溶血磷脂酸(LPA)在tpa诱导的小鼠中枢性卒中后疼痛(CPSP)中的作用

Pain Research Pub Date : 2018-12-28 DOI:10.11154/PAIN.33.269
H. Ueda, Ryusei Iwamoto
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引用次数: 0

摘要

本文介绍了最近发表的关于小鼠脑卒中后中枢性疼痛(CPSP)新动物模型的开发及其通过溶血磷脂酸(LPA)信号传导的机制的出版物(doi.org/10.116/j.ynpai.2018.07.001)。在该模型中,用孟加拉玫瑰(30mg/kg,i.v.)和绿光(5000Lx)通过硬脑膜照射10min,在小鼠大脑中动脉(MCA)产生光化学诱导的血栓形成(PIT)。当使用250(Aδ)和2000 Hz(Aβ)刺激的电刺激诱导缩爪(EPW)测试时,在PIT模型中观察到双侧痛觉过敏。由于没有观察到明显的热或机械痛觉过敏,我们将组织纤溶酶原激活剂(tPA)联合治疗,在PIT开始6小时后以10mg/kg(i.v.)的剂量进行治疗。用tPA和PIT治疗的小鼠存活了至少18天,并且在电(EPW)、热和机械伤害感受测试中表现出稳定的双侧痛觉过敏,没有显著的行为异常,这使得疼痛评估变得困难。在LPA1和LPA3缺乏的小鼠中,这些试验中的痛觉过敏被完全消除。LPA 1/3受体拮抗剂Ki 16425以30 mg/kg(i.p.)每天两次,持续一周的全身治疗在很大程度上消除了已建立的和双侧的热和机械痛觉过敏。液相色谱-串联质谱仪(LC–MS⁄MS)分析显示,PIT诱导和tPA增强了体感皮层(S–I/II)LPA的产生,但在纹状体或腹后丘脑中没有。有趣的是,tPA联合PIT观察到内侧背侧丘脑(MD)中LPA的显著产生。MD中LPA的产生是否与情绪疼痛途径方面的双侧痛觉过敏有关尚不清楚。高度需要对包括岛叶皮层在内的各个大脑区域的LPA测量结果进行进一步分析,岛叶皮层具有左右连合。
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Involvement of lysophosphatidic acid (LPA) in tPA–induced central post stroke pain (CPSP) in mice
This article introduces the recent publication (doi.org/ 10 . 1016 /j.ynpai. 2018 . 07 . 001 ) on the development of new animal model for central post stroke pain ( CPSP ) and its mechanisms through lysophosphatidic acid (LPA) signaling in mice. In this model, the photochemically induced thrombosis (PIT) at middle cerebral artery (MCA) of mouse was made by use of Rose Bengal ( 30 mg/kg, i.v.) and irradiation by green light ( 5 , 000 Lx) for 10 min through the dura mater. Bilateral hyperalgesia in the PIT model was observed when electrical stimulation–induced paw withdrawal (EPW) test using 250 (A δ ) and 2000 Hz (A β ) stimulation was used. As no significant thermal or mecha nical hyperalgesia was observed, we combined the treatment with tissue plasminogen activator (tPA), which was treated at 10 mg/kg (i.v.) 6 h after the start of PIT. Mice treated with tPA and PIT survived and showed stable bilateral hyperalgesia in electrical (EPW), thermal and mechanical nociception tests at least for 18 days without signifi cant behavioral abnormality to make the pain assessment difficult. The hyperalgesia in these tests were completely abolished in mice deficient of LPA 1 and LPA 3 . The systemic treatments of LPA 1 / 3 –receptor antagonist, Ki 16425 at 30 mg/kg (i.p.) twice daily for a week largely abolished the established and bilateral thermal and mecha nical hyperalgesia. Liquid Chromatograph–tandem Mass Spectrometer (LC– MS ⁄ MS) analysis revealed the PIT–induced and tPA–enhanced production of LPA in somato sensory cortex (S–I/II), but not in striatum or ventroposterial thalamus. Interestingly, significant production of LPA in mediodorsal thalamus (MD) was observed by tPA–combined PIT. It remains whether the LPA production in MD is related to the bilateral hyperalgesia in terms of emotional pain pathway. Further analyses of LPA measurements in various brain regions including insular cortex, which has right and left commissure, are highly required.
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Pain Research
Pain Research CLINICAL NEUROLOGY-
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