Calderón-Vallejo Denisse, Quintanar-Stephano Andrés, Hernández-Jasso Irma, Jiménez-Hernández Violeta, Ruiz-Ornelas Jannet, Jiménez Ismael, Quintanar J Luis
Laboratory of Neurophysiology, Depto. de Fisiología y Farmacología, Centro de Ciencias Básicas, Universidad Autónoma de Aguascalientes, Av. Universidad 940, Col. Ciudad Universitaria, C.P. 20131, Aguascalientes, AGS, Mexico.
Neurochem Res. 2015 Mar;40(3):455-62. doi: 10.1007/s11064-014-1486-9. Epub 2015 Jan 25.
Several studies have shown that gonadotropin-releasing hormone (GnRH) have extra-pituitary roles, including neurotrophic effects. This study was to evaluate the effects of GnRH treatment on the spinal cord injury (SCI) of rats. Ovariectomized rats were divided into: sham SCI surgery (Sham), SCI treated with saline solution (SCI + SS), and SCI treated with GnRH (SCI + GnRH). The SCI was induced by compression. One day after the lesion, SCI + GnRH group was injected with GnRH (60 µg/kg/twice/day; i.m.) for 15 days and the other groups with saline solution. To kinematic gait analysis, length and velocity of the stride were measured. In spinal cord, axonal morphometry and spared white and gray matter were analyzed by histochemistry. Protein expression of spinophilin was evaluated by western blot. The results showed that, 5 weeks after the injury, the group of animals treated with GnRH, significantly increased the length and velocity of the stride compared to SCI + SS group and they were similar to Sham group. In spinal cord, GnRH treatment increased the number and caliber of nerve axons and in the case of white matter, spared tissue was significantly higher than those animals treated with saline solution. The expression of spinophilin in spinal cord of SCI + GnRH group was slightly increased with respect to those not treated. In conclusion, GnRH treatment improves recovery of gait and decreases histopathological damage in the injured spinal cord of rat. These findings suggest that GnRH acts as a neurotrophic factor and can be used as a potential therapeutic agent for treatment of SCI.
多项研究表明,促性腺激素释放激素(GnRH)具有垂体外作用,包括神经营养作用。本研究旨在评估GnRH治疗对大鼠脊髓损伤(SCI)的影响。将去卵巢大鼠分为:假SCI手术组(Sham)、生理盐水治疗的SCI组(SCI + SS)和GnRH治疗的SCI组(SCI + GnRH)。通过压迫诱导SCI。损伤后一天,SCI + GnRH组注射GnRH(60 μg/kg/每天两次;肌肉注射),持续15天,其他组注射生理盐水。进行运动步态分析,测量步幅长度和速度。在脊髓中,通过组织化学分析轴突形态学以及保留的白质和灰质。通过蛋白质印迹法评估亲环蛋白的蛋白表达。结果显示,损伤后5周,与SCI + SS组相比,接受GnRH治疗的动物组步幅长度和速度显著增加,且与Sham组相似。在脊髓中,GnRH治疗增加了神经轴突的数量和直径,对于白质而言,保留组织明显高于接受生理盐水治疗的动物。与未治疗的动物相比,SCI + GnRH组脊髓中亲环蛋白的表达略有增加。总之,GnRH治疗可改善大鼠损伤脊髓的步态恢复并减少组织病理学损伤。这些发现表明,GnRH作为一种神经营养因子,可作为治疗SCI的潜在治疗剂。