大叶月见草中的 (2S)-Pinocembrin 对巨噬细胞系产生前列腺素 E2 的抑制作用:体外和硅学研究。

IF 2.1 Q3 PHARMACOLOGY & PHARMACY
Advances in Pharmacological and Pharmaceutical Sciences Pub Date : 2024-10-30 eCollection Date: 2024-01-01 DOI:10.1155/2024/8811022
Hilwan Yuda Teruna, Kamal Rullah, Rudi Hendra, Rahayu Utami, Deri Islami, Siti Munirah Mohd Faudzi, Mohd Fadhlizil Fasihi Mohd Aluwi, Kok Wai Lam
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引用次数: 0

摘要

皮诺雪布林(PCB)是一种具有抗炎特性的类黄酮,已被批准用于各种临床试验。为了深入评估天然多氯联苯的特定对映体的抗炎潜力,我们首次研究了纯对映体(2S)-多氯联苯在小鼠 RAW 264.7 和人类 U937 巨噬细胞系中调节脂多糖(LPS)诱导的炎症介质的功效。这种特殊的化合物是从印度尼西亚的一种本地植物 Goniothalamus macrophyllus(芒萁科)中分离出来的。这种植物在传统上被用作缓解炎症的草药。(2S)-PCB 是通过正己烷脱脂,然后用甲醇浸泡的方法从 G. macrophyllus 的茎皮中分离出来的。纯化采用了多种色谱技术。利用电子圆二色性(ECD)光谱测定了其绝对构型。然后测试了该化合物对前列腺素 E2 (PGE2) 的抑制活性,并进行了对接模拟。结果表明,(2S)-PCB 能显著抑制 LPS 诱导的 PGE2 在 RAW 264.7 和 U937 细胞系中的产生。对接模拟显示,(2S)-PCB 通过抑制 p38 和细胞外信号调节激酶 (ERK) 来抑制丝裂原活化蛋白激酶 (MAPK) 的活化,从而降低了 PGE2 的水平。这些发现表明,该化合物可防止细菌感染引起的脓毒性休克恶化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibitory Effect of (2S)-Pinocembrin From Goniothalamus macrophyllus on the Prostaglandin E2 Production in Macrophage Cell Lines: In Vitro and In Silico Studies.

Pinocembrin (PCB), a flavonoid known for its anti-inflammatory properties, has been approved for various clinical trial applications. To evaluate deeper into the anti-inflammatory potential of the specific enantiomer of natural PCB, we conducted the first investigation into the efficacy of the pure enantiomer (2S)-PCB in modulating inflammatory mediators induced by lipopolysaccharide (LPS) in both murine RAW 264.7 and human U937 macrophage cell lines. This particular compound was isolated from Goniothalamus macrophyllus (Annonaceae), a native plant of Indonesia. This plant has been used traditionally as an herbal medicine to alleviate inflammation. (2S)-PCB was isolated from the stem bark of G. macrophyllus by defatting with n-hexane followed by maceration with methanol. Purification was performed using several chromatographic techniques. The absolute configuration was determined using electronic circular dichroism (ECD) spectroscopy. This compound was then tested for its inhibitory activity on prostaglandin E2 (PGE2) and subjected to docking simulations. The results indicated that (2S)-PCB significantly suppressed the production of PGE2 induced by LPS in both RAW 264.7 and U937 cell lines. The docking simulations revealed that (2S)-PCB reduced PGE2 levels by suppressing mitogen-activated protein kinase (MAPK) activation through inhibiting p38 and extracellular signal-regulated kinases (ERK). These findings suggest that the compound may prevent worsening of septic shock caused by bacterial infection.

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来源期刊
CiteScore
4.30
自引率
3.60%
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0
审稿时长
17 weeks
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