Yu Z, Cheng G, Huang X, Li K, Cao X
National Key Laboratory of Medical Neurobiology, Shanghai Medical University, People's Republic of China.
Neuroreport. 1997 Jul 7;8(9-10):2117-9. doi: 10.1097/00001756-199707070-00006.
Substance P (SP) has been implicated in immune responses and could increase glutamate release, and inflammatory reactions are known to be able to potentiate ischemic damage. We have previously found that SP was over-expressed in cerebral ischemia and speculated that SP may play a role in exacerbating ischemic damage. In this study, we examined whether a neurokinin-1 (NK-1) receptor antagonist, SR140333, would have an effect on brain ischemia. Intra-cerebroventricular (i.c.v.) administration of SR140333 (30 micrograms) markedly reduced (37.1 +/- 7.8%, p < 0.001) infarct volume measured 24 h after focal cerebral ischemia in the rat. The SR140333-treated group also exhibited a significantly improved neurological function reflected by the neurological deficit score. The results represented the first demonstration that a NK-1 receptor antagonist may be a novel type of drug for treatment of cerebral ischemia.
P物质(SP)与免疫反应有关,并且能够增加谷氨酸的释放,而炎症反应已知可增强缺血性损伤。我们之前发现SP在脑缺血中过度表达,并推测SP可能在加重缺血性损伤中发挥作用。在本研究中,我们检测了神经激肽-1(NK-1)受体拮抗剂SR140333是否会对脑缺血产生影响。大鼠局灶性脑缺血24小时后,脑室内(i.c.v.)注射SR140333(30微克)可显著减少梗死体积(37.1±7.8%,p<0.001)。经SR140333治疗的组在神经功能缺损评分方面也表现出神经功能显著改善。这些结果首次证明NK-1受体拮抗剂可能是一种新型的脑缺血治疗药物。