内毒素对兔红细胞膜磷脂含量的影响及阳离子A对其的拮抗效应

利用高效液相色谱法分别测定正常对照组（Ⅰ组）、内毒素组（Ⅱ组）和内毒素＋阳离子A拮抗组（Ⅲ组）中兔红细胞膜磷脂酰胆碱（PC）、磷脂酰乙醇胺（PE）、磷脂酰丝氨酸（PS）和磷脂酰肌醇（PI）含量。结果显示，Ⅱ组中除PE在处理后0．5h没有明显变化外（P〉0．05），PC、PE、PS、PI含量在0，5、1、3、5、7h均低于Ⅰ组（P〈0.05，P〈0．01）；而Ⅲ组中除PS、PE和PI在处理后0．5h、PC在1h、PI在3h没有明显变化外（P〉0．05），整个时间段中上述4种磷脂的含量均高于Ⅱ组（P〈0．05，P〈0．01）。可见，内毒素能使兔红细胞膜磷脂含量降低，而阳离子A在一定程度上具有对内毒素的拮抗作用和对红细胞膜的保护效应。     

Adipocyte-derived relaxing factor,a new vasodilative factor

Although our knowledge of ADRF (adipocyte-derived relaxing factor) is extremely limited,the little that is known has already revealed a promising future in this newly found factor.Firstly,it is secreted by adipose tissue,which is a abundantly and extensively distributed in human body and has become a hot spot for research work in recent years.Secondly,ADRF has shown a significant vasodilative action in a considerable number of experiments conducted on arteries of various sizes,from different body parts of different species of animals,including human.In this article,we introduce the development of ADRF research,sum up its known properties,including its Ca2+,protein tyrosine kinase,and protein kinase A dependent releasing,K+ channel mediated functioning,and interfered effect in different pathological models,and propose problems surrounding this factor and directions for future research work.     

蒺藜苜蓿cation/H+ exchanger基因家族鉴定及表达特征分析

CPA（cation proton antiporter）超家族通过转运质子和一价金属离子调节细胞内离子和pH稳定。阳离子质子转运体（cation/H⁺ exchanger,CHX）基因家族属于CPA2（cation proton antiporter 2）超家族,其N端有一个Na⁺/H⁺ exchanger结构域,对植物维持细胞离子平衡、花器官发育起着至关重要的作用。通过生物信息学手段,系统地分析了蒺藜苜蓿CHX家族基因,通过全基因组筛选共鉴定出47个MtCHXs;染色体定位分析表明蒺藜苜蓿CHX基因分布在8条不同的染色体上;同源性分析显示蒺藜苜蓿和拟南芥亲缘关系近,而与水稻亲缘关系远;进一步进化关系分析将47个MtCHXs基因分为5组,并且各组内成员在基因结构和基序上比较保守;顺式作用元件分析发现MtCHXs基因启动子包含大量光响应元件、激素响应元件以及干旱、低温、创伤响应元件;表达特性分析发现MtCHXs在生殖器官中高表达,并且响应干旱、低温等非生物胁迫。     

秦岭南坡中山地带华北落叶松人工林对土壤的影响

秦岭南坡中山地带华北落叶松人工林对土壤的影响雷瑞德，党坤良，张硕新，谭芳林（西北林学院森林资源保护系杨陵７１２１００）关键词华北落叶松，土壤养分状况，阳离子交换量，酶活华北落叶松（Ｌａｒｉｘｐｒｉｎｃｉｐｉｓ－ｒｕｐｐｒｅｃｈｃｉｉＭａｒｙｒ．）天然...     

