Zheng Yi-Ran, Tufvesson-Alm Maximilian, Trepci Ada, Imbeault Sophie, Li Xue-Qi, Schwieler Lilly, Engberg Göran, Erhardt Sophie
Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Acta Neuropsychiatr. 2023 Aug 18;37:e18. doi: 10.1017/neu.2023.40.
We previously reported that dual injections of lipopolysaccharide (LPS) in mice constitute a valuable tool for investigating the contribution of inflammation to psychotic disorders. The present study investigated how immune activation affects the kynurenine pathway and rat behaviour of relevance for psychotic disorders.
Male Sprague Dawley rats were treated with either dual injections of LPS (0.5 mg/kg + 0.5 mg/kg, i.p.) or dual injections of saline. Twenty-four hours after the second injection, behavioural tests were carried out, including locomotor activity test, fear conditioning test, spontaneous alternation Y-maze test, and novel object recognition test. In a separate batch of animals, in vivo striatal microdialysis was performed, and tryptophan, kynurenine, quinolinic acid, and kynurenic acid (KYNA) in the dialysate were measured using ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS).
Dual-LPS treatment decreased spontaneous locomotion, exaggerated d-amphetamine-induced locomotor activity, and impaired recognition memory in male Sprague-Dawley rats. In vivo microdialysis showed that dual-LPS treatment elicited metabolic disturbances in the kynurenine pathway with increased extracellular levels of kynurenine and KYNA in the striatum.
The present study further supports the feasibility of using the dual-LPS model to investigate inflammation-related psychotic disorders and cognitive impairments.
我们之前报道过,对小鼠进行两次脂多糖(LPS)注射是研究炎症对精神障碍影响的一种有价值的工具。本研究调查了免疫激活如何影响犬尿氨酸途径以及与精神障碍相关的大鼠行为。
对雄性斯普拉格 - 道利大鼠进行两次LPS注射(0.5毫克/千克 + 0.5毫克/千克,腹腔注射)或两次生理盐水注射。第二次注射后24小时,进行行为测试,包括自发活动测试、恐惧条件反射测试、自发交替Y迷宫测试和新物体识别测试。在另一批动物中,进行体内纹状体微透析,并使用超高效液相色谱 - 串联质谱法(UPLC - MS/MS)测量透析液中的色氨酸、犬尿氨酸、喹啉酸和犬尿喹啉酸(KYNA)。
双重LPS处理降低了雄性斯普拉格 - 道利大鼠的自发活动,夸大了右旋苯丙胺诱导的活动,并损害了识别记忆。体内微透析显示,双重LPS处理引发了犬尿氨酸途径的代谢紊乱,纹状体中细胞外犬尿氨酸和KYNA水平升高。
本研究进一步支持了使用双重LPS模型来研究炎症相关精神障碍和认知障碍的可行性。