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[具体名称]深层培养物及其可能的活性化合物的抗炎作用和机制

The Anti-Inflammatory Effects and Mechanism of the Submerged Culture of and Its Possible Active Compounds.

作者信息

Huang Hsien-Chi, Shi Yu-Juan, Vo Thuy-Lan-Thi, Hsu Tai-Hao, Song Tuzz-Ying

机构信息

PhD Program of Biotechnology and Bioindustry, College of Biotechnology and Bioresources, Da-Yeh University, Changhua 515, Taiwan.

Department of Medicinal Botanicals and Foods on Health Applications, Da-Yeh University, Changhua 515, Taiwan.

出版信息

J Fungi (Basel). 2024 Jul 27;10(8):523. doi: 10.3390/jof10080523.

Abstract

The pharmacological effects of the fruiting body of () such as antioxidant, anti-virus, and immunomodulatory activities have already been described, whereas the anti-inflammatory effects and active components of the submerged culture of (SCOS) still need to be further verified. This study aimed to investigate the active compounds in the fermented liquid (FLOS), hot water (WEOS), and 50-95% (EEOS-50, EEOS-95) ethanol extracts of SCOS and their anti-inflammatory effects and potential mechanisms in lipopolysaccharide (LPS)-stimulated microglial BV2 cells. The results demonstrated that all of the SCOS extracts could inhibit NO production in BV2 cells. EEOS-95 exhibited the strongest inhibitory effects (71% inhibitory ability at 500 µg/mL), and its ergosterol, γ-aminobutyric acid (GABA), total phenolic, and total flavonoid contents were significantly higher than those of the other extracts (18.60, 18.60, 2.28, and 2.14 mg/g, < 0.05, respectively). EEOS-95 also has a strong inhibitory ability against IL-6, IL-1β, and TNF-α with an IC of 617, 277, and 507 µg/mL, respectively, which is higher than that of 1 mM melatonin. The anti-inflammatory mechanism of EEOS-95 seems to be associated with the up-regulation of PPAR-γ/Nrf-2/HO-1 antioxidant-related expression and the down-regulation of NF-κB/COX-2/iNOS pro-inflammatory expression signaling. In summary, we demonstrated that EEOS-95 exhibits neuroinflammation-mediated neurodegenerative disorder activities in LPS-induced inflammation in brain microglial cells.

摘要

(某菌)子实体的药理作用,如抗氧化、抗病毒和免疫调节活性等已有相关描述,而该菌深层培养物(SCOS)的抗炎作用及活性成分仍有待进一步验证。本研究旨在探究SCOS发酵液(FLOS)、热水提取物(WEOS)以及50 - 95%乙醇提取物(EEOS - 50、EEOS - 95)中的活性化合物及其在脂多糖(LPS)刺激的小胶质细胞BV2中的抗炎作用和潜在机制。结果表明,所有SCOS提取物均可抑制BV2细胞中一氧化氮(NO)的产生。EEOS - 95表现出最强的抑制作用(在500 μg/mL时抑制能力达71%),其麦角甾醇、γ-氨基丁酸(GABA)、总酚和总黄酮含量显著高于其他提取物(分别为18.60、18.60、2.28和2.14 mg/g,P < 0.05)。EEOS - 95对白细胞介素-6(IL - 6)、白细胞介素-1β(IL - 1β)和肿瘤坏死因子-α(TNF - α)也具有较强的抑制能力,其半数抑制浓度(IC)分别为617、277和507 μg/mL,高于1 mM褪黑素。EEOS - 95的抗炎机制似乎与过氧化物酶体增殖物激活受体-γ(PPAR - γ)/核因子E2相关因子2(Nrf - 2)/血红素加氧酶-1(HO - 1)抗氧化相关表达的上调以及核因子κB(NF - κB)/环氧化酶-2(COX - 2)/诱导型一氧化氮合酶(iNOS)促炎表达信号的下调有关。综上所述,我们证明了EEOS - 95在LPS诱导的脑小胶质细胞炎症中表现出神经炎症介导的神经退行性疾病活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3bd/11355118/dfb2f20db5b3/jof-10-00523-g001a.jpg

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