In order to observe the pathological changes of kidney in rabbits infected with the viral haemorrhagic disease, the kidney tissues from the 91 rabbits infected with the viral haemorrhagic disease were examined by light and electron microscopy. On light microscopic observation, the kidney lesions were identified as haemorrhagic glomerular necrosis (33.0 %), membranous glomerulonephritis (20.9 %), thrombotic glomerulopathy (19.8 %) membranoproliferative glomerulonephritis (8.8 %), mesangial proliferative glomerulonephritis (8.8 %) ischemic acute tubular necrosis (7.7 %), and acute serous glomerulitis (6.6 %). On electron microscopic observation, cytoplasmic degeneration of mesangial cells, and irregular thickening of basement membranes with electron dense granular materials were observed. In podocytes swelling of mitochondria, dilatation of endoplasmic reticulum and extensive fusion of foot processes were also observed. Nonenveloped round icosahedral picornaviral particles with a diameter of 28-33nm were detected in the cytoplasm of degenerative endothelial cells, polymorphonuclear leucocytes, and monocytes

The study was undertaken to obtain indirect values of volume of packed red cell (VPRC) without centrifugation, using the erythrocyte sedimentation rate (ESR) of diluted blood in dogs. ESRs of diluted blood using the diluent of autologous plasma in which formed numerous RBC-rouleau clumps, autologous serum in which formed a few RBC-rouleau clumps, and 5 % dextrose or 6 % sucrose solutions in which formed numerous RBC-aggregation clumps, were accelerated. But ESR of diluted blood using the 0.9 % saline, D-S, ACD-B, CDP or D-PBS solutions were sluggish, because erythrocytes were dispersed in these diluents. Reliable values of VPRC on the basis of the correlating regressive equation to the ESR could be derived from values of 60deg C-angled-micro-ESR/40 min in the mixture, four parts of 5 % dextrose solution and one part of whole blood. In the ESR values of diluted blood with low ratio, 1 : 1-3 : 1, 60deg C-micro-ESR was higher than 60deg C-Wintrobe-ESR. But, in the diluted blood with high ratio, 4 : 1-5 : 1, there was no different ESR values. For an aid of practical use, authors suggested a list of the 60deg C-micro-ESR/40 min in the diluted blood with equivalent VPRC of whole blood

The proteins of the ruminant erythrocyte membranes were analysed by polyacrylamide gel electrophoresis in sodium dodecyl sulfate, and their relations to the slow erythrocyte sedimentation rate (ESR) of the ruminants were investigated by treating the erythrocytes with proteinases such as trypsin, chymotrypsin and pronase, and glycosidases such as neuraminidase and galactosidase. Protein content in the erythrocyte membrane was 2.85 +- 0.28 in human, 3.60 +-0.41 in Korean cattle, 3.71 +- 0.36 in Holstein, 4.13 +-0.83 in Korean native goat and 3.94 +- 0.56 mg/ml in sheep, showing higher in ruminant animals than in human (p0.01). Although the general protein profiles of the ruminant erythrocyte membranes were almost similar to that of human, all the ruminant erythrocyte membranes showed one additional protein band, called band- Q in the previous report on proteins of bovine erythrocyte membrane, which migrated electrophoretically to the mid position between band-2 and band-3 in human erythrocyte membranes. The glycoprotein profiles of ruminant erythrocyte membranes revealed by periodic acid Schiff (PAS) stain showed a marked difference from that of human. The PAS-l (glycophorin) and PAS-2 (sialoglycoprotein) present in human erythrocyte membranes were almost absent from the ruminant animals. Instead, a strong PAS-positive band near the origin of the electrophorograms, which was named as PAS-B in the previous report on proteins of bovine erythrocyte membranes, was shown in the ruminant animals except sheep. In addition, the erythrocyte membranes of Korean native goat and sheep showed a moderate PAS-negative band near the tracking dye of the electrophorograms, which was named as PAS-G in this study. In the erythrocyte treated with the enzymes, the migration of each protein fracture of erythrocyte membranes in response to each enzyme was diverse according to different species or breed of ruminant animals. Among others, band-Q present in ruminants was slightly or moderately decreased by trypsin-, chymotrypsin-, and pronase- treatments of the erythrocytes, but not only in sheep

This study was undertaken to establish reliable diagnostic-procedures for the microbiological monitoring of laboratory animals. Murine (mice and rats) antibodies against hemagglutinating virus of Japan (HVJ), mouse hepatitis virus (MHV) and Mycoplasma pulmonis (Mp) were detected sensitively and specifically in experimentally and naturally infected animals' sera by an indirect enzyme-linked immuno-sorbent assay (ELISA), using urease conjugated antimurine immunoglobulin. The sensitivity and specificity of the complement fixation test which has been apllied widely for serodiagnosis of HVJ, MHV and Mp infections were apparently lower than those of ELISA. From these results, the ELISA was found to be available for the serodiagnosis of HVJ, MHV and Mp infections in mice and rats

These studies were carried out to investigate the changes of blood pictures, histological findings and testosterone concentrations after orchidectomy in ageing rat. The total W.B.C. counts were 9.27 +- 12 x 10** (3)/mm** (3) in the control group, 9.54 +- 34 x 10** (3)/mm** (3) in the sham-operation group and 12.08 +- 28 x 10** (3)/mm** (3) in the orchidectomy group when it was checked 50days after the operation. The number of lymphocytes after orchidectomy began to increase gradually as time passes, thereafter markedly increased 10.12 +- 03 x 10** (3)/mm** (3) at 50 days after orchidectomy. The concentration of testosterone in serum began to decrease gradually after orchidectomy showed lowest level 1.68 +- 0.61 pg/ml at 50 days after orchidectomy while it was 5.82 +- 0.39 pg/ml in control group. The histological findings of thymus after orchidectomy marked increase of thymic lymphocyte, disapearance of fat cells and appearance of mitotic figures

