Haplopine Ameliorates 2,4-Dinitrochlorobenzene-Induced Atopic Dermatitis-Like Skin Lesions in Mice and TNF-α/IFN-γ-Induced Inflammation in Human Keratinocyte
This study aimed to investigate the anti-inflammatory, antioxidant, and anti-atopic dermatitis (AD) effects of haplopine, which is one of the active components in <i>D. dasycarpus.</i> Haplopine (12.5 and 25 μM) inhibited the mRNA expressions of inflammatory cytokines IL-6, TSLP, GM-CSF,...
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MDPI AG
2021-05-01
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author | Tae-Young Kim Ye Jin Kim Jonghwan Jegal Beom-Geun Jo Han-Seok Choi Min Hye Yang |
author_facet | Tae-Young Kim Ye Jin Kim Jonghwan Jegal Beom-Geun Jo Han-Seok Choi Min Hye Yang |
author_sort | Tae-Young Kim |
collection | DOAJ |
description | This study aimed to investigate the anti-inflammatory, antioxidant, and anti-atopic dermatitis (AD) effects of haplopine, which is one of the active components in <i>D. dasycarpus.</i> Haplopine (12.5 and 25 μM) inhibited the mRNA expressions of inflammatory cytokines IL-6, TSLP, GM-CSF, and G-CSF and the protein expressions of IL-6 and GM-CSF in TNF-α/INF-γ-stimulated HaCaT cells. In H<sub>2</sub>O<sub>2</sub>-induced Jukat T cells, haplopine (25 and 50 μM) suppressed the productions of proinflammatory cytokines (IL-4, IL-13, and COX-2) and increased the mRNA and protein expressions of oxidative stress defense enzymes (SOD, CAT, and HO-1) in a concentration-dependent manner. In vivo, haplopine significantly attenuated the development of AD symptoms in 2,4-dinitrochlorobenzene (DNCB)-stimulated Balb/c mice, as evidenced by reduced clinical dermatitis scores, skin thickness measurements, mast cell infiltration, and serum IgE concentrations. These findings demonstrate that haplopine should be considered a novel anti-atopic agent with the potential to treat AD. |
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issn | 2076-3921 |
language | English |
last_indexed | 2024-03-10T11:14:58Z |
publishDate | 2021-05-01 |
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series | Antioxidants |
spelling | doaj.art-2d0683154b9f457ab01967ecdf60279e2023-11-21T20:28:50ZengMDPI AGAntioxidants2076-39212021-05-0110580610.3390/antiox10050806Haplopine Ameliorates 2,4-Dinitrochlorobenzene-Induced Atopic Dermatitis-Like Skin Lesions in Mice and TNF-α/IFN-γ-Induced Inflammation in Human KeratinocyteTae-Young Kim0Ye Jin Kim1Jonghwan Jegal2Beom-Geun Jo3Han-Seok Choi4Min Hye Yang5College of Pharmacy, Pusan National University, Busan 46241, KoreaC&D Research Team, R&D Strategy Center, Genuonesciences, Seoul 06800, KoreaCollege of Pharmacy, Pusan National University, Busan 46241, KoreaCollege of Pharmacy, Pusan National University, Busan 46241, KoreaC&D Research Team, R&D Strategy Center, Genuonesciences, Seoul 06800, KoreaCollege of Pharmacy, Pusan National University, Busan 46241, KoreaThis study aimed to investigate the anti-inflammatory, antioxidant, and anti-atopic dermatitis (AD) effects of haplopine, which is one of the active components in <i>D. dasycarpus.</i> Haplopine (12.5 and 25 μM) inhibited the mRNA expressions of inflammatory cytokines IL-6, TSLP, GM-CSF, and G-CSF and the protein expressions of IL-6 and GM-CSF in TNF-α/INF-γ-stimulated HaCaT cells. In H<sub>2</sub>O<sub>2</sub>-induced Jukat T cells, haplopine (25 and 50 μM) suppressed the productions of proinflammatory cytokines (IL-4, IL-13, and COX-2) and increased the mRNA and protein expressions of oxidative stress defense enzymes (SOD, CAT, and HO-1) in a concentration-dependent manner. In vivo, haplopine significantly attenuated the development of AD symptoms in 2,4-dinitrochlorobenzene (DNCB)-stimulated Balb/c mice, as evidenced by reduced clinical dermatitis scores, skin thickness measurements, mast cell infiltration, and serum IgE concentrations. These findings demonstrate that haplopine should be considered a novel anti-atopic agent with the potential to treat AD.https://www.mdpi.com/2076-3921/10/5/806haplopineatopic dermatitisHaCaT cellsJurkat T cells2,4-dinitrochlorobenzeneBalb/c mice |
spellingShingle | Tae-Young Kim Ye Jin Kim Jonghwan Jegal Beom-Geun Jo Han-Seok Choi Min Hye Yang Haplopine Ameliorates 2,4-Dinitrochlorobenzene-Induced Atopic Dermatitis-Like Skin Lesions in Mice and TNF-α/IFN-γ-Induced Inflammation in Human Keratinocyte Antioxidants haplopine atopic dermatitis HaCaT cells Jurkat T cells 2,4-dinitrochlorobenzene Balb/c mice |
title | Haplopine Ameliorates 2,4-Dinitrochlorobenzene-Induced Atopic Dermatitis-Like Skin Lesions in Mice and TNF-α/IFN-γ-Induced Inflammation in Human Keratinocyte |
title_full | Haplopine Ameliorates 2,4-Dinitrochlorobenzene-Induced Atopic Dermatitis-Like Skin Lesions in Mice and TNF-α/IFN-γ-Induced Inflammation in Human Keratinocyte |
title_fullStr | Haplopine Ameliorates 2,4-Dinitrochlorobenzene-Induced Atopic Dermatitis-Like Skin Lesions in Mice and TNF-α/IFN-γ-Induced Inflammation in Human Keratinocyte |
title_full_unstemmed | Haplopine Ameliorates 2,4-Dinitrochlorobenzene-Induced Atopic Dermatitis-Like Skin Lesions in Mice and TNF-α/IFN-γ-Induced Inflammation in Human Keratinocyte |
title_short | Haplopine Ameliorates 2,4-Dinitrochlorobenzene-Induced Atopic Dermatitis-Like Skin Lesions in Mice and TNF-α/IFN-γ-Induced Inflammation in Human Keratinocyte |
title_sort | haplopine ameliorates 2 4 dinitrochlorobenzene induced atopic dermatitis like skin lesions in mice and tnf α ifn γ induced inflammation in human keratinocyte |
topic | haplopine atopic dermatitis HaCaT cells Jurkat T cells 2,4-dinitrochlorobenzene Balb/c mice |
url | https://www.mdpi.com/2076-3921/10/5/806 |
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