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豆甾醇通过抑制 P 物质受体缓解哮喘小鼠的过敏性气道炎症和气道高反应性。

Stigmasterol alleviates allergic airway inflammation and airway hyperresponsiveness in asthma mice through inhibiting substance-P receptor.

机构信息

Department of Material supply, the Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, Shandong, China.

Department of Cardiology, First Ward, Yantai Yeda Hospital, Yantai, Shandong, China.

出版信息

Pharm Biol. 2023 Dec;61(1):449-458. doi: 10.1080/13880209.2023.2173252.

DOI:10.1080/13880209.2023.2173252
PMID:36788676
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9930798/
Abstract

CONTEXT

Stigmasterol has significant anti-arthritis and anti-inflammatory effects, but its role in immune and inflammatory diseases is still unclear.

OBJECTIVE

The potential advantages of stigmasterol in asthma were explored in IL-13-induced BEAS-2B cells and asthmatic mice.

MATERIALS AND METHODS

The optimal target of stigmasterol was confirmed in asthma. After detecting the cytotoxicity of stigmasterol in BEAS-2B cells, 10 μg/mL and 20 μg/mL stigmasterol were incubated with the BEAS-2B cell model for 48 h, and anti-inflammation and antioxidative stress were verified. Asthmatic mice were induced by OVA and received 100 mg/kg stigmasterol for 7 consecutive days. After 28 days, lung tissues and BAL fluid were collected for the following study. To further verify the role of NK1-R, 0.1 μM WIN62577 (NK1-R specific antagonist), and 1 μM recombinant human NK1-R protein were applied.

RESULTS

NK1-R was the potential target of stigmasterol. When the concentration of stigmasterol is 20 μg/mL, the survival rate of BEAS-2B cells is about 98.4%, which is non-toxic. Stigmasterol exerted anti-inflammation and antioxidant stress in a dose-dependent manner and decreased NK1-R expression in IL-13-induced BEAS-2B. Meanwhile, assay also indicated the anti-inflammation and antioxidant stress of stigmasterol after OVA challenge. Stigmasterol inhibited inflammation infiltration and mucus hypersecretion, and NK1-R expression.

DISCUSSION AND CONCLUSIONS

The protective effect of stigmaterol on asthma and its underlying mechanism have been discussed in depth, providing a theoretical basis and more possibilities for its treatment of asthma.

摘要

背景

豆甾醇具有显著的抗关节炎和抗炎作用,但它在免疫和炎症性疾病中的作用尚不清楚。

目的

探讨豆甾醇在白介素-13诱导的 BEAS-2B 细胞和哮喘小鼠中的潜在优势。

材料和方法

确定豆甾醇在哮喘中的最佳靶点。在 BEAS-2B 细胞模型中检测豆甾醇的细胞毒性后,用 10μg/mL 和 20μg/mL 豆甾醇孵育 BEAS-2B 细胞 48 小时,验证抗炎和抗氧化应激作用。卵清蛋白(OVA)诱导哮喘小鼠,连续 7 天给予 100mg/kg 豆甾醇。28 天后,收集肺组织和 BAL 液进行后续研究。为了进一步验证 NK1-R 的作用,应用了 0.1μM WIN62577(NK1-R 特异性拮抗剂)和 1μM 重组人 NK1-R 蛋白。

结果

NK1-R 是豆甾醇的潜在靶点。当豆甾醇浓度为 20μg/mL 时,BEAS-2B 细胞的存活率约为 98.4%,无毒性。豆甾醇呈剂量依赖性发挥抗炎和抗氧化应激作用,并降低 IL-13 诱导的 BEAS-2B 中 NK1-R 的表达。同时,实验还表明 OVA 挑战后豆甾醇具有抗炎和抗氧化应激作用。豆甾醇抑制炎症浸润和粘液分泌过度,以及 NK1-R 的表达。

讨论与结论

深入探讨了豆甾醇对哮喘的保护作用及其潜在机制,为其治疗哮喘提供了理论依据和更多可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ca/9930798/188a0b614536/IPHB_A_2173252_F0007_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ca/9930798/1c5c9944babc/IPHB_A_2173252_F0001_C.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ca/9930798/988cb08623e3/IPHB_A_2173252_F0005_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ca/9930798/36274d8ee02e/IPHB_A_2173252_F0006_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ca/9930798/188a0b614536/IPHB_A_2173252_F0007_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ca/9930798/1c5c9944babc/IPHB_A_2173252_F0001_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ca/9930798/e82624c277c2/IPHB_A_2173252_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ca/9930798/4e537645ee8d/IPHB_A_2173252_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ca/9930798/fd1178c39a08/IPHB_A_2173252_F0004_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ca/9930798/988cb08623e3/IPHB_A_2173252_F0005_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ca/9930798/36274d8ee02e/IPHB_A_2173252_F0006_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0ca/9930798/188a0b614536/IPHB_A_2173252_F0007_C.jpg

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