Acute administration of methyleugenol impairs hippocampus-dependent contextual fear memory and increases anxiety-like behavior in mice.

Methyleugenol (ME) as a natural essential oil in many plant species is widely used in human food and beverage for its fragrance and possible beneficial health effects. Previous chronic or subacute studies in rodents show that ME mainly causes liver toxicity. However, whether and how acute ME affects the central nervous system still remain elusive. Here, we found that ME administrated into the hippocampus impaired the acquisition of hippocampus-dependent contextual fear memory in mice (ME vs control: repeated-measures two-way ANOVA, F-(5,F-70) = 2.937, p < 0.05; Fisher test, p < 0.05, respectively, 53 +/- 5.2% vs 73 +/- 7.6% during trial 4 and 46.8 +/- 6% vs 74.5 +/- 9.3% during trial 5). Meanwhile, acute ME impaired hippocampal CA1 long-term potentiation (LTP; ME vs control: independent t-test, p < 0.01, 110.6 +/- 1.8% vs 133.3 +/- 5.6%) while facilitated long-term depression (LTD; p < 0.01, 75.7 +/- 3.4% vs 88.6 +/- 1.7%) in mice brain slices and inducing a decrease in learning-dependent phosphorylation of Ser831 (ME vs control: independent t-test, p < 0.001, 0.87 +/- 0.03 vs 1.23 +/- 0.03) and Ser845 (p < 0.01, 0.42 +/- 0.07 vs 0.97 +/- 0.14) sites of excitatory glutamate AMPA receptor subunit 1 (GluA1) in the hippocampus, which may be the underlying mechanisms of impairment of hippocampus-dependent learning. In addition, intrahippocampal infusion of ME also increased anxiety-like behaviors in mice. These results suggested that acute ME impaired the hippocampus function at behavioral, cellular, and molecular levels, indicating the potential risks of ME on the central nervous system.