5 mg/mL). Parallel cohorts of mice were similarly injected with equal volumes of vehicle (75% DMSO / 25% PBS). Animals were sacrificed 12 hours after their last SP600125 or vehicle
injection. For the interpretation of histology, a mouse pathologist, blinded to treatment group, read and scored liver sections from mice treated with SP600125 or vehicle as described.25 The presence of steatohepatitis was defined by the presence of steatosis, inflammation, and ballooning and changes in these features were quantified using the NAS and its components. Analysis of variance (ANOVA) was used for multiple group comparisons. When two groups were compared, unpaired t tests were used for data analysis. https://www.selleckchem.com/products/BMS-777607.html Unpaired t tests were used to compare the effect of the diet within
a strain and paired t tests were used to assess the effect of strain on mice receiving the same diet (n = 5-12 for each group). The MCD diet induces activation of the PERK pathway by increasing the phosphorylation of eiF2α (p-eIF2α) and activating its downstream targets. eIF2α phosphorylation was increased more dramatically by PD0332991 mw MCD feeding in db/db mice when compared to db/m mice. In db/db mice, p-eIF2α expression increased from 0.26 ± 0.04 to 0.6 ± 0.01 integrated density units with MCD feeding (P < 0.001) compared with db/m mice; 0.4 ± 0.06 and 0.47 ± 0.03 integrated density units for control and MCD-fed mice, respectively (P = NS). Furthermore, db/db mice had increased p-eIF2α expression compared
to db/m mice fed the MCD diet (Fig. 1A, Table 1). CHOP activation is one of the most important downstream effects of p-eIF2α particularly when it is persistent. CHOP messenger RNA (mRNA) levels increased 7.6-fold in db/db mice and 4.2-fold in db/m mice fed the MCD diet (Fig. 1B). CHOP protein expression was also more dramatically increased in db/db mice fed the MCD compared to db/m mice (Fig. 1A). Furthermore, gene expression levels of other downstream markers of eIf2α: activating transcription factor Aldol condensation 4 (ATF-4) and oxireductase endoplasmic reticulum oxidoreductin-1 alpha (ERO-1 α), were also increased in db/db mice compared to db/m mice on the MCD diet: 0.6 ± 0.09 and 3.0 ± 0.37 for ATF-4 and 0.89 ± 0.17 and 1.76 ± 0.26 for ERO-1 α in db/m versus db/db mice, respectively (Fig. 1B). The expression of GADD34 represents a negative feedback mechanism to counteract translational arrest and later inflammatory signaling initiated by the phosphorylation of eIF2α. db/db mice fed the MCD diet had reduced GADD34 protein levels compared to db/db mice on the control diet (P < 0.01). When compared to db/m mice on the MCD diet, db/db mice on the MCD diet had lower GADD34 protein expression levels that approached significance (P = 0.06) (Fig. 1A, Table 1). Both these findings suggest an inadequate compensatory response in db/db mice that is exacerbated by the MCD diet.