Effects of Taoren Honghua Jian on the hyperlipidemia without symptom

AIM: To examine the effect of traditional chinese medicine recipe, Taoren Honghua(semen persicae-flos carthami) decoction, on hyperlipidemia without symptom. METHODS: The plasma TC, TG, LDL, HDL, apolipoprotein(Apo) A, Apo Bof the patients with hyperlipidemia without symptom were measured using automatic analyzer (shimadiu CL-7200), the production of nitric oxide(NO) was detected by Greiss reaction, and SODactivity and MDAformation were examined using o-trihydroxy benzene and barbituric methotheds, respectively. RESULTS: After oral administration of Taoren Honghua decoction, the plasma levels of TC, TG, LDL, and MDAof the patients were markedly decreased, however, the plasma levels of ApoA, HDL, SODand NOwere significantly increased and almost no change was detected in the plasma level of Apo B. In control group, it was found that although the plasma level of TC, TG and LDL were decreased ( P<0.05 ) and ApoAas well as HDLwere increased, ApoB, SOD, MDA and NO production were all unchanged. CONCLUSION: The traditional chinese medicine recipe, Taoren Honghua decoction,has a significant therapeutic effect on patients with hyperlipidemia by removing blood stasis, promoting qi circulation and in turn reducing blood lipid level.     

利用RT-PCR检测库尔勒香梨苹果茎痘病毒的研究

 以库尔勒香梨新鲜、冷藏、冷冻叶片和皮层为材料,对提取双链RNA (dsRNA)的2种方法和提取总RNA的3种方法进行了分析比较,并对总RNA的提取方法进行了改进,获得了纯度较高、完整性较好的dsRNA和总RNA,在此基础上进行了反转录(RT)和PCR扩增。在国内首次完成了对苹果茎痘病毒(ASPV)的RT-PCR检测,建立了ASPV有效RT-PCR反应体系。用此体系扩增到ASPV一个长约316 bp的片段。实验表明以dsRNA和总RNA为模板均能成功进行RT-PCR检测,且dsRNA优于总RNA。     

Changes of potassium currents in rabbit ventricle with healed myocardial infarction

AIM: To elucidate the mechanism of arrhythmia in healed myocardial infarction (HMI), and to investigate the changes of action potential duration (APD),transient outward potassium current (I_to), delayed rectifier potassium current (I_K) and inward rectifier potassium current (I_K1) of left ventricular myocytes in noninfarcted zone of HMI. METHODS: 12 rabbits were randomly assigned in two groups: HMI group (thoracotomy and ligation of the circumflex coronary); sham-operated group (thoracotomy but no conorary ligation). 3 months after operation, whole cell patch clamp technique was used to record APD, I_to, I_K and I_K1 of ventricular myocytes in non-infarcted zone. RESULTS: Membrane capacitance was larger in HMI group than that in sham-operated group. Action potential duration was lengthened significantly in HMI group and early after depolarization (EAD) appeared in HMI group. The densities of I_to, I_K,tail and I_K1 were reduced significantly in HMI group (P<0.01), from (6.72±0.42) pA/pF, (1.54±0.13) pA/pF and (25.6±2.6) pA/pF in Sham-operated group to (4.03±0.33) pA/pF, (1.14±0.11) pA/pF and (17.6±2.3) pA/pF, respectively. CONCLUSION: The reduced densities of I_to, I_K,tail and I_K1 in ventricular myocytes of non-infarcted zone in HMI are responsible for the prolongation of APD and the presentation of EAD, which play important roles in the malignant arrhythmia of HMI.     

以Taichung29为背景的小麦抗条锈病近等基因系转育进展

自1988年起,系统开展了以Taichung29为背景的小麦抗条锈病近等基因系转育及其基础性研究。采用回交法和系谱法相结合的转育方法,以春性品种Taichung29为轮回亲本作母本,分别与25个抗性供体即中国小麦条锈病菌鉴别寄主和国际上重要的抗条锈基因载体品种杂交、回交和自交。通过基因推导分析、单体分析和SSR标记技术检测目的基因,选育抗条锈近等基因系,现已获得重要进展,成功选育出8个以Taichung29为背景的抗条锈病单基因近等基因系,即Taichung29*6／Yr1、Taichung29*6／Yr2、Taichung29*6／Yr5、Taichung29*6／Yr7、Taichung29*6/Yr9、Taichung29*6／Yr10、Taichung29*6/YrSpP、Taichung29*6/YrKy2。另有9个组合转育获得343个抗性稳定株系,正检测其目的基因,3个组合转至BC₆F₃,自交纯合筛选抗性稳定株系,5个组合转至BC₅,继续回交转育。     

Effects of fosinopril,captopril and valsartan on the expressionof tissue factor in human monocytes

AIM: To investigate the effects of angiotensin-converting enzyme inhibitors (ACEI), fosinopril, captopril and angiotensin II AT₁ antagonists, valsartan on tissue factor (TF) expression on monocytes induced by lipopolysaccharide (LPS). METHODS: Mononuclear leukocytes from normal delivered female umbilical veins were incubated with bacterial LPS in presence or absence of different ACE inhibitors .At the end of incubation, the cells were disrupted by 3 freeze-thaw cycles. TF procoagulant activity was assessed by a one-stage clotting assay. RT-PCR was used to check TF mRNA expression, and GAPDH mRNA was used for parallel assay. RESULTS and CONCLUSION: The results showed that increased expression of TF mRNA induced by LPS was inhibited by fosinopril, captopril and valsartan, respectively, and the procoagualant activity of monocytes was also reduced.     

