几种改进的CoMFA方法比较研究血小板活化因子拮抗剂

由于传统的比较分子场分析(CoMFA)方法本身存在一些缺陷，使得分子的叠合 规则以及叠合分子的空间取向和空间位置等因素对q~2的影响很大，因此相继提出 了几种改进的CoMFA方法。为了优化CoMFA结果，应用传统的CoMFA方法和交叉验证 的R~2引导的区域选择法(q~2-GRS)、全取向搜索法（AOS）、全空间搜索法（APS） 以及比较分子相似性指数(CoMSIA)等四种改进的CoMFA方法，对18个pinusolide类 衍生物这类新发现的血小板活化因子（PAF）拮抗剂进行了比较研究。结果表明四 种改进的CoMFA方法得到的q~2值均比传统CoMFA的高。q~2-GRS方法得到的q~2值有 所提高，但综合结果并不理想，AOS与APS得到的q~2较为理想，而在CoMSIA中， q~2几乎不受空间取向或空间位置的影响。同时我们引人基于样本的偏最小二乘法 （SAMPLS）取代原AOS／APS程序中的传统PLS进行统计分析，明显提高了其运行速 度。最后，根据q~2最高的CoMFA模型和CoMSIA模型设计了几个预测活性更高的 pinusolide类似物。     

Synthesis of positively charged lipids containing a 1,3-oxathiolane cycle

Positively charged lipids of the 1,3-oxathiolane series were synthesized by interaction of 2-pentadecyl-5-tosyloxymethyl- or -5-iodomethyl-1,3-oxathiolane with 2-(N,N-dimcthyl-amino)ethanol.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 2347–2349, September, 1996.     

血小板阻聚药物中间体N-环己基-5-氯丁基-1H-四氮唑的合成

以δ-戊内酯和环己胺为原料合成了抗血小板聚集药物西洛他唑的重要中间体N-环己基-5-氯丁基-1H-四氮唑，选择了合适的相转移催化剂及安全的叠氮试剂并获得较高的收率。     

Natural products of the medicinal fungus Ganoderma lucidum: occurrence,biological activities,and pharmacological functions

Ganoderma lucidum, a fungus used in traditional Chinese medicine, produces polysaccharides and oxygenated triterpenoids with a very broad spectrum of biological activities and pharmacological functions. Among the Ganoderma triterpenoids, many pairs of C-3 alpha/beta stereoisomers and C-3/C-15 positional isomers have been identified. Biosynthetic study has indicated that the C-3alpha series of oxygenated triterpenoids is derived from the C-3beta series via an oxidation-reduction pathway. The interaction of Ganoderma triterpenoids with human platelets in the induction of aggregation and inhibition of agonist-induced aggregation and signal transduction has been elucidated. Reduction of cellular mevalonate content to a stage in which cholesterol synthesis is strongly inhibited and cell growth is marginally arrested sensitizes hepatoma cells to the oxygenated triterpenoids. A combination treatment of lovastatin and Ganoderma triterpenoids in animal studies has exhibited a potential anticancer effect.     

Patterning Surfaces for Controlled Platelet Adhesion and Detection of Dysfunctional Platelets

Platelets play a fundamental role in thrombus formation and in the pathogenesis of arterial thrombosis. Patterning surfaces for controlled platelet adhesion paves the way for adhesion and activation mechanisms in platelets and detection of platelet functional defects. Here, a new and simple method based on controlled polymerization of 2‐methacryloyloxyethyl phosphorylcholine (MPC) on the surface of styrene‐block‐(ethylene‐co‐butylene)‐block‐styrene (SEBS) is shown. The competition between polymerization and degradation enables platelet adhesion on SEBS to be switched on and off. The adhesive sites of the platelets can be down to single cell level, and the dysfunctional platelets can be quantitatively detected.

