除颤时间与心脏性猝死除颤复苏成功率的相关性分析

目的:研究除颤时间与心脏性猝死患者除颤复苏成功率的相关性。方法:选取2015年2月至2017年6月于我院接受除颤复苏治疗的心脏性猝死患者120例为研究对象。分析除颤时间与除颤复苏成功以及心功能舒张早期充盈峰速度(E峰)、左室射血分数(LVEF)、左心室舒张末期内径(LVEDD)以及E/舒张晚期充盈峰速度(A)水平的相关性。结果:电除颤时间2 min患者的复苏成功率为60.00%(21/35),显著高于电除颤时间2~5 min、5~10 min以及10 min患者的34.21%(13/38)、11.11%(3/27)、0.00%(0/20),而电除颤时间2~5 min患者的复苏成功率又显著高于电除颤时间5~10 min患者,差异均有统计学意义(均P0.05)。电除颤时间2 min、2~5 min、5~10 min以及10 min患者的E峰、LVEF、LVEDD以及E/A水平呈逐渐下降趋势,差异均有统计学意义(均P0.05)。Pearson相关性分析结果显示心脏性猝死患者除颤时间与除颤复苏成功率、E峰、LVEF、LVEDD以及E/A均呈负相关关系(r=-0.593,P=0.000;r=-0.476,P=0.001;r=-0.523,P=0.000;r=-0.502,P=0.000;r=-0.469,P=0.001)。结论:除颤时间与心脏性猝死患者除颤复苏成功率呈负相关关系,即除颤时间越早,患者复苏成功率越高。     

白介素-6对NMDA诱导的小脑神经元放电活动的抑制作用及其机制

目的：观察白介素-6（IL-6）对N-甲基-D-天冬氨酸（NMDA）激发的神经元放电活动的影响及其可能的作用机制。方法：用含IL-6、NMDA和JAK抑制剂ACA90的人工脑脊液（ACSF）灌流小脑脑片,利用离体脑片神经元单位放电细胞外记录技术,记录药物对小脑间位核神经元放电的影响。用Western blot法测定间位核神经元NMDA受体亚单位1（NRI）的磷酸化水平。结果：单独用12．5μmol／L和25μmol／LNMDA灌流,神经元放电频率均较基础放电频率增加;用不同浓度IL-6（50,100,200μg／ml）联合NMDA作用后,神经尤的放电频率出现浓度依赖性地降低;AG490可部分阻断IL-6对NMDA兴奋神经元放电的抑制作用。与单独NMDA处理组比较,用IL-6联合NMDA处理神经元后,神经元的NR1磷酸化水平出现浓度依赖性地降低。AG490可阻断IL-6所致的神经元NR1磷酸化水平的降低。结论：IL-6可抑制NMDA激发的小脑间位核神经元的放电兴奋活动;并同时下调神经元的NR1磷酸化水平。     

Continual assembly of desmosomes within stable intercellular contacts of epithelial A-431 cells

Subclones of human carcinoma-derived A-431 cell line stably producing fusion proteins consisting of the enhanced green fluorescent protein and either human desmoglein 2 (Dsg-GFP) or human plakoglobin (GFP-Pg) were used to examine the behavior of desmosomes in living cells. Immunofluorescence microscopy of the fixed cells showed that both fusion proteins, which were expressed in significantly lower levels relative to their endogenous counterparts, were efficiently recruited into desmosomes. Time-lapse confocal imaging of these cells reveals that such GFP-labeled desmosomes (GFP desmosomes) are stable structures which exhibit various dynamic and motile activities. The most notable are independent lateral mobility and fusion. Furthermore, the continual assembly of new nascent desmosomes is observed within stable contacts located at the middle of the epithelial sheet. A new GFP desmosome appears as a closely apposed group of fine patches which after a few minutes aggregate into a single structure. These three dynamic processes resulted in constant changes of desmosome distribution, numbers, and sizes. In addition, fluorescence recovery after photobleaching experiments showed that fine patches of desmosomal proteins may participate in desmosome maintenance. Such a diverse range of dynamic activities of desmosomes apparently produces flexible but tight cell-cell adhesion required for different morphogenetic events in epithelial structures.This work was supported by grant AR44016-04 from the National Institutes of Health     

Quantitative FRET measurement based on spectral unmixing of donor,acceptor and spontaneous excitation‐emission spectra

