Experimental research on cardiac fibrosis induced by recombinant mouse interleukin-11 in mice

AIM To observe the effect of recombinant mouse interleukin-11 （rmIL-11）injected subcutaneously into mice on heart structure and function and to determine its pro-fibrotic effect. METHODS C57BL/6 mice were randomly divided into experimental group and control group.The mice in experimental group were injected subcutaneously with recombinant mouse IL-11 at the dose of 100 μg·kg^-1·d^-1 for 3 consecutive weeks, while the control group were given equal volume of normal saline in the same way. After the experiment was finished, the parameters of heart function were measured by echocardiography.The heart weight was weighed and the cardiac weight index (CWI) was calculated. HE staining and Masson's trichrome staining were performed to observe the pathological changes and the extent of myocardial fibrosis in mouse myocardia respectively, and the cardiac collagen volume fraction (CVF) was calculated. The expression levels of extracellular matrix proteins in the myocardial tissues of mice, including type Ⅰ collagen, type Ⅲ collagen and fibronectin, were determined by Western blot. RESULTS Left ventricular ejection fraction and left ventricular fraction shortening in experimental group were obviously lower than those in control group (P<0.01), however left ventricular end-diastolic diamension and left ventricular end systolic dimension were significantly higher than those in control group (P<0.05).Compared with control group, the CWI was increased (P<0.01), the myocardial arrangement was disorder, the necrosis of cardiac myocytes was increased, and excessive deposition of collagen was observed in the myocardial tissues in experimental group. Correspondingly, the CVF and protein levels of type Ⅰ collagen, type Ⅲ collagen and fibronectin in the left ventricle in experimental group were increased significantly (P<0.05). CONCLUSION Injection of rmIL-11 into the mice subcutaneously induces fibrogenesis in the heart, which implies that IL-11 is likely a novel pro-fibrotic factor.     

十个侧耳菌株的模糊综合评价初报

应用模糊数学中隶属度和模糊概率概念,对10个侧耳菌株进行了模糊综合评价。结果表明,SN1是表现最好的菌株,与实际试验结果较为一致。     

苦竹各器官主要营养元素分布及采伐的养分输出

本文根据四川长宁苦竹(Pleioblastus amarus)各器官生物量以及其主要营养元素含量和储量,研究了苦竹采伐的养分输出问题。结果表明:苦竹各器官中N、P、K、Si、Ca、Mg等6种营养元素以代谢旺盛的竹叶和竹鞭中含量最高;6种养分元素在各器官贮存量(单位:kg.hm-2)从大至小的排序为:叶(510.8)>竹根(230.62)>杆(182.14)>枝(163.77>竹鞭(59.19)>竹蔸(41.16)。苦竹采伐的养分年输出量(单位:kg.hm-2)从大至小的排序为:Si(50.23)>K(38.77)>N(35.58)>Mg(4.55)>P(3.86)>Ca(3.31)。对比该地区的降雨输入,苦竹林地养分以Si失衡最为严重;其次为K、N。若采伐时将竹叶带出竹林,6种元素的养分输出总量将增加1.48倍。可见,竹叶归还林地对维持地力具有极其重要的作用。     