In present study the transtracheal aspiration technique using a commercial polypropylene 5 fr. urinary catheter with 13-gauge 2.5 inch hypodermic needle was applied to bovine medicine in order to determine the availability of this procedure for diagnosis of lower respiratory tract disease. The subjects were forty adult cattle which consisted of thirty-one cows with respiratory signs such as cough and nasal discharge and nine cows without these signs. This procedure appeared suitable for collecting specimens of the lower respiratory tract secretions without uncontamination by the flora of the mouth, respiratory distress and any complications. The most of microorganisms isolated was Pasteurella multocida (48.7 %) and a mucopurulent inflammatory response was the most appeared accounting for 40 % of cytological basis. Most cows with severe clinical signs showed a mucopurulent inflammation (60 %) and Pasteurella multocida were isolated dominantly in severe cases (63.2 %). Cows with mild clinical signs were distributed in each of the five cytological classification and Pasteurella multocida was the most isolated accounting for 40 % of mild cases. In the cytologic examination, a few neutrophils and epithelial cells were seen in the fluid of mucoid inflammation, and many neutrophils with epithelial cells and thick mucoid exudate were seen in the fluid of mucopurulent inflammation. Various number of neutrophils, lymphocytes, macrophages and epithlial cells were examined in the fluid of mixed cell inflammation. The columnar ciliated epithelial cells were examined mainly in normal aspirates. From these results the transtracheal aspiration technique as a diagnostic aid for lower respiratory tract disease of cow is considered as a simple, safe and useful method and can be performed in the field situation

Morphological features of the vomeronasal organ of both Korean native cattle and Korean native goat were studied by gross, microscopic and histochemical examinations. Anatomical characteristics of the vomeronasal organ were similar in both Korean native cattle and Korean native goats. The vomeronasal organ is a tubular structure situated bilaterally at the base of the nasal septum, and enclosed by hyaline cartilage. Its lumen is semilunar to crescent in transverse sections. It joins with the incisive duct through narrow duct. The lumen of the vomeronasal organ is lined with sensory and respiratory epithelia. The distribution pattern of vomeronasal mucosal epithelia varied by the position. In the anterior portion joining with nasal cavity, the lumen is lined with only respiratory epithelium. In the middle portion, sensory epithelium appeared on the medial side, and respiratory epithelium on the lateral side. In the posterior, it is lined with sensory epithelium on the ventral side and lined with respiratory epithelium on the dorsal side. The vomeronasal gland composed of mucous and serous acini are distributed in the lamina propria under the respiratory epithelium, where venous sinuses are also well developed

In order to manifest the presence of Na-K pump and its property on the unfertilized egg membranes of mouse, membrane potential was recorded under the physiological condition (at 37deg C and 4mM Ca** 2+). After an induction of superovulation, the fresh eggs with zona pellucida were collected from mouse oviduct. Transient hyperpolarization as pump action was recorded after the switch into the high potassium perfusate (15mM K+) from K-free perfusate, and the difference between membrane potential observed just before the perfusion of high potassium solution and the maximal membrane potential during the perfusion of high potassium solution was regard as pump activities. Resting membrane potential was depolarized under the treatment of 10** (-5) ouabain. Pump activities of the unfertilized mouse eggs were -3.38 +- 0.61mV (Mean +- SD, n=6), recorded as transient hyperpolarization due to the electrogenic property. Pump activities were blocked by both treatment of 10** (-5)M ouabain and perfusion of Na-free solution, while increased by high Na + (300mM) perfusion (-7.45 +- 0.75mV, n=2). Hyperpolarization due to pump activity was not altered by Mn 2+. Above results confirm the presence of ouabain-sensitive Na-K pump, which affected the membrane potential directly, on the unfertilized egg membranes of mouse

The present study was carried out to determine viral antigens and its morphogenesis in the ultrathin frozen and araldite sections of cell cultures infected with ADV by protein A-gold labelling. ADV antigens were labelled with 10nm gold probes, and electron-dense gold particles were mainly present on viral nucleocapsids and viral envelopes. Immunogold labelling in the ultracryosections showed a very low degree of interaction with tissue structures. Immunogold labelling in the ultrathin cryosections can be useful tool for the detection of ADV antigens, and the technique also may provide its great potential for immunocytochemical studies on various virus-host cell interactions

To investigate the epidemiological trait of intestinal diseases of animals caused by thermophilic Campylobacter spp., isolation of etiological agent was carried out. Isolated Campylobacter spp. were biotyped, serotyped and the susceptibility of the isolates to antimicrobial agents were examined. Isolation rates of Campylobacter spp. from 649 fecal materials of 208 cattle, 300 pigs and 141 chickens were 25.5 %, 23.7 % and 38.3 %, respectively. The majority of the 130 isolates of C jejuni was classified as biotype I (50.6 %) and biotype II (34.6 %). Most of the 46 isolates of C coli were biotype I (71.7 %). Isolated C jejuni strains showed 14 different serotype, and serotype 4, 26, 36 were most frequent. Isolated C coli strains showed 5 different serotype and serotype 31 and 21 were relatively common. Isolated Campylobacter spp. were highly susceptible to nalidixic acid, amikacin, gentamycin, colistin and chlorampehnicol