Data are derived from evaluation of the hepatocyte morphology (find more Figure 2). RFS group, black box; ad-libitum-fed SC79 purchase control group, white box; 24-h-fasting control group, hatched and gray box. Results are expressed as mean ± SEM of 6 independent determinations. Significant difference between food restricted and ad-libitum fed groups [*], within the same experimental group [+], and different from 24-h fasting group [×]. Differences derived from Tukey’s post hoc test (α = 0.05). Liver glycogen The presence of glycogen in the cytoplasm of hepatocytes was detected and quantified using the periodic acid-Schiff (PAS) staining (Figures 4 and 5). Glycogen staining
intensity remained mostly constant in the groups of rats fed
ad libitum (Figure 4, panels A, C, and E, and Figure 5), with a slight tendency for glycogen levels to decline in the rats at 14:00 h (Figure 5). The group with 24-h fasting showed a dramatic reduction (≈ 82%) check details in the glycogen content (Figure 4, panel G, and Figure 5). Rats under RFS showed a significant but smaller decrease in liver glycogen (≈ 30%) during the FAA (at 11:00 h). Indeed, the reduction in glycogen in the rats expressing the FEO was less than that shown by the 24-h fasted rats, even though both groups had a similar period of fasting (Figure 4, panels D and G, and Figure 5). After food ingestion (at 14:00 h), hepatic glycogen in RFS rats reverted to normal levels. Figure 4 Periodic-acid Schiff (PAS) stained histological sections of livers of rats exposed to a restricted feeding schedule for 3 weeks (food intake from 12:00 to 14:00 h). Pink color indicates the presence of hepatic glycogen. Tissue samples from food-restricted and ad-libitum 17-DMAG (Alvespimycin) HCl fed rats were collected before (08:00 h), during (11:00 h), and after
food anticipatory activity (14:00 h). The control group with 24-h fasting was processed at 11:00 h. Panels A, C, and E, control ad-libitum fed groups; panels B, D, and F, food-restricted groups; panel G, 24-h fasted group. Images in panels A and B were taken at 08:00 h, in panels C, D and G at 11:00 h, and E and F at 14:00 h. Figure 5 Quantification of the hepatocytes’ glycogen content of rats exposed to a restricted feeding schedule for 3 weeks (food intake from 12:00 to 14:00 h). Data are derived from evaluation of the liver PAS staining from Figure 4. RFS group, black box; ad-libitum-fed control group, white box; 24-h-fasting control group, hatched and gray box. Results are expressed as mean ± SEM of 6 independent determinations. Significant difference between food restricted and ad-libitum fed groups [*], within the same experimental group [+], and different from 24-h fasting group [×]. Differences derived from Tukey’s post hoc test (α = 0.05).