4.7 Article

In Vivo Assessment of the Effects of Mono-Carrier Encapsulated Fucoxanthin Nanoparticles on Type 2 Diabetic C57 Mice and Their Oxidative Stress

期刊

ANTIOXIDANTS
卷 11, 期 10, 页码 -

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MDPI
DOI: 10.3390/antiox11101976

关键词

fucoxanthin; zein; nanoparticles; T2DM; C57; diabetes

资金

  1. State Key Laboratory of Biological Fermentation Engineering of Beer
  2. National Natural Science Foundation of China [31871786]

向作者/读者索取更多资源

Fucoxanthin (FX), a carotenoid from marine origin, plays an important role in regulating and alleviating type 2 diabetes. In this study, FX was encapsulated in hydrolyzed zein to form a stable nanocomplex (FZNP) which effectively reduced fasting blood glucose levels, repaired hepatocyte and pancreatic beta-cell damage, and regulated glucose metabolism. FZNP exhibited superior effects compared to FX, leading to improved glucose transport and decreased oxidative stress.
Fucoxanthin (FX) is a carotenoid from a marine origin that has an important role in our health, especially in the regulation and alleviation of type 2 diabetes. Its specific molecular structure makes it very unstable, which greatly affects its delivery in the body. In this study, FX was encapsulated in a mono-carrier using a hydrolyzed zein to form a nanocomplex with a stable structure and chemical properties (FZNP). Its stability was demonstrated by characterization and the efficacy of FX before and after encapsulation in alleviating diabetes in mice, which was evaluated by in vivo experiments. FZNP reduced the level of fasting blood glucose and restored it to normal levels in T2DM mice, which was not caused by a decrease in food intake, and effectively reduced oxidative stress in the organism. Both FX and FZNP repaired the hepatocyte and pancreatic beta-cell damage, increased serum SOD and reduced INS values significantly, upregulated PI3K-AKT genes as well as CaMK and GNAs expression in the pancreas. FZNP increased ADPN and GSH-PX values more significantly and it decreased serum HOMA-IR and MDA values, upregulated GLUT2 expression, promoted glucose transport in pancreatic and hepatocytes, regulated glucose metabolism and glycogen synthesis with much superior effects than FX.

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