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首页> 外文期刊>International immunopharmacology >Oral administration of ginsenoside Rh1 inhibits the development of atopic dermatitis-like skin lesions induced by oxazolone in hairless mice.
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Oral administration of ginsenoside Rh1 inhibits the development of atopic dermatitis-like skin lesions induced by oxazolone in hairless mice.

机译:人参皂甙Rh1的口服给药可抑制恶唑酮在无毛小鼠中诱发的特应性皮炎样皮肤病的发展。

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In the present study, we examined the inhibitive effect of ginsenoside Rh1 on oxazolone-induced atopic dermatitis-like skin lesions in hairless mice. Oral administration of ginsenoside Rh1 improved clinical symptoms, and it was confirmed by histophathological analysis. In ginsenoside Rh1 (20mg/kg) group, ear swellings and ear weights were significantly lower than the control group. Moreover, elevation of IL-6 and total IgE levels in serum were suppressed by ginsenoside Rh1 (20mg/kg). In addition, ginsenoside Rh1 (20mg/kg) significantly increased mRNA expression of IFNgamma and Foxp3, and slightly decreased IL-4 expression in draining lymph nodes. The results suggest that ginsenoside Rh1 can alleviate inflammatory symptoms in atopic dermatitis (AD) by reduction of IgE and IL-6 levels in peripheral blood, increase of Foxp3 expression in draining lymph nodes and suppression of inflammation in skin regions. Indeed, ginsenoside Rh1 exhibited therapeutic possibility in immune disorders.
机译:在本研究中,我们检查了人参皂苷Rh1对恶唑酮诱导的无毛小鼠特应性皮炎样皮肤损伤的抑制作用。人参皂苷Rh1的口服改善了临床症状,并通过组织病理学分析证实了这一点。人参皂苷Rh1(20mg / kg)组的耳肿胀和耳重显着低于对照组。此外,人参皂甙Rh1(20mg / kg)抑制了血清中IL-6的升高和总IgE水平。此外,人参皂苷Rh1(20mg / kg)显着增加了IFNgamma和Foxp3的mRNA表达,而引流淋巴结中的IL-4表达略有降低。结果表明人参皂苷Rh1可以通过降低外周血中IgE和IL-6水平,增加引流淋巴结中Foxp3的表达并抑制皮肤区域的炎症来缓解特应性皮炎(AD)的炎症症状。实际上,人参皂甙Rh1在免疫疾病中表现出治疗的可能性。

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