摘要
目的:建立一压力可控型椎间盘退变模型,并探讨持久的脊柱负荷对椎间盘MMP-2表达的影响。方法:选用54只成年Wistar大鼠随机分为三组,分别模拟人类在站立(A组1.12N)、坐位直立(B组1.68N)、坐位前屈(C组3.08N)三种状态下椎间盘内的负荷情况,给予大鼠尾椎Co9/10椎间盘恒定压力加压,以相邻Co8/9椎间盘不加压作为对照(D组)。三组分别在3、7、14天后取受压及对照椎间盘标本,进行HE染色组织学观察及免疫组织化学分析,观察椎间盘退变情况及MMP-2在椎间盘组织中的含量变化。结果:随时间与压力的增加,椎间盘组织学评分与MMP-2表达增高(P<0.05),MMP-2表达与椎间盘退变程度成正相关(r=0.870,P<0.05)。结论:持久的脊柱负荷可引起椎间盘退变及MMP-2表达增加,MMP-2可能在椎间盘退变的过程中发挥重要作用。
Objective: To establish an in vivo mouse model of compression-control degeneration and to investigate the effects of prolonged mecanial loading on MMP2.Methods: A total of 54 adult Wistar rats were randomly divided into three groups,group A: the pressure was 1.12N(simulating human pressure of the disc when human stand),group B: the pressure was1.68N(simulating human sit-ting),group C: the pressure was 3.08N(simulating human sitting flexion).Group D: control group without any pressure to the disc.Static compression was applied to mouse coccygeal discs in vivo for 3,7,or 14 days.The expression of MMP-2 in four groups were detected by immunohistochemical technique.Results: The degeneration of disc and the expression of MMP-2 increased with the increasing of the time and pressure(P 0.05),and a positive correlation was observed between the degeneration grade of disc and the amount of MMP-2(r=0.870,P0.05).Conclusion: Prolonged spinal loading cause the disc degeneration and the increasing expression of MMP-2,MMP-2 may be one of the important factors leading to intervertebral disc degeneration.
出处
《现代生物医学进展》
CAS
2011年第14期2730-2733,共4页
Progress in Modern Biomedicine