Zhang Siqi, Kim Joonki, Lee Gakyung, Ahn Hong Ryul, Kim Yeo Eun, Kim Hee Ju, Yu Jae Sik, Park Miso, Kang Keon Wook, Kim Hocheol, Jung Byung Hwa, Kwon Sung Won, Jang Dae Sik, Yang Hyun Ok
Natural Product Research Center, Korea Institute of Science and Technology, Gangneung 25451, Republic of Korea.
KIST-School, Korea University of Science and Technology (UST), Seoul 02792, Republic of Korea.
Biomol Ther (Seoul). 2024 Nov 1;32(6):744-758. doi: 10.4062/biomolther.2024.058. Epub 2024 Oct 7.
Asthma is a chronic inflammatory disorder of the lungs that results in airway inflammation and narrowing. BS012 is an herbal remedy containing , , and extracts. To elucidate the anti-asthma effect of BS012, this study analyzed the immune response, respiratory protection, and changes in metabolic mechanisms in an ovalbumin-induced allergic asthma mouse model. Female BALB/c mice were exposed to ovalbumin to induce allergic asthma. Bronchoalveolar lavage fluid and plasma were analyzed for interleukin and immunoglobulin E levels. Histological analyses of the lungs were performed to measure morphological changes. Apoptosis-related mediators were assayed by western blotting. Plasma and lung tissue metabolomic analyses were performed to investigate the metabolic changes. A T-helper-2-like differentiated cell model was used to identify the active components of BS012. BS012 treatment improved inflammatory cell infiltration, mucus production, and goblet cell hyperplasia in lung tissues. BS012 also significantly downregulated ovalbumin-specific immunoglobulin E in plasma and T-helper-2-specific cytokines, interleukin-4 and -5, in bronchoalveolar lavage fluid. The lungs of ovalbumin-inhaled mice exhibited nerve growth factor-mediated apoptotic protein expression, which was significantly attenuated by BS012 treatment. Ovalbumin-induced abnormalities in amino acid and lipid metabolism were improved by BS012 in correlation with its anti-inflammatory properties and normalization of energy metabolism. Additionally, the differentiated cell model revealed that -isobutyl-dodecatetraenamide is an active component that contributes to the anti-allergic properties of BS012. The current findings demonstrate the anti-allergic and respiratory protective functions of BS012 against allergic asthma, which can be considered a therapeutic candidate.
哮喘是一种肺部慢性炎症性疾病,会导致气道炎症和狭窄。BS012是一种含有[具体成分未给出]提取物的草药疗法。为了阐明BS012的抗哮喘作用,本研究在卵清蛋白诱导的过敏性哮喘小鼠模型中分析了免疫反应、呼吸道保护以及代谢机制的变化。雌性BALB/c小鼠暴露于卵清蛋白以诱导过敏性哮喘。分析支气管肺泡灌洗液和血浆中的白细胞介素和免疫球蛋白E水平。对肺部进行组织学分析以测量形态学变化。通过蛋白质印迹法检测凋亡相关介质。进行血浆和肺组织代谢组学分析以研究代谢变化。使用T辅助2样分化细胞模型来鉴定BS012的活性成分。BS012治疗改善了肺组织中的炎性细胞浸润、黏液分泌和杯状细胞增生。BS012还显著下调了血浆中卵清蛋白特异性免疫球蛋白E以及支气管肺泡灌洗液中T辅助2特异性细胞因子白细胞介素-4和-5的水平。吸入卵清蛋白的小鼠肺部表现出神经生长因子介导的凋亡蛋白表达,而BS012治疗可显著减弱这种表达。BS012改善了卵清蛋白诱导的氨基酸和脂质代谢异常,这与其抗炎特性和能量代谢的正常化相关。此外,分化细胞模型显示异丁基十二碳四烯酰胺是一种有助于BS012抗过敏特性的活性成分。目前的研究结果证明了BS012对过敏性哮喘具有抗过敏和呼吸道保护功能,可被视为一种治疗候选药物。