评估髋关节植入物的潜在肝毒性——一项体外和体内研究

Q3 Biochemistry, Genetics and Molecular Biology
Shriya Thakur , Hemalatha Kanniyappan , Puranjay Gupta , Govindaraj Perumal , Robert Hillwig , Vedant V. Bodke , Salman R. Khetani , Mathew T. Mathew
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引用次数: 0

摘要

全髋关节置换术(THR)被认为是治疗严重关节炎或髋关节问题的有效方法,每年约有250万例髋关节和膝关节置换术(AJJR, 2021)。与THR相关的一个重要临床问题是由植入物表面释放的金属颗粒和离子引起的毒性,这可能损害局部组织并可能扩散到远处器官,导致全身毒性。这种毒性受颗粒和离子的大小和浓度的影响,在肝脏中尤其重要,肝脏是人体的主要代谢器官,也是植入物积累的主要部位。在这项研究中,我们的目的是研究钴铬钼(CoCrMo)和钛(Ti)颗粒/离子(通常称为磨损产物)浓度增加对远端器官,特别是肝脏的肝毒性。我们发现这些颗粒和离子通过金属离子转运体和吞噬作用进入细胞,导致明显的细胞损伤,其中钛离子表现出最高的毒性水平,其次是钴离子和CoCrMo颗粒。我们的体外和体内联合研究支持这样的假设,即植入物中的金属颗粒和离子会造成肝细胞损伤的重大风险。这强调了解决THR患者植入物源性金属毒性的系统性影响的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluating the potential hepatotoxicity from hip implant wear products—An in-vitro and in-vivo study
Total hip replacement (THR) is recognized as an effective treatment for patients suffering from severe arthritis or hip issues, with approximately 2.5 million hip and knee replacements recorded annually (AJJR, 2021). A significant clinical concern associated with THR is the toxicity caused by metal particles and ions released from the implant surfaces, which can damage local tissue and potentially spread to distant organs, resulting in systemic toxicity. The toxicity, influenced by the size and concentration of the particles and ions, is especially critical in the liver, the body's main metabolic organ and a primary site for implant accumulation. In this study, we aim to investigate the hepatotoxicity of increasing concentrations of cobalt-chromium-molybdenum (CoCrMo) and titanium (Ti) particles/ions (generally called wear products) in remote organs, particularly the liver. We found that these particles and ions enter cells through metal ion transporters and phagocytosis, leading to significant cellular damage, with titanium ions exhibiting the highest toxicity levels, followed by cobalt ions and CoCrMo particles. Our combined in-vitro and in-vivo research supports the hypothesis that metal particles and ions from implants pose a substantial risk of liver cell damage. This underscores the importance of addressing the systemic impacts of implant-derived metal toxicity in patients with THR.
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CiteScore
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