62 resultados para NITRIC OXIDE SYNTHESIS


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We investigated the effects of Ginsenoside R-e on human sperm motility in fertile and asthenozoospermic infertile individuals in vitro and the mechanism by which the Ginsenosides play their roles. The semen samples were obtained from 10 fertile volunteers and 10 asthenozoospermic infertile patients. Spermatozoa were separated by Percoll and incubated with 0, 1, 10 or 100 mu M of Ginsenoside R-e. Total sperm motility and progressive motility were measured by computer-aided sperm analyzer (CASA). Nitric oxide synthase (NOS) activity was determined by the H-3-arginine to H-3-citrulline conversion assay, and the NOS protein was examined by the Western blot analysis. The production of sperm nitric oxide (NO) was detected using the Griess reaction. The results showed that Ginsenoside R-e significantly enhanced both fertile and infertile sperm motility, NOS activity and NO production in a concentration-dependent manner. Sodium nitroprusside (SNP, 100 nM), a NO donor, mimicked the effects of Ginsenoside R-e. And pretreatment with a NOS inhibitor N-omega-Nitro-L-arginine methyl ester (L-NAME, 100 mu M) or a NO scavenger N-Acetyl-L-cysteine (LNAC, 1 mM) completely blocked the effects of Ginsenoside R-e. Data suggested that Ginsenoside R-e is beneficial to sperm motility, and that induction of NOS to increase NO production may be involved in this benefit.

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The nitric oxide synthase (NOS) activity in the haemocytes of shrimps Fenneropenaeus chinensis (Osbeck) and Marsupenaeus japonicus (Bate) was Studied after white spot syndrome virus (WSSV) infection to determine its characteristics in response to virus infection. First, the NOS activity in haemocytes of shrimps was determined by the means of NBT reduction and changes in cell conformation. And the variations of NOS activity in shrimps after challenge with WSSV intramuscularly were evaluated through the analysis Of L-citrulline and total nitrite/nitrate (both as NO derivates) concentrations. The result showed that NOS activity in the haemocytes of F chinensis increased slightly from 0 to 12 h postchallenge, indicated by the variations Of L-Citrulline (from 11.15 +/- 0.10 to 12.08 +/- 0.64 mu M) and total nitrite/nitrate concentrations (from 10.45 +/- 0.65 to 12.67 +/- 0.52 mu M). Then it decreased sharply till the end of the experiment (84 h postchallenge), the concentrations Of L-Citrulline and total nitrite/nitrate at 84 It were 1.58 +/- 0.24 and 2.69 +/- 0.70 mu M, respectively. The LPS-stimulated NOS activity kept constant during the experiment. However, in M. japonicus, the NOS activity kept increasing during the first 72 It postchallenge, the concentrations Of L-Citrulline and total nitrite/nitrate increased from 7.82 +/- 0.77 at 0 h to 10.79 +/- 0.50 mu M at 72 h, and from 8.98 +/- 0.43 at 0 h to 11.20 +/- 0.37 mu M at 72 h, respectively. Then it decreased till the end of the experiment (216 h postchallenge), and the concentrations of L-Citrulline and total nitrite/nitrate at 216 h were 5.66 +/- 0.27 and 4.68 +/- 0.16 mu M, respectively. More importantly, an apparent increase of I-PS-stimulated NOS activity was observed in M japonicus at 48 h postchallenge, which was about 4 times higher than that in the control group of health shrimps. In correspondence with the difference of NOS activity between the two species of shrimps, the Cumulative mortalities of the shrimps were also different. All shrimps of F. chinensis in the mortality experiment died in 66 h, much more quickly than M. japonicus, Whose accumulative mortality reached 100% after 240 h. Data here reported let us hypothesize that NOS activity in the haemocytes of shrimps F chinensis and M. japonicus responses to WSSV infection differently, and this might be one of the reasons for the different susceptibility of F chinensis and M. japonicus to WSSV infection. (c) 2005 Elsevier Inc. All rights reserved.

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The coadsorption of NO and O-2 on Ag(110) surface has been studied by X-ray photoelectron spectroscopy (XPS), ultraviolet photoelectron spectroscopy (UPS) and in situ Raman spectroscopy. The existence of oxygen enhances the adsorption of NO by forming the NOx species, that is, NO2 and NO3, and the NO in turn as a promotor facilitates the cleavage of the dioxygen bond, forming the surface atomic oxygen species having the same spectral characteristics as those produced using oxygen at high pressure. The oxygen species generated by the interaction is composed of two parts. One is produced directly by the decomposition of surface NO-O-2 complex at ca 625 K, which raised an O 1s feature at 530.5 eV and is absent at ca 800 K, while the another with an O 1s binding energy of 529.2 eV emerges at higher temperatures and shows similar properties as the reported gamma-state oxygen which bound tightly on restructured silver surface. The exposure to NO and O-2 causes noticeable changes in the morphology of the Ag(110) surface and the flat terraces superseded by small (ca 0.1 mu m) pits, and particles with typical diameters of a few micrometres were formed at elevated temperatures. (C) 1999 Elsevier Science B.V. All rights reserved.

