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31.
目的探讨动脉粥样硬化性脑梗死患者血浆氧化低密度脂蛋白与血管内皮损伤及血小板活化程度的关系。方法用酶联免疫吸附测定(ELISA)的方法检测49例脑梗死患者和50例相匹配的对照组血浆氧化低密度脂蛋白(OX-LDL)、血管性假血友病因子(VWF)、血浆颗粒膜蛋白(GMP-140)水平,同时用硝酸还原酶比色法测定血清一氧化氮(NO)水平,并把、VWF、GMP-140、NO与OX-LDL作相关分析。结果脑梗死组血浆OX-LDL、、VWF、GMP-140明显高于对照组(t=2.91,P〈0.01;t=3.94,P〈0.001;t=2.08,P〈0.05),而脑梗死组血清NO水平明显低于对照组(t=4.02,P〈0.001);相关分析表明血浆OX-LDL水平与血清NO水平呈负相关(r=-0.204,P〈0.05),与血浆懈呈正相关(r=0.60,P〈0.01),与血浆GMP-140呈正相关(r=0.430,P〈0.01)。结论脑梗死患者的血浆OX-LDL明显增高,而OX-LDL增高可能是脑梗死的危险因素。  相似文献   
32.
生物体内的一氧化氮 (NO)作为一种反应极强的效应分子 ,不仅参与免疫调控 ,而且也是造血祖细胞生长和分化不可缺少的调节因子 [1 ]。本文通过对再生障碍性贫血 (AA)患者血清 NO与白细胞介素 - 2 (IL- 2 )、肿瘤坏死子 (TNF)、血小板生成素 (TPO)、红细胞生成素 (EPO)、GM- CSF、5种细胞因子水平测定 ,分析其与外周血象及各细胞因子间的相互关系 ,并探讨 NO及 IL- 2等细胞因子在 AA发生发展过程中的作用。1 材料和方法1.1 材料1.1.1 标本来源  AA患者 5 0例 ,以 2 0 0 2年 3月至 2 0 0 4年4月我院确诊为 AA的患者为研究对象…  相似文献   
33.
一氧化氮与胚胎异常发育的相关性研究   总被引:3,自引:0,他引:3  
李勇  朱惠刚 《卫生研究》1997,26(3):162-166
为了解开一氧化氮(NO)是否与畸胎发生有关这一谜团和进一步阐明砷致畸作用机理,本实验应用诱生型NO合成酶(iNOS)组织化学、扫描电镜(SEM)及体内致畸试验等方法研究了砷对小鼠卵黄囊胎盘(YSP)和胚胎发育的影响。结果表明YSP细胞iNOS表达与砷浓度之间存在明显的剂量—反应关系(P<0.05);SEM观察可见YSP内皮层和间皮层细胞受损;光镜下可见YSP变小、萎缩和微血管分化不良;随着染毒剂量的升高,畸胎率和死胎率亦逐步增加,最高分别达到56.8%和24.7%;畸胎的主要表现是神经管未闭,心包积液和体位异常等。研究结果率先提示过量NO与畸胎发生及致畸机理关系密切;推荐在致畸研究中iNOS可作为一种有效的生物标志物。  相似文献   
34.
Over the last two decades, nitric oxide (NO) has been established as a novel mediator of biological processes, ranging from vascular control to long-term memory, from tissue inflammation to penile erection. This paper reviews recent research which shows that NO and its derivatives also are synthesized within skeletal muscle and that NO derivatives influence various aspects of muscle function. Individual muscle fibres express one or both of the constitutive NO synthase (NOS) isoforms. Type I (neuronal) NOS is localized to the sarcolemma of fast fibres; type III (endothelial) NOS is associated with mitochondria. Isolated skeletal muscle produces NO at low rates under resting conditions and at higher rates during repetitive contraction. NO appears to mediate cell–cell interactions in muscle, including vasodilation and inhibition of leucocyte adhesion. NO also acts directly on muscle fibres to alter cell function. Muscle metabolism appears to be NO-sensitive at several sites, including glucose uptake, glycolysis, mitochondrial oxygen consumption and creatine kinase activity. NO also modulates muscle contraction, inhibiting force output by altering excitation–contraction coupling. The mechanisms of NO action are likely to include direct effects on redox-sensitive regulatory proteins, interaction with endogenous reactive oxygen species, and activation of second messengers such as cyclic guanosine monophosphate (cGMP). In conclusion, research published over the past few years makes it clear that skeletal muscle produces NO and that endogenous NO modulates muscle function. Much remains to be learned, however, about the physiological importance of NO actions and about their underlying mechanisms.  相似文献   
35.
