纳米分散氧化锰的毒理学特征:不同暴露类型下的物理化学特性、生物积累和形态功能特性

Nina Vladimirovna Zaitseva, Marina Alexandrovna Zemlyanova
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引用次数: 8

摘要

纳米氧化锰具有良好的应用前景。一些数据表明,当以各种方式引入时,它的颗粒可能是有毒的,这需要进一步检查这种纳米材料。作者通过对纳米分散二氧化锰水悬浮液的灌胃、吸入和皮肤吸收引入小啮齿动物进行了研究,获得了其毒性作用的深刻特征,确定了靶器官,揭示了剂量依赖性效应。该物质具有急性毒性,在长期接触下其生物积累导致脑形态功能紊乱、脂质过氧化激活和抗氧化系统活性降低。作者发现血管充血,蛛网膜下腔出血,脑水肿伴血管周围和细胞周围间隙扩张,神经纤维脱髓鞘和血管内皮局灶性营养不良改变。长期以0.25 ~ 2.5 mg/kg剂量给药后,出现氧化-抗氧化失衡,神经递质和电解质平衡被破坏,刷边上皮功能不全。以2.5和0.25 mg/kg剂量的纳米二氧化锰水悬浮液灌胃Wistar大鼠没有胚胎毒性和致畸作用。10.3和5.15 mg/kg的剂量对Wistar雄性大鼠没有诱变作用,10.3 - 5.15 mg/kg的剂量通过胃管给药也没有促性腺毒性作用。
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Toxicologic Characteristics of Nanodisperse Manganese Oxide: Physical-Chemical Properties, Biological Accumulation, and Morphological-Functional Properties at Various Exposure Types
Nanosized manganese oxide has excellent prospects. Some data imply that its particles can be toxic when introduced in various ways, and it requires further examination of this nanomaterial. The authors conducted research of nanodisperse MnO 2 water suspension at intragastric, inhalation, and skin-resorptive introduction into small rodents and obtained profound characteristics of its toxic effects, determined target organs and revealed dose-dependent effects. The substance was characterized with acute toxicity, and its bioaccumulation under long-term exposure caused morphofunctional disorders in brain, lipid peroxidation activation, and lower antioxidant system activity. The authors detected vessel hyperemia, subarachnoid hemorrhages, brain edema with perivascular and pericellular spaces dilatation, nerve fiber demyelinization, and focal dystrophic changes in vessels endothelium. After a long-term introduction in doses from 0.25 to 2.5 mg/kg, oxidizing-antioxidant imbalance occurred, neurotransmitters and electrolytes balance was violated, and there was also brush border epithelium insufficiency. Nanodisperse MnO 2 water suspension in doses equal to 2.5 and 0.25 mg/kg at intragastric introduction into Wistar rats did not have embryotoxic or teratogenic effects. It did not have any mutagenic effects in doses equal to 10.3 and 5.15 mg/kg or gonadotoxic effects either when introduced into Wistar male rats in doses equal to 10.3–5.15 mg/kg via gastric tube.
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