Abstract | OBJECTIVES: In the present study, we aimed to examine the anti-atopic properties of bile from the cat fish, Silurus asotus, to determine its possible use as a pharmaceutical product. METHODS: RESULTS: The results of these experiments revealed that Silurus asotus bile (SAB) scavenges radicals and protects proteins from superoxide attacks, suggesting that SAB suppresses the T helper (Th) type 2-skewed immune response. Th1/Th2 mRNA cytokines ( interleukin (IL)-2, interferon (IFN)-γ and IL-4) from mouse splenocytes were effectively inhibited, and the release of β- hexosaminidase in RBL-2H3 mast cells was significantly suppressed by SAB. These results were supported by screening the Th1/Th2 cytokine mRNAs (IL-2, IFN-γ and IL-4) from lymph nodes in DNCB-treated mice. More dramatic results were observed in the histological changes at higher SAB concentrations (5%) compared to the therapeutic control, visualized using hematoxylin- eosin (H&E) staining. CONCLUSIONS: The results presented in this study suggest that SAB may provide functional advantages with regard to treating atopic dermatitis because of its antioxidant and immune-suppressive effects.
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Authors | Do Ik Lee, Yoon Joo Huh, Kwang Woo Hwang, YoungWook Choi, Jae-Seok Choi, Sam-Yong Han, Young-Soo Gyoung, Seong Soo Joo |
Journal | The Journal of pharmacy and pharmacology
(J Pharm Pharmacol)
Vol. 63
Issue 10
Pg. 1327-35
(Oct 2011)
ISSN: 2042-7158 [Electronic] England |
PMID | 21899549
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2011 The Authors. JPP © 2011 Royal Pharmaceutical Society. |
Chemical References |
- Antioxidants
- Biological Products
- Cytokines
- Dinitrochlorobenzene
- RNA, Messenger
- Superoxides
- beta-N-Acetylhexosaminidases
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Topics |
- Animals
- Antioxidants
(pharmacology, therapeutic use)
- Bile
- Biological Products
(pharmacology, therapeutic use)
- Catfishes
- Complementary Therapies
- Cytokines
(antagonists & inhibitors, genetics)
- Dermatitis, Atopic
(immunology, metabolism, therapy)
- Dinitrochlorobenzene
- Lymph Nodes
(drug effects, metabolism)
- Mast Cells
(drug effects, metabolism)
- Mice
- Mice, Inbred BALB C
- Protein Carbonylation
(drug effects)
- RNA, Messenger
(metabolism)
- Skin
(drug effects, pathology)
- Spleen
(cytology, drug effects, metabolism)
- Superoxides
(metabolism)
- T-Lymphocytes
(metabolism)
- Th1 Cells
(drug effects, metabolism)
- Th2 Cells
(drug effects, metabolism)
- beta-N-Acetylhexosaminidases
(antagonists & inhibitors)
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