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脑桥网状结构神经元参与了由听源性点燃强化的全身性阵挛性癫痫发作的神经网络。

Pontine reticular formation neurons are implicated in the neuronal network for generalized clonic seizures which is intensified by audiogenic kindling.

作者信息

Raisinghani Manish, Faingold Carl L

机构信息

Department of Pharmacology, Southern Illinois University School of Medicine, PO Box 19629, Springfield, IL 62794-9629, USA.

出版信息

Brain Res. 2005 Dec 7;1064(1-2):90-7. doi: 10.1016/j.brainres.2005.09.047. Epub 2005 Dec 5.

Abstract

The caudal pontine reticular formation nucleus (cPRF) is implicated in seizure propagation to the spinal cord in several forms of generalized convulsive seizures, including audiogenic seizures (AGS). Focal microinjection studies implicate cPRF as a requisite neuronal network site subserving generalized AGS in the moderate severity substrain of genetically epilepsy-prone rats (GEPR-3s). AGS in GEPR-3s culminate in generalized clonus, but daily repetition of AGS (AGS kindling) results in an additional seizure behavior, facial and forelimb (F and F) clonus, not seen prior to kindling. This study examined cPRF neuronal firing changes and seizure behaviors during AGS in GEPR-3s. We examined extracellular cPRF neuronal responses to acoustic stimuli (12 kHz) and observed neuronal firing during AGS. cPRF neurons exhibited onset responses to acoustic stimuli before and after AGS kindling. After AGS kindling, increased neuronal firing occurred, and response latencies were prolonged. Tonic neuronal firing occurred during generalized clonus, which changed to burst firing after AGS kindling. Burst firing also occurred during F and F clonus. Increased neuronal firing and the change from tonic to burst firing suggest that AGS kindling involves increased cPRF excitability. These data support an important role for cPRF neurons in generation of generalized clonus in unkindled GEPR-3s, which is increased by AGS kindling. The increased cPRF response latency might reflect a greater role of rostral components of the AGS neuronal network in transmission of acoustic responses to cPRF. This study also suggests that cPRF neurons may be involved in F and F clonus, which was unexpected since F and F clonus is thought to originate primarily in forebrain structures.

摘要

尾侧脑桥网状结构核(cPRF)在多种全身性惊厥发作形式中,包括听源性惊厥(AGS),与癫痫发作向脊髓的传播有关。局灶性微量注射研究表明,在遗传易癫痫大鼠(GEPR - 3s)的中度严重亚系中,cPRF是全身性AGS所必需的神经网络位点。GEPR - 3s中的AGS最终会导致全身性阵挛,但每天重复AGS(AGS点燃)会导致一种额外的癫痫发作行为,即面部和前肢(F和F)阵挛,这在点燃之前是看不到的。本研究检查了GEPR - 3s中AGS期间cPRF神经元放电变化和癫痫发作行为。我们检查了cPRF神经元对听觉刺激(12 kHz)的细胞外反应,并观察了AGS期间的神经元放电。cPRF神经元在AGS点燃前后对听觉刺激均表现出起始反应。AGS点燃后,神经元放电增加,反应潜伏期延长。在全身性阵挛期间出现强直性神经元放电,在AGS点燃后变为爆发性放电。在F和F阵挛期间也出现爆发性放电。神经元放电增加以及从强直性放电到爆发性放电的变化表明,AGS点燃涉及cPRF兴奋性增加。这些数据支持cPRF神经元在未点燃的GEPR - 3s全身性阵挛产生中起重要作用,而AGS点燃会增强这种作用。cPRF反应潜伏期的增加可能反映了AGS神经网络的头侧成分在将听觉反应传递到cPRF中的更大作用。本研究还表明,cPRF神经元可能参与F和F阵挛,这是出乎意料的,因为F和F阵挛被认为主要起源于前脑结构。

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