直接利用传递函数对分叉结构进行模态综合

建立了一种直接利用传递函数对分叉结构进行模态综合的方法。传统的方法一般都需要对大矩阵进行求逆运算,而此方法只涉及分叉结构结合部的传递函数矩阵的求逆,因此求逆计算量很小,特别是当直接采用传递函数的测量值进行模态综合时,就更体现出它的优越性。     

鸡实验性急性有机磷中毒血清酶活性变化分析

选取临床健康体质量为0.8±0.07kg的三黄肉鸡24只,随机分成3个试验组和1个对照组,每组6只,其中试验、和组分别皮下一次注射氧乐果攻毒,剂量分别为35mg/kg体质量、70mg/kg体质量和140mg/kg体质量;对照组注射生理盐水。攻毒后系统观察动物急性有机磷中毒症状,采血测定体内胆碱酯酶(CHE)、碱性磷酸酶(ALP)、乳酸脱氢酶(LDH)、谷丙转氨酶(ALT)以及谷草转氨酶(AST)的活力。试验结果表明:鸡急性有机磷中毒主要表现为精神沉郁,共济失调,口角大量流涎,呼吸困难,严重腹泻和粪便带血等临床症状。攻毒组CHE3活性显著低于对照组,ALP的活性也有所降低,LDH活性升高,但ALT和AST的活性无显著变化。     

补饲不同配方酶制剂对犊牛断奶后生产性能的影响

选择健康无病、6- 7月龄间断奶的公牛犊 30头 ,随机分成 3组 ,即对照组 CK、试验组 TE1和 TE2 ,每组 1 0头。对照 CK组饲喂基础日粮 ;试验 TE1和 TE2 组分别补饲0 .1 %由纤维素酶、果胶酶、蛋白酶与淀粉酶组成的酶制剂 E1和由木聚糖酶、果胶酶、蛋白酶与淀粉酶组成的酶制剂 E2 ;试验 60 d,测定加酶对生产性能的影响。结果表明 ,与 CK组相比 ,TE1组日增重提高 7.51 % (P<0 .0 5) ,混合精料、粗料与增重比各下降 7.0 0 % (P<0 .0 5)、1 .2 3% (P<0 .0 5) ;TE2 组增重提高 4.2 0 % (P<0 .0 5) ,混合精料、粗料与增重比各下降 3.86% (P<0 .0 5)和 0 .31 % (P>0 .0 5) ;试验组犊牛断奶后对粗饲料的适应性有所增强 ;两组酶配方中 ,以纤维素酶为主的 E1效果优于 E2     

左旋肉碱对生长肥育猪消化酶活力的影响

用分别添加0、50和100mg/kg 左旋肉碱 (L—肉碱 )的饲粮 ,饲喂“杜大长”三元猪。试验结束屠宰收集十二指肠内容物、血液和肝脏等样品。实验结果表明 :与对照组相比 ,50、100mg/kg肉碱处理提高或趋向于提高十二指肠内容物总蛋白酶、脂肪酶和淀粉酶活力 ,其中100mg/kg肉碱组显著提高总蛋白酶63.49 % (P<0.05)、淀粉酶活力285.85 % (P<0.05)、脂肪酶活力360.86 % (P<0.01)。肉碱处理刺激肝脏酮体生成 ,促进脂肪酸β-氧化利用 ;50mg/kg和100mg/kg肉碱处理使血清β-羟丁酸分别趋向升高 (P>0.05)和升高27.80 % (P<0.05) ;肝β-羟丁酸浓度提高9.80 % (P<0.05)和16.95 % (P<0.01)。结论 :肉碱处理促进脂肪酸氧化 ,用利于机体蛋白质沉积 ,增加消化酶的分泌 ,提高消化酶活力 ,改善生长肥育猪的消化性能。     

实验性脾虚证大白鼠酶组织化学研究

将45只大白鼠随机分成3组，即实验组、治疗组及对照组，每组15只。以利血平致大白鼠脾虚证模型，分阶段捕杀动物，取肝脏、胃、十二指肠，用酶组织化学方法测定酸性磷酸酶(ACP)、碱性磷酸酶(ALP)、葡萄糖-6-磷酸酶(G-6-Pase)活性的变化。结果表明：实验组、治疗组、正常对照组各酶活性均发生了变化，在第7天、第14天时组内各酶存在着动态学上的变化。治疗组各酶活性接近正常对照组，说明四君子汤具明显的治疗作用。     

猪血浆蛋白(酶)多态性与杂种优势的关系

为探讨血浆蛋白 (酶 )多态性与杂种优势的关系 ,测定了杜洛克、长白、大白、杜×长大、大×长大、长×大、大×长共 7个品种 (组合 )的 8个血浆蛋白 (酶 )位点的多态性及部分生长和胴体性状 ,计算了平均基因杂合度与部分经济性状实测值和杂优率的相关关系 .结果表明 ,平均基因杂合度与遗传距离呈正相关 ,与日增重、屠宰率、背膘厚、后腿比例的实测值或杂优率呈正相关 ,与眼肌面积的实测值和杂优率呈负相关 .平均基因杂合度和亲本间遗传距离可为预测杂种优势提供依据 .     

