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131.
本文应用系统分析方法,建立了一种一级吸收药物的生物利用度的简便估计的两点法。这种方法,只需测量血管内和血管外给药后的两个相同时点的血药浓度值。不论该药的处置系统是多少室,均能得到较好的结果。这种方法不仅比目前常用的点一点法和点一面法简单,而且结果更精确。 相似文献
132.
133.
津白_3侏儒小鼠(dW~t)是1982年从津白_3纯系小鼠(TA_3)中发现,进而培育成侏的变种。本实验应用免疫细胞化学技术,对dw ̄t小鼠垂体前叶生长激素(GH)细胞进行观察,并根据体视学原理进行定量分析,以探讨dw~t小鼠是否存在垂体发育缺陷。实验结果显示,dw~t小鼠GH细胞的体积密度(Vv)和数密度(Nv)值均低于正常对照组,P<0.01~0.001。表明dw~t小鼠由于垂体前叶GH细胞数量减少,导致GH分泌不足,从而形成侏儒。 相似文献
134.
HBIG,无环鸟苷,干扰素联合对慢性乙型肝炎抗病毒效应观察 总被引:1,自引:0,他引:1
本文报道血清HBV复制标志阳性的慢乙肝54例,随机分为治疗组及对照组各27例进行HBIG、无环鸟苷、干扰素联合近、远期抗病毒效应观察。治疗组为无环鸟苷第一周按25~20mg/kg/d计后改17~15mg/kg/d×53天,共60天;人白细胞干扰素1×106U肌注每周3次×4周,后改1.0×106U肌注每周2次×6周,共10周;HBIG400U肌注隔日1次,共10周,对照组仅给予一般“保肝”药物。其中治疗组18例,对照组19例进行治后半年到2年追踪观察,结果近、远期HBcAg、DNAP、HBV-DNA阴转率治疗组均高于对照组,其中治疗组近、远期HBcAg,HBV-DNA阴转率均达40%以上,明显高于对照组(P<0.05~0.01),治疗组近、远期各有4例及2例HBsAg阴转,而对照组则无一例阴转,从近、远期综合抗病毒效应观察,治疗组全阴率分别为33.3%、44.4%,而对照组分别为3.79%及0%,P<0.01,治疗组无明显毒副反应。对比单用无环鸟苷,全阴率31.8%;无环鸟苷加干扰素两药联合全阴率37.5%,均有所提高,达到44.4%,值得进一步研究。 相似文献
135.
冷锻炼和ABA诱导水稻幼苗提高抗冷性期间膜保护系统的变化 总被引:16,自引:1,他引:15
冷锻炼和ABA处理提高了水稻幼苗叶绿体SOD和GR活性及叶片抗氧化剂AsA和GSH的含量,降低了膜电解质泄漏,增强了幼苗的抗冷性.等电聚焦电泳分析表明,冷锻炼和ABA处理苗叶绿体SOD三条同工酶带和GR1、2、3和6同工酶带都有不同程度的增强.低温胁迫后,处理和未处理首的SOD、GR活性和ASA、GSH含量均有所下降.但处理苗的水平仍维持在未处理苗之上.亚胺环已酮可抑制因冷锻炼和ABA诱导增加的SOD和GR活性,并使叶片电解质泄漏增大.本试验结果表明冷锻炼或ABA诱导水稻幼苗抗冷性提高时,对防御活性氧的保护系统有类似的影响。 相似文献
136.
岩豆凝集素的圆二色性与生物学活性关系的研究 总被引:1,自引:0,他引:1
岩豆凝集素(MDL)的远紫外圆二色性谱(CD谱)显示216-217nm处的单一负峰。此时MDL分子含有16.2%的α螺旋,46.3%的β折叠和37.5%的无规卷曲。pH9.0时负峰红移至220nm,且在217-222nm处的峰值几乎相同;在20-40℃范围内,CD谱的变化甚微;60℃时谱峰蓝移;在80℃或100℃时,212nm处出现一大负峰。1mol/L或2mol/L脲时,MDL的CD谱已发生明显变化,二级结构单元也有变化,凝集兔红细胞的活性也随之减弱;随脲浓度的增加,MDL的谱峰蓝移,最终在212nm处出现大负峰。当胍浓度为0.75mol/L时,MDL的CD谱即有明显变化和活性丧失;胍浓度继续增加,CD谱逐渐成为特征的无规卷曲的谱形。在pH9.0、温度超过80℃、脲或胍浓度分别高于2mol/L和0.75mol/L时,MDL的CD谱发生显著变化的同时,其凝集兔红细胞的生物学活性全部丧失,分子的二级结构单元也发生很大改变。 相似文献
137.
