Bo-Kyung Park1, Yang-Chun Park2, In Chul Jung3, Seung-Hyung Kim4, Jeong June Choi4, Moonho Do5, Sun Yeou Kim5, Mirim Jin6. 1. Laboratory of Pharmacology, College of Korean Medicine, Daejeon University, Daejeon 300-706, Republic of Korea. 2. Department of Internal Medicine, Daejeon Korean Medicine Hospital of Daejeon University, Daejeon 301-724, Republic of Korea. 3. Department of Neuropsychiatry, Dunsan Korean Medicine Hospital of Daejeon University, Daejeon 302-122, Republic of Korea. 4. Institute of Traditional Medicine and Bioscience, Daejeon University, Daejeon 300-706, Republic of Korea. 5. College of Pharmacy, Gachon University, Incheon 406-799, Republic of Korea. 6. Laboratory of Pharmacology, College of Korean Medicine, Daejeon University, Daejeon 300-706, Republic of Korea. Electronic address: mirimj@dju.ac.kr.
Abstract
ETHNOPHARMACOLOGICAL RELEVANCE: Gamisasangja-tang (GST) is a traditional herbal formula prescribed for patients with intractable pruritus in association with various inflammatory skin diseases. To evaluate the effects of GST on pruritic skin inflammation and investigate its cellular and molecular mechanisms. MATERIALS AND METHODS: We orally administered GST to NC/Nga (NC) mice, an animal model of atopic dermatitis. Scratching frequency and the dermatitis index were evaluated, and histological examination was performed using hematoxylin and eosin and toluidine blue staining. The levels of interleukin (IL)-31 and T-helper cell type 2 (TH2) cytokines were determined in both the dorsal skin and cultured splenocytes by real-time polymerase chain reaction (PCR) and enzyme-linked immunosorbent assay (ELISA), respectively. The serum levels of chemokines and immunoglobulin E (IgE) were determined by ELISA. Changes in the inflammatory cell population were analyzed by a hemocytometer. RESULTS: GST significantly lowered scratching frequency and inhibited increases in dermatitis index, thickness of epidermis/dermis and infiltration of chemokine (C-C motif) receptor 3 (CCR3)(+) and cluster of differentiation (CD)117(+)/FcεRIα (Fc fragment of IgE, high affinity I, receptor for; alpha polypeptide)(+) cells in atopic skin. Both IL-31 mRNA expression and production were significantly reduced by GST, which was accomrease in the levels of IL-4, IL-5, and IL-13. Further, GST treatment suppressed the secretion of eotaxin, TARC (thymus and activation-regulated chemokine), IgE, and increases in the number of basophils and eosinophils in the blood. CONCLUSION: GST may have potential as an effective treatment for pruritic skin disease such as atopic dermatitis.
ETHNOPHARMACOLOGICAL RELEVANCE: Gamisasangja-tang (GST) is a traditional herbal formula prescribed for patients with intractable pruritus in association with various inflammatory skin diseases. To evaluate the effects of GST on pruritic skin inflammation and investigate its cellular and molecular mechanisms. MATERIALS AND METHODS: We orally administered GST to NC/Nga (NC) mice, an animal model of atopic dermatitis. Scratching frequency and the dermatitis index were evaluated, and histological examination was performed using hematoxylin and eosin and toluidine blue staining. The levels of interleukin (IL)-31 and T-helper cell type 2 (TH2) cytokines were determined in both the dorsal skin and cultured splenocytes by real-time polymerase chain reaction (PCR) and enzyme-linked immunosorbent assay (ELISA), respectively. The serum levels of chemokines and immunoglobulin E (IgE) were determined by ELISA. Changes in the inflammatory cell population were analyzed by a hemocytometer. RESULTS: GST significantly lowered scratching frequency and inhibited increases in dermatitis index, thickness of epidermis/dermis and infiltration of chemokine (C-C motif) receptor 3 (CCR3)(+) and cluster of differentiation (CD)117(+)/FcεRIα (Fc fragment of IgE, high affinity I, receptor for; alpha polypeptide)(+) cells in atopic skin. Both IL-31 mRNA expression and production were significantly reduced by GST, which was accomrease in the levels of IL-4, IL-5, and IL-13. Further, GST treatment suppressed the secretion of eotaxin, TARC (thymus and activation-regulated chemokine), IgE, and increases in the number of basophils and eosinophils in the blood. CONCLUSION: GST may have potential as an effective treatment for pruritic skin disease such as atopic dermatitis.
Authors: Ju Hyun Lee; Eun Heui Jo; Jee Youn Jung; Young-Eun Kim; Mi-Ju Son; Su Jin Kang; Geum Jin Yang; Yu Hwa Shim; Min Cheol Park Journal: Front Pharmacol Date: 2020-11-26 Impact factor: 5.810
Authors: Jin Mo Ku; Se Hyang Hong; Soon Re Kim; Han-Seok Choi; Hyo In Kim; Dong Uk Kim; So Mi Oh; Hye Sook Seo; Tai Young Kim; Yong Cheol Shin; Chunhoo Cheon; Seong-Gyu Ko Journal: BMC Complement Altern Med Date: 2018-07-13 Impact factor: 3.659
Authors: Bo-Kyung Park; Yu Ri Kim; Young Hwa Kim; Changsop Yang; Chang-Seob Seo; In Chul Jung; Ik-Soon Jang; Seung-Hyung Kim; Mi Young Lee Journal: Biomed Res Int Date: 2018-06-26 Impact factor: 3.411
Authors: Bo-Kyung Park; Young Hwa Kim; Yu Ri Kim; Jeong June Choi; Changsop Yang; Ik-Soon Jang; Mi Young Lee Journal: Evid Based Complement Alternat Med Date: 2019-04-01 Impact factor: 2.629