TY - JOUR
T1 - Bifidobacterium longum HY8004 attenuates TNBS-induced colitis by inhibiting lipid peroxidation in mice
AU - Lee, In Ah
AU - Bae, Eun Ah
AU - Lee, Jung Hee
AU - Lee, Hoyong
AU - Ahn, Young Tae
AU - Huh, Chul Sung
AU - Kim, Dong Hyun
N1 - Copyright:
Copyright 2010 Elsevier B.V., All rights reserved.
PY - 2010/5
Y1 - 2010/5
N2 - Objective To investigate the mechanisms of the preventive activity of lactic acid bacteria in colitis, the inhibitory effect of Bifidobacterium longum HY8004, which potently inhibited lipid peroxidation in vitro, was examined in 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitic mice. Methods We measured the ability of lactic acid bacteria (LAB) to inhibit lipid peroxidation in vitro and to inhibit colitis outcomes, colon shortening, and myeloperoxidase activity in TNBS-induced colitis in C3H/HeN and C3H/HeJ mice. We also measured levels of the inflammatory markers interleukin (IL)-1β and tumor necrosis factor (TNF)-α and their transcription factor, NF-κB, in the colon by enzyme-linked immunosorbent assay and immunoblot analysis. Results Among the LAB tested, B. logum HY8004 most potently inhibited lipid peroxidation in vitro but did not inhibit TLR-4-linked NF-κB activation in HEK cells. Oral administration of HY8004 inhibited TNBS-induced colon shortening and myeloperoxidase activity in the colon of C3H/HeN and C3H/HeJ mice as well as IL-1β and TNF-α expression. B. longum HY8004 also inhibited TNBSinduced lipid peroxidation, TLR-4 expression, and NF-κB activation in the colon of C3H/HeN and C3H/HeJ mice. Conclusion B. longum HY8004 can improve colitis via the inhibition of lipid peroxidation as well as NF-κB activation.
AB - Objective To investigate the mechanisms of the preventive activity of lactic acid bacteria in colitis, the inhibitory effect of Bifidobacterium longum HY8004, which potently inhibited lipid peroxidation in vitro, was examined in 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitic mice. Methods We measured the ability of lactic acid bacteria (LAB) to inhibit lipid peroxidation in vitro and to inhibit colitis outcomes, colon shortening, and myeloperoxidase activity in TNBS-induced colitis in C3H/HeN and C3H/HeJ mice. We also measured levels of the inflammatory markers interleukin (IL)-1β and tumor necrosis factor (TNF)-α and their transcription factor, NF-κB, in the colon by enzyme-linked immunosorbent assay and immunoblot analysis. Results Among the LAB tested, B. logum HY8004 most potently inhibited lipid peroxidation in vitro but did not inhibit TLR-4-linked NF-κB activation in HEK cells. Oral administration of HY8004 inhibited TNBS-induced colon shortening and myeloperoxidase activity in the colon of C3H/HeN and C3H/HeJ mice as well as IL-1β and TNF-α expression. B. longum HY8004 also inhibited TNBSinduced lipid peroxidation, TLR-4 expression, and NF-κB activation in the colon of C3H/HeN and C3H/HeJ mice. Conclusion B. longum HY8004 can improve colitis via the inhibition of lipid peroxidation as well as NF-κB activation.
KW - 2,4,6-trinitrobenzene sulfonic acid
KW - Bifidobacterium longum
KW - Inflammatory bowel disease
KW - Lipid peroxidation
KW - NF-κB
KW - Toll-like receptor-4
UR - http://www.scopus.com/inward/record.url?scp=77953363389&partnerID=8YFLogxK
U2 - 10.1007/s00011-009-0108-5
DO - 10.1007/s00011-009-0108-5
M3 - Article
C2 - 19882302
AN - SCOPUS:77953363389
SN - 1023-3830
VL - 59
SP - 359
EP - 368
JO - Inflammation Research
JF - Inflammation Research
IS - 5
ER -