刺梨汁对慢性氟中毒的影响及机理研究

用高氟饲料喂养大鼠６个月，复制出慢性氟中毒模型，再自由饮用刺梨汁３个月，探讨刺梨汁对慢性氟中毒的影响及机理。结果表明：刺梨汁可明显改善氟中毒的一般状况，对已形成的氟斑牙影响不大，但可促进尿氟排泄，降低血清和骨氟含量及尿羟脯氦酸含量，提高血清中维生素Ｃ、维生素Ｅ和血清、肝、肾ＧＳＨ含量，增强血、肝、肾ＧＳＨ－Ｐｘ和ＳＯＤ活性，降低血清、肝和肾ＬＰＯ含量，降低尿γ－ＧＴ和血清ＧＰＴ活性及肝ＴＧ含量，提示：刺梨汁具有明显桔抗慢性氟中毒作用，其机理可能是通过促进尿氟排泄和抗氧化作用。     

Absence of donor-type major histocompatibility complex class I antigen-bearing microglia in the rat central nervous system of radiation bone marrow chimeras

Localization of bone marrow-originated cells in the central nervous system (CNS) of the rat was investigated by using bone marrow chimeras. In order to do this, Lewis rats which carry major histocompatibility complex (MHC) class I antigens haplotype 1 (RT1.Al) were reconstituted with (Lew X PVG)F1 (RT1.Al/c) bone marrow cells after lethal irradiation. Transferred bone marrow cells were detected by immunohistochemical staining using a monoclonal antibody, OX27, specific for haplotype c of rat MHC class I antigens (RT1.Ac). The spleen and thymus of chimeric rats were fully reconstituted with transferred F1 cells 4 weeks after bone marrow transplantation. At this stage, mononuclear cells in the subarachnoid space of the CNS expressed OX27 antigen indicating that they were of bone marrow origin. A few OX27-positive blood cells were scattered in the CNS parenchyma 4-12 weeks after reconstitution. Ramified microglia, however, remained OX27-negative. Bone marrow-derived microglia were not observed throughout the period of examination until 24 weeks. In addition, experimental allergic encephalomyelitis (EAE) was induced in chimeric rats in order to augment the expression of MHC class I antigens on microglia. Even under this condition, no OX27-positive microglia were observed. Taken together, ramified microglia might be of neuroectodermal origin and there is little possibility that the microglia are derived from the bone marrow. However, if the ramified microglia are derived from blood cells, the microglia may be expected to have characteristic cell kinetics from the following points: (1) the precursor cells of the microglia may enter the CNS only at the perinatal stage; and (2) even under the condition in which lymphocytes and macrophages enter the CNS as observed in EAE, the precursor cells of the microglia are not supplied from the blood.     

山楂结块体外凝结、离解的实验研究

目的:探讨山楂结块形成的机制,以指导预防和治疗。方法:配制以胃蛋白酶为基本液的模拟胃液,对60个山楂糊团和500g山楂糊进行酸凝实验。使用6％和8％浓度的碳酸氢钠溶液对酸凝后的山楂糊团、山楂糊做碱离解试验。设搅拌、非搅拌组和清水对照组作对比。结果:酸凝实验:山楂团硬度增加。清水对照组山楂团硬度明显低于酸凝组。散放入模拟胃液中的山楂糊相互接触处发生凝结,形态仍呈不规则片块状。碱离解实验:6h后碳酸氢钠溶液中均出现酸碱中和现象。非搅拌组:结块表面有碎屑脱落,至第10天碳酸氢钠溶液和清水中的结块均未自行碎解。搅拌组:搅拌时有较多碎屑脱落。第3天,1个结块碎解。至第10天,20个结块全部碎解。清水对照组:仅1个结块在第8天碎解。结论:山楂团酸凝后硬度增大。散放入的山楂糊酸凝后形态仍呈不规则片块状。碱溶液通过酸碱中和可使山楂结块表面松解,无外力作用时不能使结块碎解。     

