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作 者:黄金兰[1] 陆璐[2] 黄丹[2] 冯颖琴 崔雯[2] 张雯艳[2] 钟振国[1]
机构地区:[1]广西医科大学,南宁530021 [2]广西中医药大学,南宁530001
出 处:《中国实验方剂学杂志》2013年第8期171-174,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家自然科学基金项目(30960489;81160512);广西中医药大学中药药效研究重点实验室开放课题(09-007-06-07)
摘 要:目的:研究三七总皂苷(PNS)对快速老化痴呆模型小鼠(SAMP8)炎症因子及小胶质细胞的影响。方法:采用SAMP8小鼠,将其随机分为模型组、PNS高剂量组(200 mg·kg-1)、PNS低剂量组(100 mg·kg-1)和石杉碱甲组(0.3 mg·kg-1),8只/组,模型组ig给予给药组相同容积的双蒸水。每天ig 1次,连续给药2个月。用ELISA双抗体夹心法法测定PNS对各组SAMP8小鼠血清中的细胞因子白介素(IL)-1β,IL-6、肿瘤坏死因子(TNF-α)及补体(C1q)表达的影响;HE染色光镜观察小胶质细胞的形态变化。结果:PNS高剂量组的IL-1β(23.14±12.58)ng·L-1水平低于模型组(47.44 ng·L-1)(P<0.05);IL-6 PNS高、低剂量组(243.3±133.9),(269.0±75.1)ng·L-1低于模型组(582.5±144.6)ng·L-1(P<0.05);模型组小鼠血清中补体C1q(280.4±49.75)mg·L-1含量均高于阳性组C1q(144.71±21.78)mg·L-1和PNS高剂量组C1q(187.7±65.56)mg·L-1;模型组小鼠海马区的小胶质细胞被激活,吞噬神经细胞;用药组海马区小胶质细胞没有被激活,为静息状态。血清中TNF-α各组间无显著差异。结论:PNS对SAMP8小鼠的免疫炎症反应有一定的抑制作用。Objective:To study the effect of Panax notoginseng saponins(PNS) on the inflammatory factors and microglia cell of senescence-accelerated mouse prone 8(SAMP8) mice.Method:SAMP8 mice were randomly divided into four groups:PNS high-dosage group,PNS low-dosage group,huperzine A group and model control group.The high-dosage group and low-dosage group were treated with 200,100 mg·kg-1 PNS respectively per day and the huperzine A group was treated with 0.3 mg·kg-1 huperzine A by intragastric administration,per day for 8 consecutive weeks.The serum cytokines of SAMP8 like interleukin(IL)-1β,IL-6,tumor necrosis factor-α(TNF-α),complement 1q(C1q) were measured by ELISA.The morphological changes of microglia cells were observed by light microscopy with HE staining.Result:The level of IL-1β in the high-dose group was lower than that in the model group(P0.05),and compared to the model group,the content of IL-6 in PNS high,low-dose groups showed significantly different(P0.05).The level of C1q in the blank group was higher than that in the high-dose group and positive group.HE staining showed that microglia in the hippocampus of the model group was over-activation,and swallowed nerve cells,while the microglia in the treatment groups was not activated.Conclusion:PNS can reduce the inflammatory response in SAMP8 mice.
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