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源自(L)DC的生物活性肽豆豉在消化模拟中作为血管紧张素转换酶(ACE)的抑制剂。

Bioactive Peptide Tempe Made from (L) DC as an Inhibitor of Angiotensin-I-Converting Enzyme (ACE) in a Digestion Simulation.

作者信息

Rizkaprilisa Windy, Marsono Yustinus, Indrati Retno

机构信息

Department of Food and Agricultural Product Technology, Faculty of Agriculturural Technology, Universitas Gadjah Mada, Yogyakarta 55281, Indonesia.

出版信息

Prev Nutr Food Sci. 2020 Mar 31;25(1):93-97. doi: 10.3746/pnf.2020.25.1.93.

DOI:10.3746/pnf.2020.25.1.93
PMID:32292761
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7143009/
Abstract

(L) DC tempe is a food that functions as an inhibitor of the angiotensin-I-converting enzyme (ACE). The purpose of this research was to study the activity of tempe peptides during the digestive process with pepsin-pancreatin, and absorption of peptides in the small intestine using the inverted intestinal sac method. Our results show that had the highest ACE-inhibiting activity after digestion after fermentation for 72 h (F72). F72 peptide absorption (%) and ACE-inhibitory activity of the absorbed peptides did not significantly differ between the different segments of the small intestine (duodenum, jejunum, and ileum). These results demonstrate that F72 tempe maintains ACE-inhibitory activity in each segment of the small intestine after both digestion and absorption.

摘要

豆豉是一种可作为血管紧张素转换酶(ACE)抑制剂的食物。本研究的目的是利用胃蛋白酶 - 胰酶研究豆豉肽在消化过程中的活性,并采用翻转肠囊法研究肽在小肠中的吸收情况。我们的结果表明,发酵72小时(F72)后的豆豉在消化后具有最高的ACE抑制活性。F72肽的吸收百分比以及吸收肽的ACE抑制活性在小肠的不同节段(十二指肠、空肠和回肠)之间没有显著差异。这些结果表明,F72豆豉在消化和吸收后在小肠的每个节段中都保持ACE抑制活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/7143009/a66ea3cdd579/PNFS-25-093-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/7143009/9c8e06ecb89e/PNFS-25-093-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/7143009/a66ea3cdd579/PNFS-25-093-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/7143009/9c8e06ecb89e/PNFS-25-093-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a33/7143009/a66ea3cdd579/PNFS-25-093-f2.jpg

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