Hataedock Treatments for Dermatophagoides Farinae-induced Atopic Dermatitis in NC/Nga Mice Treated with High-fat Diet
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Hataedock (HTD) treatment is a traditional preventive therapy for the fetal toxicosis- the acute allergic disease after childbirth, mainly manifested by a variety of skin allergies such as scab, phlegm. The aim of this study was to investigate the efficacy of HTD treatments for the alleviation of inflammation in Dermatophagoides farinae-induced obese NC/Nga mice. 20 mg/kg of Coptidis Rhizoma, Glycyrrhizae Radix (CRGR) extracts as a remedy of HTD treatments were orally administered to NC/Nga mice. We induced obesity in the mice by high-fat diet. To induce skin allergies, the extracts of Dermatophagoides farinae were topically applied on the NC/Nga mice at 4th-6th and 8th-10th weeks. Structural and molecular changes in the skin tissues were measured by immunohistochemical staining. HTD treatment decreased the atopic dermatitis (AD)-like symptoms including hemorrhage, erythema, erosion, edema, and dryness. HTD treatment suppressed the mast cell activation confirmed by reduction of FcɛRI, substance P, and serotonin. The expression of several inflammatory mediators including nuclear factor-kappa B (NF-κB) p65, inducible nitric oxide synthase (iNOS), vascular endothelial growth factors (VEGFs) was also decreased by HTD treatment. HTD treatment suppressed the allergic, inflammatory responses in the skin tissues of the NC/Nga mice by reducing mast cells and down-regulating several inflammatory mediators.
Abstract
Hataedock (HTD) treatment is a traditional preventive therapy for the fetal toxicosis- the acute allergic disease after childbirth, mainly manifested by a variety of skin allergies such as scab, phlegm. The aim of this study was to investigate the efficacy of HTD treatments for the alleviation of inflammation in Dermatophagoides farinae-induced obese NC/Nga mice. 20 mg/kg of Coptidis Rhizoma, Glycyrrhizae Radix (CRGR) extracts as a remedy of HTD treatments were orally administered to NC/Nga mice. We induced obesity in the mice by high-fat diet. To induce skin allergies, the extracts of Dermatophagoides farinae were topically applied on the NC/Nga mice at 4th-6th and 8th-10th weeks. Structural and molecular changes in the skin tissues were measured by immunohistochemical staining. HTD treatment decreased the atopic dermatitis (AD)-like symptoms including hemorrhage, erythema, erosion, edema, and dryness. HTD treatment suppressed the mast cell activation confirmed by reduction of FcɛRI, substance P, and serotonin. The expression of several inflammatory mediators including nuclear factor-kappa B (NF-κB) p65, inducible nitric oxide synthase (iNOS), vascular endothelial growth factors (VEGFs) was also decreased by HTD treatment. HTD treatment suppressed the allergic, inflammatory responses in the skin tissues of the NC/Nga mice by reducing mast cells and down-regulating several inflammatory mediators.
