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首页> 外文期刊>Toxicology in vitro: an international journal published in association with BIBRA >Mitigative action of monoisoamyl-2,3-dimercaptosuccinate (MiADMS) against cadmium-induced damage in cultured rat normal liver cells.
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Mitigative action of monoisoamyl-2,3-dimercaptosuccinate (MiADMS) against cadmium-induced damage in cultured rat normal liver cells.

机译:2,3-二巯基琥珀酸单异戊酯(MiADMS)对镉诱导的大鼠正常肝细胞损伤的缓解作用。

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摘要

Cadmium is non-essential, carcinogenic and multitarget pollutant in the environment. Monoisoamyl-2,3-dimercaptosuccinate (MiADMS) is an ester of dimercaptosuccinic acid that acts as an antioxidant and chelator. Therefore, the mitigative action of MiADMS on viability, morphology, antioxidative enzymes and cell cycle were studied on rat liver cells treated with cadmium chloride (CdCl2). The cells were treated with 150 muM CdCl2 alone or cotreated with 300 muM MiADMS (concurrently, 2 h or 4 h post-CdCl2 treatment) for 24 h. The viability of cells treated with CdCl2 alone was decreased in comparison to the control cells. Cotreatment with MiADMS resulted in an increase in cell viability in comparison to the CdCl2 alone treated cells. The CdCl2 treatment altered the morphological shape of the cells, while cotreatment with MiADMS restored the shape. Antioxidative enzymes activities were decreased in the cells treated with CdCl2 alone, while MiADMS cotreatment resulted in an increase in enzyme activities. The CdCl2 arrested the cells in S phase of the cell cycle. Cotreatment with MiADMS alleviated cell cycle arrest by shifting to G1 phase. These results clearly show the mitigative action of MiADMS on CdCl2 toxicity and may suggest that MiADMS can be used as an antidote against cadmium.
机译:镉是环境中不必要的,致癌的多目标污染物。 2,3-二巯基琥珀酸单异戊酯(MiADMS)是二巯基琥珀酸的酯,可作为抗氧化剂和螯合剂。因此,在用氯化镉(CdCl2)处理的大鼠肝细胞中,研究了MiADMS对存活率,形态,抗氧化酶和细胞周期的缓解作用。将细胞单独用150μMCdCl2处理或与300μMMiADMS共同处理(同时,在CdCl2处理后2小时或4小时)持续24小时。与对照细胞相比,仅用CdCl2处理的细胞的活力降低了。与单独使用CdCl2处理的细胞相比,与MiADMS共同处理可提高细胞活力。 CdCl2处理改变了细胞的形态,而与MiADMS共同处理则恢复了形状。在单独用CdCl2处理的细胞中,抗​​氧化酶的活性降低,而MiADMS共同处理导致酶的活性增加。 CdCl2将细胞停滞在细胞周期的S期。与MiADMS共同处理可通过转移至G1期来缓解细胞周期停滞。这些结果清楚地表明了MiADMS对CdCl2毒性的缓解作用,并且可能表明MiADMS可用作抗镉的解毒剂。

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