Cho Byoung Ok, Che Denis Nchang, Yin Hong Hua, Shin Jae Young, Jang Seon Il
Research Institute, Ato Q&A Corporation, Jeonju 55069, Republic of Korea; Department of Health Care & Science, Jeonju University, Jeonju 55069, Republic of Korea.
Department of Health Care & Science, Jeonju University, Jeonju 55069, Republic of Korea.
Biomed Pharmacother. 2017 May;89:819-826. doi: 10.1016/j.biopha.2017.01.145. Epub 2017 Mar 6.
Atopic dermatitis, a chronic relapsing and pruritic inflammation of the skin also thought to be involved in, or caused by immune system destruction is an upsetting health problem due to its continuously increasing incidence especially in developed countries. Mast cell infiltration in atopic dermatitis skin lesions and its IgE-mediated activation releases various cytokines and chemokines that have been implicated in the pathogenesis of atopic dermatitis. This study was aimed at investigating synergistic anti-inflammatory, anti-pruritic and anti-atopic dermatitis effects of Diospyros lotus leaf extract (DLE) and Muscat bailey A grapefruit stem extract (GFSE) in atopic dermatitis-like induced skin lesions in mice. Combinations of DLE and GFSE inhibited TNF-α and IL-6 production more than DLE or GFSE in PMA plus calcium ionophore A23187-activated HMC-1 cells. DLE and GFSE synergistically inhibited compound 48/80-induced dermal infiltration of mast cells and reduced scratching behavior than DLE or GFSE. Furthermore, DLE and GFSE synergistically showed a stronger ameliorative effect in skin lesions by reducing clinical scores; dermal infiltration of mast cells; ear and dorsal skin thickness; serum IgE and IL-4 production in atopic dermatitis-like mice. Collectively, these results suggest that DLE and GFSE synergistically exhibit anti-atopic dermatitis effects in atopic dermatitis-like skin lesions in mice.
特应性皮炎是一种慢性复发性瘙痒性皮肤炎症,也被认为与免疫系统破坏有关或由其引起,由于其发病率持续上升,尤其是在发达国家,它是一个令人苦恼的健康问题。肥大细胞浸润于特应性皮炎皮肤病变中,其IgE介导的激活会释放多种细胞因子和趋化因子,这些因子与特应性皮炎的发病机制有关。本研究旨在探讨柿叶提取物(DLE)和玫瑰香葡萄柚茎提取物(GFSE)对小鼠特应性皮炎样诱导皮肤病变的协同抗炎、止痒和抗特应性皮炎作用。在佛波酯加钙离子载体A23187激活的HMC-1细胞中,DLE和GFSE的组合比DLE或GFSE更能抑制TNF-α和IL-6的产生。DLE和GFSE协同抑制化合物48/80诱导的肥大细胞真皮浸润,并比DLE或GFSE减少抓挠行为。此外,DLE和GFSE通过降低临床评分、肥大细胞真皮浸润、耳部和背部皮肤厚度、特应性皮炎样小鼠血清IgE和IL-4的产生,协同显示出对皮肤病变更强的改善作用。总体而言,这些结果表明,DLE和GFSE在小鼠特应性皮炎样皮肤病变中协同表现出抗特应性皮炎作用。