Structure of bovine fungiform taste buds and their immunoreactivity for gustducin

The taste buds of bovine fungiform papillae were studied by light and electron microscopy using both histological and immunohistochemical methods. The taste buds existed in the epithelium of the apical region of the papillae. By electron microscopy, two types of taste cells, namely type I and type II cells, could be classified according to the presence of dense-cored vesicles, the cytoplasmic density and the cell shape. Type I cells were thin, had an electron-dense cytoplasm containing dense-cored vesicles, and possessed long thick apical processes in the taste pore. Type II cells were thick, had an electron-lucent cytoplasm containing many electron-lucent vesicles, rather than dense-cored vesicles, and possessed microvilli in the taste pore. Immunohistochemical staining with an antiserum against gustducin was investigated by both light and electron microscopy using the avidin-biotin complex (ABC) method. Some, but not all, of the type II cells exhibited gustducin immunoreactivity, whereas none of the type I cells showed any immunoreactivity.     

Comparative study of the innervation of acetylcholinesterase-positive nerves in the cerebral arterial tree of birds

Acetylcholinesterase (AChE) histochemistry and quantitative analysis were used to investigate and compare the projections and densities of cerebral perivascular AChE nerves in five avian species. In the society finch, AChE nerves arising from the cerebral carotid, internal ethmoidal and vertebral arteries generally have no overlap with each other. This is different from AChE neuronal projections via these three vascular routes reported previously for the pigeon, duck, chicken and quail. AChE nerves supplying the pigeon cerebral arterial tree are the highest in density, predominate in the anterior circulation (AC) rather than in the posterior circulation (PC). Similar differential supply of nerves is also found in the duck, with a marked low density in the PC. In contrast, the chicken PC has a substantial amount of AChE nerves that is larger than the fiber amount contained in the AC. The reduction of nerves is far greater in both the AC and PC of the finch. It is not so prominent as that seen in the quail. The significant difference in the distribution and density of cerebral perivascular AChE nerves presented here may indicate that there are some species-specific cholinergic controlling mechanisms responsible for the cerebral circulation of birds.     

Analyses of hemorrhagic diathesis in high-iron diet-fed rats

Iron overload has been well recognized to cause oxidant-mediated cellular/tissue injury; however, little is known about the effects of iron overload on the blood coagulation system. We encountered an unexpected bleeding tendency in rats fed a high-iron diet in a set of studies using iron-modified diets. In this study, we investigated the mechanism of hemorrhagic diathesis induced by dietary iron overload in rats. Six-week-old F344/DuCrlCrlj male rats were fed a standard (containing 0.02% iron) or a high-iron diet (containing 1% iron) for 6 weeks and were then sampled for hematological, blood biochemical, coagulation, and pathological examinations. Serum and liver iron levels increased in rats fed the high-iron diet (Fe group) and serum transferrin was almost saturated with iron. However, serum transaminase levels did not increase. Moreover, plasma prothrombin time and activated partial thromboplastin time were significantly prolonged, regardless of the presence of hemorrhage. The activity of clotting factors II and VII (vitamin K-dependent coagulation factors) decreased significantly, whereas that of factor VIII was unaltered. Blood platelet levels were not influenced by dietary iron overload, suggesting that the bleeding tendency in iron-overloaded rats is caused by secondary hemostasis impairment. In addition, hemorrhage was observed in multiple organs in rats fed diets containing more than 0.8% iron. Our results suggest that iron overload can increase the susceptibility of coagulation abnormalities caused by latent vitamin K insufficiency.     

Comparison of the amino acid sequences of acorn barnacle lectins showing different inhibitory activities toward the crystal growth of calcium carbonate

ABSTRACT: The amino acid sequence of a D -galactose-binding lectin isolated from the hemolymph of the acorn barnacle Balanus rostratus was determined. The lectin (BRL) ( M _r 120K) is a multimeric protein whose subunit consists of 182 amino acids. The amino acid sequence was compared with those of multiple lectins (BRA-2, BRA-3) from Megabalanus rosa to explore the relationship between the structures and the inhibitory activity toward the crystal growth of calcium carbonate. Although BRL was 46% identical to BRA-2 and 15% identical to BRA-3, the lectin had no inhibitory activity, unlike BRA-2 and BRA-3. Both the number and the localization of acidic amino acid residues and their amide forms were different among them. Observations by scanning electron microscopy revealed modifications in the size and morphology of the calcium carbonate crystals grown in the presence of the lectins.     

