The proteins of the bovine erythrocyte membrane were analyzed by polyacrylamide gel electrophoresis in sodium dodecyl sulfate, and their relations to the slow sedimentation rate of bovine erythrocytes were investigated by treating the erythrocytes with trypsin. The erythrocyte sedimentation rates of bovine erythrocytes from Holstein and Korean native cattle were very slow compared with the human one (1/7 as slow as the human one) as reported previously. However, when human and Holstein erythrocytes were treated with trypsin (0.2 and 0.5 mg/ml) for 1 hour at 37deg C, their sedimentation rates were markedly accelerated while the sedimentation rate of Korean native cattle's erythrocytes were not affected. Although the general protein profiles of the bovine erythrocyte membranes were almost similar to that of human, bovine erythrocyte membranes showed one additional protein band called band Q in this study, which migrated electrophoretically to the mid-position between band 2 and band 3 in human erythrocyte membranes. Treatment of Holstein and human erythrocytes with trypsin caused a decrease or disappearance of the band Q from the erythrocyte membrane. Although the band Q in Korean native cattle's erythrocyte membrane was decreased by trypsin treatment of the erythrocytes, the magnitude of the decrement was not so pronounced as in the case of human and Holstein erythrocytes. The glycoprotein profiles of the bovine erythrocyte membranes revealed by periodic acid-Schiff stain showed a marked difference from that of human. The PAS-1 (glycophorin) and PAS-2 (sialoglycoprotein) present in human erythrocyte membrane were almost absent from the bovine erythrocyte membranes. Instead, the bovine erythrocyte membranes showed a strong PAS-positive band near the origin of the electrophorograms, which is named as PAS-B in this study

The levels of the serum and colostral total protein and immunoglobulins of the Korean native cows immediately after parturition and colostrum-conferred passive immune status of the Korean native calves were studied, and the results obtained were summarized as follows: The mean total protein, total immunoglobulin, IgG, IgM, and IgA concentrations in sera of 10 Korean native cows immediately after parturition were 6.8 +- 0.4g/dl, 24.39 +- 3.41mg/ml, 19.49 +- 2.70 mg/ml, 4.56 +- 1.14mg/ml, and 0.35 +-0.08 mg/ml respectively. And the mean total protein, total immunoglobulin, IgG, IgM, and IgA concentrations in colostrum were 15.0 +- 1.1 g/dl, 116.13 +- 23.07mg/ml, 101.51 +- 22.59mg/ml, 9.46 +- 1.99mg/ml, and 5.17 +- 1.59mg/ml respectively. The mean concentrations of total protein and immunoglobulins in colostrum were 2.1 times to 14.8 times higher than those in serum. The mean concentrations of total protein, total immunoglobulins in colostrum were 2.1 times to 14.8 times higher than those in serum. The mean concentrations of total protein, total immunoglobulin, IgG, IgM and IgA in sera from 211 Korean native calves at 2 days old were 6.7 +- 0.9g/dl, 35.74 +- 9.56mg/ml, 29.06 +-8.07mg/ml, 4.91+-2.99mg/ml, and 1.9 +- 0.99mg.ml respectively. Although the calves had been suckled the dam's colostrum, each of calves was considerably various in levels of serum total protein and immunoglobulins and 16.1 percent of the calves were in a state of hypoglobulinemia

Pure separation of various leukocytes is required for the assessment of their roles in immunological and physiological function. In this study, pure separation of monocytes from canine peripheral blood was attempted. At first, mononuclear cells (PBMC) were separated by ficoll-hypaque gradient method and then monocytes were recovered from PBMC suspensions in sucrose gradient Sol. (PBMC-Sucrose), autologous plasma (PBMC-Plasma) and autologous serum (PBMC-Serum) incubated at 37deg C for 2 hours. In the separation of PBMC by ficoll-hypaque gradient method in canine blood, higher relative centrifugal force (RCF) was required, as high as more than 1,300xg RCF for 40 minutes, for clear formation of PBMC layer than that in human blood as usually used 400xg RCF for 40 minutes. In monocytes-separation from three PBMC suspensions following PBMC separation, recovery-, purity- and viability- rate of monocytes showed better results in PBMC-Plasma and PBMC-Serum than in PBMC-Sucrose suspension, particularly showing better results from PBMC suspensions performed by centrifugation at 1,500xg RCF for 40 minutes

