A reactive pattern of ischemia-induced nestin protein in the rat brain

AIM:To explore the expressive profile of nestin protein in the focal ischemic brain and to study the recovery mechanism of brain focal infarct.METHODS:Cellular morphology,time-course and distribution pattern of nestin positive response were immunohistochemically examined in different brain regions of 36 adult male SD rats. RESULTS:Nestin positive response of different brain regions in sham operated rats was present in small- and micro-vasculartures and the third ventricle bottom and ependyma. A large number of nestin positive cells were detected in ischemic brain, and were more remarkable in the cortical areas of parietal lobe and preoptic area as well as ischemic caudoputamen. Stellate nestin positive cells were located in the deep layer of ischemic cortex, but fibrillary cells were located in the shallow layer. Nestin positive cells in the ischemic caudoputamen showed the same changes of morphology as those cells in the deep layer of ischemic cortex. Morphological and number alterations of nestin positive cells were the most remarkable at 1 weeks post-ischemia, which showed more hypertrophy and proliferation in morphology, and a marked increase in number was present in the ischemic cerebral cortex and the ischemic caudoputamen. These alterations of nestin positive cells persisted up to 6 weeks post-ischemia, and then, the nestin positive response in the ischemic brain decreased gradually.CONCLUSION:Focal cerebral ischemia induces nestin re-expression on reactive astrocytes, which may be very important to the self-recovery of cerebral infarct.     

Changes of myocardial glycogen content and right ventricular function in hypoxia swimming rats

AIM: To investigate the changes of myocardium glycogen content and the relation ship between changes of the myocardial glycogen content and the myocardial function. METHODS: Male Wistar rats were placed in (hypoxia rats) and made to swim in (hypoxia swimming rats) a hypobaxic chamber simulating an altitude of 5 000 m above sea level. The content of myocardium glycogens was determined by colorimetry. RESULTS: The myocardium
glycogen content of rats significantly reduced along with the prolongation of hypoxic exposure and approached to control level in hypoxia swimming rats. The myocardial function of right ventricule was improved significantly compared with control group.CONCLUSION: Moderate exercise (swimming) is beneficial to hypoxic adaptation of rats under the condition of chronic hypoxia.     

利用ZXX-65真空循环熏蒸设备熏蒸仓储害虫的研究

用ZXX-65真空循环熏蒸设备在不同真空压力、熏蒸时间、药剂浓度条件下对选定的典型仓储实验试虫进行熏蒸，根据杀虫效果，筛选出害虫的最优熏蒸条件组合。结果表明，ZXX-65真空循环熏蒸设备可以在2h内杀死各种仓储害虫。40000Pa，60g/m^3，2h为仓储害虫的最优熏蒸条件组合。     

仔猪日粮中添加复合酸化剂的饲喂效果

选择7日龄哺乳仔猪126头，在玉米—豆粕型日粮中，分别添加6种自行研制的复合酸化剂饲喂仔猪，酸化剂的主要成分是柠檬酸、延胡索酸、磷酸、乳酸、草酸、酒石酸。结果表明，断奶仔猪的日增重比对照组分别提高11．94％、14．03％、7．46％、7．46％、17．31％、12．24％；饲料转化率分别提高13．92％、25．26％、7．73％、11．35％、21．65％、11．86％。仔猪的腹泻率也降低了。     

富铁酵母对家兔红细胞免疫功能的影响

为探讨富铁酵母对家兔红细胞免疫功能的影响,将32只家免随机分成富铁酵母高、低剂量组,FeSO4组及空白对照组,分别灌服富铁酵母(Fe元素8 mg/kg、4 mg/kg)、FeSO4(Fe元素4 mg/kg)及空白生理盐水;连续5 d后,检测红细胞C3g受体花环率和复合物(IC)花环率.结果:富铁酵母较FeSO4及空白组能显著提高红细胞C3h受体花环和红细胞复合物(IC)花环的百分率,但高、低剂量间无显著性差异.结论:富铁酵母能显著提高红细胞免疫功能.     

长期施肥条件下菜田—蔬菜生态系统变化的研究( Ⅳ) 蔬菜生态系统的变化

 以2002 年设施番茄栽培为代表计算其N、P、K投入量与携出量之间的表观平衡状态, 其结果基本上和14.5 年后的土壤实测值与设施栽培本底值之间纵向比较的增长关系一致, 前者只能说明系统养分变化的趋势, 后者才是实际的养分盈亏状态, 养分盈亏主要取决于有机肥的施用与养分元素的供给。5个代表性处理模拟了蔬菜施肥的不同现状, 从土壤肥力及产量等方面的变化真实反映出各自的系统变化及发展趋势, 在本试验条件下以ANK施肥下的系统最优。对有机肥施用、化学肥料的配施以及测土施肥等问题进行了探讨。     