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A new poly(fullerene oxide) thin film material has been fabricated by thermal activation and electron bombardment on hexanitro[60]fullerene (HNF) film deposited on a An substrate, all under vacuum conditions. The reaction products in the polymerization process are analyzed by XPS, UPS, IR, TGA-MS and LDI-MS techniques. It is found that the main effect of thermal and radiation treatments is to induce cleavage of -NO bonds from HNF molecules resulted in the release of nitric oxide gas and the formation of fullerene-bound oxyradicals, C-60-C-6. Spectroscopic evidence strongly suggests that rearrangement of fullerenic nitro moieties into nitrito groups is involved in the HNF decomposition process prior to the generation of reactive oxyradical intermediates. Consequently, the intermolecular coupling reaction of these oxyradicals leads to carbon polymer networks containing oxygen-bridged fullerenes. The thermally generated polymeric thin film is stable up to 900 K. Electron bombardment is also effective in both the decomposition of -NO2 groups and the removal of -OH groups present in HNF films. UV irradiation at 365 nm alone is shown to be not as efficient for the polymer formation. (C) 2003 Elsevier Ltd. All rights reserved.

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In this paper, we report a simple method of fabricating silver and gold nanostructures at the air - water interface, which can be spontaneously assembled through the reduction of AgNO3 and HAuCl4 with ultraviolet (UV) irradiation in the presence of polyacrylic acid (PAA), respectively. It was found that the building blocks in the silver nanostructure are mainly interwoven silver nanofilaments, while those of the gold nanostructure are mainly different sizes of gold nanoparticles and some truncated gold nanoplates, and even coalescence into networks. At the air - water interface, these silver and gold nanostructures can be easily transferred onto the surface of indium tin oxide (ITO) slides and used for electrochemical measurements. After a replacement reaction with H2PdCl4, the silver nanostructure is transformed into a Ag - Pd bimetallic nanostructure, with good electrocatalytic activity for O-2 reduction. The gold nanostructure can also show high electrocatalytic activity to the oxidation of nitric oxide (NO) with a detection limit of about 10 mu M NaNO2 at S/N = 3.

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Europium-doped Gd2O3 with an average size of similar to15 nm was coated on the surface of preformed silica nanospheres by the wet chemical method. SEM and TEM photographs showed that SiO2/Gd2O3:Eu core-shell submicrospheres are obtained. XRD patterns indicated that the Gd2O3:Eu shell is crystalline after heat treatment. FTIR and XPS spectra showed that the Gd2O3:Eu shell is linked to the silica surface by forming a Si-O-Gd bond. Photoluminescence studies showed that the luminescent properties are still retained after coating on an inert silica core; additionally, we noted that the emitting peaks are broadened, which results from size effects and interface effects of nanocrystal.

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A new comblike polymer host for polymer electrolyte was synthesized by reacting monomethyl ether of poly(ethylene glycol) with poly(vinyl methyl ether-alt-maleic anhydride) and endcapping the residual carboxylic acid with methanol. Butanone was selected as a solvent for the esterification in order to obtain a completely soluble product. The synthesis process was traced through by LR. Compared with the model compounds, the presumed structure of this comblike polymer has been proved to be valid by C-13 NMR The comb polymer is a white rubbery solid. It can be dissolved in butanone and THF, and manifests good film forming ability.

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CO2-TPD was demonstrated an effective way to investigate the phase formation during pyrolysis for the preparation of composite oxides using metal-organic molecules as precursors. Based on the CO2-TPD results, it was found that calcination condition had deep effect on the carbonate formation and the minimum firing temperature to acquire pure phase composite oxide. An optimized calcination schedule was then developed.

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In our previous work, bone cell networks with controlled spacing and functional intercellular gap junctions had been successfully established by using microcontact printing and self assembled monolayers technologies [Guo, X. E., E. Takai, X. Jiang, Q. Xu, G. M. Whitesides, J. T. Yardley, C. T. Hung, E. M. Chow, T. Hantschel, and K. D. Costa. Mol. Cell. Biomech. 3:95-107, 2006]. The present study investigated the calcium response and the underlying signaling pathways in patterned bone cell networks exposed to a steady fluid flow. The glass slides with cell networks were separated into eight groups for treatment with specific pharmacological agents that inhibit pathways significant in bone cell calcium signaling. The calcium transients of the network were recorded and quantitatively evaluated with a set of network parameters. The results showed that 18 alpha-GA (gap junction blocker), suramin (ATP inhibitor), and thapsigargin (depleting intracellular calcium stores) significantly reduced the occurrence of multiple calcium peaks, which were visually obvious in the untreated group. The number of responsive peaks also decreased slightly yet significantly when either the COX-2/PGE(2) or the NOS/nitric oxide pathway was disrupted. Different from all other groups, cells treated with 18 alpha-GA maintained a high concentration of intracellular calcium following the first peak. In the absence of calcium in the culture medium, the intracellular calcium concentration decreased slowly with fluid flow without any calcium transients observed. These findings have identified important factors in the flow mediated calcium signaling of bone cells within a patterned network.

