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黄芩中的黄酮类化合物通过阻断IκBζ/C/EBPβ信号通路抑制衰老相关分泌表型的产生:对年龄相关炎症的抑制作用。

Flavonoids from Scutellaria baicalensis inhibit senescence-associated secretory phenotype production by interrupting IκBζ/C/EBPβ pathway: Inhibition of age-related inflammation.

作者信息

Lim Hyun, Kwon Yong Soo, Kim Donghoon, Lee Jongkook, Kim Hyun Pyo

机构信息

College of Pharmacy, Kangwon National University, 1, Gangwondaehak-gil, Chuncheon 24341, Republic of Korea.

College of Pharmacy, Kangwon National University, 1, Gangwondaehak-gil, Chuncheon 24341, Republic of Korea.

出版信息

Phytomedicine. 2020 Sep;76:153255. doi: 10.1016/j.phymed.2020.153255. Epub 2020 Jun 5.

Abstract

BACKGROUND

Prolonged exposure to the senescence-associated secretory phenotype (SASP) with age leads to chronic low-grade inflammation in neighboring cells and tissues, causing many chronic degenerative diseases.

PURPOSE

The effects on SASP production of the ethanol extract from Scutellaria radix and 17 isolated flavonoid constituents were examined in vitro and in vivo.

METHODS

Cellular senescence was induced by bleomycin. Expression of the SASP and cell signaling molecules was detected using ELISA, RT-qPCR, Western blotting, and immunofluorescence staining. To investigate the in vivo effects, 21-month-old aged rats were used.

RESULTS

The ethanol extract and 5 compounds including 1 (Oroxylin A; 5,7-dihydroxy-6-methoxyflavone), 5 (2',6',5,7-tetrahydroxy-8-methoxyflavone), 8 (2',5,7-trihydroxyflavone), 10 (2',5,7-trihydroxy-8-methoxyflavone) and 11 (2',5,7-trihydroxy-6-methoxyflavone) potently reduced IL-6 and IL-8 production and gene expression of the SASP, including IL-1α, IL-1β, IL-6, IL-8, GM-CSF, CXCL1, MCP-2, and MMP-3. This finding indicates the important role of the B-ring 2'‑hydroxyl group in flavonoid molecules. Furthermore, compounds 8 and 11, the strongest SASP inhibitors, decreased the expression of IκBζ and C/EBPβ protein without affecting either BrdU uptake or the expression of senescence markers, such as pRb and p21. Finally, the oral administration of compound 8 to aged rats at 2 and 4 mg/kg/day for 10 days significantly inhibited the gene expression of SASP and IκBζ in kidneys. This is the first report of the strong SASP inhibitory action of flavonoids from Scutellaria radix on in vitro and in vivo senescence models. The inhibitory action was shown to be mediated mainly by interfering with the IκBζ/C/EBPβ signaling pathway.

CONCLUSION

Targeting production of the SASP using flavonoids from Scutellaria radix or its extract might help reduce low-grade sterile inflammation and control age-related diseases.

摘要

背景

随着年龄增长,长期暴露于衰老相关分泌表型(SASP)会导致邻近细胞和组织发生慢性低度炎症,引发多种慢性退行性疾病。

目的

在体外和体内研究黄芩乙醇提取物及其17种分离出的黄酮类成分对SASP产生的影响。

方法

用博来霉素诱导细胞衰老。采用酶联免疫吸附测定(ELISA)、逆转录定量聚合酶链反应(RT-qPCR)、蛋白质免疫印迹法和免疫荧光染色检测SASP及细胞信号分子的表达。为研究体内作用,使用21月龄的老年大鼠。

结果

乙醇提取物以及5种化合物,包括1号化合物(木犀草素;5,7-二羟基-6-甲氧基黄酮)、5号化合物(2',6',5,7-四羟基-8-甲氧基黄酮)、8号化合物(2',5,7-三羟基黄酮)、10号化合物(2',5,7-三羟基-8-甲氧基黄酮)和11号化合物(2',5,7-三羟基-6-甲氧基黄酮),能有效降低白细胞介素-6(IL-6)和白细胞介素-8(IL-8)的产生以及SASP的基因表达,SASP包括白细胞介素-1α(IL-1α)、白细胞介素-1β(IL-1β)、IL-6、IL-8、粒细胞-巨噬细胞集落刺激因子(GM-CSF)、CXC趋化因子配体1(CXCL1)、单核细胞趋化蛋白-2(MCP-2)和基质金属蛋白酶-3(MMP-3)。这一发现表明黄酮类分子中B环2'-羟基的重要作用。此外,8号和11号化合物作为最强的SASP抑制剂,可降低IκBζ和C/EBPβ蛋白的表达,而不影响5-溴脱氧尿苷(BrdU)摄取或衰老标志物如视网膜母细胞瘤蛋白(pRb)和p21的表达。最后,以2毫克/千克/天和4毫克/千克/天的剂量给老年大鼠口服8号化合物10天,可显著抑制肾脏中SASP和IκBζ的基因表达。这是关于黄芩黄酮类化合物对体外和体内衰老模型具有强大SASP抑制作用首份报告。研究表明,这种抑制作用主要是通过干扰IκBζ/C/EBPβ信号通路介导的。

结论

利用黄芩中的黄酮类化合物或其提取物靶向作用于SASP的产生,可能有助于减轻低度无菌性炎症并控制与年龄相关的疾病。

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