4.6 Article

The cannabinoid WIN55,212-2 protects against oxidized LDL-induced inflammatory response in murine macrophages

期刊

JOURNAL OF LIPID RESEARCH
卷 51, 期 8, 页码 2181-2190

出版社

ELSEVIER
DOI: 10.1194/jlr.M001511

关键词

atherosclerosis; TNF-alpha; ROS; inflammatory response; CB2 receptor; oxLDL

资金

  1. Shanghai Municipal Natural Science Foundation [09ZR1418100]
  2. Shanghai Subject Chief Scientist [08XD14026]
  3. National Natural Science Foundation of China
  4. Shanghai Jiao Tong University [YG08PETZD03]

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The endocannabinoid system has recently been attracted interest for its anti-inflammatory and anti-oxidative properties. In this study, we investigated the role of the endocannabinoid system in regulating the oxidized low-density lipoprotein (oxLDL)-induced inflammatory response in macrophages. RAW264.7 mouse macrophages and peritoneal macrophages isolated from Sprague-Dawley (SD) rats were exposed to oxLDL with or without the synthetic cannabinoid WIN55,212-2. To assess the inflammatory response, reactive oxygen species (ROS) and tumor necrosis factor alpha (TNF-alpha) levels were determined, and activation of the mitogen-activated protein kinase (MAPK) and nuclear factor (NF)-kappa B signaling pathways were assessed. We observed that: i) oxLDL strongly induced ROS generation and TNF-alpha secretion in murine macrophages; ii) oxLDL-induced TNF-alpha and ROS levels could be lowered considerably by WIN55,212-2 via inhibition of MAPK (ERK1/2) signaling and NF-kappa B activity; and iii) the effects of WIN55212-2 were attenuated by the selective CB2 receptor antagonist AM630.jlr These results demonstrate the involvement of the endocannabinoid system in regulating the oxLDL-induced inflammatory response in macrophages, and indicate that the CB2 receptor may offer a novel pharmaceutical target for treating atherosclerosis.-Hao, M-x., L-s. Jiang, N-y. Fang, J. Pu, L-h. Hu, L-H. Shen, W. Song, and B. He. The cannabinoid WIN55,212-2 protects against oxidized LDL-induced inflammatory response in murine macrophages. J. Lipid Res. 2010. 51: 2181-2190.

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