Determination of Hepatic Iron Deposition in Drug-Induced Liver Fibrosis in Rats by Confocal Micro-XRF Spectrometry.
Determination of Hepatic Iron Deposition in Drug-Induced Liver Fibrosis in Rats by Confocal Micro-XRF Spectrometry.
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共焦微型 XRF 光谱法测定大鼠药物性肝纤维化中的肝铁沉积
DOI:
10.1021/acsomega.1c06476
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发表时间:
2022-02-01
期刊:
影响因子:
4.1
通讯作者:
Li F
中科院分区:
文献类型:
--
作者:
Xu Q;Xia W;Zhou L;Zou Z;Li Q;Deng L;Wu S;Wang T;Cui J;Liu Z;Sun T;Ye J;Li F
Liver fibrosis is the intermediate process and inevitable stage of the development of chronic liver disease into cirrhosis. Reducing the degree of liver fibrosis plays an extremely important role in treating chronic liver disease and preventing liver cirrhosis and liver cancer. The formation of liver fibrosis is affected by iron deposition to a certain extent, and excessive iron deposition further induces liver cirrhosis and liver cancer. Herein, confocal microbeam X-ray fluorescence (μ-XRF) was used to determine the intensity and biodistribution of iron deposition at different time points in the process of liver fibrosis induced by thioacetamide (TAA) in rats. To our best knowledge, this is the first study using confocal μ-XRF to analyze hepatic iron deposition in hepatic fibrosis. The results showed that there are minor and trace elements such as iron, potassium, and zinc in the liver of rats. Continuous injection of TAA solution resulted in increasing liver iron deposition over time. The intensity of iron deposition in liver tissue was also significantly reduced after bone mesenchymal stem cells (BMSCs) were injected. These findings indicated that confocal μ-XRF can be used as a nondestructive and quantitative method of evaluating hepatic iron deposition in hepatic fibrosis, and iron deposition may play an important role in the progression of hepatic fibrosis induced by TAA.
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DOI:
10.1039/c2cp41858d
发表时间:
2012-10-21
期刊:
Physical chemistry chemical physics : PCCP
影响因子:
--
作者:
Chen H;Rogalski MM;Anker JN
通讯作者:
Anker JN
DOI:
10.26355/eurrev_202102_24870
发表时间:
2021-01-01
影响因子:
3.3
作者:
Chen, Z-K;Chen, D-Z;Chen, Y-P
通讯作者:
Chen, Y-P
影响因子:
7.4
作者:
Peng, Song;Liu, Zhiguo;Ding, Xunliang
通讯作者:
Ding, Xunliang
影响因子:
6.1
作者:
Mazel, Vincent;Reiche, Ina;Tchoreloff, Pierre
通讯作者:
Tchoreloff, Pierre
影响因子:
5
作者:
Alvarez-Marimon, Elena;Castillo-Michel, Hiram;Benseny-Cases, Nuria
通讯作者:
Benseny-Cases, Nuria