2019
DOI: 10.1016/j.jep.2019.111937
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Effects and mechanism of action of Huang-Lian-Jie-Du-Tang in atopic dermatitis-like skin dysfunction in vivo and in vitro

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Cited by 27 publications
(15 citation statements)
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“…In 2,4-dinitrochlorobenzene-induced atopic dermatitis mice, HLJDD down-regulated serum expression levels of IL-1α, IL-1β, IL-2, IL-4, IL-5, IL-6, interferongamma and TNF-α, normalised the splenic CD4 + /CD8 + T-lymphocyte ratio, and inactivated MAPKs (including p38, extracellular regulated protein kinases (ERK), and c-Jun N-terminal kinase (JNK)), IκB-α, and NF-κB (p65). Moreover, HLJDD inhibited LPS-induced differentiation of RAW264.7 cells, reduced LPS binding to the RAW264.7 cell membrane, as well as decreased ERK, p38, JNK, IκB-α, and p65 phosphorylation levels in the MAPKs/NF-κB pathway and inhibited p65 nuclear translocation [115]. Further, a study revealed that HLJDD had a positive effect in rat gingivitis induced by LPS.…”
Section: Anti-inflammatory and Anti-allergymentioning
confidence: 90%
See 1 more Smart Citation
“…In 2,4-dinitrochlorobenzene-induced atopic dermatitis mice, HLJDD down-regulated serum expression levels of IL-1α, IL-1β, IL-2, IL-4, IL-5, IL-6, interferongamma and TNF-α, normalised the splenic CD4 + /CD8 + T-lymphocyte ratio, and inactivated MAPKs (including p38, extracellular regulated protein kinases (ERK), and c-Jun N-terminal kinase (JNK)), IκB-α, and NF-κB (p65). Moreover, HLJDD inhibited LPS-induced differentiation of RAW264.7 cells, reduced LPS binding to the RAW264.7 cell membrane, as well as decreased ERK, p38, JNK, IκB-α, and p65 phosphorylation levels in the MAPKs/NF-κB pathway and inhibited p65 nuclear translocation [115]. Further, a study revealed that HLJDD had a positive effect in rat gingivitis induced by LPS.…”
Section: Anti-inflammatory and Anti-allergymentioning
confidence: 90%
“…5. Collagen-induced arthritis rats Regulating fatty acid oxidation and arachidonic acid metabolism [19] LPS-stimulated RAW 264.7 macrophages Suppressing the production of inflammatory mediators via inactivation of NF-κB and MAPKs, and degradation of IκBα [108] Cecal ligation and puncture-induced septic model rats Enhancing cholinergic anti-inflammatory pathway Inhibiting HMGB-1/TLR4/NF-κB signaling pathway [4] Cecal ligation and puncture-induced septic model rats Suppressing the production of proinflammatory cytokines Reversing the shift from Th1 to Th2 response and promote Th1/Th2 balance toward Th1 predominance Iinhibiting Th17 activation [112] 2,4-dinitrochlorobenzene-induced atopic dermatitis mice LPS-stimulated RAW 264.7 macrophages Inhibiting MAPKs/NF-κB pathway [115] LPS-induced gingivitis rats Inhibiting AMPK and ERK1/2 pathway [116] LPS-induced acute kidney injury mice Inhibiting NF-κB and MAPK activation Activating Akt/HO-1 pathway Ameliorating disturbances in oxidative stress and energy metabolism [26] Anti-allergy Antigen-induced RBL-2H3 cells Suppressing allergic mediators via inactivation of MAPKs and Lyn pathway [108] Modulation of blood lipid ApoE(-/-) mice Primary bone marrow-derived macrophage Foam cells…”
Section: Anti-tumormentioning
confidence: 99%
“…The regulation of Th2 differentiation was studied by measuring the extent of IL-4-, FcεR-, and p-NF-κB p65-positive reactions in the immunohistochemical analysis (Figure 5). TSLP overexpression results in allergic inflammation as well as Th2-skewed conditions after a series of processes involving IL-4, FcεR, and p-NF-κB p65 [27][28][29][30][31]. Immunohistochemistry results showed that IL-4-, FcεR-, and p-NF-κB p65-positive reactions in the LBE, PEAT, and 3HbT groups were higher than those in the Ctrl group, and those in the 3HbT group were lower than those in the LBE and PEAT groups (p < 0.05).…”
Section: Regulation Of Th2 Differentiationmentioning
confidence: 99%
“…In dextran sulphate sodium-induced mice ulcerative colitis (UC), HLJD decoction alleviates the UC symptoms and decreases inflammatory cytokines in colons [11]. HLJD decoction mitigates mice atopic dermatitis induced by 2,4-dinitrochlorobenzene [12] and decreases nitric oxide and various cytokines release in LPS-stimulated RAW264.7 cells [13]. Taken together, HLJD decoction shows its effects in various inflammatory conditions.…”
Section: Introductionmentioning
confidence: 98%