The spontaneous excitation‐emission (ExEm) spectrum is introduced to the quantitative mExEm‐spFRET methodology we recently developed as a spectral unmixing component for quantitative fluorescence resonance energy transfer measurement, named as SPEES‐FRET method. The spectral fingerprints of both donor and acceptor were measured in HepG2 cells with low autofluorescence separately expressing donor and acceptor, and the spontaneous spectral fingerprint of HEK293 cells with strong autofluoresence was measured from blank cells. SPEES‐FRET was performed on improved spectrometer‐microscope system to measure the FRET efficiency (E) and concentration ratio (R _C) of acceptor to donor vales of FRET tandem plasmids in HEK293 cells, and obtained stable and consistent results with the expected values. Moreover, SPEES‐FRET always obtained stable results for the bright and dim cells coexpressing Cerulean and Venus or Cyan Fluorescent Protein (CFP)‐Bax and Yellow fluorescent protein (YFP)‐Bax, and the E values between CFP‐Bax and YFP‐Bax were 0.02 for healthy cells and 0.14 for the staurosporine (STS)‐treated apoptotic cells. Collectively, SPEES‐FRET has very strong robustness against cellular autofluorescence, and thus is applicable to quantitative evaluation on the protein‐protein interaction in living cells with strong autofluoresence.      

珊瑚礁白化研究进展

珊瑚礁白化是由于珊瑚失去体内共生的虫黄藻和（或）共生的虫黄藻失去体内色素而导致五彩缤纷的珊瑚礁变白的生态现象。近年来,频繁发生的珊瑚礁白化导致了珊瑚礁生态系统严重退化,并已经影响到全球珊瑚礁生态系统的平衡,受到了人们的高度重视。研究认为：（1）大范围珊瑚礁白化主要是全球环境变化引起的,尤其是全球变暖和紫外辐射增强;（2）导致珊瑚礁白化的机制主要在于细胞机制和光抑制机制;（3）珊瑚礁白化后的恢复与白化程度有关,大范围白化的珊瑚礁完全恢复需要几年到几十年;（4）珊瑚礁白化的后果在于降低珊瑚繁殖能力、减缓珊瑚礁生长、改变礁栖生物的群落结构,导致大面积珊瑚死亡和改变珊瑚礁生态类型,如变为海藻型等;（5）与珊瑚共生的D系群虫黄藻更适应高温环境,珊瑚礁有可能通过D系群逐渐取代C系群的方式适应全球环境变化。     

Spontaneous insertion of plant plasma membrane (H+)ATPase into a preformed bilayer

Summary The purified (H⁺ATPase from corn roots plasma membrane inserted spontaneously into preformed bilayer from soybean lipids. The yield of the protein insertion, as measured from its H⁺-pumping activity, increased as a function of lipids and protein concentrations. In optimum conditions, all the (H⁺)ATPase molecules were closely associated with liposomes, exhibiting a high H⁺-pumping activity (150,000% quenching· min^–1·mg^–1 protein of the probe 9-amino-6-chloro-2-methoxyacridine). The insertion was achieved within a few seconds. No latency of the (H⁺)ATPase hydrolytic activity was revealed when lysophosphatidylcholine was added to permeabilize the vesicles. This indicated that the (H⁺)ATPase molecules inserted unidirectionally, the catalytic sites being exposed outside the vesicles (inside-out orientation), and thus freely accessible to Mg-ATP. The nondelipidated (H⁺)ATPase could also functionally insert into bilayer from PCPEPG or PCPEPI, due to the presence of both hydrophobic defects promoted by PE, and negative phospholipids specifically required by the (H⁺)ATPase from corn roots. The detergent octylglucoside facilitated the delipidated (H⁺)ATPase reinsertion probably by promoting both a proper protein conformation and hydrophobic defects in the bilayer. Lysophosphatidylcholine facilitated the delipidated protein insertion only when hydrophobic defects were already present, and thus seemed only capable to ensure a proper protein conformation     

