半胱胺的生物学作用及应用

半胱胺具有多种生物学功能,如耗竭生长抑素,影响糖、蛋白质和脂肪的代谢,抗氧化和氧化作用,提高免疫功能。本文综述了半胱胺的生物学功能和应用情况。     

复合酶制剂对产蛋鸡生产性能的影响

选用41周龄的海兰褐商品蛋鸡1200只,随机分成两组,每组600只。组内设3个重复,每个重复200只。对照组喂基础日粮,试验组喂基础日粮+0.1%蛋鸡用复合酶制剂,试验期28d。结果表明在产蛋鸡的基础日粮中添加0.1%的复合酶制剂可以使产蛋率平均提高6.12%(P<0.05),料蛋比降低11.69%(P<0.05)。说明在蛋鸡的基础日粮中添加适当的复合酶制剂能促进蛋鸡消化吸收,降低饲养成本,提高饲料转化率和经济效益。     

不同能量水平日粮对肉仔鸡生长及屠宰性能指标的影响研究

选择3周龄健康、无病、体重无显著差异的肉仔鸡96只,随机分为3组,每组设4 个重复,每个重复8只。分别饲喂蛋白质水平(19．5％)相同而能量水平不同(3．0 Mcal／kg、 3．08 Mcal／kg、3．16Mcal／kg)的3种饲粮。试验结果表明:前两周饲料转化(采食／增重)均以 中能量组(3．08 Mcal／kg)最好,为1．4416±0．1199,但三种不同能量水平对肉仔鸡平均日增 重、平均日耗料、饲料转化率均差异不显著(P>0．05);后两周饲料转化仍以中能量组最好,为 1．6362±0．1346,且显著优于高能量组(P<0．05),而与低能组和中能组之间差异不显著,各 能量处理组蛋白质、粗纤维、钙的代谢率均差异不显著(P>0．05),而磷的代谢率却存在显著 差异(P<0．05),其中,以中等能量组的磷代谢率最高,平均为90．73％;3种能量水平下肉仔鸡 半净膛率、全净膛率均差异不显著(P>0．05),表明能量水平并不影响肉仔鸡屠宰性能。     

苹果渣替代麦麸饲喂雏鸡效果试验

选用400只商品代尼克红母雏,随机分为4组,每组100只,设5个重复,每个重复 20只。试验组日粮分别由基础日粮和用风干未发酵苹果渣粉、半干发酵苹果渣粉、膜发酵苹果 渣粉分别替代基础日粮中5％的麸皮。试期为6周。结果显示,添加半干发酵苹果渣粉组和膜 发酵苹果渣粉组试鸡6周龄平均体重及日增重显著高于喂基础日粮的对照组和风干未发酵苹 果渣粉组(P<0．05),喂基础日粮的对照组略高于风干未发酵苹果渣粉组,差异不显著 (P>0．05)。表明发酵苹果渣粉对雏鸡生长发育有显著的促进效果。     

水稻旱作对其生长量和经济产量的影响

1998～1999年，研究了水稻旱作条件下，不同生育时期受水分胁迫后对作物生长量的影响。结果表明：不同指标对水分胁迫时期的敏感性不一，植株高度对抽穗期水分胁迫最敏感；单株绿叶面积和单株地上部干重对幼穗分化后期水分胁迫最敏感；根系干重和根冠比对幼穗分化前期水分胁迫最敏感；幼穗分化后期水分胁迫对经济产量影响程度最大，无效分蘖期水分胁迫对产量影响程度最小。     

Antisense drug targeting with VEGF mRNA designed by computer aid and inhibitory effects on K562 cell line in vitro

AIM:The effective antisense sequences targeted VEGF mRNA with computer software would be screened and designed, and effect of them on growth K562 cells and protein expression of VEGF were studied with experiments.METHODS:Seven antisense sequences were selected and synthesized, which consisted of 18-20 deoxynucleotide acid and were modified with phosphorothioate, according to principle of low free energy of overall △G₃₇ Overall. Cell growth was assayed by trypan blue dye exclusion assay and level of VEGF protien in the media was determined by ELISA.RESULTS:Six of seven sequences were capable of inhibing growth of K562 cells and downregulating the VEGF protein expression significantly, compared with Scrambed control group. It was found that there was a close correlation between low level of overall △G₃₇ and antisense effectiveness (r=0.887,P<0.01).CONCLUSION:VEGF mRNA antisense oliogdeoxynucleotides, which were designed by computer software of RNAstructure, were able to inhibit growth of K562 and its protein expression. The VEGF mRNA may be new target attached by drugs. At same time, the computer aided design is useful methods to obtain the effective antisense.     

