壳聚糖对黄瓜种子萌发和生长发育的影响

研究了壳聚糖对黄瓜种子萌发和生长发育的影响。结果表明，壳聚糖能促进种子萌发，改善根系的发育，增强超微弱发光强度和过氧化氢酶的活性，最适宜浓度为0.1%和0.05%。     

红汁乳菇多糖提取最佳工艺研究

对红汁乳菇多糖提取、纯化工艺进行了优化研究，结果表明在料液比1：30，浸提温度95％浸提时间2h,pH8．0，可获得最佳提取效果。在醇析浓度为70％，V(氯仿)：V(正丁醇)=1：0．2，V(氯仿 正丁醇)：V(样品)=1：l时，纯化含量为58％。同时用超声波法对红汁乳菇多糖的提取作了研究，其得率为6.99％，效果较佳。     

鸡腿蘑菌丝体的同工酶研究

用8种不同培养基配方，培养鸡腿蘑菌丝体，其同工酶分析结果表明，鸡腿蘑菌丝体酯酶(EST)同工酶谱差异明显，过氧化物酶(POD)同工酶谱差异明显。     

三种外检植物病毒的灭活处理

番茄环斑病毒（ＴｍＲＳＶ），烟草环斑病毒（ＴＲＳＶ），南芥菜花叶病毒（ＡｒＭＶ）的病汁液和ＰＥＧ粗提纯液，经适宜温度或甲醛处理，均丧失侵染性而有抗原性。ＴｍＲＳＶＰＥＧ粗提纯液经６０℃（水浴）处理１０分钟或２８℃７天，ＴＲＳＶ粗提纯液置２５℃一个月，Ａｒ－ＭＶ在４０℃７天条件下均可做为阳性对照的灭活处理的最佳方案。可保存抗原性在７～１２月以上。为了防止危险性检疫病毒的侵入，对入境种苗进行检疫，需建立快速、准确、标准化检疫程序，而在血清学快速诊断试验中，提供阳性对照，对提高判断准确率是必要的。因此，为了解决在诊断试剂中提供阳性对照但又不能使其检疫性病毒人为扩散这一重要问题，我们在研究三种外检病毒（ＴｍＲＳＶ，ＴＲＳＶ，ＡｒＭＶ）的检验技术的同时，又进行了一些灭活试验，用化学和物理方法钝化病毒，使其失去侵染性而保持抗原性，并应用于酶联诊断试剂盒中，本文报道了初步试验结果     

鸡球虫对机体的致病作用研究进展

球虫在鸡体内进行生命活动的同时对鸡体产生不同程度的损害，球虫感染后的致病性和病理学反应是球虫与宿主机体相互作用的结果。本文就鸡球虫致病作用及其对宿主细胞代谢的影响、及影响球虫致病性的因素的研究进展予以综述，对鸡球虫病的防治具有一定的指导意义。     

丝兰属植物提取物降低鸡舍氨气浓度的效果试验

通过在21日龄的肉用仔鸡饲料中添加丝兰属植物提取物(其有效成分为丝兰皂角苷)，研究丝兰属植物提取物对降低鸡舍中氨气浓度和提高肉仔鸡生产性能的效果。试验结果表明，试验组鸡舍内氨气平均浓度为4．75mg／L，对照组鸡舍内氨气平均浓度为13．80mgl／L，试验组比对照组鸡舍内氨气平均浓度降低了9．05mg／L，经t检验，两鸡舍内氨气平均浓度差异显著(P＜0．05)，并且试验组比对照组饲料报酬提高了8.92％。     

山羊传染性胸膜肺炎支原体和绵羊肺炎支原体对抗菌药物敏感性的研究

测定了环丙沙星、氧氟沙星、单诺沙星、红霉素、罗红霉素、泰乐菌素、泰妙菌素、四环素等8种药物对羊肺炎支原体两个标准株Y-98和Y-goat的体外抑菌浓度以及红霉素与氧氟沙星、泰乐菌素对Y-goat和四环素与氧氟沙星、泰乐菌素对Y-98的联合药敏作用.结果表明,这8种抗菌药物对Y-goat和Y-98的MIC(μg/mL)分别为:环丙沙星0.223、0.002 23,氧氟沙星0.281、0.014 0,单诺沙星0.136、0.014 0,红霉素0.021 8、无效,罗红霉素0.032 7、无效,泰乐菌素0.042 2、0.039 0,泰妙菌素0.021 7、0.052 0,四环素0.195、0.052 0.红霉素与氧氟沙星的联合药敏指数为1,是相加作用;红霉素与泰乐菌素对Y-goat的联合药敏指数为1.5,是无关作用;四环素与氧氟沙星、泰乐菌素对Y-98的联合药敏试验指数均为0.375,是协同作用.     

施肥对黔中地区混播草地牧草生长性能的影响

本文研究了氮磷钾不同配比施肥量对黑麦草和紫花苜蓿混播草地牧草生长的影响,结果表明:氮肥促进禾本科牧草叶的生长(P<0.05),增施钾肥对禾草的生长有利;磷能促进豆科牧草根的生长(P<0.05)且豆科牧草株高随着施磷量的增加各处理间差异显著(P<0.05),高氮抑制豆科牧草的生长;最高产量的施肥方式:N:P_2O_5:K_2O为20:30:20,比对照处理的草地产量增加63.92％。     

Effects of sodium ferulate on the nonenzymatic glycation and oxidation in kidneys of diabetic rats

AIM: To investigate the blocking effects of sodium ferulate (SF) on the nonenzymatic glycation and oxidation in kidneys of diabetic rats. METHODS: The diabetic rats induced by streptozotocin (STZ) were treated with SF (110 mg/kg) per day for 8 weeks. The renal weight/body weight, clearance rate of creatinine (Ccr), proteinuria, advanced glycation end products (AGEs) in renal cortex, and the malonyldialdehyde (MDA), fructosamine (FMN), antioxidant enzymes in serum and renal cortex were measured. The pathologic changes of kidneys were also observed. RESULTS: The levels of Ccr, proteinuria, FMN and AGEs in renal cortex, FMN in serum, and renal weight/body weight in diabetic control group were significantly higher than those in normal control group. In the diabetic control group, there was a highter level of MDA and a lower activity of superoxide dismutase (SOD) and catalase (CAT) in serum and renal cortex than those in normal control group. Except for FMN in renal cortex, the abnormalities were significantly ameliorated in the treatment group. The pathologic changes was significant in the diabetic control group, which was significantly ameliorated with the treatment of SF. CONCLUSIONS: SF protects the activity of antioxidant enzymes, clears away oxygen radicals and inhibits the deposit of AGEs in kindey, which may be the mechanisms of protecting effects of SF on kindey in diabetic rats.     

Comparison of different conditions inducing embryonic stem cells

AIM: To evaluate the different conditions inducing mouse embryonic stem cells (ESC) in vitro to differentiate into cardiomyocytes. METHODS: BRL conditioned medium was used to promote the growth of ESC and maintain them in an undifferentiated state. During the inducing process, retinoic acid (RA), DMSO, activin-A and TGF-β₁ were used as inducing reagents, and made up six kinds of differentiating medium. Then a three-step method inducing ESC cultured in hanging drops, in suspension and in plating was used to induce the differentiation of ESC. RESULTS: ESC were induced in vitro to differentiate into cardiomyocytes. Of all groups, the highest differentiating rate was observed in the group induced by activin-A (20 μg/L) and TGF-β₁ (2 μg/L). CONCLUSION: The inducing conditions including activin-A (20 μg/L) and TGF-β₁ (2 μg/L) is very valuable in inducing ESC differentiation into cardiomyocytes.