Siqi Zhang, Joonki Kim, Gakyung Lee, Hong Ryul Ahn, Yeo Eun Kim, Hee Ju Kim, Jae Sik Yu, Miso Park, Keon Wook Kang, Hocheol Kim, Byung Hwa Jung, Sung Won Kwon, Dae Sik Jang, Hyun Ok Yang
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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 <i>N</i>-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.</p>","PeriodicalId":8949,"journal":{"name":"Biomolecules & Therapeutics","volume":" ","pages":"744-758"},"PeriodicalIF":3.0000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11535288/pdf/","citationCount":"0","resultStr":"{\"title\":\"Phytotherapeutic BS012 and Its Active Component Ameliorate Allergic Asthma via Inhibition of Th2-Mediated Immune Response and Apoptosis.\",\"authors\":\"Siqi Zhang, Joonki Kim, Gakyung Lee, Hong Ryul Ahn, Yeo Eun Kim, Hee Ju Kim, Jae Sik Yu, Miso Park, Keon Wook Kang, Hocheol Kim, Byung Hwa Jung, Sung Won Kwon, Dae Sik Jang, Hyun Ok Yang\",\"doi\":\"10.4062/biomolther.2024.058\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Asthma is a chronic inflammatory disorder of the lungs that results in airway inflammation and narrowing. 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引用次数: 0
摘要
哮喘是一种慢性肺部炎症性疾病,会导致气道发炎和狭窄。BS012 是一种草药疗法,含有西洋菝葜、桔梗和肉桂提取物。为了阐明 BS012 的抗哮喘作用,本研究分析了卵清蛋白诱导的过敏性哮喘小鼠模型的免疫反应、呼吸保护和代谢机制的变化。雌性 BALB/c 小鼠接触卵清蛋白诱发过敏性哮喘。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。用 Western 印迹法测定与细胞凋亡相关的介质。血浆和肺组织代谢组分析用于研究代谢变化。使用 T-helper-2 样分化细胞模型来鉴定 BS012 的活性成分。BS012 治疗改善了肺组织的炎症细胞浸润、粘液分泌和上睑球细胞增生。BS012 还能显著下调血浆中的卵清蛋白特异性免疫球蛋白 E 和支气管肺泡灌洗液中的 T-helper-2 特异性细胞因子、白细胞介素-4 和白细胞介素-5。卵清蛋白吸入小鼠的肺部表现出神经生长因子介导的凋亡蛋白表达,BS012 治疗可显著减少这种表达。BS012 可改善卵清蛋白诱导的氨基酸和脂质代谢异常,这与 BS012 的抗炎特性和能量代谢正常化有关。此外,分化细胞模型显示,N-异丁基十二碳四烯酰胺是促进 BS012 抗过敏特性的活性成分。目前的研究结果表明,BS012 对过敏性哮喘具有抗过敏和呼吸保护功能,可被视为一种候选治疗药物。
Phytotherapeutic BS012 and Its Active Component Ameliorate Allergic Asthma via Inhibition of Th2-Mediated Immune Response and Apoptosis.
Asthma is a chronic inflammatory disorder of the lungs that results in airway inflammation and narrowing. BS012 is an herbal remedy containing Asarum sieboldii, Platycodon grandiflorum, and Cinnamomum cassia 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 N-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.
期刊介绍:
Biomolecules & Therapeutics (Biomolecules & Therapeutics) (Print ISSN 1976-9148, Online ISSN 2005-4483) is an international, peer-reviewed, open access journal that covers pharmacological and toxicological fields related to bioactive molecules and therapeutics. It was launched in 1993 as "The Journal of Applied Pharmacology (ISSN 1225-6110)", and renamed "Biomolecules & Therapeutics" (Biomol Ther: abbreviated form) in 2008 (Volume 16, No. 1). It is published bimonthly in January, March, May, July, September and November. All manuscripts should be creative, informative, and contribute to the development of new drugs. Articles in the following categories are published: review articles and research articles.