猪卵泡卵母细胞体外成熟与冷冻保存

研究了激素、猪卵泡液、不同类型血清对猪卵泡卵母细胞体外成熟的影响 ;比较了卵泡直径小于 2 mm、2～ 5 mm和大于 5 mm的卵母细胞体外成熟能力的差异 ,并对不同发育阶段猪卵母细胞的冷冻保存进行了研究。结果表明 :猪卵母细胞体外培养 4 8h时 ,培养的前 2 4 h培养液中加入激素 ,后 2 4 h去掉激素 ,卵母细胞的 A级成熟率 (5 1.73% )和总成熟率 (83.2 5 % )最高 ,极显著高于前 2 4 h不加激素 ,后 2 4 h添加激素培养的成熟率 (P<0 .0 1) ;也显著高于不含激素的培养液连续培养 4 8h的成熟率 (P<0 .0 5 ) ;但与添加激素连续培养 4 8h的成熟率差异不显著 (P>0 .0 5 )。在体外成熟培养液中 ,添加 10 % (体积分数 ) ECS的成熟率 (72 .86 % )显著高于添加 10 % (体积分数 ) NCS的成熟率(6 2 .2 1% ) (P<0 .0 5 ) ,而添加 10 % p FF则抑制卵母细胞的体外成熟。随着卵泡直径的增大 ,卵母细胞体外成熟能力逐渐增强。采用程序冷冻保存方法 ,成熟卵母细胞的成活率 (35 .5 9% )显著高于培养前 (2 4 .6 4 % )和培养 2 4 h(2 3.36 % ) (P<0 .0 5 )。培养 2 4 h(77.2 2 % )和培养成熟 (72 .81% )的卵母细胞解冻后的形态完整率均显著高于培养前(5 3.2 4 % ) (P<0 .0 5 )     

围产期奶牛能量代谢障碍性疾病的防治进展

奶牛代谢性疾病给奶牛饲养业造成重大经济损失。因此 ,如何搞好奶牛的饲养管理 ,减少代谢病的发生 ,充分发挥其生产潜力 ,是当前奶牛代谢病防治工作中亟待解决的问题。本文主要阐述了围产期奶牛能量代谢障碍病的危害、病因及防治措施     

动物胚胎工程技术研究进展

动物胚胎生物工程是用人工方法对动物卵母细胞或胚胎进行改造的技术,在育种中可使优良的种质特性和遗传潜力得到充分发挥,是家畜繁殖领域的一次技术革命.论述了目前国内外胚胎生物工程的研究成果.     

不同能量摄入水平对围产期奶牛生产性能及血浆瘦素浓度影响的研究

将健康的围产期奶牛30头随机分为3组, 每组10头。其中Ⅱ组为对照组, Ⅰ组和Ⅲ组分别为试验组。Ⅰ、Ⅱ、Ⅲ组均于产前28d开始分别饲喂NRC标准减少20%日粮(能量摄入80%组)、NRC标准日粮(能量摄入100%组)、NRC标准增加20%日粮(能量摄入120%组), 产后各组奶牛均饲喂标准日粮, 至产后56d结束。观察妊娠后期奶牛不同能量水平对干物质摄入量、产奶量、乳成分及体重等生产性能和血浆瘦素浓度的影响。试验结果表明: 奶牛产后干物质摄入量、产奶量、乳中蛋白质、乳脂率和非固体物质为Ⅰ组高于Ⅱ组、Ⅱ组又高于Ⅲ组(P>0 05 ); 同时血浆瘦素浓度为Ⅰ组高于Ⅱ组、Ⅱ组又高于Ⅲ组, 经统计分析组间差异极显著(P<0 01) 或差异显著(P<0 05); 但产前28~14d瘦素浓度组间差异均不显著(P>0 05 ), 此后Ⅰ组和Ⅲ组差异显著(P<0 05 )。此外, Ⅰ组体重消耗最小, Ⅲ组体重消耗最大, 各组间差异极显著(P<0 01)。可见, 围产期健康奶牛不同能量水平与干物质摄入量、产奶量、乳成分、体重等生产性能及血浆瘦素浓度之间存在着密切的关系。     

鸡呼吸道传染病基因芯片诊断方法的建立

随着养禽业集约化程度的不断提高,鸡呼吸系统疾病的发生呈逐年上升趋势.而且大多数的呼吸道疾病不是单一病原感染,而是多种病原混合感染,从临床上难以及时鉴别诊断,延误防治时机,从而给养禽业造成巨大的经济损失.因此,禽呼吸道疾病已经成为生产和研究中的一类重要疾病.目前,禽呼吸系统疾病的诊断方法主要有病毒分离、血凝（HA）、血凝抑制（HI）、琼脂扩散、ELISA、PCR等,但是传统的检测方法灵敏度较低,而且当病原发生变异或感染禽处在潜伏期时会造成误诊.PCR方法每次只能检测一种病毒,费时费力.采用基因芯片的方法可以快速、准确地同步检测多种病原体,且需要样品量少、灵敏、特异、快速、费用低廉,将生物芯片技术用于禽呼吸道疾病诊断意义重大.