TY - JOUR
T1 - Fermented rice bran supplementation prevents the development of intestinal fibrosis due to dss-induced inflammation in mice
AU - Agista, Afifah Zahra
AU - Rusbana, Tubagus Bahtiar
AU - Islam, Jahidul
AU - Ohsaki, Yusuke
AU - Sultana, Halima
AU - Hirakawa, Ryouta
AU - Watanabe, Kouichi
AU - Nochi, Tomonori
AU - Ardiansyah,
AU - Budijanto, Slamet
AU - Yang, Suh Ching
AU - Koseki, Takuya
AU - Aso, Hisashi
AU - Komai, Michio
AU - Shirakawa, Hitoshi
N1 - Funding Information:
Funding: This work was partially supported by grants from the JSPS Core-to-Core Program A (Advanced Research Networks), entitled “Establishment of international agricultural immunology research-core for quantum improvement in food safety”; the Kobayashi Foundation; the Tojuro Iijima Foundation for Food Science and Technology; the Salt Science Research Foundation (No. 20D4); and the Joint Projects of Rice Bran of Sunstar Inc.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/6
Y1 - 2021/6
N2 - Fermented rice bran (FRB) is known to protect mice intestines against dextran sodium sulfate (DSS)-induced inflammation; however, the restoration of post-colitis intestinal homeostasis using FRB supplementation is currently undocumented. In this study, we observed the effects of dietary FRB supplementation on intestinal restoration and the development of fibrosis after DSSinduced colitis. DSS (1.5%) was introduced in the drinking water of mice for 5 days. Eight mice were sacrificed immediately after the DSS treatment ended. The remaining mice were divided into three groups, comprising the following diets: control, 10% rice bran (RB), and 10% FRB-supplemented. Diet treatment was continued for 2 weeks, after which half the population of mice from each group was sacrificed. The experiment was continued for another 3 weeks before the remaining mice were sacrificed. FRB supplementation could reduce the general observation of colitis and production of intestinal pro-inflammatory cytokines. FRB also increased intestinal mRNA levels of anti-inflammatory cytokine, tight junction, and anti-microbial proteins. Furthermore, FRB supplementation suppressed markers of intestinal fibrosis. This effect might have been achieved via the canonical Smad2/3 activation and the non-canonical pathway of Tgf-β activity. These results suggest that FRB may be an alternative therapeutic agent against inflammation-induced intestinal fibrosis.
AB - Fermented rice bran (FRB) is known to protect mice intestines against dextran sodium sulfate (DSS)-induced inflammation; however, the restoration of post-colitis intestinal homeostasis using FRB supplementation is currently undocumented. In this study, we observed the effects of dietary FRB supplementation on intestinal restoration and the development of fibrosis after DSSinduced colitis. DSS (1.5%) was introduced in the drinking water of mice for 5 days. Eight mice were sacrificed immediately after the DSS treatment ended. The remaining mice were divided into three groups, comprising the following diets: control, 10% rice bran (RB), and 10% FRB-supplemented. Diet treatment was continued for 2 weeks, after which half the population of mice from each group was sacrificed. The experiment was continued for another 3 weeks before the remaining mice were sacrificed. FRB supplementation could reduce the general observation of colitis and production of intestinal pro-inflammatory cytokines. FRB also increased intestinal mRNA levels of anti-inflammatory cytokine, tight junction, and anti-microbial proteins. Furthermore, FRB supplementation suppressed markers of intestinal fibrosis. This effect might have been achieved via the canonical Smad2/3 activation and the non-canonical pathway of Tgf-β activity. These results suggest that FRB may be an alternative therapeutic agent against inflammation-induced intestinal fibrosis.
KW - Colitis
KW - Dextran sodium sulfate
KW - Fermented rice bran
KW - Intestinal fibrosis
KW - Intestinal inflammation
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U2 - 10.3390/nu13061869
DO - 10.3390/nu13061869
M3 - Article
AN - SCOPUS:85106744721
SN - 2072-6643
VL - 13
JO - Nutrients
JF - Nutrients
IS - 6
M1 - 1869
ER -