摘要
目的:观察胰岛素对急性脊髓损伤是否有保护作用及其可能的机理。方法:60只SD大鼠,雌雄不限,随机分为A组(损伤对照组)和B组(胰岛素组),每组各30只大鼠,Allen法建立脊髓损伤模型,B组给与1IU/kg的胰岛素,1日3次腹腔灌注,连续7d,A组给与等量同次数的生理盐水腹腔灌注,在伤后8h、第3d、第7d、第14d、第28d观察脊髓凋亡细胞,在第1d、第3d、第7d、第14d、第28d观察尼氏体和神经元数量、GAP-43阳性细胞、BBB评分。结果:B组神经元数量、GAP-43阳性细胞、BBB评分在多个时相点要好于A组(P<0.05或P<0.01),凋亡细胞B组明显少于A组(P<0.05或P<0.01)。结论:胰岛素能通过抑制脊髓神经细胞的凋亡坏死、促进神经轴突的修复和再生来达到保护脊髓神经细胞、促进功能恢复的目的。
Objective:To observe neuroprotective effects of insulin on traumatic spinal cord injury in rat models and discuss its potential mechanisms. Methods:60 SD rats were randomly divided into A group(control group) and B group(insulin group), with 30 rats in each group,The animal SCI model was established according to method Allen's,A group and B group were respectively infused with isotonic Na chloride or 1Iu/kg insulin through abdominal cavity,three times a day,for 7 days. apoptosis neurons were observed on 8 hours,3 days,7 days,14 days,and 28 days after SCI,and tigroid body,neurons,GAP-43 positive cells,and BBB scorn were measured on 1 day,3 days,7 days,14 days,and 28 days after SCI. Results:Neuron number, GAP-43 positive cells,and BBB score in multitude time points were significantly higher in B group than in A group(P〈0.05 or P〈0.01 ). The number of apoptosis neurons in B group was less than in A group's(P〈0.05 or P〈0.01). Conclusions:Insulin has neuroprotective effects on traumatic spinal cord injury in rat models. It can promote recovery of function by depressing apoptosis of neurons and promoting recovery and regeneration of neuraxon.
出处
《重庆医科大学学报》
CAS
CSCD
2008年第9期1103-1107,共5页
Journal of Chongqing Medical University