灌浆初期高温胁迫对水稻籽粒活性氧积累及产量形成的影响

【目的】研究灌浆初期高温胁迫对水稻籽粒活性氧积累及产量形成的影响,为耐热水稻种质资源的筛选和鉴定提供理论依据。【方法】以长江中下游地区普遍推广种植的8个水稻品种为材料,在灌浆初期进行高温胁迫（38 ℃/32 ℃,昼/夜）,研究各水稻品种在灌浆初期高温胁迫下的ROS含量、抗氧化酶活性、淀粉合成相关酶活性、产量及其构成要素以及稻米品质的差异。【结果】与对照相比,灌浆初期高温胁迫导致水稻籽粒O^-₂·和H₂O₂含量及抗氧化酶活性显著增加。在不同水稻品种中,淀粉合成相关酶活性对灌浆初期高温胁迫的响应具有差异性。高温胁迫下,产量损失较大水稻品种的O^-₂·和H₂O₂含量增幅较大,淀粉合成酶活性受高温胁迫影响也较大。灌浆初期高温胁迫导致水稻结实率、千粒质量、收获指数和产量显著下降,其中黄华占和湘两优900的产量损失较小,在灌浆初期的耐热性较强;粤王丝苗、泰优390和湘两优2号的产量损失较大,在灌浆初期的耐热性弱。灌浆初期高温胁迫导致糙米率、精米率和淀粉含量显著下降,垩白粒率和垩白度增加。高温胁迫下,产量损失较大水稻品种的淀粉含量下降幅度较大,稻米品质受高温胁迫影响也较大。在高温胁迫下,水稻产量与ROS含量显著负相关,而与抗氧化酶活性显著正相关。产量、籽粒加工指标、淀粉含量和淀粉合成酶活性的抗逆系数与ROS含量的抗逆系数显著负相关,而与抗氧化酶活性的抗逆系数显著正相关。【结论】灌浆初期高温胁迫导致水稻籽粒ROS过量积累是降低淀粉合成酶活性和淀粉含量,进而导致产量和稻米外观加工品质下降的重要因素。ROS的增加量可作为灌浆初期水稻耐热性评价的参考指标。     

瓦埠湖沉积物氮的赋存特征以及环境因子对NH4+-N释放的影响

采用现场采样和室内测试的方法,研究了瓦埠湖沉积物各层的TN、NH4^＋-N、NO3^--N的赋存特征。结果发现,TN上层比底层低,随着沉积深度的增加,硝化作用相对减弱,NO3^-N随着沉积深度的增加而减少,NH4^＋-N的含量随着沉积深度的增加而增加。pH〈9时,pH对NH4^＋-N释放的影响规律不是很明显,pH〉9时,NH4^＋-N释放随着pH的增加而增加。随着温度的升高,NH4^＋-N的释放量增大。好氧、厌氧条件下,NH4^＋-N都有释放,且在好氧条件下NH4^＋-N呈低释放状态,厌氧状态下NH4^＋-N呈高释放状态。     

PubMed系统特殊服务功能应用概述

美国医学图书馆（NLM）开发的PubMed是我国医学科技人员最常使用的一个生物医学文献检索系统,本文针对PubMed实际应用中的问题,主要介绍了该系统几项特殊服务功能的应用方法,包括期刊数据库、医学主题词数据库、单引文匹配器、批引文匹配器、临床咨询、外部链接和存储器等,旨在为需求者提供一些有益的帮助。     

蚯蚓粪与化肥配施对红小豆生长与品质的影响

为探究蚯蚓粪与化肥配施对陕西关中地区红小豆产量及品质的影响,以红小豆新品种保红947为研究对象,设置T1(纯化肥)、T2(20％蚯蚓粪+80％化肥)、T3(50％蚯蚓粪+50％化肥)、T4(80％蚯蚓粪+20％化肥)和CK(不施肥)5个处理,研究了不同处理下红小豆成熟期农艺性状、产量性状及品质性状的差异.结果表明:蚯蚓...     

Relationship between Th1/Th2 balance and CD28/CTLA-4 expression on peripheral blood T cells in patients with systemic lupus erythematosus

