Pak So-Won, Lee Ik Soo, Kim Woong-Il, Lee Se-Jin, Kim Jong-Choon, Shin In-Sik, Kim Taesoo
College of Veterinary Medicine and BK21 FOUR Program, Chonnam National University, Gwangju, Republic of Korea.
KM Convergence Research Division, Korea Institute of Oriental Medicine (KIOM), Daejeon, Republic of Korea.
Anim Cells Syst (Seoul). 2024 Aug 1;28(1):381-391. doi: 10.1080/19768354.2024.2383254. eCollection 2024.
Allergic asthma, a type of chronic airway inflammation, is a global health concern because of its increasing incidence and recurrence rates. L. yields a variety type of teas, which are also used as medicinal plants in East Asia and are known to have antioxidant, anti-inflammatory, and immune-potentiating properties. Here, we examined the constituents of L. extract (CSE) and evaluated the protective effects of CSE on allergic asthma by elucidating the underlying mechanism. To induce allergic asthma, we injected the sensitization solution (mixture of ovalbumin (OVA) and aluminum hydroxide) into mice intraperitoneally on days 0 and 14. Then, the mice were exposed to 1% OVA by a nebulizer on days 21 to 23, while intragastric administration of CSE (30 and 100 mg/kg) was performed each day on days 18 to 23. We detected five compounds in CSE, including (-)-epigallocatechin, caffeine, (-)-epicatechin, (-)-epigallocatechin gallate, and (-)-epicatechin gallate. Treatment with CSE remarkably decreased the airway hyperresponsiveness, OVA-specific immunoglobulin E level, and inflammatory cell and cytokine levels of mice, with a decrease in inflammatory cell infiltration and mucus production in lung tissue. Treatment with CSE also decreased the phosphorylation of nuclear factor-κB (NF-κB) and the expression of matrix-metalloproteinase (MMP)-9 in asthmatic mice. Our results demonstrated that CSE reduced allergic airway inflammation caused by OVA through inhibition of phosphorylated NF-κB and MMP-9 expression.
过敏性哮喘是一种慢性气道炎症,因其发病率和复发率不断上升,已成为全球关注的健康问题。L. 能产出多种类型的茶,在东亚地区这些茶也被用作药用植物,已知具有抗氧化、抗炎和增强免疫的特性。在此,我们研究了L. 提取物(CSE)的成分,并通过阐明其潜在机制评估了CSE对过敏性哮喘的保护作用。为诱导过敏性哮喘,我们在第0天和第14天给小鼠腹腔注射致敏溶液(卵清蛋白(OVA)和氢氧化铝的混合物)。然后,在第21天至23天通过雾化器让小鼠暴露于1% OVA中,同时在第18天至23天每天对小鼠进行CSE(30和100 mg/kg)灌胃。我们在CSE中检测到五种化合物,包括(-)-表没食子儿茶素、咖啡因、(-)-表儿茶素、(-)-表没食子儿茶素没食子酸酯和(-)-表儿茶素没食子酸酯。CSE处理显著降低了小鼠的气道高反应性、OVA特异性免疫球蛋白E水平以及炎症细胞和细胞因子水平,同时肺组织中的炎症细胞浸润和黏液分泌减少。CSE处理还降低了哮喘小鼠中核因子-κB(NF-κB)的磷酸化以及基质金属蛋白酶(MMP)-9的表达。我们的结果表明,CSE通过抑制磷酸化的NF-κB和MMP-9的表达减轻了OVA引起的过敏性气道炎症。