Department of Food Nutritional Science, Tokushima Bunri University, 180 Nishihama, Yamashiro, Tokushima 770-8514, Japan; Department of Nutritional Science, Okayama Prefectural University, 111 Kuboki, Soja, Okayama 719-1197, Japan.
Department of Nutritional Science, Okayama Prefectural University, 111 Kuboki, Soja, Okayama 719-1197, Japan.
Int Immunopharmacol. 2021 May;94:107394. doi: 10.1016/j.intimp.2021.107394. Epub 2021 Feb 11.
Black soybean hull extract (BSHE) exhibits a variety of biological activities. However, little is known about the effects of BSHE on immunoglobulin E (IgE)-mediated type I allergic reactions. The anti-allergic effect of BSHE was assessed with the degranulation assay using rat basophilic leukemia RBL-2H3 cells and the passive cutaneous anaphylaxis (PCA) reaction in mice. An active compound in BSHE was identified by ultra-performance liquid chromatography coupled to diode array detection and electrospray ionization tandem mass spectrometry analysis. BSHE inhibited the release of β-hexosaminidase and histamine in RBL-2H3 cells, and cyanidin-3-O-glucoside (C3G) was identified as one of its active compounds. Oral administering of 200 μmol/kg of C3G to IgE-sensitized mice prior to antigen injection suppressed the PCA reaction, as compared with control (p < 0.01). Intravenous administration of BSHE (C3G content, 5.4%) more strongly inhibited PCA responses at lower doses (100 mg/kg, p < 0.01) than oral administration (1,000 mg/kg, p = 0.059). Intravenous C3G also suppressed PCA response at a low dose (40 mg/kg, p < 0.05), showing the same trend as BSHE. This information can be useful to design appropriate formulations of anthocyanin-based drug products to suppress allergic reactions. This study provides evidence for the potential use of BSHE and C3G for the prevention or the treatment of type I allergies.
黑豆皮提取物(BSHE)具有多种生物活性。然而,BSHE 对免疫球蛋白 E(IgE)介导的 I 型过敏反应的影响知之甚少。使用大鼠嗜碱性白血病 RBL-2H3 细胞的脱颗粒测定法和小鼠被动皮肤过敏反应(PCA)反应评估 BSHE 的抗过敏作用。通过超高效液相色谱-二极管阵列检测和电喷雾串联质谱分析鉴定 BSHE 中的活性化合物。BSHE 抑制 RBL-2H3 细胞中β-己糖胺酶和组胺的释放,鉴定出矢车菊素-3-O-葡萄糖苷(C3G)是其活性化合物之一。在抗原注射前,用 200 μmol/kg 的 C3G 对 IgE 致敏的小鼠进行口服给药,与对照组相比(p < 0.01),抑制了 PCA 反应。BSHE(C3G 含量为 5.4%)静脉给药在较低剂量(100 mg/kg,p < 0.01)比口服给药(1000 mg/kg,p = 0.059)更能强烈抑制 PCA 反应。静脉内 C3G 也在低剂量(40 mg/kg,p < 0.05)下抑制 PCA 反应,表现出与 BSHE 相同的趋势。这些信息可用于设计基于花色苷的药物产品的适当制剂,以抑制过敏反应。本研究为 BSHE 和 C3G 预防或治疗 I 型过敏反应提供了证据。