Pulmonary and Critical Care Medicine, Yantai Yuhuangding Hospital, Yantai, 264000, China.
Pulmonary and Critical Care Medicine, Central Hospital Affiliated to Shandong First Medical University, Jinan, 250000, China.
Pulm Pharmacol Ther. 2023 Feb;78:102183. doi: 10.1016/j.pupt.2022.102183. Epub 2022 Dec 5.
In most asthma patients, symptoms are controlled by treatment with glucocorticoid, but long-term or high-dose use can produce adverse effects. Therefore, it is crucial to find new therapeutic strategies. β-sitosterol could suppress type Ⅱ inflammation in ovalbumin (OVA)-induced mice, but its mechanisms have remained unclear.
A binding activity of β-sitosterol with glucocorticoid receptor (GR) was analyzed by molecular docking. Human bronchial epithelial cells (BEAS-2B) and human bronchial smooth muscle cells (HBSMC) were treated with different concentrations (0, 1, 5, 10, 20, and 50 μg/mL) of β-sitosterol for suitable concentration selection. In transforming growth factor (TGF)-β1 treated BEAS-2B and HBSMC, cells were treated with 20 μg/mL β-sitosterol or dexamethasone (Dex) to analyze its possible mechanism. In OVA-induced mice, 2.5 mg/kg β-sitosterol or Dex administration was performed to analyze the therapeutic mechanism of β-sitosterol. A GR antagonist RU486 was used to confirm the mechanism of β-sitosterol in the treatment of asthma.
A good binding of β-sitosterol to GR (score = -8.2 kcal/mol) was found, and the GR expression was upregulated with β-sitosterol dose increase in BEAS-2B and HBSMC. Interleukin (IL)-25 and IL-33 secretion was significantly decreased by β-sitosterol in the TGF-β1-induced BEAS-2B, and the levels of collagen 1A and α-smooth muscle actin (SMA) were reduced in the TGF-β1-induced HBSMC. In the OVA-challenged mice, β-sitosterol treatment improved airway inflammation and remodeling through suppressing type Ⅱ immune response and collagen deposition. The therapeutic effects of β-sitosterol were similar to Dex treatment in vitro and in vivo. RU486 treatment clearly hampered the therapeutic effects of β-sitosterol in the TGF-β1-induced cells and OVA-induced mice.
This study identified that β-sitosterol binds GR to perform its functions in asthma treatment. β-sitosterol represent a potential therapeutic drug for allergic asthma.
在大多数哮喘患者中,通过糖皮质激素治疗可控制症状,但长期或大剂量使用会产生不良反应。因此,寻找新的治疗策略至关重要。β-谷甾醇可抑制卵清蛋白(OVA)诱导的小鼠的 2 型炎症,但具体机制尚不清楚。
通过分子对接分析β-谷甾醇与糖皮质激素受体(GR)的结合活性。用不同浓度(0、1、5、10、20 和 50μg/mL)β-谷甾醇处理人支气管上皮细胞(BEAS-2B)和人支气管平滑肌细胞(HBSMC),以选择合适的浓度。在转化生长因子(TGF)-β1 处理的 BEAS-2B 和 HBSMC 中,用 20μg/mLβ-谷甾醇或地塞米松(Dex)处理细胞,以分析其可能的机制。在 OVA 诱导的小鼠中,给予 2.5mg/kgβ-谷甾醇或 Dex 给药以分析β-谷甾醇的治疗机制。用 GR 拮抗剂 RU486 证实β-谷甾醇治疗哮喘的机制。
发现β-谷甾醇与 GR 具有良好的结合(评分=-8.2kcal/mol),并且随着 BEAS-2B 和 HBSMC 中β-谷甾醇剂量的增加,GR 表达上调。β-谷甾醇显著降低 TGF-β1 诱导的 BEAS-2B 中白细胞介素(IL)-25 和 IL-33 的分泌,并降低 TGF-β1 诱导的 HBSMC 中胶原 1A 和α-平滑肌肌动蛋白(SMA)的水平。在 OVA 挑战的小鼠中,β-谷甾醇通过抑制 2 型免疫反应和胶原沉积来改善气道炎症和重塑。β-谷甾醇在体外和体内的治疗效果与 Dex 治疗相似。RU486 处理明显阻碍了 TGF-β1 诱导的细胞和 OVA 诱导的小鼠中β-谷甾醇的治疗效果。
本研究确定了β-谷甾醇通过与 GR 结合在哮喘治疗中发挥作用。β-谷甾醇可能成为治疗过敏性哮喘的潜在治疗药物。