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. Author manuscript; available in PMC: 2013 Aug 1.
Published in final edited form as: Neurotoxicology. 2011 Dec 14;33(4):763–768. doi: 10.1016/j.neuro.2011.12.004

Figure 2.

Figure 2

Effects of IIIM1 on the F2 – IsoPs formation in cultured astrocytes in the presence and absence of MeHg treatment. Rat primary astrocytes cultures were incubated for 66 hours at 37°C with IIIM1 (5 µg/ml; 4.95 µM) followed by 6 hour exposure to MeHg (5 µM) or vehicle. Total F2-IsoPs were determined with a stable isotope dilution method with detection by gas chromatography/mass spectrometry and selective ion monitoring. Data represent the mean ± S.E.M. from three independent experiments. * p<0.05 versus control by one-way ANOVA followed by Bonferroni’s multiple comparison tests.