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低聚合度原花青素因其能够形成特定相互作用而成为消化酶的良好抑制剂:一种假设。

Proanthocyanidins with a Low Degree of Polymerization are Good Inhibitors of Digestive Enzymes Because of their Ability to form Specific Interactions: A Hypothesis.

机构信息

Dept. of Chemical Biological Sciences, Universidad Autónoma de Ciudad Juárez, Anillo Envolvente del PRONAF y Estocolmo s/n, Ciudad Juárez, Chihuahua, CP 322310, México.

Coordinación en Tecnología de Alimentos de Origen Vegetal, Centro de Investigación en Alimentación y Desarrollo, A. C. (CIAD, AC), Carretera a la Victoria Km. 0.6, La Victoria, Hermosillo, Sonora, CP 83000, México.

出版信息

J Food Sci. 2018 Dec;83(12):2895-2902. doi: 10.1111/1750-3841.14386. Epub 2018 Nov 16.

Abstract

Inhibition of target digestive enzymes is an accepted strategy to prevent diseases such as obesity and diabetes. Proanthocyanidins (PACs) are known for their ability to bind, inhibit, and precipitate enzymes, which makes them potential bioDrugs with an impact on the digestive process. PAC degree of polymerization (DP) is one of the structural features responsible for their differential inhibitory potency but the explanation for this phenomenon is still unclear. Pecan nut (Carya illinoinensis L.) kernels and nutshells are rich in oligomeric and polymeric PACs. We have used thiolysis and HPLC analyses to propose four theoretical model structures of PACs representative of four semipurified fractions obtained from pecan kernel and shell, which showed different inhibitory activity against intestinal lipases, amylases, and proteases. The noncovalent interactions between PACs and digestive enzymes were predicted by in silico methods through computational software. These observations are discussed in view of current literature on the biological effects of PACs with different DPs and allowed us to propose the hypothesis that "small oligomeric PACs could be digestive enzyme inhibitors due to their capacity to enter and bind the enzymes' specific cavities better than polymers and oligomers of medium and high molecular weight."

摘要

抑制靶消化酶是预防肥胖症和糖尿病等疾病的一种公认策略。原花青素 (PACs) 以其结合、抑制和沉淀酶的能力而闻名,这使它们成为具有潜在影响消化过程的生物药物。PAC 的聚合度 (DP) 是决定其差异抑制效力的结构特征之一,但对这一现象的解释仍不清楚。山核桃(Carya illinoinensis L.)果仁及其外壳富含低聚和聚合 PACs。我们使用硫解和 HPLC 分析,提出了四个理论 PAC 模型结构,代表从山核桃仁壳中获得的四个半纯化级分,它们对肠道脂肪酶、淀粉酶和蛋白酶显示出不同的抑制活性。通过计算软件的计算方法预测了 PAC 与消化酶之间的非共价相互作用。根据不同 DP 的 PAC 生物学效应的现有文献讨论了这些观察结果,并提出了“小分子寡聚 PAC 可能是消化酶抑制剂,因为它们比中高分子量的聚合物和寡聚物更有能力进入并结合酶的特定腔室”的假设。

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