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作 者:胡微煦[1] 向勤[2] 付爱珍 文珠 何丹[5] 胡国柱[5]
机构地区:[1]复旦大学附属中山医院肿瘤放疗科,上海200032 [2]南昌大学研究生院医学部,南昌330006 [3]樟树市人民医院,樟树331200 [4]江西省医学科学研究院,南昌330006 [5]江西省人民医院,南昌330006
出 处:《中药药理与临床》2014年第3期89-91,共3页Pharmacology and Clinics of Chinese Materia Medica
基 金:江西省科技厅社会发展计划(2007BS22602)
摘 要:目的:探讨白术多糖的毒性及抗神经细胞缺氧性凋亡作用。方法:研究分为正常对照组、凋亡阳性组、白术多糖0.025g/L组、白术多糖0.05g/L组、白术多糖0.1g/L组、白术多糖0.25g/L组。采用"Neurobasal+B27"体外神经细胞无血清培养,免疫细胞化学鉴定神经细胞,MTT测定药物毒性,AnnexinV/PI荧光双染流式细胞仪及Hochest33342荧光染色检测细胞凋亡。结果:白术多糖在1.0g/L之内预处理神经细胞对其无毒性作用。白术多糖在0.025g/L^0.05g/L范围显著地改善缺氧对神经细胞生长的抑制,在0.025g/L^0.25g/L范围内显著地抑制缺氧复氧诱导的神经细胞早期凋亡。结论:白术多糖在一定浓度范围内具有抗缺氧复氧诱导的细胞凋亡作用。Objective: To explore the effect of Atractylodes macrocephalaon polysaccharides( AMPS) on cytotoxicity and preventing the neuron apoptosis indued by hypoxia. Methods: The study was divided into normal control group( group C),apoptosis positive group induced by hypoxia( group A),experiment 1 group treated by 0. 025g /L AMPS( AMPS1),experiment 2 group treated by 0. 05g /L AMPS group( AMPS2),experiment3 group treated by0.1g/L AMPS group( AMPS3),experiment4 group treated by0.25 g/L AMPS group( AMPS4).Neurons were cultured by Neurobasal + B27 in serum-free in vitro. Neurons were identified by immunocytochemistry. Drug toxicity was determined by MTT assay,Neuron apoptosis was examined by Annexin V- FITC /PI in flow cytometry and Hoechst 33342 fluorescent staining under fluorescence microscope. Results: The AMPS was non-toxic for neurons pretreated within 1. 0 g /L. The AMPS significantly prevented the inhibition of neuron growth from hypoxia from 0. 025g /L to 0. 05g /L,( P 〈 0. 05). Early apoptosis of neurons induced by hypoxia-reoxygenation was significantly inhibited by AMPS from 0. 025g /L to 0. 25g /L( P 〈 0. 05). Conclusion: The AMPS has an effect on inhibitting early apoptosis of neurons induced by hypoxia-reoxygenation in a certain concentration range.
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