Jiao Yiqun, Nadler J Victor
Department of Pharmacology and Cancer Biology, Duke University Medical Center, Box 3813, Durham, North Carolina 27710, USA.
Exp Neurol. 2007 Jun;205(2):569-82. doi: 10.1016/j.expneurol.2007.03.025. Epub 2007 Mar 30.
Mossy fiber sprouting and the genesis of ectopic granule cells contribute to reverberating excitation in the dentate gyrus of epileptic brain. This study determined whether the extent of sprouting after status epilepticus in rats correlates with the seizure-induced degeneration of GluR2-immunoreactive (GluR2+) hilar neurons (presumptive mossy cells) and also quantitated granule cell-like GluR2-immunoreactive hilar neurons. Stereological cell counting indicated that GluR2+ neurons account for 57% of the total hilar neuron population. Prolonged pilocarpine-induced status epilepticus killed 95% of these cells. A smaller percentage of GluR2+ neurons (74%) was killed when status epilepticus was interrupted after 1-3.5 h with a single injection of phenobarbital, and the number of residual GluR2+ neurons varied among animals by a factor of 6.2. GluR2+ neurons were not necessarily more vulnerable than other hilar neurons. In rats administered phenobarbital, the extent of recurrent mossy fiber growth varied inversely and linearly with the number of GluR2+ hilar neurons that remained intact (P=0.0001). Thus the loss of each GluR2+ neuron was associated with roughly the same amount of sprouting. These findings support the hypothesis that mossy fiber sprouting is driven largely by the degeneration of and/or loss of innervation from mossy cells. Granule cell-like GluR2-immunoreactive neurons were rarely encountered in the hilus of control rats, but increased 6- to 140-fold after status epilepticus. Their number did not correlate with the extent of hilar cell death or mossy fiber sprouting in the same animal. The morphology, number, and distribution of these neurons suggested that they were hilar ectopic granule cells.
苔藓纤维发芽和异位颗粒细胞的产生有助于癫痫大脑齿状回中的反复性兴奋。本研究确定了大鼠癫痫持续状态后发芽的程度是否与癫痫发作诱导的GluR2免疫反应性(GluR2+)海马门区神经元(假定的苔藓细胞)的退化相关,并且还对颗粒细胞样的GluR2免疫反应性海马门区神经元进行了定量分析。体视学细胞计数表明,GluR2+神经元占海马门区神经元总数的57%。长时间匹罗卡品诱导的癫痫持续状态杀死了这些细胞中的95%。当癫痫持续状态在1 - 3.5小时后通过单次注射苯巴比妥中断时,较小比例的GluR2+神经元(74%)被杀死,并且残留的GluR2+神经元数量在不同动物之间相差6.2倍。GluR2+神经元不一定比其他海马门区神经元更易受损。在给予苯巴比妥的大鼠中,反复的苔藓纤维生长程度与保持完整的GluR2+海马门区神经元数量呈反比且呈线性关系(P = 0.0001)。因此,每个GluR2+神经元的损失与大致相同数量的发芽相关。这些发现支持了苔藓纤维发芽主要由苔藓细胞的退化和/或神经支配丧失所驱动的假说。颗粒细胞样的GluR2免疫反应性神经元在对照大鼠的海马门区很少见,但在癫痫持续状态后增加了6至140倍。它们的数量与同一动物中海马门区细胞死亡程度或苔藓纤维发芽程度无关。这些神经元的形态、数量和分布表明它们是海马门区异位颗粒细胞。