RESUMO
AIM: To study the protective effects of nimodipine liposomes for injection (NDLI) on injuries of total cerebral ischemia/reperfusion(I/R) in rats and anoxia in mice. METHODS: Acute anoxia in mice was produced by hypoxia under normal pressure and decapitation. In these two models the survival time and persistent time of gasping were observed. Ameliorated pulsinelli four-vessel occlusion method was used to make global brain ischemia model. The EEG, the time of righting reflex recovery and Evans blue content in the homogenate of the brain tissues were recorded. RESULTS: NDLI obviously prolonged the survival time and persistent time of gasping in mice subjected to acute anoxia, remarkably shortened the time of EEG recovery and righting reflex recovery, and reduced Evens blue content in the homogenate. CONCLUSION: NDLI has significantly protective effects on injuries of total cerebral I/R and anoxia.
RESUMO
AIM Protective effects of extract of astragalus on injuries of global cerebral ischemia/reperfusion in rats and anoxia in mice. METHODS Acute anoxia in mice were produced by hypoxia under normal pressure and decapitation. In these two models the survival time and persistent time of gasping were observed. The global ischemia and reperfusion in rats was made by four-vessel occlusion (4-VO). After 20 min ischemia and 24 h reperfusion, the brain index and water content in brain was detected. MDA content and SOD activity of brain homogenate were tested. Endothelin concentration was determined both in plasma and hippocampus. The pathological changes of cortex tissue were observed by light microscope. RESULTS EA(50,100 mg?kg -1) significantly prolonged the survival time and persistent time of gasping in mice subjected to acute anoxia. EA(20,40,80 mg?kg -1) markedly reduced brain edema induced by global ischemia and reperfusion. EA(40,80 mg?kg -1) decreased MDA content and increased SOD activity in brain homogenate, and also inhibited ET concentration both in plasma and hippocampus. The pathological changes of cortex tissue were less serious in rats treated with EA. CONCLUSION EA has protective effects on cerebral ischemia and anoxia injuries that may relate to anti-oxidation and inhibition of ET production.