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单次灌胃杂色曲霉素对小鼠大脑细胞的影响
引用本文:刘晋红,张祥宏,左连富,严霞,王俊灵,黄向华,邢凌霄,李月红,王凤荣. 单次灌胃杂色曲霉素对小鼠大脑细胞的影响[J]. 中国药理学与毒理学杂志, 2004, 18(1): 57-61
作者姓名:刘晋红  张祥宏  左连富  严霞  王俊灵  黄向华  邢凌霄  李月红  王凤荣
作者单位:河北医科大学实验病理室,河北,石家庄,050017
摘    要:目的 探讨单次ig杂色曲霉素 (ST)对小鼠大脑细胞的影响。方法 采用形态学观察和流式细胞术定量检测方法 ,研究ST对BALB/c小鼠大脑神经细胞的影响。结果 病理形态学观察可见 ,ig小剂量ST(3μg·kg-1 )后 1 2h或大剂量ST(3mg·kg-1 )后6h即可见小鼠大脑皮质、丘脑、海马CA2区神经元出现胞核固缩深染、胞浆嗜酸性变、空泡变性等病理变化 ,且随剂量增大和作用时间延长 ,病变神经元逐渐增多 ;光镜下对海马CA2区病变神经元进行计数分析 ,结果表明ST处理组发生病理变化的神经元比例均高于相应对照组 ,且呈剂量和时间依赖性增高 ;流式细胞术定量检测结果表明 ,igST 3,30 ,30 0和30 0 0 μg·kg-1 1 2h后 ,小鼠脑细胞的凋亡率呈剂量依赖性增高 ;ig3mg·kg-1 的ST后 6~48h,随ST作用时间的延长 ,脑细胞凋亡率也明显增高。结论经口给予ST可导致小鼠大脑皮质、丘脑、海马CA2区神经元发生退行性病变 ,诱导并促进小鼠大脑细胞凋亡

关 键 词:杂色曲霉素    凋亡  流式细胞术
收稿时间:2003-01-22

Effects of sterigmatocystin on cerebral cells in BALB/c mice after single intragastral administration
LIU Jin-Hong, ZHANG Xiang-Hong, ZUO Lian-Fu, YAN Xia, WANG Jun-Ling, HUANG Xiang-Hua, XING Ling-Xiao, LI Yue-Hong, WANG Feng-Rong. Effects of sterigmatocystin on cerebral cells in BALB/c mice after single intragastral administration[J]. Chinese Journal of Pharmacology and Toxicology, 2004, 18(1): 57-61
Authors:LIU Jin-Hong   ZHANG Xiang-Hong   ZUO Lian-Fu   YAN Xia   WANG Jun-Ling   HUANG Xiang-Hua   XING Ling-Xiao   LI Yue-Hong   WANG Feng-Rong
Affiliation:(Laboratory of Experimental Pathology, Hebei Medical University, Shijiazhang 050017, China)
Abstract:AIM To investigate the effects of sterigmatocystin(ST) on cerebral cells in BALB/c mice after single intragastral administration. METHODS The effect of ST, with different dosages and at different times after intragastral administration, on cerebral cells was studied with HE staining and flow cytometric (FCM) methods. RESULTS Pathologically, degenerated changes were observed in cortex, thalamus, hippocampus at 12 h in group with ST 3 μg•kg-1 ig and at 6 h in group with ST 3 mg•kg-1 ig. The nuclei in degenerated cells were shrunk in size with dark and condense chromatin staining, while the nuclear membrane and nucleoli structures were not clearly distinguished. The degenerated changes increased gradually along with the increases in ST dosage and treatment time period. The degenerated cells in the neurons of CA2 region of hippocampus was counted. The result showed that the percentage of degenerated neurons in the ST treatment group was significantly higher than that in control group. FCM analysis revealed that 12 h after ig 3, 30, 300 and 3000 μg•kg-1, the apoptosis rates of cerebral cells in all ST treatment groups were significantly higher than that in control group in a dose effect correlation fashion. Apoptosis rates also increased with treatment time 6-48 h after ig ST 3 mg•kg-1. CONCLUSION Oral ST exposure causes some degenerated changes in neurons in cortex, thalamus, CA2 of hippocampus, induces and promotes apoptosis of cerebral cells in mice.
Keywords:sterigmatocystin  brain  apoptosis  flow cytometry
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