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桔梗根皂苷通过抑制NF-κB和STAT1以及激活Nrf2/ARE介导的血红素加氧酶-1来减轻特应性皮炎样皮肤损伤。

Platycodon grandiflorum root-derived saponins attenuate atopic dermatitis-like skin lesions via suppression of NF-κB and STAT1 and activation of Nrf2/ARE-mediated heme oxygenase-1.

作者信息

Choi Jae Ho, Jin Sun Woo, Han Eun Hee, Park Bong Hwan, Kim Hyung Gyun, Khanal Tilak, Hwang Yong Pil, Do Minh Truong, Lee Hyun-Sun, Chung Young Chul, Kim Hee Suk, Jeong Tae Cheon, Jeong Hye Gwang

机构信息

Department of Toxicology, College of Pharmacy, Chungnam National University, Daejeon, Republic of Korea.

Department of Toxicology, College of Pharmacy, Chungnam National University, Daejeon, Republic of Korea; Department of Pharmaceutical Engineering, International University of Korea, Jinju, Republic of Korea.

出版信息

Phytomedicine. 2014 Jul-Aug;21(8-9):1053-61. doi: 10.1016/j.phymed.2014.04.011. Epub 2014 May 20.

DOI:10.1016/j.phymed.2014.04.011
PMID:24854572
Abstract

PURPOSE

The consequences of precipitously rising allergic skin inflammation rates worldwide have accelerated the risk of atopic dermatitis (AD). Natural product-based agents with good efficacy and low risk of side effects offer promising prevention and treatment strategies for inflammation-related diseases. We have already reported that Platycodon grandiflorum root-derived saponins (Changkil saponins, CKS) have many pharmacological effects, including anti-inflammatory and anti-allergic effects, but its influence on AD remains unclear. Therefore, we evaluated the inhibitory effect of CKS, mainly platycodin D, on AD-like skin symptoms in mice and the possible mechanisms in cells.

METHODS

Mice were sensitized and challenged with 2,4-dinitrochlorobenzene (DNCB). Four weeks after challenge, mice were treated with oral administration of CKS for 4 weeks. In addition, cells were used to evaluate the effect of CKS, mainly platycodin D, on the TARC expression regulated mechanism.

RESULTS

CKS attenuated DNCB-induced dermatitis severity, serum levels of IgE and TARC, and mRNA expression of TARC, TNF-α, IFN-γ, IL-4, IL-5, and IL-13 in mice. Histopathological examination showed reduced thickness of the epidermis/dermis and dermal infiltration of inflammatory cells and mast cells in the ears. Moreover, CKS and platycodin D inhibited TNF-α/IFN-γ-induced TARC expression through the suppression of NF-κB and STAT1 and induction of Nrf2/ARE-mediated hemeoxygenase-1 (HO-1) expression in cells.

CONCLUSION

We suggest that CKS and platycodin D inhibited the development of AD-like skin symptoms by regulating cytokine mediators and may be an effective alternative therapy for AD-like skin symptoms.

摘要

目的

全球过敏性皮肤炎症发生率急剧上升的后果加速了特应性皮炎(AD)的发病风险。具有良好疗效且副作用风险低的天然产物类药物为炎症相关疾病提供了有前景的预防和治疗策略。我们已经报道过桔梗根皂苷(长梗皂苷,CKS)具有多种药理作用,包括抗炎和抗过敏作用,但其对AD的影响仍不清楚。因此,我们评估了CKS(主要是桔梗皂苷D)对小鼠AD样皮肤症状的抑制作用以及在细胞中的可能机制。

方法

用2,4 -二硝基氯苯(DNCB)对小鼠进行致敏和激发。激发4周后,给小鼠口服CKS治疗4周。此外,使用细胞评估CKS(主要是桔梗皂苷D)对胸腺和活化调节趋化因子(TARC)表达调控机制的影响。

结果

CKS减轻了DNCB诱导的小鼠皮炎严重程度、血清IgE和TARC水平,以及TARC、肿瘤坏死因子-α(TNF-α)、干扰素-γ(IFN-γ)、白细胞介素-4(IL-4)、白细胞介素-5(IL-5)和白细胞介素-13的mRNA表达。组织病理学检查显示耳朵表皮/真皮厚度变薄,炎症细胞和肥大细胞的真皮浸润减少。此外,CKS和桔梗皂苷D通过抑制核因子-κB(NF-κB)和信号转导子和转录激活子1(STAT1)以及诱导细胞中核因子E2相关因子2(Nrf2)/抗氧化反应元件(ARE)介导的血红素加氧酶-1(HO-1)表达来抑制TNF-α/IFN-γ诱导的TARC表达。

结论

我们认为CKS和桔梗皂苷D通过调节细胞因子介质抑制了AD样皮肤症状的发展,可能是AD样皮肤症状的一种有效替代疗法。

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