[The protective effect of propofol pretreatment on glutamate injury of neonatal rat brain slices].

Xiao-feng Zhou, Ding-ding Huang, Di-fen Wang, Jiang-quan Fu
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引用次数: 2

Abstract

OBJECTIVE To study the protective effect of propofol precondition against glutamate (Glu) neurotoxicity to neonatal rat cerebrocortical slices. METHODS Brain slices of Sprague-Dawley (SD) rats were cultured in vitro and observed the morphologic changes. Brain slices were randomly divided into three groups: blank control group, Glu injury group (1 mmol/L Glu for 0.5 hour), propofol precondition group (20 mg/L propofol for 24 hours), each n=12. Changes in pathological and ultra-structure of cells were observed using microscope. Lactate dehydrogenase (LDH) leakage rate was measured. Meanwhile, the expression of glial fibrillary acidic protein (GFAP) was detected by immunohistochemical technology, then the positive cell were counted. RESULTS Cultured brain slices of cell were intact and survived well. Hematoxylin-eosin (HE) staining, electron microscopy and LDH test results showed that cerebral film neuron severely damage, gliosis, edema, LDH leakage rate in Glu injury group were significantly more severe compared with blank control group [(68.5±2.0)% vs. (16.0±2.5)%, P<0.01]. Reduce the brain slice of the propofol pretreatment group of neuronal cell jury, cell shape recovery significantly reduced LDH leakage rate compared with the Glu injury group [(38.5±2.4)% vs. (68.5±2.0)%, P<0.05]. Immunohistochemical detection of GFAP expression of Glu injury group glial cell body swelling, producing increase in the number of GFAP positive reaction strong, the number of positive cells compared with blank control group was significantly increased (50±5 cells/HP vs. 10±3 cells/HP, P<0.01). The recovery of propofol pretreatment group glial cell morphology, cell processes slender GFAP positive reaction decreased the number of positive cells compared with the Glu injury group was significantly decreased (30±4 cells/HP vs. 50±5 cells/HP, P<0.05). CONCLUSION Propofol pretreatment has protective effect against Glu injured rat cerebrocortical slices.
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[异丙酚预处理对新生大鼠脑片谷氨酸损伤的保护作用]。
目的研究异丙酚预处理对新生大鼠脑皮质片谷氨酸(Glu)神经毒性的保护作用。方法体外培养SD大鼠脑切片,观察其形态学变化。将脑切片随机分为空白对照组、Glu损伤组(1 mmol/L Glu持续0.5 h)、异丙酚预处理组(20 mg/L异丙酚持续24 h),每组n=12。显微镜下观察细胞病理及超微结构的变化。测定乳酸脱氢酶(LDH)渗漏率。同时采用免疫组化技术检测胶质原纤维酸性蛋白(GFAP)的表达,并对阳性细胞计数。结果脑细胞切片完整,存活良好。苏木精-伊红(HE)染色、电镜及LDH检测结果显示,Glu损伤组大鼠脑膜神经元严重损伤、胶质细胞增生、水肿、LDH漏出率显著高于空白对照组[(68.5±2.0)%比(16.0±2.5)%,P<0.01]。减少脑切片异丙酚预处理组神经元细胞损伤后,细胞形态恢复较Glu损伤组显著降低LDH漏出率[(38.5±2.4)%比(68.5±2.0)%,P<0.05]。免疫组化检测GFAP表达使Glu损伤组胶质细胞体肿胀,产生GFAP阳性反应的细胞数量增加,阳性细胞数量较空白对照组显著增加(50±5个细胞/HP vs. 10±3个细胞/HP, P<0.01)。异丙酚预处理组神经胶质细胞形态恢复,细胞突起细长GFAP阳性反应减少,阳性细胞数较Glu损伤组明显减少(30±4个细胞/HP比50±5个细胞/HP, P<0.05)。结论异丙酚预处理对Glu损伤大鼠脑皮质片有保护作用。
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