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The aim of the study was the examine atrophy and degenerative brain changes of nine elderly animals (three monkeys, two wild cats, a likaon, a bear, a fox and horse) and to find an animal model for researching Alzheimer disease in humans. Brain hemispheres were dissected into hemispheric slabs 4.0-4.8 mm thick. Tissue samples from the brains were fixed in 10% neutral formalin, and embedded in paraffin, and then stained with hematoxylin an eosin, Nissl method, and monoclonal antibody 4G8 mAb against b-polipeptyde and neurofibrillary tangles (NFT) were stained with anti-tau monoclonal antibody. The examined animals revealed various degrees of brain atrophy neuron loss in layer III-VI in particular, lipofuscin deposit, status lacunaris, degenerative changes in the white matter, and gliosis. Lafora-like bodies were observed in licaon, horse and bear brains. The monkeys, cats, licaon, foxes, with the exception of the horse developed brain parenchymal amyloidosis-b. Two types of plaque were present, with the diffuse form being predominant. Congophilic amyloid angiopathy was observed in all the animals with the exception of the horse. NFT and amyloidosis-b was observed only in the bear brain and the latter is a good model for Alzheimer's pathology.
Провели морфометрический сравнительный анализ яичек и придатков яичек молодых 1,5—3-летних хряков с правильным семенем и старых 4—8-летыих хряков, показывающих различного рода расстройства в составе семени. Отметили, что наиболее сильными изменениями в яичках старых неплодных хряков были: уменьшение их массу, дегенерация эпителия семенных канальцев с одновременным утолщением основной мембраны, образование сперматоцелей и отрофия семенных канальцев с разрастанием интерстициальных клеток. В придатках яичек наблюдали гиперплазию эпителия протока, образование интраэпителиальных кист, реже дегенерацию эпителия протока. Другие часто встречаемые у остальных видов старические изменения яичек были здесь слабо выражены либо не появлялись.
The article presents atherosclerotic and inflammatory changes in brain vessels and perivascular tissue leading to ischemic and hypoxic changes which, in consequence, produce strokes and brain hemorrhages. The aim of the study was to examine the morphology of the brain vessels of seven elderly animals from 7-21 years of age (three monkeys, a likaon, wolf and two pigs). The brain vessels of the investigated animals demonstrated atherosclerotic changes such as: fibroid changes and amyloidal angiopathy (CAA) in the cortical and leptomeningeal vessels of the three monkeys, likaon and wolf brain. Fibroid arteritis was present in the meningeal arteries of the two sows. These atherosclerotic and inflammatory processes in the CNS vessels led to strokes and hemorrhages. Subarachnoid (Cebus apella) and intraventricular (Lemur mongoz) hemorrhages were noted in two of the monkey’s brains and fibrinotic arteritis produced massive mesencephalon hemorrhaging in the two 7-year old sows. The advanced stages of infarct necrosis were characterized by a predominance of vacuolated macrophages with proliferating mesodermal and glial components. Small post infarct and post hemorrhages lesions in nervous tissue produced scarring, with astrocytes, whereas large foci liquefied and formed cysts, marked by the presence of macrophages with hemosyderin in their margins. No atheromatosis changes were observed in the brain vessels.
The structure and functions of the oligodendrocytes in different areas of the brain in the normal process of aging in mammals is poorly known. The purpose of this study was to investigate three types of oligodendrocytes, their ultrastructure as well as morphology of myelin sheaths of nerve fibers in the central gray matter (substantia grisea centralis-SGC). The study was conducted on adult rats, 25-week-old and140-week-old rats. The animals were perfused with fixative through the left ventricle and the midbrain containing SGC were collected. Ultrathin sections were observed and photographed in an electron microscope. In both tested age groups oligodendrocytes were usually arranged in pairs. In adult rats, the SGC survey revealed a clear advantage and medium oligodenrocytów, and, rarely, dark cells with normal ultrastructure. In old rats, oligodendrocytes were dominated by medium and dark cytoplasm and less commonly with clear cells. The cytoplasm of the few bright and medium oligodendrocytes expressed the morphological changes manifested by the presence of varying electron densities and size of inclusions and the insulation of nerve fibers were also changed. The presence of the few bright oligodendrocytes in the SGC in old rats suggests that a few of their young forms of progenitor cells may arise, as in other areas of the brain normally aging in mammals. These new cells may participate in remielinization nerve fibers affecting the proper connections SGC with other brain areas.
Currently the structure and function of oligodendrocytes in the central nervous system (cns) in young individuals is known; however, there is no information about their morphology in the central gray matter (substantia grisea centralis-SGC) in old animals. The aim of this study was to investigate the morphology of oligodendrocytes in the semithin SGC sections of 6-month (5 pcs) and 3-year-old (5 pcs) male Wistar rats. The animals were anaesthetized with ketamine, perfused with fixative through the left ventricle, and the midbrains containing SGC were taken. Semithin sections were analyzed morphologically and photographs were made in light microscope Axiolab (Zeiss). In the semithin sections of the SGC of 6-month-old adult rats oligodendrocytes with mostly light and medium density cytoplasm were observed. Oligodendrocytes were located by different structures: blood vessels, neurons and astrocytes. Sometimes two cells with dark cytoplasm were side by side or near oligodendrocytes with a medium cytoplasm density. In old male rats oligodendrocytes with dark cytoplasm located at the capillary blood vessels, neurons and astrocytes were dominant in the SGC. Cells with light cytoplasm, which occurred mainly in blood vessels, were rarely encountered. The results indicate that in the SGC of 3-years-old individuals older forms with a dark cytoplasm are dominant, in contrast to 6-month-old rats which have younger oligodendrocytes with light cytoplasm.
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