TY - JOUR
T1 - Protective effect of Lagerstroemia speciosa against dextran sulfate sodium induced ulcerative colitis in C57BL/6 mice
AU - Chaudhary, Ghanshyam
AU - Mahajan, Umesh B.
AU - Goyal, Sameer N.
AU - Ojha, Shreesh
AU - Patil, Chandragouda R.
AU - Subramanya, Sandeep B.
N1 - Funding Information:
The authors would like to acknowledge Dr. S. J. Surana, Principal, R. C. Patel Institute of Pharmaceutical Education and Research, Shirpur, Dist. Dhule for providing necessary facilities to carry out the study. The authors also acknowl edge the financial support to the research works in the laboratory of Dr. Shreesh Ojha and Dr. Sandeep B Subramanya from United Arab Emirates University, United Arab Emirates.
Publisher Copyright:
© 2017, E-Century Publishing Corporation. All rights reserved.
PY - 2017
Y1 - 2017
N2 - The protective effect of methanolic extract of Lagerstroemia speciosaleaves (LS) was evaluated against dextran sulfate sodium (DSS) induced ulcerative colitis in C57BL/6 mice. The administration of DSS (2.5% in drinking water ad libitum) in C57BL/6 mice induced ulcerative colitis in 7 days. The LS was orally administered for 7 days at daily doses of 100 and 200 mg/kg. At the end of 7 days of treatment the animals were sacrificed, colonic tissues were removed and processed for further analysis of oxidative stress, and histopathology. In DSS treated mice the oxidative stress markers were elevated compared to controls. There was also significant reduction in the anti-oxidant defense levels marked by reduced cellular glutathione, catalase, and superoxide dismutase. The DSS-induced damage to the colon epithelium was evident from a significant increase in the lipid peroxidation. The histology of colon sections revealed inflammatory changes and marked impairment in the integrity of the mucosal lining with inflammatory changes. Both the doses of LS significantly prevented DSS-induced inflammatory and ulcerative damages of the colon, reduced lipid peroxidation and also restored the levels of innate antioxidants in the colon tissue. These findings indicate the protective effects of LS against the DSS-induced inflammatory and oxidative damage in the mouse colon. Further investigation involving bioactivity guided fractionation of the LS can yield potent constituent which may have a significant role in the treatment of inflammatory bowel disease and ulcerative colitis.
AB - The protective effect of methanolic extract of Lagerstroemia speciosaleaves (LS) was evaluated against dextran sulfate sodium (DSS) induced ulcerative colitis in C57BL/6 mice. The administration of DSS (2.5% in drinking water ad libitum) in C57BL/6 mice induced ulcerative colitis in 7 days. The LS was orally administered for 7 days at daily doses of 100 and 200 mg/kg. At the end of 7 days of treatment the animals were sacrificed, colonic tissues were removed and processed for further analysis of oxidative stress, and histopathology. In DSS treated mice the oxidative stress markers were elevated compared to controls. There was also significant reduction in the anti-oxidant defense levels marked by reduced cellular glutathione, catalase, and superoxide dismutase. The DSS-induced damage to the colon epithelium was evident from a significant increase in the lipid peroxidation. The histology of colon sections revealed inflammatory changes and marked impairment in the integrity of the mucosal lining with inflammatory changes. Both the doses of LS significantly prevented DSS-induced inflammatory and ulcerative damages of the colon, reduced lipid peroxidation and also restored the levels of innate antioxidants in the colon tissue. These findings indicate the protective effects of LS against the DSS-induced inflammatory and oxidative damage in the mouse colon. Further investigation involving bioactivity guided fractionation of the LS can yield potent constituent which may have a significant role in the treatment of inflammatory bowel disease and ulcerative colitis.
KW - 5-amino salicylic acid
KW - DSS
KW - Lagerstroemia
KW - Oxidative stress
KW - Ulcerative colitis
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M3 - Article
AN - SCOPUS:85018317247
SN - 1943-8141
VL - 9
SP - 1792
EP - 1800
JO - American Journal of Translational Research
JF - American Journal of Translational Research
IS - 4
M1 - AJTR0041102
ER -