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. 2018 Jul 16;9:2735. doi: 10.1038/s41467-018-05131-6

Fig. 1.

Fig. 1

Inhibition of AON-projecting hippocampal neurons impairs context-dependent odour memory recall. a Coronal section depicting site of AAV-ChR2-YFP and -mCherry injections in the hippocampus (top) and the resulting innervation pattern at the AON (bottom). Coordinates mark anteroposterior position from bregma. Scale bars represent 1 mm; ac, anterior commissure; pc, piriform cortex; l, lateral AON; m, medial AON; vp, ventroposterior AON. b Schematic diagram depicting experimental approach. CAV2-Cre was infused into the AON, whereas Cre-responsive AAV-hM4D-mCherry was injected in the hippocampus. c Representative sections depicting AON-projecting HPC neurons expressing hM4D-mCherry. Magnification is indicated on the bottom right of each panel. Scale bars represent 1 mm (black) or 10 μm (white). d The olfactory spatial memory test paradigm. CNO-treated hM4D mice investigated the familiar and novel odour location to a largely equal extent, indicative of impaired spatial odour memory (Independent-samples t-test, t(16) = 3.194, **P < 0.01). e The olfactory temporal order memory test paradigm. CNO-treated hM4D mice were impaired in memory for the temporal occurrence of encountered odours (Independent-samples t-test, t(16) = 2.795, *P < 0.05). f Both groups showed normal performance in a context-independent novel odour recognition test (Independent-samples t-test, t(16) = 0.05644, NS, P = 0.9557). For all behavioural tests, CNO was injected 15 min before the retrieval phase. The odour in the novel spatiotemporal configuration is numbered in red. Positive discrimination ratios indicate preference for the novel odour-context configuration. mCherry control group: n = 8, hM4D group: n = 10. Data are presented as mean ± SEM