Kanter Mehmet
Department of Histology and Embryology, Faculty of Medicine, Trakya University, Edirne, Turkey.
Neurochem Res. 2008 Nov;33(11):2241-9. doi: 10.1007/s11064-008-9702-0. Epub 2008 Apr 22.
The goal of this study was designed to evaluate the possible protective effects of Nigella sativa (NS) on the neuronal injury in the frontal cortex and brain stem after chronic toluene exposure in rats. The rats were randomly alotted into one of three experimental groups: A (control), B (toluene treated) and C (toluene treated with NS); each group contain 10 animals. Control group received 1 ml serum physiologic and toluene treatment was performed by inhalation of 3,000 ppm toluene, in a 8 h/day and 6 day/week order for 12 weeks. The rats in NS treated group was given NS (in a dose of 400 mg/kg body weight) once a day orally by using intra gastric intubation for 12 weeks starting just after toluene exposure. Tissue samples were obtained for histopathological investigation. To date, no histopathological changes of neurodegeneration in the frontal cortex and brain stem after chronic toluene exposure in rats by NS treatment have been reported. In this study, chronic toluene exposure caused severe degenerative changes, shrunken cytoplasma, severely dilated cisternae of endoplasmic reticulum, markedly swollen mitochondria with degenerated cristae and nuclear membrane breakdown with chromatin disorganization in neurons of the frontal cortex and brain stem. The nerve cells showing the pathologic changes were almost absent in the NS-treated rats. We conclude that NS therapy causes morphologic improvement on neurodegeneration in frontal cortex and brain stem after chronic toluene exposure in rats. We believe that further preclinical research into the utility of NS may indicate its usefulness as a potential treatment on neurodegeneration after chronic toluene exposure in rats.
本研究旨在评估黑种草(NS)对大鼠慢性甲苯暴露后额叶皮质和脑干神经元损伤的可能保护作用。将大鼠随机分为三个实验组之一:A组(对照组)、B组(甲苯处理组)和C组(甲苯加NS处理组);每组包含10只动物。对照组接受1毫升生理盐水,甲苯处理组通过吸入3000 ppm甲苯进行处理,每天8小时,每周6天,持续12周。NS处理组的大鼠在甲苯暴露后立即开始,每天经胃内插管口服给予NS(剂量为400毫克/千克体重),持续12周。获取组织样本进行组织病理学研究。迄今为止,尚未有关于NS治疗大鼠慢性甲苯暴露后额叶皮质和脑干神经退行性变的组织病理学变化的报道。在本研究中,慢性甲苯暴露导致额叶皮质和脑干神经元出现严重的退行性变化、细胞质萎缩、内质网池严重扩张、线粒体明显肿胀且嵴退化以及核膜破裂和染色质紊乱。在NS处理的大鼠中,几乎没有显示出病理变化的神经细胞。我们得出结论,NS治疗可使大鼠慢性甲苯暴露后额叶皮质和脑干的神经退行性变在形态上得到改善。我们认为,对NS效用的进一步临床前研究可能表明其作为大鼠慢性甲苯暴露后神经退行性变潜在治疗方法的有用性。