참고문헌 (28)
- 강기수, "Nutritional Counseling for Obese Children with Obesity-Related Metabolic Abnormalities in Korea", Pediatric Gastroenterology, Hepatology & Nutrition, 20(2), pp.71~78 (2017), 대한소아소화기영양학회
- Kelishadi R, "Association of Childhood Obesity and the Immune System: A Systematic Review of Reviews", Child Obes, 13(4), pp.332~346 (2017)
- Mraz M, "The role of adipose tissue immune cells in obesity and low-grade inflammation", J Endocrinol, 222(3), pp.R113~R127 (2014)
- Guttman-Yassky E, "Systemic immune mechanisms in atopic dermatitis and psoriasis with implications for treatment", Exp Dermatol, 27(4), pp.409~417 (2018)
- Silverberg JI, "Central obesity and high blood pressure in pediatric patients with atopic dermatitis", JAMA Dermatol, 151(2), pp.144~152 (2015)
- Romieu I, "Maternal fish intake during pregnancy and atopy and asthma in infancy", Clin Exp Allergy, 37(4), pp.518~525 (2007)
- Moon M, "Coptidis Rhizoma Prevents Heat Stress-Induced Brain Damage and Cognitive Impairment in Mice", Nutrients, 9(10), pp.1057~ (2017)
- Kim BB, "7,3',4'-Trihydroxyisoflavone Ameliorates the Development of Dermatophagoides farinae-Induced Atopic Dermatitis in NC", Nga Mice, 2013, pp.2013, 636597~
- Jung AR, "Douchi (fermented Glycine max Merr.) alleviates atopic dermatitis-like skin lesions in NC", Nga mice by regulation of PKC and IL-4, 2016, pp.16(1), 416~
- Cha HY, "Hataedock Treatment Has Preventive Therapeutic Effects in Atopic Dermatitis-Induced NC", Nga Mice under High-Fat Diet Conditions, 2016, pp.2016, 1739760~
- Proksch E, "Role of the epidermal barrier in atopic dermatitis", J Dtsch Dermatol Ges, 7(10), pp.899~910 (2009)
- Liu J, "Genetic deficiency and pharmacological stabilization of mast cells reduce diet-induced obesity and diabetes in mice", Nat Med, 15(8), pp.940~945 (2009)
- Poglio S, "Adipose tissue as a dedicated reservoir of functional mast cell progenitors", Stem Cells, 28(11), pp.2065~2072 (2010)
- Zhang J, "Mast cells and metabolic syndrome", Biochim Biophys Acta, 1822(1), pp.14~20 (2012)
- Shoelson SE, "Obesity, Inflammation, and Insulin Resistance", Gastroenterology, 132(6), pp.2169~2180 (2007)
- Kanchongkittiphon W, "Child with atopic dermatitis", Ann Allergy Asthma Immunol, 114(1), pp.6~11 (2015)
- Benelli R, "Cytokines and chemokines as regulators of angiogenesis in health and disease", Curr Pharm Des, 12(24), pp.3101~3115 (2006)
- Charo IF, "Chemokines in the pathogenesis of vascular disease", Circ Res, 95(9), pp.858~866 (2004)
- Theoharides TC, "Mast cells and inflammation", Biochim Biophys Acta, 1822(1), pp.21~33 (2012)
- Suzuki H, "Substance P induces degranulation of mast cells and leukocyte adhesion to venular endothelium", Peptides, 16(8), pp.1447~1452 (1995)
- Baram D, "Human Mast Cells Release Metalloproteinase-9 on Contact with Activated T Cells: Juxtacrine Regulation by TNF-alpha", J Immunol, 167(7), pp.4008~4016 (2001)
- Chen TL, "Protective effects of isorhamnetin on apoptosis and inflammation in TNF-alpha-induced HUVECs injury", Int J Clin Exp Pathol, 8(3), pp.2311~2320 (2015)
- Li J, "Nitric oxide suppresses apoptosis via interrupting caspase activation and mitochondrial dysfunction in cultured hepatocytes", J Biol Chem, 274(24), pp.17325~17333 (1999)
- Chen L, "The progression of inflammation parallels the dermal angiogenesis in a keratin 14 IL-4-transgenic model of atopic dermatitis", Microcirculation, 15(1), pp.49~64 (2008)
- Zhang Y, "Increased production of vascular endothelial growth factor in the lesions of atopic dermatitis", Arch Dermatol Res, 297(9), pp.425~429 (2006)
- Genovese A, "Angiogenesis, lymphangiogenesis and atopic dermatitis", Chem Immunol Allergy, 96, pp.50~60 (2012)
- Samochocki Z, "Expression of vascular endothelial growth factor and other cytokines in atopic dermatitis, and correlation with clinical features", Int J Dermatol, 55(3), pp.e141~e146 (2016)
- 김희연, "Effect of Skin Lipid Barrier Formation on Hataedock Treatment with Douchi", 대한한의학회지, 38(2), pp.41~52 (2017), 대한한의학회[DOI]
