Isolation of Apigenin from Sungkai ( Peronema canescens) Leaves and Its Immunomodulatory Effects: An In Vivo Study on Granzyme B, Interferon-γ, and Perforin Expression with Supporting In Silico Analysis.

Q2 Pharmacology, Toxicology and Pharmaceutics
F1000Research Pub Date : 2025-08-08 eCollection Date: 2025-01-01 DOI:10.12688/f1000research.167153.1
Dwisari Dillasamola, Yufri Aldi, Najmiatul Fitria, Biomechy Oktomalioputri, Uce Lestari, Risma Multia
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引用次数: 0

Abstract

Background: Paronema canescens Jack., commonly known as sungkai, is a medicinal plant native to Southeast Asia, particularly abundant in the forests of Sumatra and Borneo, Indonesia. Traditionally, sungkai has been used to treat various ailments, likely due to its rich content of bioactive secondary metabolites. This study aimed to isolate, characterize, and evaluate the immunostimulatory and anti-inflammatory potential of compounds from sungkai leaves based on in silico and in vivo analyses.

Methods: Apigenin was isolated from Paronema canescens leaves via ethanol extraction, liquid-liquid partitioning, and chromatographic purification, then characterized by UV-Vis, FT-IR, and NMR spectroscopy. Molecular docking was conducted using MOE software to assess apigenin's binding to granzyme B, perforin, and IFN-γ, with levamisole as a reference. In vivo, 25 male mice were randomized into five groups and administered apigenin (1, 25, or 50 mg/kg BW) intramuscularly for seven days, alongside COVID-19 vaccination. Granzyme B and IFN-γ serum levels were quantified using ELISA. Statistical analysis employed one-way ANOVA with Duncan's test ( p < 0.05).

Results: The in silico analysis demonstrated that apigenin exhibited favorable binding affinities and multiple stabilizing interactions with granzyme B, perforin, and interferon-γ, supporting its potential role in enhancing cellular immune responses through direct molecular modulation of key cytotoxic effector proteins. To assess its immunostimulatory activity in vivo, apigenin was orally administered to mice ( Mus musculus) at doses of 1, 25, and 50 mg/kg body weight. Mice were pre-induced with a COVID-19 vaccine to simulate immune system activation. Immunological responses were evaluated through the measurement of granzyme B, perforin, and interferon-γ expression levels. The results demonstrated that apigenin significantly increased the expression of all three markers in a dose-dependent manner.

Conclusion: Collectively, the chemical, computational, and biological data confirm that apigenin from sungkai leaves holds strong immunostimulant and selective anti-inflammatory potential, supporting its development as a natural immune booster or vaccine adjuvant.

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sunonema canescens叶片中芹菜素的分离及其免疫调节作用:颗粒酶B、干扰素-γ和穿孔素表达的体内研究
背景:Paronema canescens Jack。通常被称为sungkai,是一种原产于东南亚的药用植物,在印度尼西亚苏门答腊岛和婆罗洲的森林中尤其丰富。传统上,生葵被用来治疗各种疾病,可能是因为它含有丰富的生物活性次级代谢物。本研究旨在通过体外和体内分析,分离、表征和评价生葵叶中化合物的免疫刺激和抗炎作用。方法:采用乙醇提取、液-液分流、色谱纯化等方法从芫荽叶中分离得到芹菜素,并用紫外可见光谱、红外光谱、核磁共振光谱对其进行表征。采用MOE软件进行分子对接,以左旋咪唑为参比,评估芹菜素与颗粒酶B、穿孔素和IFN-γ的结合情况。在体内,将25只雄性小鼠随机分为5组,在接种COVID-19疫苗的同时,肌肉注射芹菜素(1、25或50 mg/kg BW) 7天。ELISA法测定血清颗粒酶B和IFN-γ水平。统计分析采用Duncan检验的单因素方差分析(p < 0.05)。结果:计算机分析表明,芹菜素与颗粒酶B、穿孔素和干扰素-γ具有良好的结合亲和力和多重稳定相互作用,支持其通过直接分子调节关键细胞毒性效应蛋白来增强细胞免疫应答的潜在作用。为了评估其在体内的免疫刺激活性,芹菜素以1、25和50 mg/kg体重的剂量口服给药小鼠(小家鼠)。用COVID-19疫苗预先诱导小鼠以模拟免疫系统激活。通过测量颗粒酶B、穿孔素和干扰素-γ表达水平来评估免疫反应。结果表明,芹菜素显著增加了这三种标志物的表达,并呈剂量依赖性。综上所述,化学、计算和生物学数据证实,芹菜素具有很强的免疫刺激和选择性抗炎潜能,支持其作为天然免疫增强剂或疫苗佐剂的发展。
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
F1000Research
F1000Research Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
5.00
自引率
0.00%
发文量
1646
审稿时长
1 weeks
期刊介绍: F1000Research publishes articles and other research outputs reporting basic scientific, scholarly, translational and clinical research across the physical and life sciences, engineering, medicine, social sciences and humanities. F1000Research is a scholarly publication platform set up for the scientific, scholarly and medical research community; each article has at least one author who is a qualified researcher, scholar or clinician actively working in their speciality and who has made a key contribution to the article. Articles must be original (not duplications). All research is suitable irrespective of the perceived level of interest or novelty; we welcome confirmatory and negative results, as well as null studies. F1000Research publishes different type of research, including clinical trials, systematic reviews, software tools, method articles, and many others. Reviews and Opinion articles providing a balanced and comprehensive overview of the latest discoveries in a particular field, or presenting a personal perspective on recent developments, are also welcome. See the full list of article types we accept for more information.
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