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51.
眼内异物合并外伤性白内障是眼外伤常见的致盲原因之一,各地报告的致盲率为20%~48.9%。本文对88例眼内异物合并外伤性白内障患者采用联合手术治疗,收到较好疗效,术前视力0.05以下占85.2%,术后矫正视力0.05以下占27.3%,矫正视力0.06~1.5占73.7%,其中矫正视力0.6~1.5者占22.8%。根据异物的性质、在眼内部位和晶体损伤情况选择不同的手术方式一次联合手术摘出异物和白内障,术后采用中西药配合治疗。联合手术可提高疗效,减少术后并发症.减少手术次数,减轻病人的痛苦,缩短病程,减少医疗费用.眼科学报1993;9:216—218. 相似文献
52.
H. M. Wisniewski C. Bancher M. Barcikowska G. Y. Wen J. Currie 《Acta neuropathologica》1989,78(4):337-347
Summary Immunocytochemical staining with monoclonal antibodies to the -protein on tissue sections which have been pretreated with formic acid is not only a very specific but also a highly sensitive method for the detection of amyloid deposits in the brains of Alzheimer's disease victims. We report here a spectrum of morphological appearance of the brain amyloid deposits which are one of the main histopathological correlates of this disorder. Deposits of the -protein are not only found in the well-known lesions [congophilic angiopathy and senile (neuritic) plaques] but are also seen under various morphological forms for which the word plaques does not appear an appropriate term: amyloid fibrils are found as large areas of diffuse infiltration of the neuropil, as ribbon-like infiltration in the subpial layer of the cerebral cortex, as granular deposits in the white matter, as diffuse deposits in the molecular layer of the cerebellum and the basal ganglia and as star-shaped deposits in the cerebellar Purkinje cell layer. The morphology of these deposits seems to depend on the cyto-and fibroarchitectonics of the brain region in which they are found, on the amount of amyloid deposited, and also on the type of staining technique used. It is only under specific circumstances that the deposition of amyloid in the neuropil is accompanied by the formation of paired helical filaments in nerve cell processes and their parent perikarya. In conclusion, our studies suggest that the extent of brain amyloidosis in Alzheimer's disease is much wider than so far appreciated.Supported in part by grants 5-AGO-4220-05 and 5-HD-22634-02 from the National Institutes of Heath 相似文献
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A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor 总被引:6,自引:0,他引:6
Ramser J Abidi FE Burckle CA Lenski C Toriello H Wen G Lubs HA Engert S Stevenson RE Meindl A Schwartz CE Nguyen G 《Human molecular genetics》2005,14(8):1019-1027
The renin-angiotensin system (RAS) is essential for blood pressure control and water-electrolyte balance. Until the discovery of the renin receptor, renin was believed to be mainly a circulating enzyme with a unique function, the cleavage of angiotensinogen. We report a unique mutation in the renin receptor gene (ATP6AP2) present in patients with X-linked mental retardation and epilepsy (OMIM no. 300423), but absent in 1200 control X-chromosomes. A silent mutation (c.321C>T, p.D107D) residing in a putative exonic splicing enhancer site resulted in inefficient inclusion of exon 4 in 50% of renin receptor mRNA, as demonstrated by quantitative RT-PCR. Analysis of membrane associated-receptor molecular forms showed the presence of full-length and truncated proteins in the patient. Functional analysis demonstrated that the mutated receptor could bind renin and increase renin catalytic activity, similar to the wild-type receptor, but resulted in a modest and reproducible impairment of ERK1/2 activation. Thus, our findings confirm the importance of the RAS in cognitive processes and indicate a novel specific role for the renin receptor in cognitive functions and brain development. 相似文献
56.
作者对抗体包被的红为性进行研究,发现抗体包被改变了红细胞的变形性,在我们研究的抗体量范围内,抗体量越多,红细胞的变形性越小,作者从血液流变学的角度对上述结果作了讨论,并提出了通过测定其对红细胞变形性的影响来比较准确地标定抗体效价的可能性。 相似文献
57.
