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. 2019 Oct 11;9:14669. doi: 10.1038/s41598-019-51183-z

Figure 6.

Figure 6

ZINC40099027 promotes the healing of indomethacin-induced small intestine injury in mice and does not affect murine kidney and liver morphology. (a) Typical macroscopic small intestinal ulcerative lesions induced by a single administration of indomethacin at a dose of 15 mg/kg subcutaneously at 24 hours after administration. (b) Hematoxylin and eosin staining of a typical indomethacin-induced small intestinal ulcer at day 4. (c) Representative images of ulcers from DMSO-treated mice and ZINC40099027-treated mice at day 4 suggest that ZINC40099027-treated mice have smaller ulcer areas than mice treated with only the DMSO vehicle. (d) Quantitation of total small intestinal ulcer area in DMSO-treated mice and ZINC40099027-treated mice demonstrates that ZINC40099027 reduces the total ulcer area after 3 days of intraperitoneal injection every 6 hours, (n = 22 in DMSO, n = 25 in ZINC40099027, *p < 0.05). (e) There is no obvious difference in renal or (f) liver morphology between typical hematoxylin and eosin stains of kidneys from mice treated with DMSO or ZINC40099027 for three days beginning one day after ulcer induction by subcutaneous injection of 15 mg/kg indomethacin, (50× magnification kidney, 100× magnification liver).