RPLM对泌乳后期奶牛血液代谢物、产乳量和乳成分的影响

选用 8头经产荷斯坦种乳牛 ,分为对照和瘤胃保护赖氨酸 蛋氨酸 (RPLM )组 ,以二乘反转法 ,研究了RPLM对泌乳后期奶牛瘤胃发酵、血液指标、产乳量和乳成分的影响。对照日粮中添加 10 0 g/d保护材料 ,RPLM组日粮中添加 10 0g/d含Lys 11 6g、Met 4 7g的保护制品。RPLM组与对照组比较 ,血浆游离Lys、Met浓度略有增加 (P >0 1) ,血浆葡萄糖浓度有增加趋势 (P <0 1) ,干物质采食量无明显变化 ,乳量和 4%的标准乳量分别增加 0 5kg/d(2 2 %)和 0 8kg/d(3 5 %) ,乳蛋白率、乳脂率和乳糖率均略高于对照组 (0 0 1%0 0 6%) ,乳蛋白质和乳脂肪生产量分别增加 2 0g/d和 40 g/d ,饲料蛋白质转化为乳蛋白质的效率提高5 9%,但均无明显差异 (P >0 1)。以上结果表明 :泌乳后期奶牛日粮中添加瘤胃保护赖氨酸和蛋氨酸 ,没有明显地提高产乳量和改善乳成分的效果。     

A collision tumor consisting of granular cell tumor and adenocarcinoma in the uterus of an aged djungarian hamster

A neoplastic nodular lesion consisting of an admixture of granular cell tumor and adenocarcinoma was found in the uterus of a 26-month-old Djungarian hamster. Neoplastic cells of the uterine adenocarcinoma showed an epithelial nature in their growth patterns and by cytokeratin-immunopositive reaction, exhibiting nuclear pleomorphism. The granular cells had an abundant amount of fine granular eosinophilic cytoplasm and eccentric or central nuclei with no nuclear atypia; the granular structures were positive for periodic acid-Schiff with diastase resistance and were confirmed as lysosomes/autophagosomes by electron microscopy; immunohistochemically, the cells reacted to desmin, vimentin and α-smooth muscle actin and negatively for neurogenic, histiocyte/macrophage or epithelial markers, indicating smooth muscle origin. Because these tumors were generated from different cell origins, a diagnosis of collision tumor was made.     

A survey of Blastocystis sp. in livestock,pets, and zoo animals in Japan

The prevalence of Blastocystis sp. was examined in fecal samples collected from cattle, pigs, dogs, and a variety of zoo animals (primates, carnivores, herbivores, pheasants, and ducks) by direct observation of fresh fecal suspensions or cultured materials, using light microscopy. The cattle and pigs were randomly sampled from 11 and 12 commercial farms, respectively, located in the western region of Japan. The dog material used in this study was obtained from pets housed in an animal shelter in the city of Osaka. Zoo animals were chosen based on housing conditions that minimized the possibility of intra-zoo transmission of the organism. The prevalence rate among the groups varied greatly. A high prevalence of infection was observed in the farm animal group, ranging from 95% (58/61) in pigs to 71% (39/55) in cattle, whereas the dog fecal samples were completely free of the organism. Prevalence of the organism in the zoo animal were 85% (29/34) in primates, 80% (8/10) in pheasants, 56% (9/16) in ducks, and 0% (0/58) in various carnivores and herbivores. Among the zoo animals infected with Blastocystis, eight species of primates, eight species of pheasants, and four species of ducks were confirmed as new hosts. Since Blastocystis organisms isolated from various animals were morphologically indistinguishable from Blastocystis hominis by light microscopy, further genomic studies are required for analysis of the zoonotic potential or etiological significance of these isolates.