del Cerro S, Arai A, Kessler M, Bahr B A, Vanderklish P, Rivera S, Lynch G
Center for the Neurobiology of Learning and Memory, University of California, Irvine 92717-3800.
Neurosci Lett. 1994 Feb 14;167(1-2):149-52. doi: 10.1016/0304-3940(94)91049-9.
The hypothesis that intense stimulation of NMDA receptors activates calpain was tested in long-term cultures of hippocampus. Slices prepared from 10-day-old rats were maintained for periods of up to 6 weeks and then assayed for a stable breakdown product that results from the proteolysis of spectrin by calpain. The breakdown product increased dramatically during the first 24 h after tissue preparation and then decreased to a low level that remained unchanged for weeks. NMDA caused a 2- to 3-fold increase in breakdown product that rose linearly with time (5-30 min) and was blocked by the receptor antagonist MK-801. The effect of NMDA was the same throughout the culture period and was dependent upon the concentration of extracellular calcium with no effect at 2 mM and maximal effect at 4 mM calcium. These results indicate that rapid activation of calpain occurs in undamaged hippocampal neurons following stimulation of NMDA receptors.
在海马体长期培养物中对强烈刺激NMDA受体激活钙蛋白酶的假说进行了测试。从10日龄大鼠制备的脑片维持长达6周的时间,然后检测一种由钙蛋白酶对血影蛋白进行蛋白水解产生的稳定降解产物。该降解产物在组织制备后的最初24小时内急剧增加,然后降至低水平并在数周内保持不变。NMDA使降解产物增加2至3倍,其随时间(5 - 30分钟)呈线性上升,并被受体拮抗剂MK - 801阻断。在整个培养期间,NMDA的作用相同,且依赖于细胞外钙的浓度,在2 mM钙时无作用,在4 mM钙时作用最大。这些结果表明,在未受损的海马神经元中,NMDA受体受到刺激后会迅速激活钙蛋白酶。