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首页> 外文期刊>Neuropharmacology >Trigeminal neuroplasticity underlies allodynia in a preclinical model of mild closed head traumatic brain injury (cTBI)
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Trigeminal neuroplasticity underlies allodynia in a preclinical model of mild closed head traumatic brain injury (cTBI)

机译:在轻度闭合性颅脑外伤(cTBI)的临床前模型中,三叉神经可塑性是异常性疼痛的基础

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Post-traumatic headache (PTH) following TBI is a common and often persisting pain disability. PTH is often associated with a multimodal central pain sensitization on the skin surface described as allodynia. However, the particular neurobiology underlying cTBI-induced pain disorders are not known. These studies were performed to assess trigeminal sensory sensitization and to determine if sensitization measured behaviorally correlated with detectable changes in portions of the trigeminal sensory system (TSS), particularly trigeminal nucleus, thalamus, and sensory cortex. Thermal stimulation is particularly well suited to evaluate sensitization and was used in these studies. Recent advances in the use of reward/conflict paradigms permit use of operant measures of behavior, versus reflex-driven response behaviors, for thermal sensitization studies. Thus, to quantitate facial thermal sensitization (allodynia) in the setting of acute TBI, the current study utilized an operant orofacial pain reward/conflict testing paradigm to assess facial thermal sensitivity in uninjured control animals compared with those two weeks after cTBI in a rodent model. Significant reductions in facial contact/lick behaviors were observed in the TBI animals using either cool or warm challenge temperatures compared with behaviors in the normal animals. These facial thermal sensitizations correlated with detectable changes in multiple levels of the TSS. The immunohistochemical (IHC) studies revealed significant alterations in the expression of the serotonin (5 HT), neurokinin 1 receptor (NK1R), norepinephrine (NE), and gamma-aminobutyric acid (GABA) in the caudal trigeminal nucleus, thalamic VPL/VPM nucleus, and sensory cortex of the orofacial pain pathways. There was a strong correlation between increased expression of certain IHC markers and increased behavioral markers for facial sensitization. The authors conclude that TBI-induced changes observed in the TSS are consistent with the expression of generalized facial allodynia following cTBI. To our knowledge, this is the first report of orofacial sensitization correlated with changes in selected neuromodulatorseurotransmitters in the TSS following experimental mild TBI. Published by Elsevier Ltd.
机译:TBI后的创伤后头痛(PTH)是常见且经常持续的疼痛残疾。 PTH通常与皮肤表面多态性中枢敏化有关,称为异常性疼痛。但是,尚不知道cTBI引起的疼痛障碍的具体神经生物学。进行这些研究是为了评估三叉神经感觉增敏作用,并确定在行为上测得的增敏作用是否与三叉神经感觉系统(TSS)部分,尤其是三叉神经核,丘脑和感觉皮层的可检测变化相关。热刺激特别适合评估敏化度,并已用于这些研究中。在奖励/冲突范式的使用方面的最新进展允许将行为的操作量度与反射驱动的反应行为进行热敏化研究。因此,为了量化急性TBI情况下的面部热敏性(异常性疼痛),当前的研究采用了操作性的脸部疼痛奖励/冲突测试范式来评估未受伤对照组动物的面部热敏性,与在啮齿类动物模型中进行cTBI后的两周相比。与正常动物的行为相比,在使用凉爽或温暖的挑战温度的TBI动物中,观察到的面部接触/舔行为明显减少。这些面部热敏化与TSS多个水平中的可检测变化相关。免疫组化(IHC)研究显示尾端三叉神经核,丘脑VPL / VPM中血清素(5 HT),神经激肽1受体(NK1R),去甲肾上腺素(NE)和γ-氨基丁酸(GABA)的表达发生了显着变化核和口面部疼痛途径的感觉皮层。某些IHC标记物的表达增加与面部敏化的行为标记物之间存在很强的相关性。作者得出的结论是,在TSS中观察到的TBI诱导的变化与cTBI后全身性异常性疼痛的表达一致。据我们所知,这是在轻度TBI实验后与TSS中所选神经调节剂/神经递质变化相关的口部增敏的首次报道。由Elsevier Ltd.发布

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