激素性股骨头缺血坏死MRI诊断的实验研究

目的：建立股骨头缺血坏死(ANFH)动物模型，将磁共振成像(MRI)表现与组织病理学结果对照，探讨早期ANFH的病理变化和删表现的病理学基础。方法：成年新西兰兔36只，随机均分成三组。A组：为正常对照组，静脉注射生理盐水。B、C组为实验组，B组：单纯静脉注射地塞米松10mg／kg／d连续7天，间隔两周再重复一次。C组；马血清与激素共用，先静脉注射马血清10g／kg，间隔2周再重复一次；继之重复B组给药。之后4、8、16、26周后分别从3组随机各取3只，先拍X线平片再进行删，然后取双侧股骨头做组织病理检查。结果：实验组兔股骨头第8周T1WI信号强度明显降低，T2WI呈不均匀高信号，对应病理改变为骨髓水肿，骨髓腔内少量出血和少量骨细胞坏死。16、26周T1WI信号强度增高，病理显示骨髓脂肪细胞肥大并融合成大泡状，大量骨细胞坏死，骨小梁变细、中断。16、26周兔股骨头X线平片示骨质稀疏，骨小梁模糊。C组上述变化较B组显著。结论：1．采用马血清和肾上腺皮质激素共用，比单纯用肾上腺皮质激素更易诱导出较典型的ANFH动物模型。2．删能够较全面反映早期激素性ANFH的病理变化。     

Selective localisation of neuro-specific T lymphocytes in the central nervous system

Using experimental autoimmune encephalomyelitis (EAE) in the rat as a model of central nervous system (CNS) inflammation, activated and quiescent T lymphocytes with different antigen specificities were labelled with the fluorescent dye Hoechst 33342 and tested by fluorescence microscopy for their ability to accumulate in different regions of the spinal cord and in other organs at varying times post inoculation. With this highly sensitive assay it was found that activated myelin basic protein (MBP)-specific T cell lines accumulated in the spinal cord (a 1000-fold increase in the lumbar/sacral region by day 4) and caused clinical signs of EAE. In contrast, interleukin-2 (IL-2)-maintained (quiescent) MBP-specific T cell lines failed to accumulate in the CNS and cause disease. Activated ovalbumin (OA)-specific and purified protein derivative of tuberculin (PPD)-specific T cell lines were also found at significantly higher levels in the spinal cord than non-activated cells although they failed to accumulate to a substantial degree when injected alone. When injected with activated MBP-specific T cells the activated OA- and PPD-specific cell lines accumulated in the spinal cord following initial accumulation of the MBP-specific cells, demonstrating that during the inflammatory process there is considerable non-specific recruitment of cells into the inflammatory site. CNS accumulation of activated MBP-specific T cell lines occurred 1-2 days later in irradiated animals than in non-irradiated recipients. This was consistent with irradiated animals also exhibiting a later onset of disease and suggests that irradiation may directly affect the endothelium in a way that makes it less adhesive. In conclusion, this study demonstrates that activated lymphocytes of any specificity enter the spinal cord, and that the neuro-antigen specific cells accumulate there and lead to the recruitment of other cells. Non-activated cells, even those with neural antigen specificity fail to enter the cord. Understanding the nature of what an 'activated' lymphocyte is may allow us to design strategies to inhibit such immune-mediated inflammation.     

Expression of ɛBP, a β-galactoside-binding soluble lectin, in normal and neoplastic epidermis

Abstract The study of animal lectins and glycoconjugates has become an important area of research in biomedical sciences, as these molecules are believed to play important roles in a variety of biological processes. This report describes a study of the expression of an animal lectin, IgE-binding protein (?BP), also known as Mac-2 and CBP35, in human skin. We have analyzed cultured human keratinocytes as well as normal human skin and a number of epidermal neoplasms, by immunoblotting. immuno-fluorescence and immunohistochemistry. We showed that ?BP is expressed in human keratinocytes, hair follicles, sebaceous and sweat glands. We found that cBP expression retains in various epidermal neoplasms, including basal cell carcinoma, squamous cell carcinoma and keratoacan-thoma, although the level of expression appears to be reduced as compared to normal epidermis. The immunohistochemical analysis also suggests that the level of ?BP expression appears to be dependent on the degree of cellular differentiation of keratinocytes.     

