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川陈皮素作为一种新型 PDE4B 抑制剂,通过激活 cAMP-PKA-CREB 信号通路缓解哮喘症状。

Nobiletin, as a Novel PDE4B Inhibitor, Alleviates Asthma Symptoms by Activating the cAMP-PKA-CREB Signaling Pathway.

机构信息

School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China.

Marine Biomedical Research Institute of Qingdao, Qingdao 266071, China.

出版信息

Int J Mol Sci. 2024 Sep 27;25(19):10406. doi: 10.3390/ijms251910406.

Abstract

Asthma is a chronic airway inflammation that is considered a serious public health concern worldwide. Nobiletin (5,6,7,8,3',4'-hexamethyl flavonoid), an important compound isolated from several traditional Chinese medicines, especially Citri Reticulatae Pericarpium, is widely used for a number of indications, including cancer, allergic diseases, and chronic inflammation. However, the mechanism by which nobiletin exerts its anti-asthmatic effect remains unclear. In this research, we comprehensively demonstrated the anti-asthmatic effects of nobiletin in an animal model of asthma. It was found that nobiletin significantly reduced the levels of inflammatory cells and cytokines in mice and alleviated airway hyperresponsiveness. To explore the target of nobiletin, we identified PDE4B as the target of nobiletin through pharmacophore modeling, molecular docking, molecular dynamics simulation, SPR, and enzyme activity assays. Subsequently, it was found that nobiletin could activate the cAMP-PKA-CREB signaling pathway downstream of PDE4B in mouse lung tissues. Additionally, we studied the anti-inflammatory and anti-airway remodeling effects of nobiletin in LPS-induced RAW264.7 cells and TGF-β1-induced ASM cells, confirming the activation of the cAMP-PKA-CREB signaling pathway by nobiletin. Further validation in PDE4B-deficient RAW264.7 cells confirmed that the increase in cAMP levels induced by nobiletin depended on the inhibition of PDE4B. In conclusion, nobiletin exerts anti-asthmatic activity by targeting PDE4B and activating the cAMP-PKA-CREB signaling pathway.

摘要

哮喘是一种慢性气道炎症,被认为是全球范围内严重的公共卫生问题。川陈皮素(5,6,7,8,3',4'-六甲基黄酮)是从几种中药中分离出来的一种重要化合物,特别是陈皮,广泛用于多种适应症,包括癌症、过敏疾病和慢性炎症。然而,川陈皮素发挥其抗哮喘作用的机制尚不清楚。在这项研究中,我们全面证实了川陈皮素在哮喘动物模型中的抗哮喘作用。结果发现,川陈皮素能显著降低哮喘小鼠炎症细胞和细胞因子的水平,减轻气道高反应性。为了探索川陈皮素的作用靶点,我们通过药效团建模、分子对接、分子动力学模拟、SPR 和酶活性测定,鉴定 PDE4B 为川陈皮素的作用靶点。随后发现川陈皮素可以激活小鼠肺组织中 PDE4B 下游的 cAMP-PKA-CREB 信号通路。此外,我们研究了川陈皮素在 LPS 诱导的 RAW264.7 细胞和 TGF-β1 诱导的 ASM 细胞中的抗炎和抗气道重塑作用,证实了川陈皮素激活 cAMP-PKA-CREB 信号通路。在 PDE4B 缺陷 RAW264.7 细胞中的进一步验证证实,川陈皮素诱导的 cAMP 水平增加依赖于 PDE4B 的抑制。综上所述,川陈皮素通过靶向 PDE4B 并激活 cAMP-PKA-CREB 信号通路发挥抗哮喘活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8578/11477036/93e1c2e0302e/ijms-25-10406-g001.jpg

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