Figures & data
Figure 1. Expression of the GLP-1 and GLP-2 mRNA of PGDPs+/+ and PGDPs−/− mice. Expressions of GLP-1 and GLP-2 are not observed in the PGDPs−/− mice.
![Figure 1. Expression of the GLP-1 and GLP-2 mRNA of PGDPs+/+ and PGDPs−/− mice. Expressions of GLP-1 and GLP-2 are not observed in the PGDPs−/− mice.](/cms/asset/8f8b7ff3-0e2f-427f-b39c-1ad8898fb046/oamd_a_1215783_f0001_b.gif)
Figure 2. (A) Villous height of the duodenum and three parts of the small intestine. No significant differences in villous height in each section are observed between the PGDPs−/− and PGDPS+/+ mice. A decrease in villous height is observed in both groups; the villous height of the small intestine is 34% of that in the duodenum in the PGDPs−/− mice and 40% in the PGDPS+/+ mice. (B) Crypt depth of the duodenum and three parts of the small intestine. No significant differences in crypt depth in each section are observed between the PGDPs−/− and PGDPS+/+ mice. Crypt depth shows no decline from the oral to anal side.
Each bar represents the mean height or depth and standard deviation.
![Figure 2. (A) Villous height of the duodenum and three parts of the small intestine. No significant differences in villous height in each section are observed between the PGDPs−/− and PGDPS+/+ mice. A decrease in villous height is observed in both groups; the villous height of the small intestine is 34% of that in the duodenum in the PGDPs−/− mice and 40% in the PGDPS+/+ mice. (B) Crypt depth of the duodenum and three parts of the small intestine. No significant differences in crypt depth in each section are observed between the PGDPs−/− and PGDPS+/+ mice. Crypt depth shows no decline from the oral to anal side.Each bar represents the mean height or depth and standard deviation.](/cms/asset/1220f8ee-6d10-4008-856d-8ce6fbe5cc95/oamd_a_1215783_f0002_b.gif)
Figure 3. (A) Time-dependent changes in disease activity index. The increases after the administration of dextran sodium for 5 days in the disease activity index until day 6 and the decline by day 12 are shown. Each point represents the mean ± SD of 7 PGDPs−/− and 7 PGDPS+/+ mice. (B) Time-dependent changes in BW. The decline in BW until day 9 and the recovery to 95% by day 20 are shown. Each point represents the mean ± SD of 7 PGDPs−/− and 7 PGDPS+/+ mice.
![Figure 3. (A) Time-dependent changes in disease activity index. The increases after the administration of dextran sodium for 5 days in the disease activity index until day 6 and the decline by day 12 are shown. Each point represents the mean ± SD of 7 PGDPs−/− and 7 PGDPS+/+ mice. (B) Time-dependent changes in BW. The decline in BW until day 9 and the recovery to 95% by day 20 are shown. Each point represents the mean ± SD of 7 PGDPs−/− and 7 PGDPS+/+ mice.](/cms/asset/6747b8d6-1fc6-4dfb-b515-73b56899a3e3/oamd_a_1215783_f0003_b.gif)
Figure 4. (A) Histological score of distal small intestine on colitis no significant differences were observed in histological score of distal small intestine between the PGDPs−/− and PGDPS+/+ mice. (B) Histological score of distal colon on colitis was not different on day 7 between the PGDPs−/− and PGDPS+/+ mice. On day 21, however, histological score of distal colon of PGDPs−/− was significantly higher than that of PGDPs−/−.
*p < 0.05.
![Figure 4. (A) Histological score of distal small intestine on colitis no significant differences were observed in histological score of distal small intestine between the PGDPs−/− and PGDPS+/+ mice. (B) Histological score of distal colon on colitis was not different on day 7 between the PGDPs−/− and PGDPS+/+ mice. On day 21, however, histological score of distal colon of PGDPs−/− was significantly higher than that of PGDPs−/−.*p < 0.05.](/cms/asset/af516fac-ae80-49a6-97e1-5acb847bbb9f/oamd_a_1215783_f0004_b.gif)