Abstract |
Soyasaponins (SSs) abundant in soybean have anti-inflammatory activities; however, their therapeutic effects on allergic contact dermatitis (ACD) remain unknown. To assess the effects of SS-enriched diets on ACD, we used a mouse model of contact hypersensitivity (CHS). Mice were fed low-dose or high-dose SS-containing diets for 3 weeks prior to CHS induction with 2,4-dinitrofluorobenzene ( DNFB). The low-dose SS diet attenuated DNFB-induced ear swelling and tissue oedema, and reduced the number of infiltrating Gr-1-positive myeloid cells. Low-dose, but not high-dose, SSs decreased chemokine (C-X-C motif) ligand 2 (CXCL2) and triggering receptor expressed on myeloid cells (TREM)-1 production in ear tissues, compared to a control. Taxonomic 16S rRNA analysis revealed significant alterations in faecal microbiota caused by CHS, which were reversed by low-dose SSs. The low-dose SS and non-CHS groups clustered together, while the high-dose SS group split between CHS and non-CHS clusters. Our results demonstrated that low-dose SSs alleviated CHS symptoms by attenuating inflammation and improving the intestinal microbiota composition, suggesting that dietary SSs may have beneficial effects on ACD.
|
Authors | Takao Nagano, Mitsuru Katase, Kazunobu Tsumura, Mineki Saito, Tsukasa Matsuda |
Journal | Experimental dermatology
(Exp Dermatol)
Vol. 26
Issue 3
Pg. 249-254
(03 2017)
ISSN: 1600-0625 [Electronic] Denmark |
PMID | 27618807
(Publication Type: Journal Article)
|
Copyright | © 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. |
Chemical References |
- Chemokine CXCL2
- Cxcl2 protein, mouse
- Saponins
- TREM1 protein, mouse
- Triggering Receptor Expressed on Myeloid Cells-1
- Dinitrofluorobenzene
|
Topics |
- Animals
- Chemokine CXCL2
(metabolism)
- Dermatitis, Contact
(drug therapy, pathology)
- Dietary Supplements
- Dinitrofluorobenzene
- Feces
(microbiology)
- Female
- Mice
- Mice, Inbred BALB C
- Saponins
(administration & dosage, therapeutic use)
- Glycine max
- Triggering Receptor Expressed on Myeloid Cells-1
(metabolism)
|