中国苜蓿育成品种遗传多样性及亲缘关系研究

以苜蓿的种子贮藏蛋白的多态性为研究指标,对中国14个审定登记的苜蓿育成品种的遗传多样性及亲缘关系进行了研究。研究结果表明:蛋白单体的分子量介于21.2～85.1kD之间,蛋白单体电泳图谱多态性品种间无显著的特异性;在参试的14个育成品种中,品种内基因多样性平均值(HS)为0.3136,总基因多样度(HT)为0.3741,基因分化系数(GST)为0.162;以λ=3.700为标准划分,14个育成品种划分为六个组群,各组群划分结果主要与参试品种的亲本来源有关,而与其种植地、育种地关系不大。     

三肽囊素对环磷酰胺诱导的鸡红细胞免疫功能低下的阻断作用

本文研究了三肽囊素对环磷酰胺诱导的墟岗黄鸡红细胞免疫功能的抑制模型的影响。180只一日龄墟岗黄母鸡随机分成对照组,三肽囊素组,三肽囊素 环磷酰胺组,环磷酰胺组四个组,三肽囊素组和环磷酰胺 三肽囊素组每只鸡肌注0.01mg/kg剂量的三肽囊素;环磷酰胺组和环磷酰胺 三肽囊素组每只鸡肌注40mg/kg剂量的环磷酰胺,对照组鸡注射等量的生理盐水。结果表明,14日龄和35日龄时各试验组鸡的红细胞总数没有显著差异,而在56日龄时,环磷酰胺组显著低于其它三组(P<0.05);从14日龄开始,环磷酰胺纽的RBC-C3bR花环率显著低于其它三组,而环磷酰胺组的RBC-IC花环率显著高于其它三组,并持续到实验结束。结果提示,三肽囊素可阻断由环磷酰胺诱导的鸡红细胞免疫功能低下。     

大豆黄酮对肉仔鸡生长相关激素水平与免疫机能的影响

将640只1日龄艾维茵肉鸡公母分养,分别随机分为4组,分别饲喂添加大豆黄酮0、5、10、15mg/kg的4种饲粮,于试验28、49d采血和屠宰,探讨了日粮中添加不同水平大豆黄酮对肉仔鸡生长相关激素水平及免疫机能的影响。结果显示,日粮中添加大豆黄酮28、49d,均可显著提高公鸡血清生长激素(GH)、胰岛素样生长因子-1(IGF-1)、睾酮(TESTO)的含量(P<0.05或P<0.01),显著降低公鸡血清尿素氮水平(P<0.05或P<0.01),而对母鸡血清GH、IGF-1、尿素氮水平无明显影响;添加大豆黄酮49d,显著提高公鸡T淋巴细胞ANAE阳性率(P<0.05或P<0.01),添加大豆黄酮28d,显著提高公鸡NDV抗体效价(P<0.05),而对母鸡无明显影响(P>0.05);添加大豆黄酮28、49d,对公母鸡免疫器官重量有增加的趋势,但差异不显著(P>0.05)。     

Canine GM2‐Gangliosidosis Sandhoff Disease Associated with a 3‐Base Pair Deletion in the HEXB Gene

Background

GM2‐gangliosidosis is a fatal neurodegenerative lysosomal storage disease (LSD) caused by deficiency of either β‐hexosaminidase A (Hex‐A) and β‐hexosaminidase B (Hex‐B) together, or the GM2 activator protein. Clinical signs can be variable and are not pathognomonic for the specific, causal deficiency.

Objectives

To characterize the phenotype and genotype of GM2‐gangliosidosis disease in an affected dog.

Animals

One affected Shiba Inu and a clinically healthy dog.

Methods

Clinical and neurologic evaluation, brain magnetic resonance imaging (MRI), assays of lysosomal enzyme activities, and sequencing of all coding regions of HEXA, HEXB, and GM2A genes.

Results

A 14‐month‐old, female Shiba Inu presented with clinical signs resembling GM2‐gangliosidosis in humans and GM1‐gangliosidosis in the Shiba Inu. Magnetic resonance imaging (MRI) of the dog's brain indicated neurodegenerative disease, and evaluation of cerebrospinal fluid (CSF) identified storage granules in leukocytes. Lysosomal enzyme assays of plasma and leukocytes showed deficiencies of Hex‐A and Hex‐B activities in both tissues. Genetic analysis identified a homozygous, 3‐base pair deletion in the HEXB gene (c.618‐620delCCT).

Conclusions and Clinical Importance

Clinical, biochemical, and molecular features are characterized in a Shiba Inu with GM2‐gangliosidosis. The deletion of 3 adjacent base pairs in HEXB predicts the loss of a leucine residue at amino acid position 207 (p.Leu207del) supporting the hypothesis that GM2‐gangliosidosis seen in this dog is the Sandhoff type. Because GM1‐gangliosidosis also exists in this breed with almost identical clinical signs, genetic testing for both GM1‐ and GM2‐gangliosidosis should be considered to make a definitive diagnosis.