Atopic dermatitis;
prebiotics;
inflammation;
gut microbiome;
GUT MICROBIOTA;
INTESTINAL MICROBIOTA;
BETA-GLUCAN;
DISEASE;
CONSEQUENCES;
CHILDREN;
HEALTH;
ASTHMA;
INFLAMMATION;
METABOLISM;
D O I:
10.4168/aair.2023.15.3.303
中图分类号:
R392 [医学免疫学];
学科分类号:
100102 ;
摘要:
Purpose: Recently, interest is increasing in using prebiotics, which are nutrient ingredients of live microorganism that improve the intestinal environments by promoting the growth of beneficial gut microflora. Although numerous studies have demonstrated the beneficial effects of probiotics on atopic dermatitis (AD) development, few have examined preventive and therapeutic effects of prebiotics on the onset and progression of AD.Methods: In this study, we investigated therapeutic and preventive effect of prebiotics, including fl-glucan and inulin, using an oxazolone (OX)-induced AD-like mouse model. Prebiotics were orally administered 2 weeks after the end of sensitization period (therapeutic study) and 3 weeks before the initial sensitization (prevention study). The physiological and histological alterations in the skin and gut of the mice were investigated.Results: In the therapeutic study, the severity of skin lesions and inflammatory responses were effectively reduced after administering fl-glucan and inulin, respectively. The expression level of calprotectin was significantly decreased by approximately 2-fold (P < 0.05) in the skin and gut of prebiotics-treated mice compared to the control. In addition, epidermal thickness and the number of infiltrated immune cells were markedly reduced in the dermis of prebiotics-treated mice compared with to those in the OX-induced mice (P < 0.05). These findings were same as in the prevention study. Importantly, pre-administration of fl-glucan and inulin prevented the progression of AD by promoting the growth of good bacteria in the gut of OX-induced AD mice. However, the co-administration of fl-glucan and inulin did not show enhanced preventive effects on these alterations. Conclusions: Prebiotics has a therapeutic effect on AD in OX-induced AD mouse model. Moreover, our study suggests that prebiotics prevents the development of AD and this effect is associated with a change in gut microbiome.
机构:
Kyungpook Natl Univ, Sch Med, Dept Pharmacol, Cell & Matrix Res Inst, 680 Gukchaebosang Ro, Daegu 41944, South KoreaKyungpook Natl Univ, Sch Med, Dept Pharmacol, Cell & Matrix Res Inst, 680 Gukchaebosang Ro, Daegu 41944, South Korea
Choi, Jin Kyeong
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机构:
Jang, Yong Hyun
Lee, Soyoung
论文数: 0引用数: 0
h-index: 0
机构:
Korea Res Inst Biosci & Biotechnol, Immunoregulatory Mat Res Ctr, Jeongeup 56212, Jeollabuk Do, South KoreaKyungpook Natl Univ, Sch Med, Dept Pharmacol, Cell & Matrix Res Inst, 680 Gukchaebosang Ro, Daegu 41944, South Korea
Lee, Soyoung
Lee, Sang-Rae
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机构:
Korea Res Inst Biosci & Biotechnol, Natl Primate Res Ctr, Cheongju 28116, Chungcheongbuk, South KoreaKyungpook Natl Univ, Sch Med, Dept Pharmacol, Cell & Matrix Res Inst, 680 Gukchaebosang Ro, Daegu 41944, South Korea
Lee, Sang-Rae
Choi, Jung Ho
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h-index: 0
机构:
Korean Drug Co Ltd, R&D Ctr, Pharmaceut Lab, Seoul 06300, South KoreaKyungpook Natl Univ, Sch Med, Dept Pharmacol, Cell & Matrix Res Inst, 680 Gukchaebosang Ro, Daegu 41944, South Korea
Choi, Jung Ho
Park, Jee Hun
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h-index: 0
机构:
Korean Drug Co Ltd, R&D Ctr, Pharmaceut Lab, Seoul 06300, South KoreaKyungpook Natl Univ, Sch Med, Dept Pharmacol, Cell & Matrix Res Inst, 680 Gukchaebosang Ro, Daegu 41944, South Korea
Park, Jee Hun
Shin, Tae-Yong
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机构:
Woosuk Univ, Coll Pharm, Dept Pharm, 443 Samrye Ro, Samrye 55338, Jeollabuk Do, South KoreaKyungpook Natl Univ, Sch Med, Dept Pharmacol, Cell & Matrix Res Inst, 680 Gukchaebosang Ro, Daegu 41944, South Korea
机构:
Hallym Univ, Inst New Frontier Res Team, Hallym Clin & Translat Sci Inst, Chunchon, South KoreaHallym Univ, Inst New Frontier Res Team, Hallym Clin & Translat Sci Inst, Chunchon, South Korea
Jung, Harry
Son, Gil Myeong
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机构:
Hallym Univ, Chuncheon Sacred Heart Hosp, Coll Med, Dept Otorhinolaryngol Head & Neck Surg, 77 Sakju Ro, Chunchon 24253, Gangwon Do, South KoreaHallym Univ, Inst New Frontier Res Team, Hallym Clin & Translat Sci Inst, Chunchon, South Korea
Son, Gil Myeong
Lee, Jae Jun
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h-index: 0
机构:
Hallym Univ, Coll Med, Dept Anesthesiol & Pain Med, Chunchon, South KoreaHallym Univ, Inst New Frontier Res Team, Hallym Clin & Translat Sci Inst, Chunchon, South Korea
机构:
MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02142 USA
MIT, Dept Chem Engn, Cambridge, MA 02139 USAMIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02142 USA
Urbanska, Aleksandra M.
Karagiannis, Emmanouil D.
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机构:
MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02142 USA
MIT, Dept Chem Engn, Cambridge, MA 02139 USAMIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02142 USA
Karagiannis, Emmanouil D.
Guajardo, Gonzalo
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MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02142 USAMIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02142 USA
Guajardo, Gonzalo
Langer, Robert S.
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h-index: 0
机构:
MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02142 USA
Childrens Hosp Boston, Dept Anesthesiol, Boston, MA 02115 USA
MIT, Dept Chem Engn, Cambridge, MA 02139 USA
MIT, Harvard MIT Div Hlth Sci Technol, Cambridge, MA 02142 USAMIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02142 USA
Langer, Robert S.
Anderson, Daniel G.
论文数: 0引用数: 0
h-index: 0
机构:
MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02142 USA
Childrens Hosp Boston, Dept Anesthesiol, Boston, MA 02115 USA
MIT, Dept Chem Engn, Cambridge, MA 02139 USA
MIT, Harvard MIT Div Hlth Sci Technol, Cambridge, MA 02142 USAMIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02142 USA