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局部大麻素受体1激动剂减轻恶唑酮诱导的特应性皮炎模型中的皮肤炎症反应。

Topical cannabinoid receptor 1 agonist attenuates the cutaneous inflammatory responses in oxazolone-induced atopic dermatitis model.

作者信息

Kim Hyun Jong, Kim Bongwoo, Park Bu Man, Jeon Jeong Eun, Lee Sin Hee, Mann Shivtaj, Ahn Sung Ku, Hong Seung-Phil, Jeong Se Kyoo

机构信息

Department of Dermatology, Atopy Clinic, Seoul Medical Center, Seoul, Korea.

CRID Center, NeoPharm Co., Ltd., Daejeon, Korea.

出版信息

Int J Dermatol. 2015 Oct;54(10):e401-8. doi: 10.1111/ijd.12841. Epub 2015 Jun 20.

Abstract

BACKGROUND

Even with the widespread clinical use of cannabinoid receptor (CBR) stimulating compounds, such as palmitoylethanolamine, the role of CBR agonists on inflammatory skin diseases is not yet fully understood. This study was performed to investigate the effects of CBR agonists on skin inflammation, using acute and chronic inflammation animal models.

METHODS

The effectiveness of the newly synthesized cannabinoid receptor 1 (CB1R) agonists was determined using in vitro assays. Markers for epidermal permeability barrier function and skin inflammation were measured, and histological assessments were performed for evaluation.

RESULTS

Topical application of CB1R-specific agonist significantly accelerated the recovery of epidermal permeability barrier function and showed anti-inflammatory activity in both acute and chronic inflammation models. Histological assessments also confirmed the anti-inflammatory effects, which is consistent with previous reports.

CONCLUSIONS

All of the results suggest that topical application of CB1R-specific agonist can be beneficial for alleviating the inflammatory symptoms in chronic skin diseases, including atopic dermatitis.

摘要

背景

即使诸如棕榈酰乙醇胺等大麻素受体(CBR)刺激化合物已在临床上广泛使用,但CBR激动剂在炎症性皮肤病中的作用尚未完全明确。本研究旨在利用急慢性炎症动物模型,探究CBR激动剂对皮肤炎症的影响。

方法

通过体外试验确定新合成的大麻素受体1(CB1R)激动剂的有效性。测量表皮渗透屏障功能和皮肤炎症的标志物,并进行组织学评估以作评价。

结果

局部应用CB1R特异性激动剂可显著加速表皮渗透屏障功能的恢复,并在急慢性炎症模型中均显示出抗炎活性。组织学评估也证实了抗炎作用,这与先前的报道一致。

结论

所有结果表明,局部应用CB1R特异性激动剂可能有助于减轻包括特应性皮炎在内的慢性皮肤病的炎症症状。

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