AIM: To investigate the pattern of Th1/Th2 balance in systemic lupus erythematosus(SLE) patients and the relationship between CD28/CTLA-4(cytotoxic T-lymphocyte antigen-4) molecule expression and Th1/Th2 balance.METHODS: Eighteen SLE patients met the ARA 1997 updated SLE criteria were selected in the study. According to Bombardier's SLEDAI criteria, all patients were classified into two groups: active group(12 cases) and static group(6 cases). Fourteen normal individuals, matched for age and sex of the patients, served as controls. The peripheral blood mononuclear cells(PBMCs) were isolated by density gradient centrifugation and cultured in RPMI-1640 culture medium. After treated with PMA(5 μg/L) and ionomycin(500 μg/L) for 72 h, the PBMCs were collected, the contents of IFN-γ and IL-10 in the supernatant of cultured PBMCs were detected using enzyme linked immunosorbent assay(ELISA). The expression of CD28 and CTLA-4 molecules on T cells were detected by flow cytometric technique with double staining by FITC or PE labeled monoclonal antibodies. RESULTS: The level of IL-10 was higher in the PBMCs of active and static SLE patients(351.29 ng/L±153.31 ng/L and 319.37 ng/L±153.39 ng/L) than that in controls(254.48 ng/L±120.69 ng/L), but the difference did not reach statistical significance(P>0.05). The level of IFN-γ was significantly lower in the PBMCs of active SLE patients(25.76 ng/L±16.09 ng/L) than that in controls(50.71 ng/L±27.92 ng/L, P＜0.05). The ratio of IL-10/IFN-γ was significantly higher in active SLE patients(18.74±13.77) than that in controls(6.66±4.95, P<0.05). Either before or after culture, the expression of CD28 molecule on CD3⁺and CD8⁺ T cells from all SLE patients was not remarkably different from that in the cells of controls. Before culture, the expression of CTLA-4 molecule on CD3⁺T cells of active SLE patients(0.79%+0.37%) was significantly lower than that in the cells of controls(1.31%+0.61%, P<0.05). After culture, the expression of CTLA-4 molecule on CD3⁺ T cells of SLE patients was still lower than that in the cells of normal controls without statistical significance(P＞0.05).The expression level of CD28 molecule on CD3⁺ or CD8⁺ T cells in active SLE patients and controls was not correlated with the levels of IFN-γ and IL-10 in the supernatants(P＞0.05). The level of CTLA-4 molecule expression on CD3⁺ T cells of active SLE patients was positively correlated with IFN-γ level(r=0.681, P<0.05), while was negatively correlated with IL-10 levels(r=-0.624,P＜0.05) and the ratio of IL-10/IFN-γ(r=-0.738, P<0.01). The level of CTLA-4 molecule expression on CD3⁺ or CD8⁺ T cells of controls showed no correlation with IFN-γ levels, while showed negative correlations with IL-10 level(r=-0.587, P<0.05; r=-0.563, P<0.05, respectively).CONCLUSION: There is a bias in the differentiation of Th0 cells towards Th2 in SLE patients. CTLA-4 probably plays an important role in this mechanism through suppressing the signal transmitted by CD28.     

1980-2007年喜马拉雅东段洛扎地区冰川和冰湖变化研究

利用1980年地形图、1988/1990年Landsat TM、2000年Landsat ETM＋、2007年ALOS AVNIR-2遥感资料和近41年（1967-2007年）的气温、降水量资料对喜马拉雅东段洛扎地区的冰川、冰湖变化特征及变化原因进行了研究。结果表明：1）1980-2007年,本区冰川面积从491.64...     

Effects of exosomes derived from hypoxia-preconditioned umbilical cord mesenchymal stem cells on function of endothelial cells

AIM To investigate the effect of exosomes derived from hypoxia-preconditioned human umbilical cord mesenchymal stem cells (hUCMSCs) on proliferation, migration and tube formation of human umbilical vein endothelial cells (HUVECs). METHODS hUCMSCs and HUVECs were isolated, cultured and identified. Exosomes derived from hUCMSCs were extracted by ultracentrifugation. The morphological change of exosomes was observed under transmission electron microscope. The particle size and concentration of exosomes were detected by nanoparticle tracking analysis, and the surface specific marker proteins of exosomes were determined by Western blot. hUCMSCs were divided into normoxia group and hypoxia group. The viability of hUCMSCs was measured by CCK-8 assay. HUVECs were divided into control group, normoxic exosome group and hypoxic exosome group. The proliferation of HUVECs was detected by EdU assay. The migration ability was detected by cell scratch assay and Transwell experiment. Tube formation ability was evaluated by tube formation experiment. RESULTS Compared with normoxia group, hypoxia pretreatment enhanced the viability and exosome release of hUCMSCs. Compared with normoxic exosome group, hypoxic exosomes enhanced the proliferation, migration and tube formation of HUVECs. CONCLUSION Exosomes derived from hUCMSCs under hypoxia enhances the proliferation, migration and tube formation of HUVECs.