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Evidence of functional mossy fiber sprouting in hippocampal formation of kainic acid-treated rats

机译:海藻酸治疗大鼠海马结构中功能性苔藓纤维出芽的证据

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摘要

In the rat hippocampal formation, degeneration of CA4-derived afferent fibers provokes the growth of mossy fiber collaterals into the fascia dentata. These aberrant fibers subsequently form granule cell-granule cell synapses. The hippocampal slice preparation was employed to determine whether these recurrent connections are electrophysiologically functional. Hippocampal slices were prepared 12 to 21 days after the bilateral destruction of CA4 neurons with either intracerebroventricular or intravenous kainic acid (KA). In slices from control rats, antidromic stimulation of the mossy fibers elicited a single population spike in the granular layer of the fascia dentata. In contrast, when slices from some KA-treated rats were similarly tested, antidromic stimulation elicited multiple population spikes. This effect was not reproduced by blocking inhibitory transmission with bicuculline methiodide. Slices from other KA-treated rats fired a single population spike, but an antidromic conditioning volley increased the amplitude of a subsequent antidromic population spike by 5 to 15%. In slices from control rats, on the other hand, an antidromic conditioning volley always either decreased or failed to alter the amplitude of an antidromic test response. Superfusion with Ca2+-free medium containing 3.8 mM Mg2+ reversibly abolished all effects of KA administration. Abnormal responses to antidromic stimulation correlated with the loss of CA4 neurons and the growth of supragranular mossy fiber collaterals in the same animals. These results suggest that supragranular mossy fiber collateral sprouts form a functional recurrent excitatory circuit. These aberrant connections may further compromise hippocampal function already disrupted by neuronal degeneration, such as by facilitating seizure activity.
机译:在大鼠海马结构中,源自CA4的传入纤维的变性促使苔藓纤维侧支生长到齿状筋膜中。这些异常纤维随后形成颗粒细胞-颗粒细胞突触。使用海马切片制剂来确定这些复发性连接是否具有电生理功能。在用脑室内或静脉内的海藻酸(KA)双向破坏CA4神经元后的12至21天,准备海马切片。在来自对照大鼠的切片中,对苔藓纤维的抗皮肤刺激在齿状筋膜的颗粒层中引起单个种群峰值。相反,当对来自一些用KA治疗的大鼠的切片进行类似测试时,抗皮肤刺激会引起多个种群峰值。通过用双瓜氨酸甲硫脲阻断抑制性传播不能重现这种效果。来自其他用KA治疗的大鼠的切片发射单个种群尖峰,但是抗病态性抽空使随后的抗蠕虫性种群峰值的幅度增加了5%至15%。另一方面,在来自对照大鼠的切片中,抗体质性排球总是会降低或无法改变抗体质测试反应的幅度。含3.8 mM Mg2 +的无Ca2 +培养基的可逆性可逆地消除了KA施用的所有作用。在同一只动物中,对抗线刺激的异常反应与CA4神经元的丢失和肾上苔藓纤维侧支的生长有关。这些结果表明,肌上苔藓纤维侧芽形成了功能性的反复性兴奋回路。这些异常连接可能进一步损害已经被神经元变性破坏的海马功能,例如通过促进癫痫发作活动。

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