Taoka Y, Okajima K, Uchiba M, Murakami K, Kushimoto S, Johno M, Naruo M, Okabe H, Takatsuki K
Department of Laboratory Medicine, Kumamoto University Medical School, Japan.
Crit Care Med. 1997 May;25(5):874-9. doi: 10.1097/00003246-199705000-00026.
Gabexate mesilate is a synthetic protease inhibitor capable of inhibiting both coagulation and cytokine production by monocytes. To investigate whether gabexate mesilate is useful for the prevention of posttraumatic spinal cord injury, we examined its effect on compression trauma-induced spinal cord injury in rats.
Prospective, randomized, blinded, controlled study.
Research laboratory at a university medical center.
Male Wistar rats weighing 300 to 350 g.
Spinal cord injury was induced by applying a 20-g weight extradurally to the spinal cord at the level of the 12th thoracic vertebra for 20 mins. Spinal cord injury was evaluated by assessing the motor function of the rats 24 hrs posttrauma. The accumulation of leukocytes and histologic changes in the injured spinal cord tissue also were examined. Rats received gabexate mesilate (10 or 20 mg/kg i.p.) 30 mins before or after the compressive trauma. The effects of heparin or an inactive derivative of activated factor X (a selective inhibitor of thrombin generation) on compressive trauma-induced spinal cord injury also were examined. Leukocytopenia was induced by the administration of nitrogen mustard.
The motor disturbances observed following traumatic spinal cord compression, evaluated by Tarlov's score, and the accumulation of leukocytes in the injured tissue, evaluated by measuring tissue myeloperoxidase activity, were markedly reduced by leukocyte depletion induced by nitrogen mustard and by pre- or posttreatment of animals with gabexate mesilate. Neither heparin nor the inactive derivative of activated factor X prevented the motor disturbances and the accumulation of leukocytes. Histologic examination demonstrated that intramedullary hemorrhages observed 24 hrs after trauma at the 12th thoracic vertebra were significantly attenuated by nitrogen mustard-induced leukocytopenia and the administration of gabexate mesilate.
The compression trauma-induced spinal cord injury demonstrated by this model was mainly mediated by leukocytes. Gabexate mesilate prevented spinal cord injury not by inhibiting coagulation, but by inhibiting the activation of leukocytes.
甲磺酸加贝酯是一种合成的蛋白酶抑制剂,能够抑制单核细胞的凝血和细胞因子生成。为研究甲磺酸加贝酯是否有助于预防创伤后脊髓损伤,我们检测了其对大鼠压迫性创伤诱导的脊髓损伤的影响。
前瞻性、随机、盲法、对照研究。
大学医学中心的研究实验室。
体重300至350克的雄性Wistar大鼠。
在第12胸椎水平硬膜外施加20克重物压迫脊髓20分钟,诱导脊髓损伤。创伤后24小时通过评估大鼠的运动功能来评价脊髓损伤。还检测了损伤脊髓组织中白细胞的聚集和组织学变化。大鼠在压迫性创伤前或后30分钟接受甲磺酸加贝酯(10或20毫克/千克腹腔注射)。还检测了肝素或活化因子X的无活性衍生物(凝血酶生成的选择性抑制剂)对压迫性创伤诱导的脊髓损伤的影响。通过给予氮芥诱导白细胞减少。
通过塔尔洛夫评分评估创伤性脊髓压迫后观察到的运动障碍,通过测量组织髓过氧化物酶活性评估损伤组织中白细胞的聚集,氮芥诱导的白细胞减少以及甲磺酸加贝酯对动物的预处理或后处理均使其明显减轻。肝素和活化因子X的无活性衍生物均不能预防运动障碍和白细胞聚集。组织学检查表明,第12胸椎创伤后24小时观察到的脊髓内出血因氮芥诱导的白细胞减少和甲磺酸加贝酯的给药而明显减轻。
该模型所显示的压迫性创伤诱导的脊髓损伤主要由白细胞介导。甲磺酸加贝酯预防脊髓损伤不是通过抑制凝血,而是通过抑制白细胞的活化。