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地榆日本变种乙醇提取物对 NC/Nga 小鼠和人角质形成细胞特应性皮炎样反应的抑制作用。

Inhibitory effect of Sanguisorba hakusanensis Makino ethanol extract on atopic dermatitis-like responses in NC/Nga mice and human keratinocytes.

机构信息

KM Convergence Research Division, Korea Institute of Oriental Medicine, Yuseong-daero 1672, Yuseong-gu, Daejeon, 34054, Republic of Korea.

College of Pharmacy, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul, 08826, Republic of Korea.

出版信息

Sci Rep. 2023 Sep 5;13(1):14594. doi: 10.1038/s41598-023-41676-3.

DOI:10.1038/s41598-023-41676-3
PMID:37670127
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10480230/
Abstract

Atopic dermatitis (AD) is an allergic, inflammatory skin disease caused by immune dysregulation. In this study, we investigated anti-atopic and anti-inflammatory activities of Sanguisorba hakusanensis ethanol extract (SHE) both in vivo using NC/Nga mice and in vitro using human HaCaT keratinocytes. Oral administration of SHE suppressed several atopic symptoms associated with house dust mites (induced with Dermatophagoides farinae extract) in NC/Nga mice and decreased serum levels of inflammatory mediators such as immunoglobulin E, histamine, and inflammatory chemokines. Additionally, SHE treatment reduced the infiltration of immune cells such as mast cells and macrophages in AD skin lesions. In vitro, interferon-γ- and tumor necrosis factor-α-stimulated HaCaT cells exhibited increased expression of T helper 1 and 2 chemokines; their expression was inhibited by SHE treatment. The anti-inflammatory effects of SHE treatment involved blocking of the mitogen-activated protein kinase and signal transducer and activator of transcription 1 signaling pathways. In conclusion, SHE exerts potent anti-atopic and anti-inflammatory effects and should be considered for the clinical treatment of AD.

摘要

特应性皮炎(AD)是一种由免疫失调引起的过敏性炎症性皮肤病。在这项研究中,我们使用 NC/Nga 小鼠进行体内研究,使用人 HaCaT 角质形成细胞进行体外研究,研究了黄耆乙醇提取物(SHE)的抗特应性和抗炎活性。SHE 口服给药可抑制 NC/Nga 小鼠与尘螨(用屋尘螨提取物诱导)相关的几种特应性症状,并降低血清中免疫球蛋白 E、组胺和炎症趋化因子等炎症介质的水平。此外,SHE 治疗可减少 AD 皮肤病变中免疫细胞如肥大细胞和巨噬细胞的浸润。体外研究显示,干扰素-γ和肿瘤坏死因子-α刺激的 HaCaT 细胞中 T 辅助 1 和 2 趋化因子的表达增加;SHE 治疗可抑制其表达。SHE 治疗的抗炎作用涉及阻断丝裂原活化蛋白激酶和信号转导及转录激活因子 1 信号通路。总之,SHE 具有强大的抗特应性和抗炎作用,应考虑用于 AD 的临床治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0b/10480230/27620cfa154f/41598_2023_41676_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0b/10480230/ad920e252d03/41598_2023_41676_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0b/10480230/65290fe642fc/41598_2023_41676_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0b/10480230/67c1bc6fe9fc/41598_2023_41676_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0b/10480230/27620cfa154f/41598_2023_41676_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0b/10480230/ad920e252d03/41598_2023_41676_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0b/10480230/1e4c92b10b00/41598_2023_41676_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0b/10480230/84a12c7b294e/41598_2023_41676_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0b/10480230/65290fe642fc/41598_2023_41676_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0b/10480230/67c1bc6fe9fc/41598_2023_41676_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0b/10480230/27620cfa154f/41598_2023_41676_Fig6_HTML.jpg

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