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首页> 外文期刊>Journal of trace elements in medicine and biology: Organ of the Society for Minerals and Trace Elements (GMS) >The chemical speciation, spatial distribution and toxicity of mercury from Tibetan medicine Zuotai, beta-HgS and HgCl2 in mouse kidney
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The chemical speciation, spatial distribution and toxicity of mercury from Tibetan medicine Zuotai, beta-HgS and HgCl2 in mouse kidney

机译:来自小鼠肾脏藏,β-HGS和HGCL2含有藏的化学品质,空间分布和毒性

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摘要

Zuotai, a famous Tibetan medicinal mixture containing beta-HgS, has been used to combine with herbal remedies for treating diseases for more than 1 300 years. The target organ for inorganic mercury toxicity is generally considered to be the kidney. Therefore, it is crucial to reveal the chemical speciation, spatial distribution and potential nephrotoxicity of mercury from Zuotai in kidney. To date, this remains poorly understood. We used Xray absorption spectroscopy (XAS) and micro X-ray fluorescence (mu-XRF) imaging based on synchrotron radiation to study mercury chemical forms and mercury special distribution in kidney after mice were treated orally with Zuotai, beta-HgS or HgCl2. Meanwhile, the histopathology of kidney was observed. Mice exposed with Zuotai showed kidney with significant proportion of mercury ions bound to sulfydryl biomolecules (e.g. Cys-S-lig-S-Cys) plus some of unknown species, but without methylmercury cysteine, which is the same as beta-HgS and HgCl2. The mercury is mainly deposited in renal cortex in mouse treated with Zuotai, beta-HgS or HgCl2, but with a low level of mercury in medulla. The total mercury in kidney of mice treated with HgCl2 was much higher than that of beta-HgS, and the later was higher than that of Zuotai. And, HgCl2 cause severe impairments in mouse kidney, but that was not observed in the Zuotai and beta-HgS groups. Meanwhile, the bio-metals (Ca, Zn, Fe and Cu) micro distributions in kidney were also revealed. These findings elucidated the chemical nature, spatial distribution and toxicity difference of mercury from Zuotai, beta-HgS and HgCl2 in mouse kidney, and provide new insights into the appropriate methods for biological monitoring.
机译:含有β-HGS的着名藏药物混合物的Zuotai已被用于与草药治疗疾病组合超过1 300年。无机汞毒性的目标器官通常被认为是肾脏。因此,揭示肾脏祖先汞的化学品质,空间分布和潜在肾毒性至关重要。迄今为止,这仍然明白很差。我们使用基于同步辐射的X射线吸收光谱(XAS)和微X射线荧光(MU-XRF)成像,以研究小鼠的汞化学形式和肾脏的汞特殊分布与Zuotai,β-Hgs或HgCl2口服。同时,观察到肾的组织病理学。用Zuotai暴露的小鼠显示肾脏,肾脏与磺酰霉菌生物分子(例如Cys-S-Lig-S-Cys)结合的汞离子比例,以及一些未知物种,但没有甲基汞半胱氨酸,其与β-Hgs和HgCl2相同。汞主要沉积在用Zuotai,β-Hgs或HgCl2处理的小鼠中肾皮质,但在髓质中汞水平较低。用HgCl2处理的小鼠肾脏的总汞远高于β-Hgs,后来高于Zuotai的小鼠。并且,HGCL2在小鼠肾脏造成严重的损伤,但在祖泰和β-HGS组中未观察到。同时,还揭示了肾脏中的生物金属(Ca,Zn,Fe和Cu)微分布。这些研究结果阐明了小鼠肾脏的玉米,β-Hgs和HgCl2的汞的化学性质,空间分布和毒性差异,并为生物监测的适当方法提供了新的见解。

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