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. 2021 Sep 28;26(12):7403–7416. doi: 10.1038/s41380-021-01304-w

Fig. 5. Neutral sphingomyelinase-2 (NSM) controls alcohol effects on emotional behaviour.

Fig. 5

a Free-choice alcohol consumption reversed the advantageous low-depression phenotype in female mice with reduced NSM activity (fro) in the novelty supressed feeding (NSF) test, but not in (b) the forced swim test (FST). Alcohol drinking eliminated the advantageous low anxiety phenotype of female fro mice in (c) the light–dark box test (LDB), (d) in the elevated plus maze test (EPM), and in (e) the open field test (OF) (n = 6–8 per group). Data are expressed as means + s.e.m. (*P < 0.05; **P < 0.01 vs. wild type (WT). f Fro mice show an enlarged volume of the dorsal hippocampus (DH) measured by magnet resonance imaging. Voluntary alcohol drinking reduced DH size in fro mice to WT levels mice. g–k There was no significant effect of reduced NSM activity or voluntary alcohol consumption on the size of other brain areas (n = 7–8 per group). Data are expressed as means + s.e.m. (***P < 0.001). l Superoxide dismutase (SOD) in the DH was significantly reduced in fro mice after water drinking. This effect was reversed after voluntary alcohol consumption (n = 7–8 per group). m, n There was no effect of NSM or alcohol on catalase activity or lipid peroxidation in the DH. All results show mean + SEM (*P < 0.05; **P < 0.01).