Department of Neurosurgery, Henry Ford Health System, Detroit, Michigan 48202, USA.
J Neurotrauma. 2010 Sep;27(9):1625-34. doi: 10.1089/neu.2010.1359.
Traumatic brain injury (TBI) elicits a strong inflammatory response that contributes to the acute pathological processes seen following TBI, including cerebral edema and disruption of the blood-brain barrier (BBB), in addition to longer-term neurological damage and cognitive impairment. Proteasome inhibitors reduce vascular thrombotic and inflammatory events and consequently protect vascular function. In the present study we evaluated the neuroprotective effect of Velcade (bortezomib), a potent and selective inhibitor of proteasomes, which is in clinical use for the treatment of multiple myeloma. When administered within 2 h after TBI onset, Velcade reduced inflammatory responses, lesion volume, and neurological functional deficits, and enhanced neuronal survival. Western blot and ELISA showed that Velcade decreased the expression of NF-κB. These results suggest that in the experimental setting, Velcade is an effective neuroprotective agent for the treatment of TBI.
创伤性脑损伤 (TBI) 会引发强烈的炎症反应,这有助于解释 TBI 后出现的急性病理过程,包括脑水肿和血脑屏障 (BBB) 破坏,以及更长期的神经损伤和认知障碍。蛋白酶体抑制剂可减少血管血栓形成和炎症事件,从而保护血管功能。在本研究中,我们评估了 Velcade(硼替佐米)的神经保护作用,Velcade 是一种有效的蛋白酶体抑制剂,目前用于治疗多发性骨髓瘤。在 TBI 发作后 2 小时内给药,Velcade 可降低炎症反应、损伤体积和神经功能缺陷,并增强神经元存活。Western blot 和 ELISA 显示 Velcade 降低了 NF-κB 的表达。这些结果表明,在实验环境中,Velcade 是治疗 TBI 的有效神经保护剂。