Rebel Andrew A, Urquhart Siri A, Puig Kendra L, Ghatak Atreyi, Brose Stephen A, Golovko Mikhail Y, Combs Colin K
Department of Biology, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota.
Department of Basic Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota.
J Neurosci Res. 2015 Aug;93(8):1279-92. doi: 10.1002/jnr.23578. Epub 2015 Feb 22.
The purpose of this study was to characterize behavioral and physiological effects of a selective thromboxane (TP) receptor antagonist, SQ 29,548, in the C57Bl/6 mouse model. At 6 months of age, male mice were given either sham or drug i.p. injections for 3 days at a dose of 2 mg/kg each day. On the day after the final injection, mice were subjected to behavioral testing before brain collection. Left hemisphere hippocampi were collected from all mice for protein analysis via Western blot. Right brain hemispheres were fixed and embedded in gelatin and then serially sectioned. The sections were immunostained with anti-c-Fos antibodies. Prostaglandin analysis was performed from remaining homogenized brain samples, minus the hippocampi. Injection of SQ 29,548 decreased selective brain prostaglandin levels compared with sham controls. This correlated with robust increases in limbic-region c-Fos immunoreactivity in the SQ 29,548-injected mice. However, drug-treated mice demonstrated no significant changes in relevant hippocampal protein levels compared with sham treatments, as determined from Western blots. Surprisingly, injection of SQ 29,548 caused mixed changes in parameters of depression and anxiety-like behavior in the mice. In conclusion, the results indicate that administration of peripheral TP receptor antagonists alters brain levels of prostanoids and influences neuronal activity, with only minimal alterations of behavior. Whether the drug affects neurons directly or through a secondary pathway involving endothelium or other tissues remains unclear.
本研究的目的是在C57Bl/6小鼠模型中表征选择性血栓素(TP)受体拮抗剂SQ 29,548的行为和生理效应。6月龄雄性小鼠每天腹腔注射2mg/kg的生理盐水或药物,持续3天。末次注射后次日,小鼠在取脑前接受行为测试。收集所有小鼠的左侧海马用于蛋白质印迹法进行蛋白质分析。右侧脑半球固定并包埋于明胶中,然后进行连续切片。切片用抗c-Fos抗体进行免疫染色。从剩余的匀浆脑样本(不含海马)中进行前列腺素分析。与假手术对照组相比,注射SQ 29,548可降低选择性脑前列腺素水平。这与注射SQ 29,548的小鼠边缘区c-Fos免疫反应性的显著增加相关。然而,从蛋白质印迹法测定结果来看,与假手术处理相比,药物处理小鼠的相关海马蛋白水平没有显著变化。令人惊讶的是,注射SQ 29,548导致小鼠抑郁和焦虑样行为参数出现混合变化。总之,结果表明外周TP受体拮抗剂的给药会改变脑内前列腺素水平并影响神经元活动,而行为改变极小。该药物是直接影响神经元还是通过涉及内皮或其他组织的次要途径发挥作用仍不清楚。