Chemical Composition and Analgesic and Antidiabetic Activity of Chenopodium ambrosioides L

IF 2.8 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Cell Biochemistry and Function Pub Date : 2024-11-21 DOI:10.1002/cbf.70016
Soufiane Drioua, Mouna Ameggouz, Abdelmounaim Laabar, Abderrahim Aasfar, Moulay El Abbes Faouzi, Ahmed Zahidi, Riaz Ullah, Amal Alotaibi, Abdelhakim Bouyahya, Gokhan Zengin, Abdelaali Balahbib, Hanane Benzied, Anass Doukkali
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Abstract

This study focuses on identifying active compounds within Chenopodium ambrosioides extracts and fractions, with a specific emphasis on their potential analgesic and antidiabetic properties. The motivation arises from the reported therapeutic effects of the plant and the desire to pinpoint the compounds responsible for these benefits. Gas chromatography–mass spectrometry spectrophotometric analysis was employed to characterize chemical constituents in the aqueous extracts (infused aqueous extract and macerated aqueous extract) and fractions (cyclohexane fraction, ethyl acetate fraction, butanol fraction, remaining aqueous fraction) of C. ambrosioides. Animal models were used to examine the analgesic activity, while α-glucosidase and α-amylase enzyme assays were used to investigate the antidiabetic effect. Throughout the investigation, several chemical families were found, including phenolic compounds, alcohols, acids, terpenes, steroids, and others. Trans-ascaridol glycol, palmitic acid, phenol, octadecadienoic acid, isoascaridol, eicosanoic acid, 2-methoxy-4-vinyl phenol, mexiletine, and thymol were among the significant chemicals found. At a dose of 500 mg/m, starting with α-amylase inhibition, among the extracts, EAF (59 ± 0.7 μg/mL) showed the highest potency, followed by FA (129 ± 0.22 μg/mL), FB (140 ± 0.9 μg/mL), and EAM (178 ± 0.9 μg/mL). Interestingly, EAI demonstrated a relatively weak inhibition (430 ± 0.2 μg/mL), and no result was reported for FCH in this category. Regarding α-glucosidase inhibition, the most potent activity was observed with EAM (1.4 ± 0.7 μg/mL), The other extracts demonstrated varying levels of inhibition, with EAI (4.4 ± 0.5 μg/mL) and EAF (140 ± 1.9 μg/mL) showing moderate activity. FA (25 ± 0.9 μg/mL) and FB (34 ± 0.3 μg/mL) exhibited lower inhibition compared to EAM but still outperformed acarbose in this test. The observed synergistic effects of phenolic compounds in Chenopodium ambrosioides provide insights into the biological properties contributing to its reported analgesic and antidiabetic effects. The study underscores the potential of natural plant products for pharmaceutical applications, especially in enzymatic inhibition. All things considered, these results add to the expanding corpus of information about substances originating from plants and their uses in industry and health.

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陈皮的化学成分及镇痛和抗糖尿病活性
本研究的重点是确定伏牛花提取物和馏分中的活性化合物,特别强调其潜在的镇痛和抗糖尿病特性。研究动机源于该植物据报道具有的治疗效果,以及确定这些功效的化合物的愿望。研究人员采用气相色谱-质谱分光光度法分析伏牛芝水提取物(浸泡水提取物和浸渍水提取物)和馏分(环己烷馏分、乙酸乙酯馏分、丁醇馏分和剩余水馏分)中的化学成分。研究人员使用动物模型来检测其镇痛活性,并使用α-葡萄糖苷酶和α-淀粉酶酶测定法来检测其抗糖尿病作用。在整个研究过程中,发现了多个化学家族,包括酚类化合物、醇类、酸类、萜类、类固醇等。其中发现的重要化学物质包括反式猩红醇乙二醇、棕榈酸、苯酚、十八碳二烯酸、异猩红醇、二十酸、2-甲氧基-4-乙烯基苯酚、麦西来坦和百里酚。在 500 毫克/米的剂量下,从抑制α-淀粉酶开始,在各种提取物中,EAF(59 ± 0.7 μg/mL)的效力最高,其次是FA(129 ± 0.22 μg/mL)、FB(140 ± 0.9 μg/mL)和EAM(178 ± 0.9 μg/mL)。有趣的是,EAI 的抑制作用相对较弱(430 ± 0.2 μg/mL),而 FCH 在这一类别中没有结果报告。关于α-葡萄糖苷酶抑制作用,EAM 的活性最强(1.4 ± 0.7 μg/mL),其他提取物表现出不同程度的抑制作用,EAI(4.4 ± 0.5 μg/mL)和 EAF(140 ± 1.9 μg/mL)表现出中等活性。与 EAM 相比,FA(25 ± 0.9 μg/mL)和 FB(34 ± 0.3 μg/mL)的抑制率较低,但在该试验中仍优于阿卡波糖。在伏牛花中观察到的酚类化合物的协同效应使人们对其所报道的镇痛和抗糖尿病作用的生物特性有了更深入的了解。这项研究强调了天然植物产品在制药方面的应用潜力,尤其是在酶抑制方面。总之,这些研究成果为不断扩大的有关植物物质及其在工业和健康领域的应用的信息库增添了新的内容。
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来源期刊
Cell Biochemistry and Function
Cell Biochemistry and Function 生物-生化与分子生物学
CiteScore
6.20
自引率
0.00%
发文量
93
审稿时长
6-12 weeks
期刊介绍: Cell Biochemistry and Function publishes original research articles and reviews on the mechanisms whereby molecular and biochemical processes control cellular activity with a particular emphasis on the integration of molecular and cell biology, biochemistry and physiology in the regulation of tissue function in health and disease. The primary remit of the journal is on mammalian biology both in vivo and in vitro but studies of cells in situ are especially encouraged. Observational and pathological studies will be considered providing they include a rational discussion of the possible molecular and biochemical mechanisms behind them and the immediate impact of these observations to our understanding of mammalian biology.
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