Ong Wei-Yi, Lu Xin-Rong, Ong Benjamin Kian-Chung, Horrocks Lloyd A, Farooqui Akhlaq A, Lim Sai-Kiang
Department of Anatomy, National University of Singapore, Singapore 119260.
Exp Brain Res. 2003 Feb;148(4):521-4. doi: 10.1007/s00221-002-1315-2. Epub 2002 Dec 11.
The present investigation was carried out to study the possible effects of quinacrine in modulating cytoplasmic phospholipase A(2) (cPLA(2)) mRNA levels in rat hippocampus after kainate treatment. Injections of kainate into the right lateral ventricle resulted in significant increases in cPLA(2) mRNA levels in the hippocampus, at 3 days and 7 days after injection. The elevation in cPLA(2) mRNA levels is consistent with previous observations of increased cPLA(2) immunoreactivity in degenerating neurons and astrocytes at these times. Rats that received once daily intraperitoneal injections of quinacrine (5 mg/kg) after the intracerebroventricular kainate injections showed almost complete attenuation of increased cPLA(2) expression, at both 3 and 7 days after kainate injection. These results show that in addition to its well-known effect of inhibition of PLA(2) activity, quinacrine could also inhibit cPLA(2) expression, and further supports a role for PLA(2) in kainate-induced neuronal injury.
本研究旨在探讨奎纳克林对海藻酸处理后大鼠海马中细胞质磷脂酶A2(cPLA2)mRNA水平的可能调节作用。向右侧脑室注射海藻酸后,在注射后3天和7天,海马中cPLA2 mRNA水平显著升高。cPLA2 mRNA水平的升高与之前在这些时间点退化的神经元和星形胶质细胞中cPLA2免疫反应性增加的观察结果一致。在脑室内注射海藻酸后,每天一次腹腔注射奎纳克林(5 mg/kg)的大鼠在海藻酸注射后3天和7天,cPLA2表达增加几乎完全被抑制。这些结果表明,除了其众所周知的抑制磷脂酶A2(PLA2)活性的作用外,奎纳克林还可以抑制cPLA2表达,并进一步支持PLA2在海藻酸诱导的神经元损伤中的作用。