Aescin 对银屑病诱发动物模型的影响:免疫组织化学和病理学研究

Rafal Wadhah, Basma Talib, Ghaith Ali, Wamidh H Talib
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引用次数: 0

摘要

背景介绍七叶皂苷(Aescin)是从七叶树(Aesculus hippocastanum)种子中提取的一种三萜皂苷混合物。七叶皂苷具有静脉补液、抗炎、抗氧化和抗风湿等特性,这些特性大多与药剂分子机制有关:本研究旨在探讨 Aescin 对 Imiquimod 诱导的雄性大鼠银屑病的潜在影响,包括对肿瘤坏死因子α、Ki-67 水平和银屑病皮肤组织病理学特征的影响:将 36 只白化雄性大鼠分为 6 组,每组 6 只,其中 5 组使用咪喹莫特诱发银屑病,最后一组使用凡士林,作为对照组。结果:在 Ki-67 水平方面,仅接受咪喹莫特治疗的组中 Ki-67 表达较强,其他组中 Ki-67 的评分明显降低。然而,外用阿司匹林和氯倍他索联合治疗组的 Ki-67 表达最低。仅接受咪喹莫特治疗的诱导组中 TNF-α 阳性细胞的数量和免疫染色的强度较高,而外用艾司馨和氯倍他索联合治疗的组中 TNF-α 阳性细胞的数量和免疫染色的强度最低。最后,组织病理学分析表明,银屑病的组织病理学特征明显受到阿司匹林和氯倍他索抗炎作用的影响,这表现在抑制促炎标志物和降低毛细血管通透性:结论:单独外用安乃近或与氯倍他索联合外用均能成功降低 Ki-67 的表达;此外,与其他组相比,安乃近和氯倍他索联合外用能降低 TNF-评分,并具有最强的抗炎活性。最后,Aescin 通过其抗炎、静脉舒张和抗水肿活性,能够改变银屑病皮肤的组织病理学特征。
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Effect of Aescin in Psoriatic-Induced Animal Model: Immunohistochemical and Pathological Study
Background: Aescin is a mixture of the triterpene saponins extracted from the seeds of the horse chestnut tree Aesculus hippocastanum. Aescin has a venotonic, anti-inflammatory, antioxidant and anti-edematous characteristics that are mostly connected to the agent molecular mechanism. Objective: The present study aim to investigate the potential effects of Aescin on psoriasis induced by Imiquimod in male rats, ncluding its effect on the level of tumor necrosis factor alpha, Ki-67 and the histopathologic features of the psoriatic skin. Methods: Thirty-six albino male rats were divided into six groups each group containing 6 animals, psoriasis was induced by Imiquimod to five of the groups, while for the last group vasaline was applied and the group served as a control group. The animals were then treated with topical Aescin, topical clobetasol, combination of topical Aescin and clobetasol and oral Aescin, finally all animals were sacrificed and the dorsal back skin was taken to perform histopathological and immunohistochemical analysis. Results: regarding the level of Ki-67, Strong expression of Ki-67 was seen in the group who received Imiquimod only, where the scoring of Ki-67 was notably lowered among the other groups. However, the lowest expression was noticed in the group that were treated with the combination of topical Aescin and clobetasol. While the number of TNF-α positive cells and the intensity of immunostaining were higher in the induction group who received Imiquimod only and the lowest among the group who received the combination of topical Aescin and Clobetasol. Lastly the histopathologic analysis shows that the histopathologic features of psoriasis was markedly affected by the anti-inflammatory effect of Aescin and clobetasol, which was noticed through inhibition of proinflammatory markers, and the decrease in capillary permeability. Conclusion: Topical Aescin alone or in combination with clobetasol reduced Ki-67 expression successfully; furthermore, the combination of topical Aescin and Clobetasol decreased TNF- score and had the strongest anti-inflammatory activity more than the other groups. Lastly Aescin was able to alter the histopathologic features of the psoriatic skin through its anti-inflammatory, venotonic and anti-edematous activity.
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