This study was carried out to determine suitable selection factors for recipients and embryos which could improve pregnancy rates following bovine embryo transfer. The experiment included 52 surgical transfers from February, 1985 through June, 1986 performed on Kyongbuk Breeding Center in southern Korea. The pregnancy rate was highest when recipients were in estrus within 6 hours before the donor to 12 hours after the donor (78.3 % versus 50 % for recipients in estrus earlier or later). Pregnancy rates were acceptable following culture under field conditions for up to 17 hours. More recipients over 15 months of age (76.1 %) remained pregnant than those under 15 months (66.7 %). Embryos transferred during the months from February to July resulted in higher pregnancy rates than those transferred during the remaining 6 months (77.3 % versus 57.1 %). Transferrable embryos were classified A (best) to C (worst); those graded A or B resulted in significantly higher pregnancy rates than those graded C (81.8 % and 73.3 % versus 25.0 %, p0.05). Pregnancy rates among recipients of the Korean native breed tended to be higher than among Holstein recipients (100 % versus 71.1 %). Similarly, when the embryo was transferred to the right uterine horn, pregnancy rates tended to be higher than when it was transferred to the left (81.3 % versus 65 %). Pregnancy rates did not differ according to the stage of development of the embryo; they were for morulae, tight morulae, blastocysts, and advanced blastocysts, respectively : 75.0 %, 66.7 %, 75.0 %, and 77.4 %

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

The change of plasma prostaglandin E2 level, natural killer cell activity and tumor cell growth were assayed after transplantation of EL-4 leukemia cells in C57BL/6 mice. Plasma prostaglandin E2 level was increased in EL-4 bearing mice, but indomethacin treated mice group showed low level. The tumor-derived prostaglandin E2 inhibited the post-target binding cytolytic process of natural killer activity. Indomethacin inhibited the growth of prostaglandin secreting EL-4 solid tumor

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

This experiment was carried out to investigate the influence of Aloe vera in the pancreatic islets of streptozotocin diabetic mice. Experimental diabetes was induced in ICR mice with a single injection of SZ (140mg/Kg body weight, ip). The mice demonstrating hyperglycemia 48 hours after SZ injection were treated for 16 days with Aloe vera (300, 800mg/Kg). Plasma glucose was measured, and for morphological studies of the islets specimens were staind with hematoxylin-eosin and by immunocytochemical methods. Then we observed the morphological changes of islets. Polymorphonuclear cells were infiltrated at the periphery of the islets 48 hours after SZ injection in SZ-treated ICR mice, but no prominent WBC infiltration was observed throughout the experiment. Blood glucose in mice treated with Aloe vera after SZ injection was higher than that of SZ injected mice, and mononuclear cells were heavily infiltrated at the islets 16 days after Aloe vera treatment (300mg/Kg), and significant islets infiltration of mononuclear cells was observed 30 days after Aloe vera treatment (800mg/Kg). Islets of ICR mice treated with Aloe vera after SZ injection showed severer insulitis, degranulation and necrosis of B cells than those of SZ injected mice. These studies indicate that Aloe in SZ injected mice increases vascular permeability and number of WBC in pancreatic islets, and potentiates destruction of B cells by cell-mediated immune system

This study was conducted in order to observe the changes in cellular association of seminiferous tubules from 4 to 22 weeks of age and to obtain the cycle and relative duration of seminiferous epithelia from 24 weeks of age in male ducks. Fifety-five male ducks were used in the experiment and divided into 11 groups, consisting of 5 male ducks each, with 2 weeks intervals from 4 to 24 weeks of age. The body and tests weight showed most rapid increase during 4 to 6 weeks and 18 to 22 weeks of age, respectively. The seminiferous tubules were abruptly enlarged in diameter of tubules during 18 to 22 weeks of age. Gonocytes were seen from 4 to 6 weeks of age, however they were not observed as from 8 weeks of age. Both type Ap spermatogonia and type Ad spermatogonia occurred from 8 to 12 weeks of age, while spermatocytes and spermatids were beginning to appear at 16 weeks and 18 weeks of age, respectively. Spermatozoa were first observed at 20 weeks of age. Full spermatogenic activity was completed at the age of 20 weeks. Average paired weight of the testes in male ducks was 78g at 24 weeks of age and its ratio spermatogenic activity was completed at the age of 20 weeks. Average diameter of seminiferous epithelium at 22 weeks of age was 232 micro m, and average numbers of Sertoli cell, spermatogonia, spermatocyte, spermatids and spermatozoa in the cross section of seminiferous epithelium were 15.30, 59.08, 41.78, 71.11 and 165.30, respectively. Spermatogonia and spermatids were classified into 2 and 4 types, respectively. The cycle of the seminiferous epithelium could be divided into 5 stages at 24 weeks of age. The relative frequencies of stages from I to V were 13.5 %, 25.0 %, 22.3 %, 20.6 % and 18.7 %, respectively. Thus, establishment of spermatogenesis in male ducks were beginning to appear at 20 weeks of age