Enriched uranium(UO2F2) accumulated in organism could cause chromosome aberrations in somatic cells, its rates on bone marrow cells were elevated when the dose of 235UO2F2 was increased. Among the types of induced abe...Enriched uranium(UO2F2) accumulated in organism could cause chromosome aberrations in somatic cells, its rates on bone marrow cells were elevated when the dose of 235UO2F2 was increased. Among the types of induced aberrations, chromatid breakage was predominant, accompanied with a few chromosome breakage and translocation. At the same time mitosis index of metaphase cells was depressed. Chromatid delation and chromatid exchange were induced in peripheral blood lymphocytes. The important type of aberrations in spermatogonia was break. For primary spermatocytes the most significant aberration was multivalents which resulted either from chromatid interchanges or reciprocal translocations. 235UO2F2 could result in DNA breakage in germ cells. The sensitivity of germ cells at various stages to 235UO2F2. was different. At 12d after exposure the amount of sperm DNA eluted reached the peak. When the treating time was fixed, elution of sperm DNA from treated animals increased with the increasing doses. 235UO2F2. could also result in sperm abnormalities. Especially at 13 to 36 d after treatment the rates of sperm abnormalities were significantly elevated.展开更多
Studies show that 235UO2F2 was chiefly localized in kidneys, then in skeleton and liver. Its radioactivity in skeleton rose steadily while the concentration in kidneys and liver droped. 235UO2F2 was difficult to pass ...Studies show that 235UO2F2 was chiefly localized in kidneys, then in skeleton and liver. Its radioactivity in skeleton rose steadily while the concentration in kidneys and liver droped. 235UO2F2 was difficult to pass through the blood- testes barrier. With 1 to 6 h contact period, only 1.4-1.6 % 235UO2F2 was found in the intact skin, but 41-54 % in the abrasive skin. The dynamic retention of 235UO2F2 through intact or abrasive skins was also dominantly localized in kidneys, skeleton and liver. Accumulation of insoluble 235U3O8 in gastrointestinal tract was well described by a double- exponential- term expression. Values of retention were estimated for fast component T1= 0.34 d, and for relatively long term component T2= 4.05 d.展开更多
基金The Subject Supported by National Natural Science Foundation of China
文摘Enriched uranium(UO2F2) accumulated in organism could cause chromosome aberrations in somatic cells, its rates on bone marrow cells were elevated when the dose of 235UO2F2 was increased. Among the types of induced aberrations, chromatid breakage was predominant, accompanied with a few chromosome breakage and translocation. At the same time mitosis index of metaphase cells was depressed. Chromatid delation and chromatid exchange were induced in peripheral blood lymphocytes. The important type of aberrations in spermatogonia was break. For primary spermatocytes the most significant aberration was multivalents which resulted either from chromatid interchanges or reciprocal translocations. 235UO2F2 could result in DNA breakage in germ cells. The sensitivity of germ cells at various stages to 235UO2F2. was different. At 12d after exposure the amount of sperm DNA eluted reached the peak. When the treating time was fixed, elution of sperm DNA from treated animals increased with the increasing doses. 235UO2F2. could also result in sperm abnormalities. Especially at 13 to 36 d after treatment the rates of sperm abnormalities were significantly elevated.
基金The Project Supported by National Natural Science Foundation of China
文摘Studies show that 235UO2F2 was chiefly localized in kidneys, then in skeleton and liver. Its radioactivity in skeleton rose steadily while the concentration in kidneys and liver droped. 235UO2F2 was difficult to pass through the blood- testes barrier. With 1 to 6 h contact period, only 1.4-1.6 % 235UO2F2 was found in the intact skin, but 41-54 % in the abrasive skin. The dynamic retention of 235UO2F2 through intact or abrasive skins was also dominantly localized in kidneys, skeleton and liver. Accumulation of insoluble 235U3O8 in gastrointestinal tract was well described by a double- exponential- term expression. Values of retention were estimated for fast component T1= 0.34 d, and for relatively long term component T2= 4.05 d.
