Suppr超能文献

二十二碳六烯酸通过大黄鱼TLR22-MAPK-PPARγ/Nrf2途径减轻棕榈酸诱导的巨噬细胞炎症()

Docosahexaenoic Acid Alleviates Palmitic Acid-Induced Inflammation of Macrophages via TLR22-MAPK-PPARγ/Nrf2 Pathway in Large Yellow Croaker ().

作者信息

Xu Dan, Cui Kun, Li Qingfei, Zhu Si, Zhang Junzhi, Gao Shengnan, Hao Tingting, Mai Kangsen, Ai Qinghui

机构信息

Key Laboratory of Aquaculture Nutrition and Feed (Ministry of Agriculture and Rural Affairs), Key Laboratory of Mariculture (Ministry of Education), Ocean University of China, 5 Yushan Road, Qingdao 266003, China.

Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, 1 Wenhai Road, Qingdao 266237, China.

出版信息

Antioxidants (Basel). 2022 Mar 31;11(4):682. doi: 10.3390/antiox11040682.

Abstract

Palmitic acid (PA) is a saturated fatty acid (SFA) that can cause an inflammatory response, while docosahexaenoic acid (DHA) is always used as a nutritional modulator due to its anti-inflammatory properties. However, the potential molecular mechanism is still not completely elucidated in fish. Herein, the PA treatment induced an inflammatory response in macrophages of large yellow croaker (). Meanwhile, the mRNA expression of Toll-like receptor (TLR)-related genes, especially , and the phosphorylation of the mitogen-activated protein kinase (MAPK) pathway were significantly upregulated by PA. Further investigation found that the PA-induced inflammatory response was suppressed by knockdown and MAPK inhibitors. Moreover, the results of the peroxisome proliferator-activated receptor γ (PPARγ) agonist and inhibitor treatment proved that PPARγ was involved in the PA-induced inflammation. PA treatment decreased the protein expression of PPARγ, while knockdown and MAPK inhibitors recovered the decreased expression. Besides, the PA-induced activation of Nrf2 was regulated by p38 MAPK. Furthermore, DHA-executed anti-inflammatory effects by regulating the phosphorylation of the MAPK pathway and expressions of PPARγ and Nrf2. Overall, the present study revealed that DHA alleviated PA-induced inflammation in macrophages via the TLR22-MAPK-PPARγ/Nrf2 pathway. These results could advance the understanding of the molecular mechanism of the SFA-induced inflammatory response and provide nutritional mitigative strategies.

摘要

棕榈酸(PA)是一种饱和脂肪酸(SFA),可引发炎症反应,而二十二碳六烯酸(DHA)因其抗炎特性常被用作营养调节剂。然而,鱼类中潜在的分子机制仍未完全阐明。在此,PA处理诱导了大黄鱼巨噬细胞的炎症反应。同时,PA显著上调了Toll样受体(TLR)相关基因的mRNA表达,尤其是 ,以及丝裂原活化蛋白激酶(MAPK)途径的磷酸化。进一步研究发现,敲低 和MAPK抑制剂可抑制PA诱导的炎症反应。此外,过氧化物酶体增殖物激活受体γ(PPARγ)激动剂和抑制剂处理的结果证明PPARγ参与了PA诱导的炎症。PA处理降低了PPARγ的蛋白表达,而敲低 和MAPK抑制剂可恢复降低的表达。此外,PA诱导的Nrf2激活受p38 MAPK调节。此外,DHA通过调节MAPK途径的磷酸化以及PPARγ和Nrf2的表达发挥抗炎作用。总体而言,本研究揭示了DHA通过TLR22-MAPK-PPARγ/Nrf2途径减轻PA诱导的巨噬细胞炎症。这些结果可促进对SFA诱导炎症反应分子机制的理解,并提供营养缓解策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e050/9032456/d2e232fcb77b/antioxidants-11-00682-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验