Phytochemical Analysis of Triphala Extract, In Vitro and In Silico Evaluation of Pancreatic Lipase Inhibition for Obesity Management.

IF 3.1 2区 农林科学 Q2 CHEMISTRY, APPLIED
Sanjay Kottekad, Usharani Dandamudi
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引用次数: 0

Abstract

Pancreatic lipase (PL) inhibition is a prominent pharmacological strategy for managing obesity, as it reduces the hydrolysis of dietary triglycerides (TAG) into free fatty acids and monoglycerides. Orlistat, an FDA-approved drug, achieves a 30% reduction in body fat through irreversible covalent inhibition of PL. However, the gastrointestinal side effects limit its long-term use. To address these issues, we explored inhibition using natural compounds from Triphala (TRI), a renowned Ayurvedic formulation comprising three plants - Emblica officinalis (EO), Terminalia bellirica (TB), and Terminalia chebula (TC). This study investigated PL inhibition by an 80% hydro-ethanolic extract of individual herbs (EO, TB, TC) as well as, Triphala (TRI) and its fractions and identified key bioactive compounds - Ellagic acid, Chebulic acid and Corilagin via LC-MS/MS. Qualitative and quantitative phytochemical analyses revealed that TF1 is rich in phenols and tannins and exhibited significant PL inhibition compared to individual herb extracts. Additionally, Ellagic acid, Chebulic acid and Corilagin of TF1 demonstrated notable PL-inhibition, with IC50 values 58.41 ± 1.92 µg/mL, 125.33 ± 2.80 and 257.81 ± 2.10 µg/mL respectively. Furthermore, the PL inhibition kinetics showed that these bioactives and TRI fractions exhibited mixed inhibition, in contrast to the competitive inhibition of Orlistat (positive control). Molecular docking and 100 ns molecular dynamic simulations of PL-inhibitor complexes revealed that the bioactives bind to key residues in the PL active site. Among the three bioactives, Chebulic acid has better binding energy, primarily due to its substantial electrostatic interactions with the gatekeeper residue D80 of the PL active site. These findings highlight the potential of Triphala bioactives, particularly Chebulic acid and Ellagic acid, to effectively inhibit PL and provide a strategy to manage obesity.

tritria提取物的植物化学分析,体外和计算机评价胰腺脂肪酶抑制肥胖的作用。
胰脂肪酶(PL)抑制是控制肥胖的重要药理学策略,因为它减少了膳食甘油三酯(TAG)水解为游离脂肪酸和单甘油三酯。奥利司他是一种fda批准的药物,通过对PL的不可逆共价抑制,使体脂减少30%,但其胃肠道副作用限制了其长期使用。为了解决这些问题,我们探索了从Triphala (TRI)中提取的天然化合物的抑制作用,Triphala (TRI)是一种著名的印度草药配方,由三种植物- Emblica officinalis (EO), Terminalia bellirica (TB)和Terminalia chebula (TC)组成。本研究采用液相色谱-质谱联用技术(LC-MS/MS)研究了不同药材(EO、TB、TC)和Triphala (TRI)及其组分80%乙醇提取物对PL的抑制作用,并鉴定了主要活性成分鞣花酸(Ellagic acid)、Chebulic acid和芫花素(Corilagin)。定性和定量植物化学分析表明,TF1富含酚类物质和单宁,与单个草药提取物相比,具有显著的PL抑制作用。此外,鞣花酸、Chebulic酸和Corilagin对TF1有明显的抑制作用,其IC50值分别为58.41±1.92µg/mL、125.33±2.80和257.81±2.10µg/mL。此外,PL抑制动力学表明,这些生物活性物和TRI组分表现出混合抑制,与奥利司他(阳性对照)的竞争性抑制相反。分子对接和100 ns分子动力学模拟表明,这些生物活性物质与PL活性位点的关键残基结合。在三种生物活性物质中,Chebulic acid具有更好的结合能,这主要是由于它与PL活性位点的gatekeeper残基D80有大量的静电相互作用。这些发现强调了Triphala生物活性物质的潜力,特别是Chebulic酸和鞣花酸,可以有效地抑制PL,并为控制肥胖提供了一种策略。
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
Plant Foods for Human Nutrition
Plant Foods for Human Nutrition 工程技术-食品科技
CiteScore
6.80
自引率
7.50%
发文量
89
审稿时长
12-24 weeks
期刊介绍: Plant Foods for Human Nutrition (previously Qualitas Plantarum) is an international journal that publishes reports of original research and critical reviews concerned with the improvement and evaluation of the nutritional quality of plant foods for humans, as they are influenced by: - Biotechnology (all fields, including molecular biology and genetic engineering) - Food science and technology - Functional, nutraceutical or pharma foods - Other nutrients and non-nutrients inherent in plant foods
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