摘要
建立大白鼠全脑缺血动物模型,用RIA法及荧光分光光度计检测了缺血脑组织匀浆的LEK、β-EP.DynA1-13及 5-HT和 5-HIAA的含量,LEK在脑组织缺血 60 min时含量略下降,但无统计学意义;β-EP在脑组织缺血 30 min时显著下降(P<0. 05),缺血 60 min时下降非常显著(P<0. 01);DynA1-13和 5-HIAA含量在缺血 60 min时明显上升,而 5-HT含量则显著下降。上述结果提示内啡肽和单胺类介质均参与了缺血性脑损伤的病理过程。
Rats were used to establish an animal model of cerebral ischemia and the change of endogenous opiate peptides (LEK, β-EP, DynA1-13) and monoamines (5-HT, 5-HIAA) levels in the ischemia cerebral tissue were measured. The main findings were as follows: The levels of LEK reduced slightly in cerebral ischemia for 60 minutes, but the levels of DynA1-13 and 5-HIAA increased obviously in cerebral ischemia for 60 minutes. At the same time the levels of β-EP and 5-HT decreased obviously. The results suggest that the endogenous opiate peptides and monomines play a possible role in the development of cerebral ischemic damage.
出处
《临床神经病学杂志》
CAS
1995年第4期197-199,共3页
Journal of Clinical Neurology
关键词
脑缺血
内啡肽
单胺类介质
Cerebral ischemia LEK β-EP DynA1-13 5-HT 5-HIAA