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氧化米糠蛋白诱导酸败对小鼠肝功能的影响。

Effects of oxidized rice bran protein induced by rancidity on the hepatic function in mice.

机构信息

College of Food Science and Engineering, Central South University of Forestry and Technology, 498 Southern Shaoshan Road, Changsha, Hunan 410004, P. R. China.

National Engineering Research Center of Rice and Byproduct Deep Processing, 498 South Shaoshan Road, Changsha, Hunan 410004, P. R. China.

出版信息

Food Funct. 2022 Jun 6;13(11):6089-6102. doi: 10.1039/d2fo00976e.

Abstract

Rice bran protein (RBP) is a great resource of premium protein. However, rice bran (RB) rancidity, which inevitably occurs during rice milling, can induce RBP oxidation, further affecting the nutritional value of RBP. This study focused on the impact of RBP rancidity on the nutritional value of oxidized RBP. RBP with varying oxidation degrees and doses was given to mice a 12-week intragastric administration. Oxidized RBP interfered with hepatic function and inflammation, and decreased the antioxidant capacities of the liver. Oxidized RBP also disturbed the hepatic lipid metabolism, and excessively oxidized RBP caused intrahepatic lipid accumulation and hepatic damage. Furthermore, oxidized RBP triggered the MyD88/NF-κB pathway but inhibited the Keap1-Nrf2/ARE pathway in the liver. Correlation analysis revealed that the protein expression of the Nrf2 pathway was negatively correlated with the NF-κB pathway. Results implied that oxidized RBP induced hepatic damage and hepatic dysfunction, indicating the deteriorating nutrition of oxidized RBP. The results exhibited the nutritional value of RBP after oxidative modification, and implied the importance of optimizing food-processing strategies to reduce the degree of protein oxidation, thereby avoiding the nutritional loss of dietary protein.

摘要

米糠蛋白(RBP)是优质蛋白质的重要来源。然而,在碾米过程中不可避免会发生米糠(RB)酸败,这会导致 RBP 氧化,进一步影响 RBP 的营养价值。本研究主要关注 RBP 酸败对氧化 RBP 营养价值的影响。将不同氧化程度和剂量的 RBP 通过灌胃方式给予小鼠 12 周。氧化 RBP 干扰肝功能和炎症,降低肝脏的抗氧化能力。氧化 RBP 还扰乱了肝脏的脂质代谢,过度氧化的 RBP 导致肝内脂质堆积和肝损伤。此外,氧化 RBP 激活了 MyD88/NF-κB 通路,但抑制了肝脏中的 Keap1-Nrf2/ARE 通路。相关性分析表明,Nrf2 通路的蛋白表达与 NF-κB 通路呈负相关。结果表明,氧化 RBP 诱导了肝损伤和肝功能障碍,表明氧化后的 RBP 营养价值下降。该结果展示了 RBP 经氧化修饰后的营养价值,提示优化食品加工策略以降低蛋白质氧化程度的重要性,从而避免膳食蛋白质的营养损失。

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