The dependence of blastocyst development on the extracellular Na+/K+ ratio was investigated in an in vitro system. Hatching and outgrowth of mouse blastocysts was enhanced at Na+/K+ ratios between 3 and 10 compared to the ratio of about 25 typical for most culture media and serum. At a Na+/K+ ratio of 2, blastocyst hatching and outgrowth were inhibited. The requirement of blastocyst development for relatively high extracellular K+ concentrations agrees with the fact that K+ concentrations in oviduct and uterine secretions are higher than in serum. The findings can also be relevant in optimizing in vitro culturing techniques for blastocysts. 相似文献
138.
Y. Li M. M. Bhargava A. Joseph L. Jin E. M. Rosen I. D. Goldberg 《In vitro cellular & developmental biology. Animal》1994,30(2):105-110
Summary Using an automated cell analyzer system, the effect of hepatocyte growth factor/scatter factor (HGF/SF), epidermal growth
factor (EGF), basic fibroblast growth factor (bFGF), endothelial acidic fibroblast growth factor (a-FGF), platelet derived
growth factor (PDGF), and recombinant human insulinlike growth factor (IGF) on the motility and morphology of Madin-Darby
canine kidney (MDCK), rat hepatomas, C2, and H5–6 and murine mammary carcinoma (EMT-6) cells was investigated. Treatment of MDCK cells with HGF/SF, bFGF, EGF, and a-FGF resulted
in an increase in average cell velocity and in the fraction of moving cells. Cells treated with the PDGF and IGF did not show
significant alterations in velocity. MDCK cells treated with each growth factor were classified into groups of “fast” and
“slow” moving cells based on their average velocities, and the average morphologic features of the two groups were quantitated.
Fast-moving cells had larger average area, circularity, and flatness as compared to slow-moving cells. Factors that stimulated
cell movement also induced alterations in cell morphologic parameters including spreading, flatness, area, and circularity.
HGF/SF also scattered and stimulated motility of C2 and H5–6 hepatoma cells. In contrast to MDCK cells, there was no significant difference between the morphology of the fast moving
and slow moving C2 and H5–6 cells. These studies suggest that growth factor cytokines have specific effects on motility of normal and tumor cells. 相似文献
139.
Xin-Min Li† Jin Qi Augusto V. Juorio Alan A. Boulton 《Journal of neurochemistry》1993,61(4):1573-1576
Abstract: Gliosis is commonly observed in the CNS following tissue damage, and it also occurs in aging and in many neurodegen-erative diseases. Glial fibrillary acidic protein (GFAP) accumulation is a prominent feature of astrocytic gliosis. An inhibition or delay in GFAP synthesis could mitigate scar formation and thus reduce the formation of a physical barrier. The consequence of this would be to allow neurons and oligodendrocytes to reestablish a functional environment. (—)-Deprenyl, a specific monoamine oxidase (MAO) B inhibitor, has been used as an effective antipar-kinsonian drug, and it has been reported to possess neuroprotective and neurorescue properties. Using northern and slot blots to detect GFAP mRNA in C6 glioma cells, we have demonstrated that (—)-deprenyl decreases the abundance of GFAP mRNA in a time- and dose-dependent manner. The effect seems to be specific to MA0 B inhibitors because (+)-deprenyl and clorgyline exhibit no effect. This study indicates therefore that (-)-deprenyl may be useful for regulating astrogliosis following CNS injury as well as in some neurodegenerative diseases. 相似文献
140.
Vntr Allele Frequency Distributions under the Stepwise Mutation Model: A Computer Simulation Approach 总被引:10,自引:9,他引:1
Variable numbers of tandem repeats (VNTRs) are a class of highly informative and widely dispersed genetic markers. Despite their wide application in biological science, little is known about their mutational mechanisms or population dynamics. The objective of this work was to investigate four summary measures of VNTR allele frequency distributions: number of alleles, number of modes, range in allele size and heterozygosity, using computer simulations of the one-step stepwise mutation model (SMM). We estimated these measures and their probability distributions for a wide range of mutation rates and compared the simulation results with predictions from analytical formulations of the one-step SMM. The average heterozygosity from the simulations agreed with the analytical expectation under the SMM. The average number of alleles, however, was larger in the simulations than the analytical expectation of the SMM. We then compared our simulation expectations with actual data reported in the literature. We used the sample size and observed heterozygosity to determine the expected value, 5th and 95th percentiles for the other three summary measures, allelic size range, number of modes and number of alleles. The loci analyzed were classified into three groups based on the size of the repeat unit: microsatellites (1-2 base pair (bp) repeat unit), short tandem repeats [(STR) 3-5 bp repeat unit], and minisatellites (15-70 bp repeat unit). In general, STR loci were most similar to the simulation results under the SMM for the three summary measures (number of alleles, number of modes and range in allele size), followed by the microsatellite loci and then by the minisatellite loci, which showed deviations in the direction of the infinite allele model (IAM). Based on these differences, we hypothesize that these three classes of loci are subject to different mutational forces. 相似文献