Yu C G, Marcillo A E, Fairbanks C A, Wilcox G L, Yezierski R P
The Miami Project, University of Miami School of Medicine, FL, 33136, USA.
Neuroreport. 2000 Sep 28;11(14):3203-7. doi: 10.1097/00001756-200009280-00031.
Clinically effective drug treatments for spinal cord injury (SCI) remain unavailable. Agmatine, an NMDA receptor antagonist and inhibitor of nitric oxide synthase (NOS), is an endogenous neuromodulator found in the brain and spinal cord. Evidence is presented that agmatine significantly improves locomotor function and reduces tissue damage following traumatic SCI in rats. The results suggest the importance of future therapeutic strategies encompassing the use of single drugs with multiple targets for the treatment of acute SCI. The therapeutic targets of agmatine (NMDA receptor and NOS) have been shown to be critically linked to the pathophysiological sequelae of CNS injury and this, combined with the non-toxic profile, lends support to agmatine being considered as a potential candidate for future clinical applications.
目前仍没有临床上有效的脊髓损伤(SCI)药物治疗方法。胍丁胺是一种N-甲基-D-天冬氨酸(NMDA)受体拮抗剂和一氧化氮合酶(NOS)抑制剂,是一种存在于大脑和脊髓中的内源性神经调节剂。有证据表明,胍丁胺能显著改善大鼠创伤性脊髓损伤后的运动功能,并减少组织损伤。结果表明,未来治疗策略中使用具有多个靶点的单一药物治疗急性脊髓损伤具有重要意义。胍丁胺的治疗靶点(NMDA受体和NOS)已被证明与中枢神经系统损伤的病理生理后遗症密切相关,再加上其无毒特性,这支持将胍丁胺视为未来临床应用的潜在候选药物。