Eells J B, Clough R W, Browning R A
Department of Physiology, Southern Illinois University, School of Medicine, Carbondale 62901, USA.
Brain Res Bull. 1998 Sep 15;47(2):155-61. doi: 10.1016/s0361-9230(98)00055-0.
Generalized tonic-clonic seizures of brain stem origin in rats are associated with acute induction of neuronal Fos in several discrete regions of the brain. One particular site in the dorsal pons shows remarkable Fos induction following generalized tonic seizures induced by maximal electroshock in normal rats or by audiogenic stimulation in genetically epilepsy-prone rats (GEPRs). Although this area shows the most intense Fos induction of any brain area following generalized tonic seizures, its identity has been uncertain. Based on its general location, we hypothesized that this nucleus was either 1) a component of the pedunculopontine tegmentum nucleus-pars compacta (PPTn-pc) or 2) the superior lateral subnucleus of lateral parabrachial area (LPBsl). The present study used Fos-protein immunocytochemistry in combination with the reduced form of nicotinamide-adenine dinucleotide phosphate (NADPH)-diaphorase histochemistry, cholecystokinin (CCK) immunocytochemistry, and neuronal tract-tracing to determine the identity of this cluster of Fos-immunoreactive neurons in the dorsal pons. Following maximal electroshock seizure (MES), Fos labeling was compared to NADPH diaphorase staining (a marker for cholinergic neurons of the PPTn-pc); retrograde transport of wheat germ agglutinin-horseradish peroxidase (WGA-HRP) injected into the ventromedial nucleus of the hypothalamus (VMH; to identify the LPBsl) or CCK immunoreactivity (also a marker for LPBsl neurons). Results showed this cluster of Fos immunoreactive (FI) neurons to be closely associated, but not overlapping, with the lateral and most caudal aspect of the PPTn-pc. Alternatively, WGA-HRP retrograde-labeled neurons corresponded precisely with the seizure-induced FI neurons. Additionally, the location of CCK immunoreactive neurons directly overlapped with the FI neurons, although they were not nearly as prevalent. These results demonstrate that the seizure-induced FI neurons in this area are neurons of the LPBsl and not cholinergic neurons of the PPTn-pc. This is the first report of seizure-induced Fos expression specifically localized to the superior lateral subnucleus of the lateral parabrachial area.
大鼠脑干起源的全身性强直阵挛性发作与大脑几个离散区域中神经元Fos的急性诱导有关。在正常大鼠中通过最大电休克或在遗传性癫痫易感大鼠(GEPRs)中通过听源性刺激诱导全身性强直发作后,脑桥背侧的一个特定部位显示出显著的Fos诱导。尽管该区域在全身性强直发作后显示出比任何脑区都更强的Fos诱导,但它的身份一直不确定。根据其大致位置,我们推测这个核要么是1)脚桥被盖核致密部(PPTn-pc)的一个组成部分,要么是2)臂旁外侧区上外侧亚核(LPBsl)。本研究使用Fos蛋白免疫细胞化学结合还原型烟酰胺腺嘌呤二核苷酸磷酸(NADPH)-黄递酶组织化学、胆囊收缩素(CCK)免疫细胞化学和神经束追踪来确定脑桥背侧这群Fos免疫反应性神经元的身份。在最大电休克发作(MES)后,将Fos标记与NADPH黄递酶染色(PPTn-pc胆碱能神经元的标志物)进行比较;将注射到下丘脑腹内侧核(VMH;用于识别LPBsl)的小麦胚凝集素-辣根过氧化物酶(WGA-HRP)的逆行运输或CCK免疫反应性(也是LPBsl神经元的标志物)进行比较。结果显示这群Fos免疫反应性(FI)神经元与PPTn-pc的外侧和最尾端部分密切相关,但不重叠。另外,WGA-HRP逆行标记的神经元与癫痫诱导的FI神经元精确对应。此外,CCK免疫反应性神经元的位置与FI神经元直接重叠,尽管它们的数量没有那么多。这些结果表明该区域癫痫诱导的FI神经元是LPBsl的神经元,而不是PPTn-pc的胆碱能神经元。这是首次报道癫痫诱导的Fos表达特异性定位于臂旁外侧区上外侧亚核。