2021
DOI: 10.1007/s11418-021-01566-2
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Orengedokuto exerts anti-allergic effects via inhibition of effector T cell activation in a murine model of contact hypersensitivity

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Cited by 3 publications
(3 citation statements)
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“…In addition, skin inflammation and itch-related behavior in animal models of atopic dermatitis were also improved by repetitive oral administration of Orengedokuto [7] and berberine [8]. Orengedokuto also attenuates the inflammatory symptoms in mite-induced allergic dermatitis [9] and chemical allergen-induced contact dermatitis [10,11]. In addition to our report [8], berberine also exerts an anti-inflammatory effect in 12-O-tetradecanoylphorbol-13-acetate-induced dermatitis [12], allergic contact dermatitis [13,14] and fungus-induced dermatitis [5] in animals.…”
Section: Tsugunobu Andoh and Tadamichi Shimizumentioning
confidence: 99%
“…In addition, skin inflammation and itch-related behavior in animal models of atopic dermatitis were also improved by repetitive oral administration of Orengedokuto [7] and berberine [8]. Orengedokuto also attenuates the inflammatory symptoms in mite-induced allergic dermatitis [9] and chemical allergen-induced contact dermatitis [10,11]. In addition to our report [8], berberine also exerts an anti-inflammatory effect in 12-O-tetradecanoylphorbol-13-acetate-induced dermatitis [12], allergic contact dermatitis [13,14] and fungus-induced dermatitis [5] in animals.…”
Section: Tsugunobu Andoh and Tadamichi Shimizumentioning
confidence: 99%
“…Kampo medicines are gaining attention as an alternative or complementary treatment option to Western medicines, particularly for chronic conditions that may not be fully addressed using conventional medicine alone. In recent years, there has been increasing research on Kampo medicines, with studies focusing on their efficacy, safety, and mechanism of action [15][16][17]. As part of our ongoing research to scientifically clarify the effectiveness of Kampo medicines [18][19][20][21], this study evaluated the anti-glycation activity of a total of 147 prescriptions of oral Kampo medicines covered by health insurance in Japan.…”
Section: Introductionmentioning
confidence: 99%
“…Figure 8. MS/MS fragmentation pathway of compounds 12 and 16.Peaks 5 (tR 5.76 min), 8 (tR 6.57 min), 15 (tR 10.38 min), 22 (tR 14.86 min), and 23 (tR 15.20 min) were identified as characteristic monoterpenoids in Paeoniae radix[39].Peaks 5, 15, and 8 were identified as albiflorin (5), 4-epi-albiflorin(15), and peoniflorin(8), with the same molecular formula (C23H28O11 each), and they were deduced from the ions of m/z 498.1966 [M+NH4] + , 481.1699 [M+H] + , and m/z 481.1704 [M+H] + , respectively. Fragmentation of 5 and 15 generated ions 5a and 15a via the loss of a glucose, followed by the loss of H2O and the benzoyl group to generate product ions 5b and 15b (Figure9).…”
mentioning
confidence: 99%