飞机草地理分布、危害、传播和防治技术的研究进展

飞机草是一种入侵性杂草,在我国已大面积发生并且仍未得到有效控制。文章对飞机草的地理分布及其对畜牧业、农产品、人畜方面的危害进行阐述,分析其传播途径,并从农业、物理、化学、生物防治技术方面进行探讨并研究其进展,为飞机草的综合防治提供参考资料。     

Expression of TMEM16A as a calcium-activated chloride channel in Fischer rat thyroid follicular epithelial cells and its electrophysiologic pro-perties

AIM：To investigate the expression of transmembrane protein 16A(TMEM16A) in Fischer rat thyroid follicular epithelial (FRT) cells and its electrophysiologic properties. METHODS：The eukaryotic expression vector of pUB6/V5-TMEM16A was constructed and transfected into FRT cells by liposome-mediated transfection. In order to obtain the high efficiency of gene transfection and expression, the quantity and ratio of lipid/DNA complexes were optimized. The FRT cells stably expressing TMEM16A were gained by the selection with blasticidin and confirmed by the techniques of RT-PCR and immunofluorescence. The expression and location of TMEM16A in the FRT cells were observed under an inverted fluorescence microscope. TMEM16A protein was associated with calcium-dependent chloride current, as measured with halide-sensitive fluorescent protein and patch-clamp technique. RESULTS：The results of double digestion and sequencing indicated that TMEM16A was cloned into pUB6/V5. The results of RT-PCR and immunofluorescence confirmed that TMEM16A was expressed in the FRT cells after transfection with TMEM16A. The classical calcium-activated chloride channel currents were recorded in the FRT cells stably expressing TMEM16A by the technique of patch-clamp and halide-sensitive fluorescent protein YFP-H148Q/I152L. CONCLUSION：The protein expression of TMEM16A in the FRT cells was observed. TMEM16A is the molecular identity of calcium-activated chloride channels.     

Effects of Kv1.5 on proliferation and apoptosis of rat PASMCs under hypoxia+hypercapnia condition and relationship with MAPK pathway

AIM：To investigate the effects of voltage-dependent K＋ channel 1.5 (Kv1.5) on the proliferation and apoptosis of rat pulmonary artery smooth muscle cells (PASMCs) under hypoxia+hypercapnia condition and the relationship with mitogen-activated protein kinase(MAPK) signal pathway. METHODS：The PASMCs isolated from the male SD rat were cultured under hypoxia+hypercapnia condition, and randomly divided into normal group (N group), hypoxia+hypercapnia group (HH group), hypoxia+hypercapnia+DMSO incubation group (HD group), hypoxia+hypercapnia+U0126 (an extracellular signal-regulated kinase 1/2 inhibitor) incubation group (HU group), hypoxia+hypercapnia+SB203580 (a p38 mitogen-activated protein kinase inhibitor) incubation group (HS group), and hypoxia+hypercapnia+anisomycin (an agonist of MAPK) incubation group (HA group). Cell Counting Kit-8 was used to detect the cell viability. The protein expression of Kv1.5, PCNA and Bax was detected by Western blotting. RESULTS：Compared with N group, the cell viability and PCNA protein expression in HH group and HD group were significantly raised (P<001), but Kv1.5 and Bax proteins were significantly decreased (P<0.01). No difference between HH group and HD group was observed (P>005). Compared with HD group, the cell viability and PCNA protein expression in HU group, HS group and HA group were decreased (P<0.05 or P<0.01), but Kv1.5 protein and Bax protein were raised (P<0.01), with the most significant changes in HA group. ^{CONCLUSION：}The regulation of Kv1.5 to the proliferation and apoptosis of PASMCs under hypoxia+hypercapnia condition might have a relationship with the activation of MAPK signal pathway.     

Action of Clathrodin and Analogues on Voltage-Gated Sodium Channels

Clathrodin is a marine alkaloid and believed to be a modulator of voltage-gated sodium (Na_V ) channels. Since there is an urgent need for small molecule Na_V channel ligands as novel therapeutics, clathrodin could represent an interesting lead compound. Therefore, clathrodin was reinvestigated for its potency and Na_V channel subtype selectivity. Clathrodin and its synthetic analogues were subjected to screening on a broad range of Na_V channel isoforms, both in voltage clamp and patch clamp conditions. Even though clathrodin was not found to exert any activity, some analogues were capable of modulating the Na_V channels, hereby validating the pyrrole-2-aminoimidazole alkaloid structure as a core structure for future small molecule-based Na_V channel modulators.