植物源农用杀菌剂银泰对作物刺激生长作用

本文通过应用植物源农用杀菌剂银泰的不同浓度处理草莓和菠菜，测定绿色面积指数、叶面积指数、根冠比、叶绿素含量、硝酸还原本科活性、生物产量、经济产量。结果表明，银泰对草莓和菠菜均具有明显的刺激生长作用。     

Study on relationship between expression of PKCα in glomeruli and development of nephropathy in diabetic rats

AIM:To observe the dynamic changes of expression of PKCα, TGF-β₁ and α-SMA in glomeruli of diabetic rats induced by the alloxon and to invesitigate their roles in the diabetic nephropathy(DN).METHODS:Rats were randomly divided into four groups: normal control group (group A), diabetic group of one week (group B), diabetic group of one month (group C), diabetic group of two months (group D). Immunohistochemistry and Western blotting were used to detect the expression of PKCα, TGF-β₁ and α-SMA in renal tissue of all groups. Blood glucose, triglycerides, cholesterol, creatinine and urine protein were analysed by chemical methods. The morphological changes of renal tissue were checked through microscopy.RESULTS:The expression of PKCα and TGF-β₁ in renal tissue of diabetic groups were increased comparing with those of nomal control group(P<0.05). The mesangial cells expressed α-SMA in two months group. Chronologically the expression of PKCα, TGF-β₁ and α-SMA were positively correlative with each other and the impairment of kidney was also observed.CONCLUSIONS: During the DN process the expression of PKCα increased. PKCα raised GFR and the permeability of glomerular filtration membrane which enhanced urinary albumin excretion. PKCα also increased expression of TGF-β and therefore to induce the expression of α-SMA. The appearance of α-SMA was a marker of the phenotypic transform of renal cells.     

Effects of TGF-β1 and TNF-α antisense PS-ODNS on ex vivo expansion of hematopoietic stem/progenitor cells(HSPC)

AIM:To study the effect of TGF-β₁ and TNF-α antisense PS-ODNS on ex vivo expansion of hematopoietic stem/progenitor cells (HSPC). METHODS:CD₃₄⁺cells were purified from fresh umbilical cord blood by immunomagnetic beads, and mononuclear cells were purified from bone marrow by Ficoll-hypaque. The effects of TGF-β₁ and /or TNF-α antisense PS-ODNS on ex vivo expansion of CD₃₄⁺ cells、CFU-GEMM、CFU-GM、CFU-E and BFU-E were detected by using liquid and semi-solid culture systems.RESULTS:TGF-β₁ antisense PS-ODNS cooperated with cytokines increased the number of CD₃₄⁺ cells, CFU-GEMM, CFU-GM, CFU-E and BFU-E, which was as 4, 2.6, 2.7, 1.8, 2.1 times as that of the control (the cytokines combination), respectively. TNF-α antisense PS-ODNS cooperated with cytokines respectively increased the number of CD₃₄⁺ cells, CFU-GEMM, CFU-GM, CFU-E and BFU-E by 4, 2.9, 2.6, 1.7, 1.8 times as that of the control. The above two antisense PS-ODNS cooperated with cytokines could respectively increased the number of CD₃₄⁺ cells, CFU-GEMM, CFU-GM, CFU-E and BFU-E by 5.3, 2.1, 2.7, 1.9, 1.8 times as that of the control.CONCLUSION:Inhibition of endogenous TGF-β₁ and TNF-α by antisense PS-ODNS will be one of the effective methods to expand HSPC ex vivo.     

Effect of tea-polyphenols on the activation of NF-κB and the expression of TGF-β1 mRNA in THP-1 cells incubated with VLDL,LDL or ox-LDL

AIM:To investigate the effect of tea-polyphenols (TP) on the activation of NF-κB and the expression of TGF-β₁ mRNA in THP-1 cells (a human acute monocytic leukemia cell line). METHODS:THP-1 cells were incubated with the different concentrations of TP, VLDL, LDL or ox-LDL. In the THP-1 cellls, the nuclear malposition rate of NF-κB was detected with immunohistochemistry technique, the positive index of the TGF-β₁ mRNA expression was detected by hybridization in situ, and accumulation of total cholesterol (TC) in cells incubated with 0.4-40 μg/L TP was determined with oxidase assay. RESULTS:The nuclear malposition rate of NF-κB, the positive index of the TGF-β₁ mRNA expression and TC in THP-1 cells incubated with 0.4-40 μg/L of TP were lower than those with 0 μg/L of TP in TP-V group, TP-L group and TP-O (P＜0.05). The differences of these markers in THP-1 cells incubated with more than 40 μg/L TP in TP-V group, TP-L group and TP-O were not statistically significant, compared with TP-C group (P＞0.05). CONCLUSION:TP inhibited the activation of NF-κB, the expression of TGF-β₁ mRNA and the foam cell formation in the mono-macrophage.