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. 2021 Mar 24;37(7):905–920. doi: 10.1007/s12264-021-00662-3

Fig. 5.

Fig. 5

Knock-down of TRPV4 with siRNA-attenuated NMDA-induced cytotoxicity and calcium accumulation in primary cultured hippocampal neurons. Neurons were pretreated with TRPV4 siRNA (10 nmol/L) for 24 h, and then exposed to NMDA (100 μmol/L) for 24 h. A Cell viability evaluated by MTT assays (mean ± SD, n = 6; *P <0.05 vs NC siRNA group, #P <0.05 vs NMDA 0 μmol/L group. B, C Intracellular Ca2+ concentrations measured using Fluo-4 Direct Calcium Assay kits (green, Fluo-4; blue, Hoechst; original magnification ×200; scale bars, 50 μm; mean ± SD, n = 7; *P <0.05 vs negative siRNA group, #P <0.05 vs NMDA group, ANOVA and Dunnett’s multiple comparison test).