Hesperidin inhibits development of atopic dermatitis-like skin lesions in NC/Nga mice by suppressing Th17 activity
Hesperidin inhibits development of atopic dermatitis-like skin lesions in NC/Nga mice by suppressing Th17 activity
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橙皮苷通过抑制 Th17 活性来抑制 NC/Nga 小鼠特应性皮炎样皮肤病变的发展
DOI:
10.1016/j.jff.2013.07.005
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发表时间:
2013
期刊:
影响因子:
5.6
通讯作者:
Tanabe S.
中科院分区:
文献类型:
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作者:
Nagashio Y;Matsuura Y;Miyamoto J;Kometani T;Suzuki T;Tanabe S.
Hesperidin (previously called vitamin P) is a predominant flavanone present in citrus fruits, and is presumed to have a role in their beneficial effect for human health because it possesses various physiological activities. In this study, we investigated the anti-allergic and anti-inflammatory effects of hesperidin and α-glucopyranosyl (αG)-hesperidin, its derivative with enhanced water-solubility, in NC/Nga mice, a human-like mouse model of atopic dermatitis. NC/Nga mice were fed a 0.1% αG-hesperidin or hesperidin diet for 8 weeks. αG-hesperidin and hesperidin feeding effectively inhibited skin lesions and immunoglobulin E (IgE) elevation. At the end of the 8-week-experimental period, the production of inflammatory cytokine interleukin (IL)-17 and interferon-gamma (IFN-γ) from splenocytes was lower in the αG-hesperidin/hesperidin-fed group than in the control group. Changes in mRNA expression in splenocytes are also examined using DNA microarray and real-time RT-PCR. It was revealed that cytotoxic T-lymphocyte antigen 4 (CTLA4), a regulatory T-cell (Treg) marker, was markedly upregulated in splenocytes, particularly by αG-hesperidin feeding. These results suggest that αG-hesperidin attenuated exacerbation of AD-like symptoms, decreased systemic immune hyper-responsiveness in part through the reduction of IgE, IL-17 and IFN-γ, and also modulated Th17/Treg balance in NC/Nga mice. Therefore, αG-hesperidin may be useful in the management of Th17-mediated allergic disorders.
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DOI:
10.1073/pnas.0500098102
发表时间:
2005-02-22
影响因子:
11.1
作者:
Mohamadzadeh, M;Olson, S;Klaenhammer, TR
通讯作者:
Klaenhammer, TR
影响因子:
20.3
作者:
Zapata, Juan M.;Llobet, David;Reed, John C.
通讯作者:
Reed, John C.
影响因子:
14.2
作者:
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通讯作者:
J. Pestel
影响因子:
5.4
作者:
Tanabe, Soichi;Hochi, Satomi
通讯作者:
Hochi, Satomi
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发表时间:
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期刊:
影响因子:
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