Neuroprotective effects of 2-heptyl-3-hydroxy-4-quinolone in HT22 mouse hippocampal neuronal cells

被引:5
|
作者
Selvaraj, Baskar [1 ,5 ,6 ]
Kim, Dae Woon
Park, Jin-Soo [2 ,3 ]
Kwon, Hak Cheol [3 ]
Lee, Heesu [4 ]
Yoo, Ki-Yeon [4 ]
Lee, Jae Wook [1 ,5 ,6 ]
机构
[1] Korea Inst Sci & Technol, Inst Nat Prod, Nat Prod Res Ctr, Gangnueng 25451, South Korea
[2] Gangneung Wonju Natl Univ, Coll Dent, Res Inst Oral Sci, Dept Biochem & Mol Biol, Kangnung, South Korea
[3] Korea Inst Sci & Technol, Inst Nat Prod, Nat Prod Informat Res Ctr, Gangnueng 25451, South Korea
[4] Gangneung Wonju Natl Univ, Inst Oral Sci, Coll Dent, Dept Oral Anat, Kangnung, South Korea
[5] Korea Inst Sci & Technol, Brain Sci Inst, Convergence Res Ctr Dementia, Gangnueng 02792, South Korea
[6] Univ Sci & Technol, Div Biomed Sci & Technol, Daejun 34113, South Korea
关键词
Quinolone; Glutamate; Neuroprotective effects; HT22 hippocampal neuronal cells; MAPK; OXIDATIVE STRESS; GLUTAMATE; KINASE; DEATH; AIF; MITOCHONDRIA; INHIBITION; ACTIVATION; APOPTOSIS; TOXICITY;
D O I
10.1016/j.bmcl.2021.128312
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The neuroprotective activity of 2-heptyl-3-hydroxy-4(1H)-quinolone (compound 1) was evaluated using the neurotoxicity of glutamate in the HT22 cell line. Compound 1, known as a signal molecule of the bacterial quorum-sensing system, protects neuronal cells from glutamate-induced neurotoxicity by inhibiting cellular Ca2+ uptake and glutamate-triggered ROS accumulation. MAPK signaling pathway inhibition by compound 1 was evaluated by immunoblotting the phosphorylation status of the proteins. Furthermore, pro-apoptotic protein levels and AIF translocation to the nucleus were found to be reduced by compound 1. In conclusion, compound 1 showed neuroprotective effects by inhibiting apoptotic neuronal cell death.
引用
收藏
页数:5
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