Inflammatory responses of C57BL/6NKorl mice to dextran sulfate sodium-induced colitis: comparison between three C57BL/6 N sub-strains

被引:9
作者
Kim, Sou Hyun [1 ]
Kwon, Doyoung [1 ]
Son, Seung Won [1 ]
Jeong, Tae Bin [1 ]
Lee, Seunghyun [1 ]
Kwak, Jae-Hwan [2 ]
Cho, Joon-Yong [3 ]
Hwang, Dae Youn [4 ]
Seo, Min-Soo [5 ]
Kim, Kil Soo [5 ,6 ]
Jung, Young-Suk [1 ]
机构
[1] Pusan Natl Univ, Coll Pharm, Busan 46241, South Korea
[2] Kyungsung Univ, Coll Pharm, Brain Busan 21 Plus Program, Busan, South Korea
[3] Korea Natl Sport Univ, Exercise Biochem Lab, Seoul, South Korea
[4] Pusan Natl Univ, Dept Biomat Sci, Coll Nat Resources & Life Sci, Life & Ind Convergence Res Inst, Miryang, South Korea
[5] Daegu Gyeongbuk Med Innovat Fdn, Lab Anim Ctr, Daegu, South Korea
[6] Kyungpook Natl Univ, Coll Vet Med, Daegu, South Korea
关键词
C57BL; 6NKorl; Inflammatory bowel disease; Dextran sulfate sodium; Colitis; Inflammation;
D O I
10.1186/s42826-021-00084-2
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background Inflammatory bowel disease (IBD), including both Crohn's disease and ulcerative colitis, are chronic human diseases that are challenging to cure and are often unable to be resolved. The inbred mouse strain C57BL/6 N has been used in investigations of IBD as an experimental animal model. The purpose of the current study was to compare the inflammatory responsiveness of C57BL/6NKorl mice, a sub-strain recently established by the National Institute of Food and Drug Safety Evaluation (NIFDS), with those of C57BL/6 N mice from two different sources using a dextran sulfate sodium (DSS)-induced colitis model. Results Male mice (8 weeks old) were administered DSS (0, 1, 2, or 3%) in drinking water for 7 days. DSS significantly decreased body weight and colon length and increased the colon weight-to-length ratio. Moreover, severe colitis-related clinical signs including diarrhea and rectal bleeding were observed beginning on day 4 in mice administered DSS at a concentration of 3%. DSS led to edema, epithelial layer disruption, inflammatory cell infiltration, and cytokine induction (tumor necrosis factor-alpha, interleukin-6, and interleukin-1 beta) in the colon tissues. However, no significant differences in DSS-promoted abnormal symptoms or their severity were found between the three sub-strains. Conclusions These results indicate that C57BL/6NKorl mice responded to DSS-induced colitis similar to the generally used C57BL6/N mice, thus this newly developed mouse sub-strain provides a useful animal model of IBD.
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页数:7
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