Yao Lu, Fan Zhuoyan, Han Shiwen, Sun Na, Che Huilian
Beijing Advanced Innovation Center for Food Nutrition and Human Health, College of Food Science and Nutritional Engineering, China Agricultural University, Beijing, China.
National Engineering Research Center of Seafood, School of Food Science and Technology, Dalian Polytechnic University, Dalian, China.
Front Pharmacol. 2020 Jul 16;11:1046. doi: 10.3389/fphar.2020.01046. eCollection 2020.
Apigenin (API) is a natural phytoestrogen with properties including anti-inflammatory and other abilities. This study aims to 1) systematically validate that excessive estrogen exacerbates allergic reactions; 2) explore the anti-allergic effects and mechanisms of API. We conduct a survey of college students, indicating that of the 505 effective results, 70 individuals were self-reported allergic and 74.1% of them were women, which proved the gender difference in allergic reactions. BALB/c mice are grouped into the negative control group (N-Ctrl), the OVA-sensitized group (P-Ctrl), the estrogenized OVA-sensitized group (E2), and three treatment groups administrating different dose of API (E2 + API/L/M/H). data indicated that API treatment significantly inhibited the enhancement of estradiol on clinical symptoms. Moreover, we found that high doses of API inhibited Th2 type humoral response and mast cell degranulation levels and . Additionally, medium, and high doses of API significantly reduced the potentiation of estradiol on ER expression, attenuated the transmission of estrogen/ER signaling, thereby inhibiting the phosphorylation of ERK1/2 and JNK1/2/3 in the MAPK. Besides, we found that API competitively bound to ER with estradiol, and showed a weak selectivity to ERβ. Overall, we identified API can be beneficial in allergic disease.
芹菜素(API)是一种天然植物雌激素,具有抗炎等特性。本研究旨在:1)系统验证过量雌激素会加剧过敏反应;2)探索API的抗过敏作用及其机制。我们对大学生进行了一项调查,结果显示,在505份有效结果中,有70人自述过敏,其中74.1%为女性,这证明了过敏反应存在性别差异。将BALB/c小鼠分为阴性对照组(N-Ctrl)、卵清蛋白致敏组(P-Ctrl)、雌激素化卵清蛋白致敏组(E2)以及三个给予不同剂量API的治疗组(E2 + API/L/M/H)。数据表明,API治疗显著抑制了雌二醇对临床症状的增强作用。此外,我们发现高剂量的API抑制了Th2型体液反应和肥大细胞脱颗粒水平。另外,中、高剂量的API显著降低了雌二醇对ER表达的增强作用,减弱了雌激素/ER信号的传递,从而抑制了MAPK中ERK1/2和JNK1/2/3的磷酸化。此外,我们发现API与雌二醇竞争性结合ER,并且对ERβ表现出较弱的选择性。总体而言,我们确定API对过敏性疾病有益。