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延迟使用利鲁唑治疗能够挽救受伤的大鼠脊髓运动神经元。

Delayed riluzole treatment is able to rescue injured rat spinal motoneurons.

作者信息

Nógrádi A, Szabó A, Pintér S, Vrbová G

机构信息

Laboratory of Neuromorphology, Department of Ophthalmology, Faculty of General Medicine, University of Szeged, Korányi fasor 10-11, 6720 Szeged, Hungary.

出版信息

Neuroscience. 2007 Jan 19;144(2):431-8. doi: 10.1016/j.neuroscience.2006.09.046. Epub 2006 Nov 2.

Abstract

The effect of delayed 2-amino-6-trifluoromethoxy-benzothiazole (riluzole) treatment on injured motoneurons was studied. The L4 ventral root of adult rats was avulsed and reimplanted into the spinal cord. Immediately after the operation or with a delay of 5, 10, 14 or 16 days animals were treated with riluzole (n=5 in each group) while another four animals remained untreated. Three months after the operation the fluorescent dye Fast Blue was applied to the proximal end of the cut ventral ramus of the L4 spinal nerve to retrogradely label reinnervating neurons. Three days later the spinal cords were processed for counting the retrogradely labeled cells and choline acetyltransferase immunohistochemistry was performed to reveal the cholinergic cells in the spinal cords. In untreated animals there were 20.4+/-1.6 (+/-S.E.M.) retrogradely labeled neurons while in animals treated with riluzole immediately or 5 and 10 days after ventral root avulsion the number of labeled motoneurons ranged between 763+/-36 and 815+/-50 (S.E.M.). Riluzole treatment starting at 14 and 16 days after injury resulted in significantly lower number of reinnervating motoneurons (67+/-4 and 52+/-3 S.E.M., respectively). Thus, riluzole dramatically enhanced the survival and reinnervating capacity of injured motoneurons not only when treatment started immediately after injury but also in cases when riluzole treatment was delayed for up to 10 days. These results suggest that motoneurons destined to die after ventral root avulsion are programmed to survive for some time after injury and riluzole is able to rescue them during this period of time.

摘要

研究了延迟给予2-氨基-6-三氟甲氧基苯并噻唑(利鲁唑)对损伤运动神经元的影响。将成年大鼠的L4腹侧神经根撕脱并重新植入脊髓。术后立即或延迟5、10、14或16天用利鲁唑治疗动物(每组n = 5),另有4只动物未治疗。术后三个月,将荧光染料固蓝应用于L4脊神经切断腹支的近端,以逆行标记再支配神经元。三天后,对脊髓进行处理以计数逆行标记的细胞,并进行胆碱乙酰转移酶免疫组织化学以显示脊髓中的胆碱能细胞。在未治疗的动物中,有20.4±1.6(±标准误)个逆行标记的神经元,而在腹侧神经根撕脱后立即或5天和10天用利鲁唑治疗的动物中,标记的运动神经元数量在763±36至815±50(标准误)之间。在损伤后14天和16天开始用利鲁唑治疗导致再支配运动神经元的数量显著降低(分别为67±4和52±3标准误)。因此,利鲁唑不仅在损伤后立即开始治疗时,而且在利鲁唑治疗延迟长达10天的情况下,都能显著提高损伤运动神经元的存活和再支配能力。这些结果表明,腹侧神经根撕脱后注定要死亡的运动神经元在损伤后被编程存活一段时间,利鲁唑能够在此期间挽救它们。

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