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补充肉桂醛可逆转饮食诱导肥胖大鼠模型中的内皮功能障碍:NF-E2相关因子2的作用

Cinnamaldehyde Supplementation Reverts Endothelial Dysfunction in Rat Models of Diet-Induced Obesity: Role of NF-E2-Related Factor-2.

作者信息

Sena Cristina M, Pereira Ana, Seiça Raquel M

机构信息

Institute of Physiology, iCBR, Faculty of Medicine, University of Coimbra, Sub-unidade 1, Pólo III, Azinhaga de Santa Comba, Celas, 3000-548 Coimbra, Portugal.

出版信息

Antioxidants (Basel). 2022 Dec 30;12(1):82. doi: 10.3390/antiox12010082.

Abstract

Cinnamaldehyde (CN) is an activator of NF-E2-related factor 2 (Nrf2), which has the potential to reduce endothelial dysfunction, oxidative stress and inflammation in metabolic disorders. Our main purpose was to evaluate the effects of CN on vascular dysfunction in metabolic syndrome rats. Normal Wistar (W) rats were divided into eight groups: (1) Wistar (W) rats; (2) W rats fed with a high-fat diet (WHFD); (3) W rats fed with a sucrose diet (WS); (4) WHFD fed with a sucrose diet (WHFDS); (5) W treated with CN (WCn); (6) WS treated with CN (WSCn); (7) WHFD treated with CN (WHFDCn); (8) WHFDS treated with CN (WHFDSCn). CN treatment with 20 mg/kg/day was administered for 8 weeks. Evaluation of metabolic profile, inflammation, endothelial function, oxidative stress, eNOS expression levels and Nrf2 activation was performed. The metabolic dysfunction was greatly exacerbated in the WHFDS rats, accompanied by significantly higher levels of vascular oxidative stress, inflammation, and endothelial dysfunction. In addition, the WHFDS rats displayed significantly reduced activity of Nrf2 at the vascular level. CN significantly reverted endothelial dysfunction in the aortas and the mesenteric arteries. In addition, CN significantly decreased vascular oxidative damage, inflammation at vascular and perivascular level and up-regulated Nrf2 activity in the arteries of WHFDS rats. Cinnamaldehyde, an activator of Nrf2, can be used to improve metabolic profile, and to revert endothelial dysfunction in obesity and metabolic syndrome.

摘要

肉桂醛(CN)是核因子E2相关因子2(Nrf2)的激活剂,它有可能减轻代谢紊乱中的内皮功能障碍、氧化应激和炎症。我们的主要目的是评估CN对代谢综合征大鼠血管功能障碍的影响。正常Wistar(W)大鼠分为八组:(1)Wistar(W)大鼠;(2)高脂饮食喂养的W大鼠(WHFD);(3)蔗糖饮食喂养的W大鼠(WS);(4)高脂饮食加蔗糖饮食喂养的大鼠(WHFDS);(5)用CN处理的W大鼠(WCn);(6)用CN处理的WS大鼠(WSCn);(7)用CN处理的WHFD大鼠(WHFDCn);(8)用CN处理的WHFDS大鼠(WHFDSCn)。以20mg/kg/天的剂量给予CN处理,持续8周。进行代谢谱、炎症、内皮功能、氧化应激、内皮型一氧化氮合酶(eNOS)表达水平和Nrf2激活的评估。WHFDS大鼠的代谢功能障碍大大加剧,同时伴有血管氧化应激、炎症和内皮功能障碍水平显著升高。此外,WHFDS大鼠在血管水平上Nrf2的活性显著降低。CN显著逆转了主动脉和肠系膜动脉的内皮功能障碍。此外,CN显著降低了血管氧化损伤、血管和血管周围水平的炎症,并上调了WHFDS大鼠动脉中的Nrf2活性。肉桂醛作为Nrf2的激活剂,可用于改善代谢谱,并逆转肥胖和代谢综合征中的内皮功能障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7457/9854673/c1e15d9d4cf4/antioxidants-12-00082-g001.jpg

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