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1.
AIM:To study the effect of environment of liver regeneration on the proliferation of rat fetal hepatocytes after intrasplenical transplantation. METHODS:Fetal hepatocytes isolated from 3-week SD rat fetuses bred were transplanted into the spleens of liver regeneration model rats with 70% partial hepatectomy. The cell cycle of the hepatocytes in the remnants liver was analyzed by flow cytometer and the density dimensions of the donor fetal hepatocytes in spleen were measured by image analysis system 7 and 30 days post-transplantation, respectively. RESULTS:Compared with the control group, the proportions of S and G2 /M cells in the remnants liver were obviously decreased (P<0.05), but the density dimensions of the donor fetal hepatocytes in spleen increased significantly (P<0.05) in rats with hepatectomy 7 days post-transplantation. CONCLUSION:The environment of liver regeneration is propitious to the proliferation of fetal hepatocytes after transplantation into spleen.  相似文献   
2.
选择新生仔猪15头,分别于出生当日(0 d)、出生后3d及7d屠宰取样,制作肝脏电镜切片进行组织学分析,并测定肝脏中DNA、RNA含量及常规生化指标。结果显示:新生仔猪肝细胞中内质网、线粒体等细胞器都很丰富,而且各细胞器的结构已经发育成熟。肝脏质量在仔猪出生后1周尤其是3d内迅速增加(P<O.01),远远快于体重增加的速度。仔猪肝脏的蛋白质含量在生后1周也迅速增加(P<O.01);而肝糖原贮备在刚出生时较高,出生后迅速下降(P<O.01)。仔猪出生后肝脏中DNA和RNA浓度的变化趋势正好相反,前者在出生后3d内明显下降(P<O.05),4~7d又有增加趋势,而RNA浓度以3d为最高。试验结果表明,仔猪到出生时肝细胞的结构和功能基本发育成熟。仔猪出生以后,肝脏的生长发育十分迅速,不仅肝细胞的数量快速增加,肝细胞的体积也不断增大。  相似文献   
3.
This experiment was conducted to investigate the liver-protective effect of Chinese herbal compound probiotics (CHCP) on acute liver injury layers.One hundred and eight 1 day old hens were divided into 4 groups with 3 replicates in each group and 9 layers per replicate in trial 1.The layers in model groups Ⅰ to Ⅲ were gavaged with 10% (V/V) soybean oil solution of carbon tetrachloride (SCCl4) according to 1,2 and 4 mL/(kg·BW) at 14,28 and 35 d,respectively.The layers in control group were gavaged with 2 mL/(kg·BW) soybean oil.In trial 2,sixty 1 d layers were divided into 5 groups:Control group (soybean oil),model control group(SCCl4)and low-dose,middle-dose and high-dose CHCP group (SCCl4+1‰ CHCP,SCCl4+2‰ CHCP and SCCl4+4‰ CHCP respectively).CHCP were used by drinking water since 7 days.SCCl4 were gavaged according to 2 mL/(kg·BW) at 14 and 28 d.The results showed as follows:The model of layers liver damage could be built by intragastric administration of 2 mL/(kg·BW) 10%(V/V) SCCl4 at 14,28 d respectively,with the signs of hepatic steatosis,severe vacuolar degeneration,nuclear condensation and necrosis.Compared to the model control group,the serum AST levels in low,medium and high dose CHCP groups were decreased by 4.35% (P > 0.05),7.57% (P > 0.05) and 9.79% (P < 0.05),the serum ALT levels in medium and high dose CHCP groups were decreased by 34.92% (P < 0.01),36.51% (P < 0.01),the serum total bilirubin content in medium and high dose CHCP groups were decreased by 25.49% (P < 0.01),27.45% (P < 0.01).The liver cell congestion was reduced to varying degrees in different dose CHCP groups,and the liver cell had no vacuoles,arranged in neat rows,abundant cytoplasm and uniform in different dose CHCP groups.In conclusion,2‰,4‰ CHCP could reduce hepatocyte necrosis,decrease the serum activities of ALT,AST and total bilirubin levels,and had protective effect on hepatic injury induced by SCCl4.  相似文献   
4.
We have shown in vitro that mechanical stretch triggers activation of quiescent satellite cells of skeletal muscle to enter the cell cycle through an intracellular cascade of events including nitric oxide (NO) synthesis that results in the release of hepatocyte growth factor (HGF) from its extracellular association and its subsequent presentation to signaling receptors. In order to explore the activation mechanism in vivo, stretch experiments were conducted in the living animal using our suspension model developed. This system used the weight of the hind portion of rats to stretch the inside muscles of the left hind limb suspended for a period of 0.5–2.0 h. At the end of the stretch period, the rats received an intraperitoneal injection of bromodeoxyuridine followed by immunocytochemistry for its incorporation as an index of satellite cell activation in vivo. Depending on the period of stretch, bromodeoxyuridine labeling was increased significantly over the contralateral unstretched leg or control muscle from untreated rats. A stretched muscle extract prepared from the 2 h stretched tissue by incubating it in PBS, showed the active form of HGF as revealed by immunoblotting and it could stimulate the activation of unstretched satellite cells. Also, administering NO synthase inhibitor L‐NAME prior to muscle stretch abolished the stretch activation of satellite cells. Therefore, the results from these experiments demonstrate that stretching muscle triggers NO synthesis and HGF release, which could activate satellite cells in vivo.  相似文献   
5.
