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231226s2022 xx |||||o 00| ||eng c |
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|a 10.1016/j.clim.2022.109102
|2 doi
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|a pubmed24n1152.xml
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|a (DE-627)NLM345668790
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|a (NLM)36049600
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|a (PII)S1521-6616(22)00183-8
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Zhang, Yi
|e verfasserin
|4 aut
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|a Vasicine alleviates 2,4-dinitrochlorobenzene-induced atopic dermatitis and passive cutaneous anaphylaxis in BALB/c mice
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|c 2022
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 12.10.2022
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|a Date Revised 11.11.2022
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a Copyright © 2022 Elsevier Inc. All rights reserved.
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|a Atopic dermatitis (AD), a type of skin inflammation, is associated with immune response mediated by T-helper 2 (Th2) cells, and mast cells. Vasicine is an alkaloid isolated from Adhatoda vasica, a popular Ayurvedic herbal medicine used for treating inflammatory conditions. In the present study, the anti-AD effects of vasicine were evaluated on 2,4-dinitrochlorobenzene-induced AD-like skin lesions in BALB/c mice. The potential anti-allergic effects of vasicine were also assessed using the passive cutaneous anaphylaxis (PCA) test. The results showed that the oral administration of vasicine improved the severity of AD-like lesional skin by decreasing histopathological changes and restoring epidermal thickness. Vasicine also inhibited the infiltration of mast cells in the skin and reduced the levels of pro-Th2 and Th2 cytokines as well as immunoglobulin E in the serum. Finally, vasicine inhibited the expression of pro-Th2 and Th2 cytokines in skin tissues, indicating the therapeutic potential of vasicine for AD
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Atopic dermatitis
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|a Mast cell
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|a Passive cutaneous anaphylaxis
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|a Th2 cytokine
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|a Vasicine
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|a Alkaloids
|2 NLM
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|a Anti-Allergic Agents
|2 NLM
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|a Cytokines
|2 NLM
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|a Dinitrochlorobenzene
|2 NLM
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|a Quinazolines
|2 NLM
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|a Immunoglobulin E
|2 NLM
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|a 37341-29-0
|2 NLM
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|a vasicine
|2 NLM
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|a 6C2ZBI733P
|2 NLM
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1 |
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|a Du, Wenxia
|e verfasserin
|4 aut
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|a Zhu, Defen
|e verfasserin
|4 aut
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|a Li, Meiling
|e verfasserin
|4 aut
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1 |
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|a Qu, Lu
|e verfasserin
|4 aut
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1 |
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|a Rao, Gaoxiong
|e verfasserin
|4 aut
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1 |
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|a Lin, Yuping
|e verfasserin
|4 aut
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1 |
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|a Tong, Xiaoyun
|e verfasserin
|4 aut
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1 |
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|a Sun, Yun
|e verfasserin
|4 aut
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|a Huang, Feng
|e verfasserin
|4 aut
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|i Enthalten in
|t Clinical immunology (Orlando, Fla.)
|d 1999
|g 244(2022) vom: 01. Nov., Seite 109102
|w (DE-627)NLM098196855
|x 1521-7035
|7 nnns
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1 |
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|g volume:244
|g year:2022
|g day:01
|g month:11
|g pages:109102
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|u http://dx.doi.org/10.1016/j.clim.2022.109102
|3 Volltext
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|a AR
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|d 244
|j 2022
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|h 109102
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