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齐墩果酸减轻体内和体外特应性皮炎样反应。

Oleanolic Acid Alleviates Atopic Dermatitis-like Responses In Vivo and In Vitro.

机构信息

Department of Pharmacology, College of Korean Medicine, Sangji University, Wonju 26339, Gangwon-do, Korea.

Department of Life Science, Dongguk University-Seoul, Ilsandong-gu, Goyang-si 10326, Gyeonggi-do, Korea.

出版信息

Int J Mol Sci. 2021 Nov 5;22(21):12000. doi: 10.3390/ijms222112000.

Abstract

Oleanolic acid (OA) is a pentacyclic triterpenoid, abundantly found in plants of the family, and is well known for its beneficial pharmacological activities. Previously, we reported the inhibitory effect of OA on mast cell-mediated allergic inflammation. In this study, we investigated the effects of OA on atopic dermatitis (AD)-like skin lesions and its underlying mechanism of action. We evaluated the inhibitory effect of OA on AD-like responses and the possible mechanisms using a 1-chloro-2,4-dinitrochlorobenzene (DNCB)-induced AD animal model and tumor necrosis factor (TNF)-α/interferon (IFN)-γ-stimulated HaCaT keratinocytes. We found that OA has anti-atopic effects, including histological alterations, on DNCB-induced AD-like lesions in mice. Moreover, it suppressed the expression of Th2 type cytokines and chemokines in the AD mouse model and TNF-α/IFN-γ-induced HaCaT keratinocytes by blocking the activation of serine-threonine kinase Akt, nuclear factor-κB, and the signal transducer and activator of transcription 1. The results demonstrate that OA inhibits AD-like symptoms and regulates the inflammatory mediators; therefore, it may be used as an effective and attractive therapeutic agent for allergic disorders, such as AD. Moreover, the findings of this study provide novel insights into the potential pharmacological targets of OA for treating AD.

摘要

齐墩果酸(OA)是一种五环三萜类化合物,大量存在于 科植物中,以其有益的药理活性而闻名。先前,我们报道了 OA 对肥大细胞介导的过敏炎症的抑制作用。在这项研究中,我们研究了 OA 对特应性皮炎(AD)样皮肤损伤的影响及其作用机制。我们使用 1-氯-2,4-二硝基氯苯(DNCB)诱导的 AD 动物模型和肿瘤坏死因子(TNF)-α/干扰素(IFN)-γ刺激的 HaCaT 角质形成细胞评估 OA 对 AD 样反应的抑制作用及其可能的机制。我们发现 OA 具有抗特应性作用,包括组织学改变,对 DNCB 诱导的 AD 样病变的小鼠。此外,它通过阻断丝氨酸-苏氨酸激酶 Akt、核因子-κB 和信号转导和转录激活因子 1 的激活,抑制 AD 小鼠模型和 TNF-α/IFN-γ诱导的 HaCaT 角质形成细胞中 Th2 型细胞因子和趋化因子的表达。结果表明,OA 抑制 AD 样症状并调节炎症介质;因此,它可能被用作治疗过敏疾病(如 AD)的有效和有吸引力的治疗剂。此外,本研究的结果为 OA 治疗 AD 的潜在药理靶点提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65b3/8584529/f996ffc0e6ae/ijms-22-12000-g002.jpg

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