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Anti-Inflammatory Effects and Mechanisms of Action of Coussaric and Betulinic Acids Isolated from Diospyros kaki in Lipopolysaccharide-Stimulated RAW 264.7 Macrophages

机译:柿柿中胆囊酸和桦木酸的抗炎作用及其作用机理对脂多糖刺激的RAW 264.7巨噬细胞的影响

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摘要

Diospyros kaki Thunb. is widely distributed in East Asian countries, its leaves being mainly used for making tea. In this study, coussaric acid (CA) and betulinic acid (BA), both triterpenoid compounds, were obtained from D. kaki leaf extracts through bioassay-guided isolation. CA and BA showed anti-inflammatory effects via inhibition of the nuclear factor-κB (NF-κB) pathway, providing important information on their anti-inflammatory mechanism. Furthermore, they markedly inhibited nitric oxide (NO) and prostaglandin E2 (PGE2) production in lipopolysaccharide (LPS)-activated RAW 264.7 macrophages, and suppressed tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and interleukin-1β (IL-1β) levels. Furthermore, they decreased protein expression of inducible nitric oxide synthase and cyclooxygenase-2. Pre-treatment with CA and BA inhibited LPS-induced NF-κB. We further examined the effects of CA and BA on heme oxygenase (HO)-1 expression in RAW 264.7 macrophages: BA induced HO-1 protein expression in a dose-dependent manner, while CA had no effect. We also investigated whether BA treatment induced nuclear translocation of Nrf2. BA inhibited LPS-induced NF-κB-binding activity, as well as pro-inflammatory mediator and cytokine production (e.g., NO, PGE2, TNF-α, IL-1β, IL-6), by partial reversal of this effect by SnPP, an inhibitor of HO-1. These findings further elucidate the anti-inflammatory mechanism of CA and BA isolated from D. kaki.
机译:柿(Diospyros kaki Thunb)。在东亚国家广泛分布,其叶子主要用于制茶。在这项研究中,库萨克酸(CA)和桦木酸(BA)都是三萜类化合物,是通过生物测定引导的分离方法从柿果叶提取物中获得的。 CA和BA通过抑制核因子-κB(NF-κB)途径表现出抗炎作用,提供了有关其抗炎机制的重要信息。此外,它们还显着抑制脂多糖(LPS)激活的RAW 264.7巨噬细胞中一氧化氮(NO)和前列腺素E2(PGE2)的产生,并抑制肿瘤坏死因子-α(TNF-α),白介素6(IL-6),和白介素1β(IL-1β)水平。此外,它们降低了诱导型一氧化氮合酶和环氧合酶-2的蛋白质表达。用CA和BA预处理可抑制LPS诱导的NF-κB。我们进一步检查了CA和BA对RAW 264.7巨噬细胞中血红素加氧酶(HO)-1表达的影响:BA以剂量依赖性方式诱导HO-1蛋白表达,而CA没有作用。我们还调查了BA治疗是否诱导Nrf2的核易位。 BA通过SnPP逆转LPS诱导的NF-κB结合活性以及促炎性介质和细胞因子的产生(例如NO,PGE2,TNF-α,IL-1β,IL-6),从而抑制了该作用。 ,HO-1的抑制剂。这些发现进一步阐明了从柿中分离出的CA和BA的抗炎机制。

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