Anti-inflammation and Anti-insulin Resistance of a Compound from Vietnamese Clerodendrum chinense Leaves.

IF 1.7 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Iranian Journal of Pharmaceutical Research Pub Date : 2026-04-20 eCollection Date: 2026-01-01 DOI:10.5812/ijpr-169136
Thu Thi Xuan Nguyen, Cuong Trinh Tat
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引用次数: 0

Abstract

Background: Clerodendrum chinense has been reported to possess several important biological activities. However, the anti-inflammation and insulin-related properties of isolated compounds from this plant have not yet been investigated.

Objectives: This study focuses on extracting compounds and evaluating improvements in insulin resistance through the anti-inflammatory potential and inhibition of reactive oxygen species (ROS) of hispidulin from Vietnamese C. chinense leaves.

Methods: Ethanol was used to separate the compounds from the leaves of Vietnamese C. chinense. 1D, 2D-NMR, and ESI-MS spectra were used to analyze the structural identity of the isolated compounds. Compound 1 (hispidulin) was evaluated for anti-inflammation and ROS in Raw 264.7 cells: Anti-inflammatory cytokine inhibition ability was analyzed by the ELISA method; Western blotting was used for the expression levels of phosphorylated ERK1/2, p38, p47phox, and GLUT4. ROS was assessed by immunofluorescence; a luminometer device was used to measure NADPH oxidase activity. The ability to absorb glucose and counteract insulin resistance was evaluated in 3T3-L1 cells via insulin-induced glucose uptake using immunofluorescence dye.

Results: One compound isolated from the leaves of Vietnamese C. chinense was identified as hispidulin. Hispidulin at a concentration of 50 μg/mL significantly inhibited tumor necrosis factor (TNF)-α, interleukin (IL)-6, and IL-8 in LPS-induced macrophages (P < 0.001). Moreover, in LPS-stimulated macrophages, the phosphorylation of p38 and ERK1/2, NADPH oxidase activity, as well as the phosphorylation of p47phox, were reduced at a concentration of 50 μg/mL of hispidulin (P < 0.001). More importantly, 3T3-L1 cells with inhibited insulin activity were able to regain glucose uptake and insulin responsiveness through GLUT4 expression when treated with 50 µg/mL of hispidulin (P < 0.001).

Conclusions: The data confirmed the presence of hispidulin in the chemical composition of Vietnamese C. chinense leaves. The results indicated that hispidulin inhibited LPS- and ROS-mediated inflammation in macrophages. More importantly, the data have shown that hispidulin enhances glucose uptake and improves insulin activity in 3T3-L1 cells.

越南松柏叶化合物的抗炎和抗胰岛素抵抗作用。
背景:据报道,中国毛竹具有多种重要的生物活性。然而,从这种植物中分离的化合物的抗炎症和胰岛素相关特性尚未被研究。目的:研究越南芫荽叶中hispidulin的抗炎活性及对活性氧(ROS)的抑制作用,研究其对胰岛素抵抗的改善作用。方法:采用乙醇法对越南三叶中各成分进行分离。利用一维、二维nmr和ESI-MS谱分析了分离化合物的结构特征。评价化合物1 (hispidulin)对Raw 264.7细胞的抗炎和ROS作用;ELISA法分析抗炎细胞因子抑制能力;Western blotting检测磷酸化ERK1/2、p38、p47phox和GLUT4的表达水平。免疫荧光法测定ROS;用光度计装置测定NADPH氧化酶活性。利用免疫荧光染料,通过胰岛素诱导的葡萄糖摄取来评估3T3-L1细胞吸收葡萄糖和抵抗胰岛素抵抗的能力。结果:从越南芫荽叶中分离得到1个化合物,经鉴定为hispidulin。50 μg/mL的Hispidulin显著抑制lps诱导的巨噬细胞中肿瘤坏死因子(TNF)-α、白细胞介素(IL)-6、IL-8的表达(P < 0.001)。此外,在lps刺激的巨噬细胞中,50 μg/mL的hispidulin降低了p38和ERK1/2的磷酸化、NADPH氧化酶活性以及p47phox的磷酸化(P < 0.001)。更重要的是,胰岛素活性被抑制的3T3-L1细胞在50µg/mL hispidulin处理后,能够通过GLUT4表达恢复葡萄糖摄取和胰岛素反应性(P < 0.001)。结论:本实验证实越南三叶化学成分中存在海鞘苷。结果表明,hispidulin抑制LPS和ros介导的巨噬细胞炎症。更重要的是,数据显示hispidulin增加了3T3-L1细胞的葡萄糖摄取并改善了胰岛素活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.40
自引率
6.20%
发文量
52
审稿时长
2 months
期刊介绍: The Iranian Journal of Pharmaceutical Research (IJPR) is a peer-reviewed multi-disciplinary pharmaceutical publication, scheduled to appear quarterly and serve as a means for scientific information exchange in the international pharmaceutical forum. Specific scientific topics of interest to the journal include, but are not limited to: pharmaceutics, industrial pharmacy, pharmacognosy, toxicology, medicinal chemistry, novel analytical methods for drug characterization, computational and modeling approaches to drug design, bio-medical experience, clinical investigation, rational drug prescribing, pharmacoeconomics, biotechnology, nanotechnology, biopharmaceutics and physical pharmacy.
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