Fig. 7: Orally administration of OCA suppresses DNL genes, PPARα activity and ER stress in liver of TCS breastfed mice.
From: Lactational delivery of Triclosan promotes non-alcoholic fatty liver disease in newborn mice

Neonatal mice receiving a normal diet or TCS through lactation for 21 days. During the course of this exposure, 16-day old mice were treated with OCA for 4 days and tissues collected on day 21. a Expression of hepatic Shp (vehicle, n = 3 per group and TCS, n = 4 per group). b Expression of genes associated with lipogenesis (vehicle, n = 3 per group and TCS, n = 4 per group). c Hepatic expression of PPARα target genes (vehicle, n = 3 per group and TCS, n = 4 per group). d Hepatic expression of Fgf21 (vehicle veh, TCS veh and TCS OCA, n = 4 per group and vehicle OCA, n = 3). e Measurement of liver TG (n = 4 per group). f Genes linked to ER stress (vehicle veh and TCS veh, n = 5 per group, TCS OCA, n = 4 and vehicle OCA, n = 3). g Hepatic IB analysis of ATF4 and FASN (n = 2 per group). h Frozen liver sections were stained with ORO (n = 3 per group). Scale bar, 20μm. (a–f) show mean ± S.E., determined by two-tailed Student’s test; *P < 0.05, **P < 0.01, ***P < 0.001.