Fig. 2From: Effects of phosphodiesterase 3A modulation on murine cerebral microhemorrhagesSurvival analysis for the different experimental groups. Significant decrease in survival of PDE3A KO mice treated with LPS compared with the WT, PDE3A KO, and LPS-treated WT mice while studying the effect of genetic deletion of PDE3A on inflammation-induced CMH development (a). No difference in the survival between any experiment groups while studying the effect of pharmacological inhibition of PDE3A with cilostazol on CAA-associated CMH development (b). LPS treatment caused a significant reduction in survival in the WT and WT-CIL treated mice compared with PBS-treated WT mice while studying the effect of pharmacological inhibition of PDE3A with cilostazol on inflammation-induced CMH development (c). Statistical test: Log-rank test for survival analysis. #p < 0.05 compared with WT, PDE3A KO, and LPS-treated WT, *p < 0.05 compared with WT-PBSBack to article page