Vascular cell adhesion molecule-1 modulation by tumor necrosis factor in experimental allergic encephalomyelitis

Anti-tumor necrosis factor (TNF) antibodies inhibit passively transferred experimental allergic encephalomyelitis (EAE) in SJL mice. The possibility that this occurs through interference in TNF's upregulation of endothelial cell adhesion molecules was investigated. Expression of both vascular cell adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1) on spinal cord vessels increased during EAE. The upregulation of VCAM-1 was markedly reduced or prevented by anti-TNF treatment. Leukocytic infiltration was 15-fold lower in anti-TNF-treated than diseased animals. Spinal cord endothelial expression of VCAM-1, though not ICAM-1 or fibronectin, positively correlated with the extent of T cell, B cell or monocyte infiltration in each animal.     

Dorsal root ganglia cocultured with macrophages: an in vitro model to study experimental demyelination

The present investigation introduces an in vitro model to study macrophage properties during demyelination. Rat dorsal root ganglia (DRG) were cultured for obtaining myelinated peripheral nerve fibers. These cultures were exposed to non-resident macrophages. In untreated control cultures, there was no indication of myelin removal by the added macrophages. DRG were exposed to enzymatically generated oxygen radicals using the xanthin/xanthin oxidase or the glucose/glucose oxidase system. Assessment of Schwann cell viability and ultrastructural morphology revealed different patterns of cell cytotoxicity and morphological changes in different experiments. High concentrations caused complete tissue necrosis of the DRG, while low concentrations did not affect either cell viability or ultrastructural morphology. Under intermediate experimental conditions, oxygen radicals caused non-lethal Schwann cell damage leading to Schwann cell retraction and myelin sheath rejection. Myelin lamellae were disrupted and decompacted. These changes were followed by a selective macrophage attack on myelin sheats, resulting in demyelination. Axons, Schwann cells and sensory ganglion cells survived this attack. The specificity of the oxygen radical effects was tested in experiments using the oxygen radical scavengers catalase and superoxide dismutase. Catalase prevented the described effects on cell morphology and subsequently blocked demyelination by non-resident macrophages.Supported by a grant from the Deutsche Forschungsgemeinschaft (DFG) (Br 1274/1-1)     

The role of macrophages in demyelination

Experimental allergic encephalomyelitis (EAE) is an autoimmune inflammatory disease of the central nervous system (CNS). In particular in the CsA-induced chronic relapsing form (CREAE), pronounced demyelination occurs, in temporal association with relapses. It is still a matter of discussion which cell type ultimately is responsible for the actual process of demyelination. Macrophages, cytotoxic T lymphocytes and also astrocytes are possible candidates. In this short overview, the role of macrophages in the pathogenesis of EAE is discussed. It is shown that in particular, newly recruited macrophages play a crucial role in the generation of clinical signs. Possible mechanisms by which macrophages are involved in the pathogenesis of demyelinating diseases are presented.     

脉冲Nd：YAG激光照射对大鼠炎症牙龈组织的作用

患实验性牙龈炎的大鼠牙龈（６例）经脉冲掺钕钇铝柘榴石激光（Ｎｄ：ＹＡＧ激光）照射后进行光镜及超微结构观察。目的在于了解低能量Ｎｄ：ＹＡＧ激光照射对牙龈炎症的治疗作用。炎症牙龈经输出能量为１．５Ｗ，脉冲数为２０ＰＰＳ的激光照射后与对照组相比较，形态学上有如下变化：上皮细胞无变性；牙龈上皮层数较炎症时减少；上皮下炎细胞浸润明显减少；上皮细胞间隙变小；上皮下结缔组织内产生大量的排列致密的胶原纤维。结果提