DHA incorporation in corneal PC and PE molecular species, from basal to treated conditions. Effect of atglistatin on gene expression, release of DHA and AA, and synthesis of hydroxy-derivatives was examined. A and B, comparison of different molecular species of PC and PE in injured corneas in mice after 1 h of topical DHA treatment in vivo analyzed by LC-MS/MS. Each plot shows the percentage of specific PC/PE species in the vehicle- (left) and DHA (right)-treated corneas. Data were collected from eight corneas individually (one cornea/sample). *, p < 0.05 with the t test statistical analysis to compare two groups at 95% of the confidence level. C, quantification of 22:6/22:6-containing PCs and PEs in the presence of PEDF, DHA, and PEDF + DHA. Single data point represents one treated cornea. *, p < 0.05 with ANOVA analysis plus Fisher post hoc test at 95% of the confidence level. D, experimental design of mice treated with atglistatin injected (i.p.) before injury and topically treated with PEDF + DHA, PEDF + DHA + atglistatin, or vehicle after injury. E and F, gene expression analysis in corneas (E) and TG (F) at 3 h after injury and treatment. G, mass spectrometry-based lipidomic analysis of mouse corneas as explained under “Experimental procedures.” *, p < 0.05 with ANOVA analysis plus Fisher post hoc test at 95% of the confidence level. For lipid analysis, a pool of six corneas/sample was used. Bars represent the mean of three experiments ± S.D.