Akdemir Osman, Berksoy Ismail, Karaoğlan Alper, Barut Seref, Bilguvar Kaya, Cirakoğlu Beyazit, Sahan Elife, Colak Ahmet
Department of Neurosurgery, Taksim Education and Research Hospital, Istanbul, Turkey.
J Clin Neurosci. 2008 Jun;15(6):672-8. doi: 10.1016/j.jocn.2007.06.014. Epub 2008 Apr 2.
We investigated the therapeutic efficacy of Ac-DMQD-CHO, a caspase-3 inhibitor, and functional recovery in spinal cord injury in a rat model. Thirty rats were randomized into three groups of 10 each. In groups 2 and 3, spinal cord trauma was produced in the thoracic region. Group 3 rats were treated with Ac-DMQD-CHO. Treatment responses were evaluated based on histopathological and TUNEL staining findings at 24 h and 5 days post-injury. Neurologic performance was assessed during and following treatment. Twenty-four hours after injury, light microscopy examination revealed diffuse hemorrhagic necrosis, edema, vascular thrombi, and polymorphonuclear leukocyte infiltration in group 2 and 3 rats, but cavitation and demyelinization were less prominent in group 3. At this time point, treatment of the rats with Ac-DMQD-CHO significantly reduced the number of apoptotic cells. Traumatic injury to the spinal cord causes apoptosis and administration of Ac-DMQD-CHO decreases apoptosis and improves functional outcome.
我们在大鼠模型中研究了半胱天冬酶-3抑制剂Ac-DMQD-CHO对脊髓损伤的治疗效果及功能恢复情况。30只大鼠被随机分为三组,每组10只。第2组和第3组在胸段造成脊髓损伤。第3组大鼠用Ac-DMQD-CHO治疗。根据损伤后24小时和5天的组织病理学和TUNEL染色结果评估治疗反应。在治疗期间及治疗后评估神经功能表现。损伤后24小时,光学显微镜检查显示第2组和第3组大鼠存在弥漫性出血性坏死、水肿、血管血栓形成和多形核白细胞浸润,但第3组的空洞形成和脱髓鞘现象不那么明显。在这个时间点,用Ac-DMQD-CHO治疗大鼠可显著减少凋亡细胞的数量。脊髓创伤会导致细胞凋亡,而给予Ac-DMQD-CHO可减少细胞凋亡并改善功能结局。