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. Author manuscript; available in PMC: 2014 Nov 1.
Published in final edited form as: J Neuroendocrinol. 2013 Nov;25(11):1151–1162. doi: 10.1111/jne.12106

Figure 5.

Figure 5

DNA methyltransferase enzymes are involved E2-induced memory enhancement. (A) Bilateral infusion of E2 (5 μg/hemisphere) into the dorsal hippocampus significantly increased levels of DNMT3B protein in the dorsal hippocampus relative to vehicle four hours after infusion (*p < 0.05). This increase was blocked by concurrent infusion of garcinol (#p < 0.05 relative to the E2 group), suggesting that histone acetylation is necessary for E2 to increase DNMT3B levels in the dorsal hippocampus. Garcinol alone had no effect on DNMT3B levels. Inset illustrates representative Western blot images. DNMT3B protein was normalized to β-actin. Reprinted with permission from (32). (B) Bilateral infusion of 5-AZA (100 μg/hemisphere) into the dorsal hippocampus administered immediately, but not three hours, after training significantly increased the time spent with the novel object relative to chance (*p < 0.05), suggesting that DNA methyltransferase enzymes regulate novel object recognition within a three-hour time window after training. 5-AZA blocked the memory enhancing effect of E2, indicating that DNMT enzymes regulate the memory-enhancing effects of E2. Reprinted with permission from (33). Bars in both panels represent the mean ± SEM.

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