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青蒿乙醇提取物对角质形成细胞的增殖抑制和银屑病的缓解作用。

Antiproliferation of keratinocytes and alleviation of psoriasis by the ethanol extract of Artemisia capillaris.

机构信息

College of Pharmacy, Kangwon National University, Chuncheon, Gangwon, 24341, Republic of Korea.

R&D Center, Radiant Ltd., Chuncheon, Gangwon, 24398, Republic of Korea.

出版信息

Phytother Res. 2018 May;32(5):923-932. doi: 10.1002/ptr.6032. Epub 2018 Jan 29.

DOI:10.1002/ptr.6032
PMID:29377339
Abstract

The therapeutic potentials of the ethanol extract of Artemisia capillaris (ACE) for psoriasis were verified in HaCaT cells (as an immortalized human keratinocyte cell line) and imiquimod (IMQ)-induced psoriasis-like mouse models. In HaCaT cells, IC value of ACE was 37.5 μg/ml after incubating for 72 hr. The antiproliferation activity of ACE in HaCaT cells was further verified by apoptosis assays. The percentage of apoptotic population in ACE-treated group was significantly higher than that of control group (p < .05). The result of cell cycle arrest assay also supported the observed antiproliferation efficacy of ACE in HaCaT cells. In IMQ-induced psoriasis-like mouse models, the Psoriasis Area and Severity Index score of ACE (50 mg/ml; ACE50)-treated group was significantly lower than that of IMQ group on Day 4 (p < .05). After topical application of ACE on psoriasis-like lesion for 4 days, the epidermal thickness of (IMQ + ACE50) group was significantly lower than that of IMQ group (p < .05). The expression levels of Ki-67 and intracellular adhesion molecule-1 in excised skin tissues of (IMQ + ACE50) group were also lower than those of IMQ group. All these findings suggest that ACE can be used as a promising antipsoriatic agent.

摘要

艾条乙醇提取物(ACE)治疗银屑病的潜力在 HaCaT 细胞(一种永生化的人角质形成细胞系)和咪喹莫特(IMQ)诱导的银屑病样小鼠模型中得到了验证。在 HaCaT 细胞中,ACE 在孵育 72 小时后,IC 值为 37.5μg/ml。ACE 在 HaCaT 细胞中的增殖抑制活性进一步通过凋亡试验得到验证。ACE 处理组的凋亡细胞比例明显高于对照组(p<0.05)。细胞周期阻滞试验的结果也支持 ACE 在 HaCaT 细胞中观察到的增殖抑制作用。在 IMQ 诱导的银屑病样小鼠模型中,ACE(50mg/ml;ACE50)处理组的银屑病面积和严重程度指数评分在第 4 天明显低于 IMQ 组(p<0.05)。在银屑病样病变处外用 ACE 4 天后,(IMQ+ACE50)组的表皮厚度明显低于 IMQ 组(p<0.05)。(IMQ+ACE50)组切除皮肤组织中的 Ki-67 和细胞间黏附分子-1 的表达水平也低于 IMQ 组。所有这些发现表明 ACE 可作为一种有前途的抗银屑病药物。

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