TY - JOUR
T1 - Methylene blue inhibits the inflammatory process of the acetic acid-induced colitis in rat colonic mucosa
AU - Dinc, Soykan
AU - Caydere, Muzaffer
AU - Akgul, Giray
AU - Yenidogan, Erdinc
AU - Hucumenoglu, Semra
AU - Rajesh, Mohanraj
PY - 2015/11/1
Y1 - 2015/11/1
N2 - Inflammatory bowel disease is a serious health problem. Although it has been widely investigated, treatment of inflammatory bowel diseases currently remains a challenging clinical problem. Overproduction of nitric oxide has been demonstrated to cause tissue damage and inflammation. In this study, the effect of methylene blue (MB), a well-known inhibitor of nitric oxide synthesis, was investigated in acetic acid (AA)-induced colitis model in Sprague-Dawley rats. Eighty male rats were randomized into 4 groups (control, control MB, colitis, colitis + MB). AA was applied to groups 3 and 4. MB was added into groups 2 and 4. Three days later, animals were killed and the 8 cm distal colonic segment was resected, and the specimens were examined using macroscopical, histological, and biochemical methods. The results of the macroscopic and microscopic examination showed that in group 4 the mucosal damage and inflammation score was significantly lower than group 3. Increased intestinal permeability in acetic acid-administered group was significantly reversed by MB application. Myeloperoxidase activity and malondialdehyde levels increased significantly, while superoxide dismutase and catalase activities were suppressed after AA-administration. These biochemical parameters were reversed in MB-treated group. Administration of acetic acid resulted in increased levels of tumor necrosis factor-α, interleukin-1, interleukin-6, total nitrite/nitrate levels, and nitric oxide synthase activity. These biochemical alterations were also significantly reversed by MB application. In conclusion, our results indicate that MB decreases the level of nitric oxide and decreases inflammation in acetic acid-induced colitis.
AB - Inflammatory bowel disease is a serious health problem. Although it has been widely investigated, treatment of inflammatory bowel diseases currently remains a challenging clinical problem. Overproduction of nitric oxide has been demonstrated to cause tissue damage and inflammation. In this study, the effect of methylene blue (MB), a well-known inhibitor of nitric oxide synthesis, was investigated in acetic acid (AA)-induced colitis model in Sprague-Dawley rats. Eighty male rats were randomized into 4 groups (control, control MB, colitis, colitis + MB). AA was applied to groups 3 and 4. MB was added into groups 2 and 4. Three days later, animals were killed and the 8 cm distal colonic segment was resected, and the specimens were examined using macroscopical, histological, and biochemical methods. The results of the macroscopic and microscopic examination showed that in group 4 the mucosal damage and inflammation score was significantly lower than group 3. Increased intestinal permeability in acetic acid-administered group was significantly reversed by MB application. Myeloperoxidase activity and malondialdehyde levels increased significantly, while superoxide dismutase and catalase activities were suppressed after AA-administration. These biochemical parameters were reversed in MB-treated group. Administration of acetic acid resulted in increased levels of tumor necrosis factor-α, interleukin-1, interleukin-6, total nitrite/nitrate levels, and nitric oxide synthase activity. These biochemical alterations were also significantly reversed by MB application. In conclusion, our results indicate that MB decreases the level of nitric oxide and decreases inflammation in acetic acid-induced colitis.
KW - Colitis
KW - Methylene blue
UR - http://www.scopus.com/inward/record.url?scp=84991728461&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84991728461&partnerID=8YFLogxK
U2 - 10.9738/INTSURG-D-15-00118.1
DO - 10.9738/INTSURG-D-15-00118.1
M3 - Article
AN - SCOPUS:84991728461
SN - 0020-8868
VL - 100
SP - 1364
EP - 1374
JO - International Surgery
JF - International Surgery
IS - 11
ER -