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利用 Caco-2 细胞作为新型食品源 DPP-IV 抑制剂鉴定工具。

Using Caco-2 cells as novel identification tool for food-derived DPP-IV inhibitors.

机构信息

Univ. Lille, EA 7394 - ICV - Institut Charles Viollette, F-59000 Lille, France.

Univ. Lille, EA 7394 - ICV - Institut Charles Viollette, F-59000 Lille, France.

出版信息

Food Res Int. 2017 Feb;92:113-118. doi: 10.1016/j.foodres.2017.01.002. Epub 2017 Jan 4.

DOI:10.1016/j.foodres.2017.01.002
PMID:28290288
Abstract

Dietary proteins have recently been investigated as a new source of DPP-IV inhibitory peptides with limited side effects and promising applications. Numerous studies have highlighted and identified peptide sequences able to inhibit DPP-IV activity in vitro, mostly from milk proteins. However, the correlation to in vivo studies remains scarce because standard in vitro assays with purified enzyme do not accurately simulate key factors impacting peptide bioactivity such as intestinal and brush border enzymes or cellular permeability. Therefore, a DPP-IV activity inhibition assay is here proposed using non differentiated confluent Caco-2 cells to rapidly assess food-derived peptide inhibitory potential in approaching intestinal conditions. DPP-IV gene expression was first checked and specific DPP-IV substrate was used to implement the assay. Using a specific DPP-IV inhibitor confirmed that non differentiated Caco-2 cells express measurable DPPIV activity. This in situ assay was then applied to digests which already demonstrated a DPP-IV inhibitory potential with a standard assay using purified enzyme. Bovine hemoglobin and cuttlefish hydrolysate digests from simulated gastrointestinal digestion exerted a dose response inhibition on DPP-IV activity but displayed different inhibitory potentials.

摘要

最近,人们研究了膳食蛋白质作为一种新的 DPP-IV 抑制肽来源,其副作用有限,具有广阔的应用前景。大量研究强调并确定了能够在体外抑制 DPP-IV 活性的肽序列,这些肽序列主要来自乳蛋白。然而,与体内研究的相关性仍然很少,因为用纯化酶进行的标准体外测定不能准确模拟影响肽生物活性的关键因素,如肠道和刷状缘酶或细胞通透性。因此,本研究提出了一种使用未分化的紧密连接 Caco-2 细胞的 DPP-IV 活性抑制测定法,以快速评估接近肠道条件的食物来源肽的抑制潜力。首先检查 DPP-IV 基因表达,并使用特定的 DPP-IV 底物来实施测定。使用特定的 DPP-IV 抑制剂证实,未分化的 Caco-2 细胞表达可测量的 DPPIV 活性。然后将该原位测定法应用于已用纯化酶的标准测定法显示出 DPP-IV 抑制潜力的消化物。来自模拟胃肠消化的牛血红蛋白和乌贼水解物消化物对 DPP-IV 活性表现出剂量反应抑制,但显示出不同的抑制潜力。

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