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随着现代工农业的发展,环境污染日益加剧。农用土壤作为我们赖以生存的基础,大量含砷(Arsenic, As)和铜(Copper, Cu)的化肥和农药的应用造成As、Cu及其他重金属的复合污染日趋加重。蜈蚣草作为一种天然的砷超富集植物,在清除土壤砷污染的应用中备受人们关注。然而,目前的研究多集中在蜈蚣草对单一砷污染的吸收、转运和超富集等方面,几乎没有对土壤复合污染尤其是As、Cu复合污染的的响应和生理机制的研究。本文针对As、Cu复合污染的现实,研究了不同浓度砷、铜复合污染胁迫对蜈蚣草生长和发育的影响,探讨了蜈蚣草对砷、铜复合污染抗性和富集的生理生化机制,以期为蜈蚣草在植物修复复合污染的应用提供理论基础。 主要研究结果如下: 1、以砷超富集植物蜈蚣草成熟孢子为外植体材料,建立了一套成熟的蜈蚣草孢子植株再生体系,包括配子体分化和愈伤组织分化两条途径。为蜈蚣草的生理生化机制以及将来的遗传转化奠定了基础。同时证明了蜈蚣草愈伤组织与其孢子体及配子体一样具有对砷的抗性和超富集特性以及铜抗性。 2、以组培的蜈蚣草孢子体为材料,通过比较高浓度砷、低浓度砷以及高浓度铜、低浓度铜的相互组合对孢子体毒性的差异,表明适度浓度砷可以增强蜈蚣草对铜的抗性,但高、低浓度铜都不能增强砷的抗性。同时测定了不同浓度砷、铜处理对蜈蚣草体内砷和铜的吸收分配情况,探讨了蜈蚣草对砷铜复合污染土壤的植物修复的潜在可能性 。 3、以蜈蚣草组培的配子体为材料,研究了蜈蚣草对不同浓度铜砷复合处理的生理生化响应。结果表明砷的加入可以缓解铜对蜈蚣草配子体的植物毒性,而铜的加入并没有缓解砷的植物毒性。而且随着砷浓度的提高可以显著降低铜在配子体中的积累,显著提高了配子体细胞生存能力,降低了配子体细胞膜透性,且可以改变铜砷在配子体中亚细胞定位,暗示砷对铜的积累具有拮抗作用。同时观察到适度的铜也可以降低砷在孢子体根中的积累,对砷在叶柄以及羽叶中的积累有一定的降低作用,但并不显著。 4、以蜈蚣草愈伤组织为材料,研究了蜈蚣草愈伤组织对砷和铜复合污染胁迫的生理生化响应,结果表明适度的砷可以显著提高蜈蚣草愈伤组织中抗氧化酶系统,进而提高抵御铜胁迫引起的ROS胁迫的能力而显著缓解铜对蜈蚣草愈伤组织的毒性。低浓度砷加入显著诱导POD、CAT活性的升高,提高了蜈蚣草愈伤组织抵抗ROS胁迫能力,尤其是POD与生长呈显著的正相关;SOD活性在0-1.0 mM Na3AsO4条件下并没有显著增加,暗示在相对较低的砷胁迫和铜胁迫条件下POD对蜈蚣草愈伤组织解毒起到重要作用。同时在高砷或者高铜胁迫条件下GR活性和GPx活性与之的相关系数可以达到显著水平,这说明高砷或者高铜胁迫条件下GR和GPx在蜈蚣草解毒中起到重要作用。 5、首次证明NO可能参与砷缓解铜对蜈蚣草的植物毒性的过程。发现加入0.2 μM NO加入并没有显著改善蜈蚣草砷的植物毒性,清除蜈蚣草愈伤组织内的NO后,显著增强了砷胁迫条件下对蜈蚣草愈伤组织生长的抑制作用。同时加入NO后却显著改善了蜈蚣草铜胁迫条件下愈伤组织的生长。测定了As、Cu处理后蜈蚣草愈伤组织内源NO含量的变化以及CAT抗ROS能力的变化,结果表明蜈蚣草愈伤组织NO合成显著受As诱导,但不受铜的诱导,同时内源NO浓度的升高,伴随着抵抗ROS胁迫的抗氧化的CAT活性升高。暗示砷可能是通过诱导内源NO浓度升高提高蜈蚣草愈伤组织抵抗ROS胁迫能力来缓解对铜的植物毒性。