     

急性等容性血液稀释在脊柱手术中对血小板功能的影响

目的探讨急性等容性血液稀释（ANH）在脊柱手术中对患者血小板功能的影响。方法择期全麻下行脊柱手术患者20例,术前行颈内静脉穿刺采自体血,同时于外周静脉输入等量的胶体液（万汶）,术中连续监测HR,SPO2,Bp及尿量变化,分别于采血前（T0）,采血后15 min（T1）,输血前（T2）,输血后15 min（T3）,抽取桡动脉血查HB,HCT,LAC,并采用Sonoclot分析仪测定激活凝血酶原时间（ACT）,凝血速率（CR）,血小板功能（PF）。记录术中晶胶体液输入量,出血量和尿量。结果与T0相比,T1的HB,HCT显著下降（P〈0.01）,CR、PF显著下降（P〈0.01）,与T2相比,T3的HB,HCT显著回升,CR、PF显著升高（P〈0.01）,LAC,ACT变化无统计学意义。结论急性等容性血液稀释对脊柱手术患者血小板功能有一定的保护作用,对凝血功能无明显不良影响。     

Biocompatibility of poly(carbonate urethane)s with various degrees of nanophase separation

Nanophase separation has been suggested to influence the biological performance of polyurethane. In a previous work, six different 4,4'-diphenylmethane diisocyanate (MDI)-based poly(carbonate urethane)s (PCUs) that exhibited various degrees of nanophase separation were synthesized and characterized. In the present work, these PCUs were used as a model system to study the effect of nanometric structures on the biocompatibility of polyurethane. Human blood platelet activation, monocyte activation, protein adsorption, and bacterial adhesion on PCU were investigated in vitro. It was found that human blood platelets as well as monocytes were less activated on the PCU surfaces with a greater degree of nanophase separation in general. This phenomenon was closely associated with the lower ratio of human fibrinogen/albumin competitively adsorbed on these surfaces. Bacterial adhesion was also inhibited in some nanophase-separated PCUs. [diagram in text].     

Well Crystallized α-GaOOH Nanocrystals Synthesized through Hydrothermal Routes and Their Properties

A facile hydrothermal process involving Ga(NO₃)₃·H₂O·NaN₃ solutions led to the formation of α‐GaOOH nano‐platelets. X‐ray diffraction (XRD) pattern revealed that the synthesized samples belonged to an orthorhombic crystal structure with lattice constants a=0.4510 nm, b=0.9750 nm and c=0.2965 nm. Transmission electron microscopy (TEM) studies showed that α‐GaOOH displayed the morphologies of an eccentric platelet‐like structure with 60–120 and 200–300 nm in the short and long axes, respectively. The average thickness of products was about 70 nm through scanning electron microscopy (SEM) images. The ultraviolet absorption of the samples was at 214 nm. The prepared α‐GaOOH nano‐platelets exhibited a broad emission band from 220 to 400 nm with a maximum at 343 nm under short UV excitation of 200 nm. Fourier transform infrared (FTIR) spectrum confirmed the existence of Ga₂O and Ga–OH bending modes. A possible mechanism for the formation of α‐GaOOH nano‐platelets was discussed briefly.     

Comparison of three methods for fractionation and enrichment of low molecular weight proteins for SELDI-TOF-MS differential analysis

In most diseases, the clinical need for serum/plasma markers has never been so crucial, not only for diagnosis, but also for the selection of the most efficient therapies, as well as exclusion of ineffective or toxic treatment. Due to the high sample complexity, prefractionation is essential for exploring the deep proteome and finding specific markers.In this study, three different sample preparation methods (i.e., highly abundant protein precipitation, restricted access materials (RAM) combined with IMAC chromatography and peptide ligand affinity beads) were investigated in order to select the best fractionation step for further differential proteomic experiments focusing on the LMW proteome (MW inferior to 40,000 Da). Indeed, the aim was not to cover the entire plasma/serum proteome, but to enrich potentially interesting tissue leakage proteins. These three methods were evaluated on their reproducibility, on the SELDI-TOF-MS peptide/protein peaks generated after fractionation and on the information supplied.The studied methods appeared to give complementary information and presented good reproducibility (below 20%). Peptide ligand affinity beads were found to provide efficient depletion of HMW proteins and peak enrichment in protein/peptide profiles.     

氯吡格雷抵抗机制的研究进展及临床处理策略

冠心病患者尽管接受了标准的氯吡格雷治疗，但仍有一部分患者对氯吡咯雷表现为低反应甚至无反应，称为氯吡格雷抵抗。导致这种抵抗现象的可能原因包括患者个体的基因多态性和药物之间的相互作用等。临床处理的主要对策有提高氯吡格雷的给药剂量和采用新型药物等。笔者就现有的临床研究证据对氯吡格雷抵抗的定义、发生机制及临床干预策略进行了综述。