将360只1日龄天府肉鸭随机分为6组,分别以对照日粮(Cu8mg/kg)和高铜日粮(Ⅰ组:Cu100mg/kg;Ⅱ组:Cu200mg/kg;Ⅲ组:Cu400mg/kg;Ⅳ组:Cu600mg/kg;Ⅴ组:Cu800mg/kg)饲喂6周,研究日粮铜水平对雏鸭肝氧化状态及肝细胞凋亡的影响。结果显示,与对照组比较,Ⅳ组和Ⅴ组肝铜锌SOD和谷胱甘肽过氧化物酶活性降低(P〈50.01),Ⅲ组、Ⅳ组和Ⅴ组羟自由基和丙二醛含量显著升高(P〈0.01),Ⅰ组和Ⅱ组肝铜锌SOD和谷胱甘肽过氧化物酶活性升高(P〈0.01)。高铜组肝细胞凋亡率随日粮铜水平的升高而增加。表明,日粮铜水平为400mg/kg以上时可引起肝抗氧化功能降低和肝细胞凋亡率升高。  相似文献   
6.
Freshly isolated rainbow trout hepatocytes were exposed to tert-butyl hydroperoxide (BuOOH), a substrate for glutathione peroxidase. BuOOH at a concentration approximately equimolar (1 mM) with intracellular reduced glutathione (GSH) caused a reversible increase in intracellular glutathione disulphide (GSSG) but did not compromise cell viability or damage membrane lipids. BuOOH at 10 mM caused a large irreversible increase in intracellular GSSG followed by efflux into the medium. Considerable leakage of lactate dehydrogenase and loss of highly unsaturated fatty acids, particularly docosahexaenoic acid also occurred. Dependence of hydroperoxide removal on flux through the hexose monophosphate pathway was suggested by the increased release of 14CO2 from [1-14C] glucose from hepatocytes incubated with BuOOH.  相似文献   
7.
根据牛肝细胞内PC(丙酮酸羧化酶)基因组与PCcDNA相比多含有一个内含子序列.在其中再插入一外源DNA序列.从而使最终构建的突变体片段的长度大于PCcDNA的长度,成功构建了PCcDNA的竞争DNA模板,然后应用竞争PCR方法研究了丙酸盐对体外培养新生牛单层肝细胞PCmRNA水平的影响。使单层肝细胞培养液中丙酸钠浓度分别为0、1.5、2.5、3.5、4.5、8.5、11.5mmol/L,处理24h,提取总RNA、逆转录,在同一体系中用相同引物扩增目的带和竞争模板带。结果表明.随着丙酸钠浓度的升高.PCmRNA水平呈上升趋势,提示肝细胞内PCmRNA的表达水平受培养液中丙酸钠浓度的影响。  相似文献   
8.
为阐明神经内分泌因子胰岛素、胰高血糖素在奶牛脂肪代谢过程中的调控作用,用荧光定量PCR方法检测胰岛素、胰高血糖素对肝细胞二酰基甘油酰基转移酶(DGAT2)mRNA丰度的影响。结果表明低浓度的胰岛素能促进脂肝细胞内DGAT2mRNA的表达;胰高血糖素抑制脂肝细胞内DGAT2mRNA表达。由此证明:胰岛素和胰高血糖素能直接调控肝细胞中的DGAT2基因mRNA的表达。  相似文献   
9.
取单层培养72 h生长良好的犊牛肝细胞,采用单因素重复试验,分别添加0、50、100、200、500、1000 pg/ml的羊体外合成神经肽Y(neuropeptide Y,NPY),每个处理3个重复(每重复2孔),再培养12 h后分别提取RNA和制备细胞上清液。应用荧光定量PCR方法检测外源NPY 对肝细胞糖异生关键酶丙酮酸羧化酶(pyruvate carboxylase,PC)基因表达的影响,同时用比色法检测其对肝细胞PC活性的影响。结果表明,一定浓度的NPY显著促进了肝细胞PC mRNA表达,增强了PC活性。  相似文献   
10.
斜带石斑鱼肝细胞分离及原代培养方法的建立   总被引:2,自引:2,他引:0  
本研究以斜带石斑鱼肝细胞为实验对象,在不同培养条件下进行原代培养,旨在探讨稳定可靠的斜带石斑鱼肝细胞分离及原代培养方法。采用组织块分离法和胰蛋白酶(含EDTA)消化法分离肝细胞,并通过密度梯度离心法分离纯化肝细胞,细胞悬液于DMEM/F-12、M199和L-15培养液中培养;细胞活力及数量采用血球计数板计数,并通过MTT法测定细胞增殖率;同时,测定不同时间培养上清液中乳酸脱氢酶(LDH)活性、白蛋白(ALB)和尿素氮(BUN)的含量,以分析肝细胞生长状态。结果表明,组织块方法不适于斜带石斑鱼肝细胞的培养,未见细胞从组织块中迁出,而胰蛋白酶消化法获得良好稳定的培养效果,细胞产量达到1.6×108个/g肝重,活细胞数达到95%;L-15培养基细胞生长明显优于DMEM/F-12和M199培养基;启动原代培养的48~72 h阶段肝细胞生长代谢旺盛,培养上清液中LDH活性显著降低,ALB和BUN含量显著升高。结果显示,0.25%的胰蛋白酶常温消化法适合斜带石斑鱼肝细胞的分离,斜带石斑鱼肝细胞原代培养的最适培养基为L-15培养基,肝细胞在启动原代培养的48~72 h生长代谢旺盛。  相似文献   
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