研究糙叶黄精的抗致脂潜能叶馏分的抗致脂潜力:氧化应激调节的脂肪生成级联中的 HPTLC-MS 表征、酶分析和 3T3-L1 脂肪细胞分化试验

Nikita Nayak, A. Pattnaik
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引用次数: 0

摘要

背景:肥胖症的分子发病机制是细胞氧化应激和脂肪生成增加。为了寻找更好的合成分子替代品,现有化合物自然成为研究重点。在这种情况下,Xanthium strumarium(X. strumarium)Linn.具有抗糖尿病活性,并被证明具有中和肥胖症病理目标的功效。目的:本研究旨在以生物活性为导向分离甲醇叶提取物的馏分,其中生物活性是指在体外酶解和三天转移、接种3×105细胞(3T3-L1)脂肪细胞分化试验中的抗脂肪生成和抗氧化功效。材料和方法收集和干燥原叶,然后用甲醇进行冷提取,用闪速色谱分离生物活性成分。利用 3T3-L1 细胞系对这些成分进行脂肪细胞分化试验,另一方面对体外胰脂肪酶、α-葡萄糖苷酶和α-淀粉酶进行酶学试验分析。根据所表现出的活性,对所选馏分进一步采用高效薄层色谱-质谱法(HPTLC-MS)进行表征。结果:通过 HPTLC-MS 对这些试验中最具活性的馏分进行了表征。馏分 2 和馏分 3 在所有酶测定中都表现出强大的活性(α-葡萄糖苷酶 IC50:2.48 ± 0.015、2.84 ± 0.030 µg/mL;α-淀粉酶 IC50:1.98 ± 0.050、1.79 ± 0.045 µg/mL;胰脂肪酶 IC50:3.16 ± 0.030、3.18 ± 0.040 µg/mL),并对 3T3-L1 细胞系的脂肪细胞分化有显著抑制作用。通过 HPTLC-MS 进一步鉴定,这些馏分含有β-谷甾醇和槲皮素等化合物,肯定了它们潜在的生物活性。结论这项研究强调了 X. strumarium Linn.
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigating the Anti-adipogenic Potential of Xanthium strumarium Linn. Leaves Fractions: HPTLC-MS Characterization, Enzymatic Analysis, and 3T3-L1 Adipocyte Differentiation Assay in Oxidative Stress-modulated Adipogenesis Cascade
Background: Molecular pathogenesis of obesity is initiated by cellular oxidative stress along with increased adipogenesis. For the search of better alternatives of synthetic molecules in terms of their adverse events, naturally, existing compounds are now a research focus. In this context, Xanthium strumarium ( X. strumarium) Linn. exhibited anti-diabetic activities and proved to have efficacy in neutralizing very near pathological targets to obesity. Purpose: This study is aimed toward bioactivity-guided fraction isolation of methanolic leaves extract, where bioactivity refers to anti-adipogenesis and anti-oxidant efficacy in in vitro enzymatic and three-day transfer, inoculum 3×105 cells (3T3-L1) adipocyte differentiation assay. Materials and method: Collection and drying of the raw leaves followed by cold extraction in methanol and flash chromatography for bioactive fraction isolation. 3T3-L1 cell line was utilized for adipocyte differentiation assay of those and on the other hand in vitro pancreatic lipase, α-glucosidase, and α-amylase enzymatic assays were analyzed. Based on exhibited activities, selected fractions are further characterized by high-performance thin-layer chromatography-mass spectrometry (HPTLC-MS). Results: The most active fractions from these assays underwent characterization via HPTLC-MS. Fractions 2 and 3 exhibited potent activities in all enzymatic assays (α-glucosidase IC50: 2.48 ± 0.015, 2.84 ± 0.030 µg/mL; α-amylase IC50: 1.98 ± 0.050, 1.79 ± 0.045 µg/mL; pancreatic lipase IC50: 3.16 ± 0.030, 3.18 ± 0.040 µg/mL) and displayed significant inhibition of adipocyte differentiation in 3T3-L1 cell line. These fractions further identified through HPTLC-MS, contained compounds like β-sitosterol and quercetin, affirming their potential bioactivity. Conclusion: The study underscores the potential of X. strumarium Linn. fractions as promising natural alternatives for combating obesity-related pathways, highlighting their significance in developing future anti-obesity therapeutics.
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