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花粉管是种子植物受精过程中的雄性生殖单位载体,具有典型的顶端极性生长特点,因此成为近年来研究植物细胞间相互识别、胞内外信号传递的模式系统。裸子植物花粉管与被子植物花粉管相比具有萌发时间长、生长缓慢等特点。一氧化氮(NO)作为一个重要的胞内信号分子,参与调节植物生长发育和多种生理过程,但是,有关NO对花粉管生长的作用机制目前尚不清楚。本研究以裸子植物白皮松(Pinus bungeana)花粉为材料,应用不同浓度的NO释放剂SNAP和SNP, NO清除剂cPTIO和哺乳动物一氧化氮合酶抑制剂L-NNA处理,对白皮松花粉萌发和花粉管伸长进行了细胞学研究,从而为进一步揭示NO调控裸子植物花粉管生长机理提供参考。 本论文首先研究了NO释放剂、清除剂及NOS抑制剂对白皮松花粉萌发和花粉管生长的影响。结果显示,SNAP和SNP能够促进白皮松花粉萌发和花粉管伸长,并具有浓度效用,但对其花粉管的形态特征无明显影响;cPTIO和L-NNA能够抑制白皮松花粉萌发和花粉管生长,并且具有浓度效应,同时还可使花粉管顶端膨大呈球形,并丧失花粉管的极性生长。运用NO特异探针DAF-2DA标记显示,SNAP和SNP处理可促进花粉管胞内NO产生;经cPTIO和L-NNA处理后,花粉管内荧光强度比对照花粉管明显减弱。上述结果表明,NO参与裸子植物花粉管极性生长,并且适量NO可以促进花粉管的生长。 用显微注射技术将Ca2+特异探针注射入白皮松花粉管,以检测白皮松花粉管胞内Ca2+浓度梯度。结果显示,SNAP和SNP处理后,NO荧光增加的同时,花粉管顶端Ca2+浓度梯度增加。与此相反,cPTIO和L-NNA处理后,NO荧光降低的同时,花粉管顶端Ca2+浓度梯度也相应降低。应用非损伤微测技术测定花粉管胞外Ca2+内流,结果显示,SNAP和SNP促进胞外Ca2+内流,而cPTIO和L-NNA则抑制胞外Ca2+内流。据此,我们推测,在白皮松花粉管中,NO可能通过调节胞外Ca2+内流来调节胞内Ca2+浓度梯度,然而,我们不能排除在NO信号传递过程中,胞内Ca2+库可能影响胞内Ca2+浓度梯度。 通过微丝特异探针标记的白皮松花粉管显示,SNAP和SNP可使花粉管顶端细微丝束解聚,而cPTIO和L-NNA处理后,花粉管中微丝聚合,尤其在花粉管顶端形成粗的微丝束,并一直延伸到花粉管的最顶端。结合上述Ca2+结果,我们认为,经NO处理后,白皮松花粉管微丝骨架的动态变化,可能是通过Ca2+浓度来进行调控的。通过FM4-64探针标记显示,正常生长白皮松花粉管胞吞作用主要集中在顶端和亚顶端,并且形成倒“V”形的分布模式,SNAP与SNP处理后荧光分布模式与对照花粉管类似,但达到饱和所用时间相对较短;而L-NNA处理后顶端膨大丧失极性的花粉管,荧光分布在膨大花粉管靠近质膜的区域,未见倒“V”形分布模式;经L-NNA处理后,顶端没有膨大的花粉管,荧光几乎均匀分布于整个花粉管,并且L-NNA处理后达到饱和的时间较对照长。上述结果表明,适量NO能够促进白皮松花粉管胞吞。 免疫抗体标记技术分析发现,对照花粉管的酯化果胶质和AGPs都集中在顶端,酸性果胶质分布在侧壁,胼胝质均匀分布在整个花粉管壁上。L-NNA处理后的花粉管,在其顶端出现酸性果胶和酯化果胶,以及有胼胝质积累,而AGPs则分布在花粉管的基部。运用傅里叶红外光谱技术(Fourier Transform Infared Spectroscopy, FTIR)技术分析白皮松花粉管顶端细胞壁成分,结果显示,SNAP处理后花粉管顶端酯化果胶增加而酸性果胶降低;与之相反,经L-NNA处理后的花粉管,其顶端酯化果胶降低而酸性果胶增加。 综上所述,在白皮松花粉管中,NO促进胞外Ca2+内流,从而维持胞内Ca2+浓度梯度,进而影响花粉管顶端微丝骨架的组装,促进囊泡运输,使花粉管顶端酯化果胶累积,最终促进花粉管的正常生长。