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姜黄提取物及其硒纳米粒子通过 Keap1/Nrf2/HO-1 通路对卡拉胶诱导的大鼠足肿胀的细胞保护/抗氧化作用的新见解。

New Insight on the Cytoprotective/Antioxidant Pathway Keap1/Nrf2/HO-1 Modulation by Extract and Its Selenium Nanoparticles in Rats with Carrageenan-Induced Paw Edema.

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, Princess Nourah bint Abdulrahman University, Riyadh 11671, Saudi Arabia.

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Tanta University, Tanta 31527, Egypt.

出版信息

Mar Drugs. 2023 Aug 22;21(9):459. doi: 10.3390/md21090459.

Abstract

Currently, there is growing interest in exploring natural bioactive compounds with anti-inflammatory potential to overcome the side effects associated with the well-known synthetic chemicals. Algae are a rich source of bioactive molecules with numerous applications in medicine. Herein, the anti-inflammatory effect of alone or selenium nanoparticles loaded with (UISeNPs), after being fully characterized analytically, was investigated by a carrageenan-induced inflammation model. The pretreated groups with free extract (III and IV) and the rats pretreated with UISeNPs (groups V and VI) showed significant increases in the gene expression of Keap1, with fold increases of 1.9, 2.27, 2.4, and 3.32, respectively. Similarly, a remarkable increase in the Nrf2 gene expression, with 2.09-, 2.36-, 2.59-, and 3.7-fold increases, was shown in the same groups, respectively. Additionally, the groups III, IV, V, and VI revealed a significantly increased HO-1 gene expression with a fold increase of 1.48, 1.61, 1.87, and 2.84, respectively. Thus, both extract and the UISeNPs boost the expression of the cytoprotective/antioxidant pathway Keap1/Nrf2/HO-1, with the UISeNPs having the upper hand over the free extract. In conclusion, and UISeNPs have proven promising anti-inflammatory activity through mediating different underlying mechanisms.

摘要

目前,人们越来越感兴趣的是探索具有抗炎潜力的天然生物活性化合物,以克服众所周知的合成化学品的副作用。藻类是生物活性分子的丰富来源,在医学中有许多应用。在此,通过角叉菜胶诱导的炎症模型,研究了 单独或负载 的硒纳米粒子(UISeNPs)的抗炎作用, 在经过全面的分析性特征描述后。预处理组用游离 提取物(III 和 IV)和用 UISeNPs 预处理的大鼠(V 和 VI 组)显示 Keap1 基因表达显著增加,分别增加了 1.9、2.27、2.4 和 3.32 倍。同样,Nrf2 基因表达也显著增加,分别增加了 2.09、2.36、2.59 和 3.7 倍。此外,III、IV、V 和 VI 组均显示 HO-1 基因表达显著增加,分别增加了 1.48、1.61、1.87 和 2.84 倍。因此, 提取物和 UISeNPs 都能增强细胞保护/抗氧化途径 Keap1/Nrf2/HO-1 的表达,UISeNPs 比游离提取物更有优势。总之, 和 UISeNPs 通过介导不同的潜在机制证明了具有有希望的抗炎活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73ed/10533125/fa86518c91e4/marinedrugs-21-00459-g001a.jpg

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