [13], [23], [27], [30], [32], [38] and [41]. A major problem that limits the power of these studies to simulate the situation in humans is the fact that they did not study continuous low-level dietary exposure but a less realistic oral intake of individual high doses of the pesticide once per day. We thus designed the current experiment to investigate if the more realistic scenario of a continuous intake Olopatadine of small α-cypermethrin doses spread-out over the day [33], amounting to a total daily intake comparable to the doses applied in previous studies [9], [12] and [32], would lead

to impaired antioxidant defence mechanisms and increased lipid peroxidation and if so, whether or not dietary curcumin might counteract these harmful effects. Curcumin was chosen as test compound because of its antioxidant activity in various model systems in addition to its reported safety for human consumption, even at high doses (curcumin is generally recognized as safe by the US Food and Drug Administration), its widespread use as a colorant by the food industry and the high acceptance of this natural plant compound by the consumers [21]. The daily α-cypermethrin intake in the current study was in the range of 20-35 mg/kg bodyweight (BW) and thus 8-14% of the acute oral LD50 for adult rats, which is 250 mg/kg bodyweight [3]. Since rats consume their feed in approximately 14-18 meals over the course of one day [31] and [42], the individual doses were much lower and below 1% LD50.