An enzyme immunoassay to measure canine circulating fibronectin

A competitive enzyme immunoassay has been used to detect and quantitate fibronectin in canine plasma. In this test, purified fibronectin, bound to microtiter plates, competes with plasma fibronectin for the conjugated antibody, rabbit-anticanine, fibronectin-horseradish peroxidase. The assay could detect fibronectin in purified standards from 58 ng/ml to 580 microgram/ml. The range of 1-100 microgram/ml was linear for plasma samples diluted 1:10, allowing samples with fibronectin concentrations from 10-1000 microgram/ml to be easily measured by this method. The mean normal fibronectin concentration of 132 dogs, by this method, was determined to be 320 +/- 74 microgram/ml.     

Serum lipase determination in the dog: a comparison of a titrimetric method with an automated kinetic method

An enzymatic, kinetic method for determining serum lipase activity was evaluated and compared to a standard manual method for use in dogs. The kinetic method was a commercial kit adapted for use on a tandem access clinical chemistry analyzer and utilized a series of coupled enzymatic reactions based on the hydrolysis of 1,2-diglyceride by lipase. The manual method was the Cherry-Crandall technique based on the titration of base against the acid formed by hydrolysis of an olive oil substrate by lipase. The correlation between the two methods was very good (r = 0.94). The reference range for 56 clinically healthy dogs assayed by the kinetic method was 90 to 527 U/L. Diseases associated with a greater than twofold elevation in serum lipase activity as determined by the kinetic method included pancreatitis, gastritis with liver disease, and oliguric renal failure with metabolic acidosis. In some cases, pancreatitis was seen with other clinical problems, such as gastroenteritis, diabetic ketoacidosis, duodenal mass, disseminated intravascular coagulation, and septic peritonitis. Diseases associated with serum lipase activity within the reference range or elevated less than twofold included gastritis, gastric ulcer, cholestasis, phenobarbital-induced hepatopathy, colitis, copper hepatopathy, abdominal hematoma, apocrine gland adenocarcinoma, and thrombocytopenia with pneumonia.     

Effect of live weight and dietary supplement of raw potato starch on the levels of skatole, androstenone, testosterone and oestrone sulphate in entire male pigs

This study evaluated the effect of supplement of raw potato starch (RPS) on the levels of skatole, androstenone, testosterone and oestrone sulphate in plasma from entire male pigs. The study also evaluated relationships between plasma levels of skatole and testicular steroids at three different live weights (LW) of approximately 90, 100 and 115 kg. A total of 111 entire male pigs of a crossbred (Yorkshire dams×Swedish Landrace sires) were used. Animals were raised either in mixed pens, with females and males, or single-sex pens. Each pen contained seven or nine pigs. The most fast-growing three pigs from the pens with nine pigs were slaughtered when they reached 90 kg LW, and the remaining pigs were slaughtered at 115 kg LW. All pigs were fed the same commercial diet until the average pen weight reached 100 kg. Then, 33 out of 80 remaining pigs received RPS, 0.6 kg per pig and day, for 2 weeks prior to slaughter. Blood samples were taken from the pigs at three occasions: first, the day prior to first slaughter occasion, low-weight group; second, the day prior to change in diet, middle-weight group; and third, the day prior to second slaughter occasion, high-weight group. Plasma was analysed for the levels of skatole, androstenone, testosterone and oestrone sulphate. Fat samples were taken at slaughter and analysed for the levels of skatole and androstenone. The levels of skatole and testicular steroids in plasma were significantly higher in entire male pigs from the high-weight group fed no RPS compared to those from low- and middle-weight groups. The levels of the investigated compounds did not differ between low- and middle-weight groups (P>0.1). The diet with RPS induced a decline in skatole levels in plasma and fat (P<0.001), but not plasma levels of testicular steroids and fat levels of androstenone (P>0.05). Skatole levels were positively correlated to testosterone and oestrone sulphate levels in the middle- and high-weight pigs fed no RPS as well as to testosterone in the low-weight group. In the high-weight group fed RPS, skatole levels were not correlated to any of the analysed compounds. Approximately 26% of the entire male pigs (11 out of 43) from the high-weight group fed no RPS produced skatole levels in fat above 0.20 μg/g, whereas the pigs from the low- and high-weight group fed RPS did not produce skatole levels above 0.20 μg/g in fat. Androstenone levels in fat were high in all groups. In total 47% (52 out of 111) pigs expressed androstenone levels above the rejection levels in fat of 1.0 μg/g and 88% (98 out of 111) had androstenone levels above 0.5 μg/g. It was concluded that a lower slaughter weight and the supplement of raw potato starch to the diet could be used to reduce skatole levels in entire male pigs. Androstenone levels in fat, however, could not be reduced by either a lower weight at slaughter or dietary manipulation.