Determination of erythrocyte pyrimidine 5′-nucleotidase activity by31P nuclear magnetic resonance: Comparison of normal controls and multiple sclerosis patients

Summary A technique to assay erythrocyte pyrimidine 5-nucleotidase activity in situ using³¹P nuclear magnetic resonance spectroscopy is presented. The assay is chemically specific, simple and applicable to untreated lysates. A comparison of enzyme levels in normal controls and in multiple sclerosis patients employing the assay yielded no significant differences between both groups. Difficulties encountered in the quantitative analysis of the assay using¹H-NMR spectroscopy are briefly discussed.     

螺旋藻藻蓝蛋白和藻多糖对人体外周血淋巴细胞功能的影响

从螺旋藻中提取藻蓝蛋白（ＳＰＣ）和多糖（ＳＰＳ）,研究其对人体外周血淋巴细胞功能的影响。实验结果表明,ＳＰＣ和ＳＰＳ能够促进ＰＨＡ刺激淋巴细胞转化的作用,其中ＳＰＳ的促进作用有剂量依存关系。ＳＰＣ和ＳＰＳ能恢复Ｔ细胞受环磷酰胺损伤后Ｅ玫瑰花环形成能力,特别是对活性Ｅ花环（Ｅａ）的形成能力有较好的恢复作用。     

氯丙嗪和异丙嗪抗红细胞膜脂过氧化机理初探

对具有显著抗辐照膜脂过氧化作用的两种药物氯丙嗪和异丙嗪进行了作用方式的研究。结果表明：随浓度增高,药物对辐照膜脂过氧化能达到完全抑制;药物对丙二醛产生的抑制作用大于其对脂氢过氧化物产生的抑制作用;药物不直接与丙二醛和脂氢过氧化物反应;药物能吸附在膜上,且主要在照射引发时通过清除自由基而起作用。     

运动、氧化应激与红细胞膜流动性

红细胞膜对于红细胞正常结构和功能的维持尤为重要，其与运动性疲劳的关系日益受到重视，笔者就运动与氧化应激、氧化损伤与红细胞膜流动性以及与红细胞功能的关系作一简要综述。     

Effect of hydrogen peroxide on the binding of Merocyanine 540 to human erythrocytes

The fluorescent dye Merocyanine 540 (MC540) is often used as a probe to monitor the molecular packing of phospholipids in the outer leaflet of biomembranes. In a previous study we showed that the increased staining of erythrocytes with a perturbed membrane structure was mainly due to an increase in the fluorescence yield of cell-bound MC540, rather than to an increase of the number of bound molecules. Erythrocytes and ghosts exposed to continuous fluxes of H₂O₂ exhibited pronounced lipid peroxidation. Further, red blood cells subjected to this form of oxidative stress also showed increased staining with MC540. It appeared that this was caused by a strong increase in binding of MC540, together with a slight red shift of the fluorescence emission maximum and a small increase in the fluorescence yield of bound MC540. The changed MC540 binding characteristics were not observed when lipid peroxidation was suppressed by the presence of the antioxidant BHT in the incubation medium. However, open ghosts exposed to H₂O₂ showed no increase of MC540 binding, excluding a direct involvement of lipid peroxidation. Measurement of fluorescence emission spectra and gel filtration studies showed that MC540 can bind to H₂O₂-exposed hemoglobin. Experiments with erythrocytes lysed in hypotonic medium after exposure to H₂O₂ revealed that peroxidation of lipids with H₂O₂ induced a non-specific permeabilization of the plasma membrane to MC540, thereby allowing MC540 to bind to the oxidatively denatured, more hydrophobic hemoglobin. These results indicate that conclusions about packing of phospholipids in the outer leaflet of the membrane based on increased MC540-staining should be drawn with care. Received 27 September 1996; received after revision 5 November 1996; accepted 27 November 1996     

牦牛血清转铁蛋白对人红细胞膜氧化损伤的保护作用

牦牛血清中分离纯化的转铁蛋白对人红细胞膜的抗氧化具有保护作用 .方法 :采用黄嘌呤 /黄嘌呤氧化酶、Fe2 + /H2 O2 两个体系产生的O·2 -、OH·对红细胞膜造成氧化损伤 ,通过丙二醛含量、超氧化物歧化酶和谷胱甘肽过氧化酶活性的测定研究牦牛转铁蛋白在抗氧化方面的作用与机制 .结果 :O·2 -和OH·可以造成红细胞膜丙二醛量的显著增加 ,超氧化物歧化酶和谷胱甘肽过氧化酶活性的下降 .当适量不同浓度牦牛血清转铁蛋白在黄嘌呤 /黄嘌呤氧化酶、Fe2 + /H2 O2 两个体系前处理可以抑制丙二醛的产生 ,保护红细胞膜免受丙二醛的氧化损伤并且使超氧化物歧化酶和谷胱甘肽过氧化酶活性升高 .提示 ,牦牛血清转铁蛋白对O·2 -和OH·自由基引起的氧化损伤有保护作用     

4种腹足纲动物粗蛋白的凝集作用

采用来自5种脊椎动物的8种血细胞、7种微生物单细胞、5种藻类细胞，对4种海产腹足纲动物凝集素进行筛选，均检测到凝集活性。绵羊红细胞、啤酒酵母、紫球藻对凝集反应最为敏感。4种动物凝集素普遍不耐高温，60℃或65℃下15min即全部失活，凝集反应的适宜pH为6．5-8．0，其凝集性能可能分别被不同的糖所抑制，但均可被0．02mol／LEDTA抑制。     

过氧化氢酶活性的简易测定法

本文论述与建立一种过氧化氢酶活性紫外吸收测定法。本法操作简易快速、实验误差较小。用本法测得正常成人红细胞中过氧化氢酶活性(M±SD)为24.25±4.02单位。     

高温对人红细胞的影响

高温用于恶性肿瘤的治疗是近年来颇受重视的工作,但高温处理不可避免地对肿瘤组织周围正常细胞也将产生影响。为了研究高温对正常细胞的影响,本文以人红细胞为实验模型,研究其细胞热损伤的机制。红细胞经不同温度处理二十分钟后,通过扫描电镜和生化分析方法探讨红细胞的形态变化,溶血作用和膜结合酶-乙酰胆碱酯酶、Na·K·Mg-ATP酶活性的变化。结果表明,在本实验条件下细胞形态的改变对高温最敏感:48℃高温处理后,绝大部分细胞变形,50℃保温使溶血显著增加,膜结合酶热变性温度则超过54℃。     

引入青海省乐都县小尾寒羊血钾型多态性的研究

采用火焰光度计法对引入青海省乐都县152只小尾寒羊红细胞钾浓度的多态性特征进行了研究.结果表明：①在红细胞钾浓度位点上存在高血钾（HK）和低血钾（LK）两种表型，以HK为优势表型（占80.26%）；②Kh和K1等位基因频率分别为0.8959和0.1041，以Kh为优势等位基因；③基因杂合度、有效等位基因数和基因纯合度指数分别为0.18651、.2293和0.6269.