Inflammatory sites associated with tissue destruction often contain a complex mixture of cells including macrophages as well as CD8+ and CD4+ T cells. Here, we have investigated, using islets of Langerhans as targets, if CD8+ T cells and macrophages can cooperate in tissue destruction. CD8+ T cells obtained from the islet inflammatory lesion of non-obese diabetic mice or cloned islet-specific CD8+ T cells were ineffective in destroying islets on their own. Including increasing numbers of macrophages in co-cultures of islets and islet-derived or cloned CD8+ T cells progressively increased and accelerated islet destruction. Macrophages alone were ineffective. Macrophage-depleted islets were not destroyed by islet-derived CD8+ T cells. For cooperative islet destruction to occur, beta cells, but not macrophages, needed to be able to present antigens to CD8+ T cells. CD8+ T cells triggered NO production by macrophages, while macrophages triggered IFN-gamma production by CD8+ T cells. Each of these factors was partially effective, but not sufficient, for maximal islet destruction. Antibodies specific for ICAM-1 and LFA-1 inhibited both cooperative islet destruction and cross-stimulation of CD8+ T cells and macrophages. The data suggest that if CD8+ T cells become only weakly activated by target cells, they are not able to destroy target tissue on their own. However, such CD8+ T cells and local macrophages may still cross-stimulate each other, which then facilitates target destruction. For this to occur, target cells, but not macrophages, need to present antigen to CD8+ T cells.  相似文献   
36.
37.
无菌分离小鼠腹腔巨噬细胞,制备单细胞悬液,加入不同终浓度的淫羊藿甙孵育4 h后,加入细菌脂多糖LPS(终浓度20 mg/L)48 h后以MTT法检测其增殖;加药孵育4 h后,分别加入直径1μm和2μm的微球(终浓度1×1010/L),5 h后利用流式细胞术(FCM)检测吞噬情况;加入LPS(终浓度20 mg/L)24 h后Griess试剂盒检测巨噬细胞NO的量。结果显示ICA在终浓度1.5、3.0μmol/L时能明显抑制LPS刺激的巨噬细胞增殖(P<0.01)和NO的产生,并促进其吞噬微球的功能。提示ICA可能抑制LPS信号转导从而抑制巨噬细胞增殖,并且通过抑制其活化,下调iNOS有关的炎症因子,使NO减少;对于未活化的巨噬细胞,ICA可能通过上调其吞噬功能,增强固有免疫系统来抵御病原体侵入。  相似文献   
38.
The results of cadaveric retransplantation in 55 recipients immunosuppressed with cyclosporine and prednisone were compared to 156 recipients of primary renal allografts. By 3 yr posttransplant, there is no significant difference in patient survival, but the yearly graft survival for primary (79%, 72%, 72%) as compared to retransplant (69%, 58%, 58%) recipients was significantly (p less than 0.05) better. There was no significant difference in rejection episodes or mean +/- SD serum creatinine (mg/dl) at 2 yr between primary (32%, 2.14 +/- 1.1) and retransplant (33%, 2.08 +/- 1.4) patients, respectively. Donor source, third kidneys, human leukocyte antigen AB and Dr matching, percent reactive antibody levels, and cause of first graft loss do not have significant impact on cyclosporine-treated retransplant outcome. However, retransplant patients who have lost a previous graft in less than 3 months continue to be at high risk for subsequent early graft loss. These results suggest that the combination of cyclosporine and prednisone is the preferred regimen for cadaveric retransplantation.  相似文献   
39.
Parameters of NO metabolism in the gingiva were studied during experimental periodontitis accompanied by alloxan diabetes and exogenous hypercholesterolemia. We measured activities of inducible and constitutive NO synthase and concentrations of stable NO end metabolites in rat gingival tissue (total contents of nitrite and nitrate). Under pathological conditions NO metabolism significantly differed from the control. Treatment with mexidol for 14 days significantly decreased activity of inducible NO synthase in the gingiva of experimental animals. __________ Translated from Byulleten' Eksperimental'noi Biologii i Meditsiny, Vol. 140, No. 10, pp. 384–386, October, 2005  相似文献   
40.
BACKGROUND: The aim of the present study was to gain insight into parents' own donor preferences within a system offering the choice between an anonymous and identity-registered donor. A comparison was made between recipients choosing for an anonymous donor (AD choosers) and those choosing for an identifiable donor (ID choosers) with regard to their sexual orientation, demographic characteristics, disclosure issues and infertility distress. METHODS: Data from 105 couples (61% heterosexual, 39% lesbian) were registered on a standardized form during implication counselling sessions previous to treatment. RESULTS: Sixty-three per cent of the heterosexual couples and 98% of the lesbian couples had chosen an ID donor. Major differences between ID and AD choosers were identified. Among the ID choosers secrecy towards the child was no option, whereas 83% of the AD choosers did not intend to inform their child. Compared with heterosexual ID choosers, AD choosers were more distressed about their infertility and had a lower educational level. CONCLUSION: Legislation imposing ID donors appears to be acceptable for the majority of this study population. For a vulnerable group of heterosexual couples, who remained secretive about the use of a donor, adaptation to the new system is not self-evident.  相似文献   
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