重度烫伤小鼠血清及去补体后血清诱导巨噬细胞凋亡作用的体外实验研究 总被引:1,自引:0,他引:1
目的 探讨重度烫伤小鼠血清及去补体血清在体外诱导腹腔巨噬细胞 (pMФs)凋亡及其机制。方法 采用小鼠 30 %TBSAⅢ度烫伤模型 ,分为正常对照组、烫伤组、去补体烫伤组 ,检测各组伤后 6h血清对体外培养的pMФs分泌超氧阴离子 (O2- )和一氧化氮 (NO)产量的影响 ,碘化丙锭 (PI)染色流式细胞术及凋亡电泳试验测定pMФs的凋亡情况。结果 与正常对照测值比较 ,烫伤血清诱导pMФs分泌较多的O2- 和NO ,去补体后烫伤血清诱导O2- 和NO的分泌量显著降低。烫伤血清诱导pMФs凋亡明显增加 ,去补体后烫伤血清和活性氧阻断剂PDTC及NO阻断剂AG能阻断绝大部分pMФs的凋亡。结论 重度烫伤小鼠血清补体能在体外诱导pMФs凋亡 ,O2- 和NO等炎性介质在其中发挥了重要作用 相似文献
58.
低强度脉冲电磁场对大鼠骨质疏松的影响 总被引:1,自引:0,他引:1
目的:观察低强度脉冲电磁场(pulsed electromagnetic fields,PEMFs)对去卵巢诱导骨质疏松症的大鼠生化指标和骨应力的影响。方法:雌性SD大鼠30只,随机等分为3组(n=10),分别为假手术组(Sham)、骨质疏松模型组(Model)、脉冲电磁场照射组(PEMFs)。经适应4wk后,在25mg·Kg^-1戊巴比妥钠腹腔麻醉下,Model组和PEMFs组摘除双侧卵巢.Sham组找到但不切除卵巢。各实验组均在相同环境下饲养,模型制备4wk后开始治疗,由GZY型低强度低频率脉冲电磁场发生仪产生低频脉冲磁场,根据实验要求,我们使用亥姆霍兹线圈形成均匀磁场,PEMFs组经照射刺激治疗,频率14.3Hz,场强2Gs.日照8h。Model组和Sham组正常饲养。治疗8wk后,对各组大鼠血清、尿液中ALP和Ca以及骨应力进行检测。结果:(1)ALP、Ca检测结果:与Model组相比,PEMFs组ALP值、Ca值差异均有统计学意义(P〈0.05)。其中,血清中ALP值,Model组为(275.16±228,57),PEMFs组为(179.30±87.68);Ca值,Model组为(2,66±0,13),PEMFs组为(2.52±0.05)。(2)骨应力检测结果:Model组为(923.60±34.15Pa),PEMFs组为(1152.85±118,20Pa),组间差异有统计学意义(P〈0.05)。结论:研究发现,PEMFs对于促进骨重建、提高Ca吸收和骨应力恢复具有积极作用。 相似文献
59.
Salmena L Lemmers B Hakem A Matysiak-Zablocki E Murakami K Au PY Berry DM Tamblyn L Shehabeldin A Migon E Wakeham A Bouchard D Yeh WC McGlade JC Ohashi PS Hakem R 《Genes & development》2003,17(7):883-895
Defects in death receptor-mediated apoptosis have been linked to cancer and autoimmune disease in humans. The in vivo role of caspase 8, a component of this pathway, has eluded analysis in postnatal tissues because of the lack of an appropriate animal model. Targeted disruption of caspase 8 is lethal in utero. We generated mice with a targeted caspase 8 mutation that is restricted to the T-cell lineage. Despite normal thymocyte development in the absence of caspase 8, we observed a marked decrease in the number of peripheral T-cells and impaired T-cell response ex vivo to activation stimuli. caspase 8 ablation protected thymocytes and activated T-cells from CD95 ligand but not anti-CD3-induced apoptosis, or apoptosis activated by agents that are known to act through the mitochondria. caspase 8 mutant mice were unable to mount an immune response to viral infection, indicating that caspase 8 deletion in T-cells leads to immunodeficiency. These findings identify an essential, cell-stage-specific role for caspase 8 in T-cell homeostasis and T-cell-mediated immunity. This is consistent with the recent identification of caspase 8 mutations in human immunodeficiency. 相似文献