刺激家兔尾核对丘脑束旁核痛兴奋和痛抑制单位放电的影响

在51只清醒麻痹家兔身上,记录了丘脑束旁核痛兴奋(PfPE)和痛抑制(PfPI)单位的放电。观察刺激尾核头背部(DHCN)对 PfPE 和 PfPI 单位自发放电和痛放电的影响。(1)刺激 DHCN时,在28个 PfPE 单位中,19个的自发放电发生抑制反应,7个无变化,2个增强;在6个PfPI 单位中,5个的自发放电增加,1个无变化。(2)刺激 DHCN 时,在38个 PfPE 单位中。2个的痛放电兴奋增强,6个无变化,30个被抑制。其中12个呈抑制反应的单位,8个立即发生在刺激 DHCN 之后,并延续700—1600ms,在10个 PfPI 单位中,7个的痛放电发生兴奋反应,3个无变化。这些结果提示,DHCN 对丘脑 PfPE 和 PfPI 单位在处理痛觉信息上具有调制作用。根据抑制的潜伏期短和延续时间长的特点,推测这种调制作用可能既通过直接通路又有间接环路参与。     

Microbially enhanced oil recovery from carbonate reservoirs

About half of the world's oil production is from carbonate formations. However, most of the research in microbially enhanced oil recovery (MEOR), a potentially important tertiary recovery technology, has focused on sandstone reservoirs because, in general, they are geologically simpler than carbonate reservoirs and easier to model in the laboratory. Carbonate formations have a wide range of pore geometries and distributions, resulting in complex flow dynamics. The low matrix permeabilities and the dual porosity characteristics of most carbonate formations, coupled with the chemistry of carbonates, have slowed implementation of enhanced oil recovery methods. A review of the data on carbonate reservoirs in Dwight's Energydata TOTL System indicated that 40% of the oil‐producing carbonate reservoirs surveyed in the United States have environmental, geological, and petrophysical conditions that would make them candidates for MEOR. A review of a number of MEOR field trials showed that rates of oil production could be increased by as much as 200%. Microbial activity in these trials was probably due to that of indigenous populations rather than the microorganisms injected for the trials. Detrimental effects such as loss of injectivity and increased souring were not reported. Based on analysis of the geology and petrophysical characteristics of carbonates, two common mechanisms of MEOR, microbial acid production and microbial gas production, are especially suited for application in carbonate reservoirs.     

Esterification of 2-methylalkanoic acids Catalysed by Lipase from Candida rugosa: Enantioselectivity as a Function of water Activity and Alcohol Chain Length

Esterifications catalysed by immobilised lipase from Candida rugosa (CRL) in cyclohexane at constant water activity (a_w = 0.76) were studied using 2-methyl substituted octa-, nona- or decanoic acids and n-alcohols of varying chain length as substrates. The importance of controlling the water activity and choosing the right alcohol for obtaining maximum enantioselectivity is demonstrated. The immobilised lipase was easily recovered without loss of activity and enantioselectivity.     

Polydatin promotes the neuronal differentiation of bone marrow mesenchymal stem cells in vitro and in vivo: Involvement of Nrf2 signalling pathway

Bone marrow mesenchymal stem cell (BMSC) transplantation represents a promising repair strategy following spinal cord injury (SCI), although the therapeutic effects are minimal due to their limited neural differentiation potential. Polydatin (PD), a key component of the Chinese herb Polygonum cuspidatum, exerts significant neuroprotective effects in various central nervous system disorders and protects BMSCs against oxidative injury. However, the effect of PD on the neuronal differentiation of BMSCs, and the underlying mechanisms remain inadequately understood. In this study, we induced neuronal differentiation of BMSCs in the presence of PD, and analysed the Nrf2 signalling and neuronal differentiation markers using routine molecular assays. We also established an in vivo model of SCI and assessed the locomotor function of the mice through hindlimb movements and electrophysiological measurements. Finally, tissue regeneration was evaluated by H&E staining, Nissl staining and transmission electron microscopy. PD (30 μmol/L) markedly facilitated BMSC differentiation into neuron‐like cells by activating the Nrf2 pathway and increased the expression of neuronal markers in the transplanted BMSCs at the injured spinal cord sites. Furthermore, compared with either monotherapy, the combination of PD and BMSC transplantation promoted axonal rehabilitation, attenuated glial scar formation and promoted axonal generation across the glial scar, thereby enhancing recovery of hindlimb locomotor function. Taken together, PD augments the neuronal differentiation of BMSCs via Nrf2 activation and improves functional recovery, indicating a promising new therapeutic approach against SCI.