School of Geography and Biological Information, Nanjing University of Posts and Telecommunications, Nanjing, China.
Key Laboratory for Organic Electronics and Information Displays & Jiangsu Key Laboratory for Biosensors, Institute of Advanced Materials (IAM), Nanjing University of Posts and Telecommunications, Nanjing, China.
J Appl Toxicol. 2020 Aug;40(8):1131-1140. doi: 10.1002/jat.3972. Epub 2020 Mar 13.
The potential toxicity of cadmium-containing quantum dots (QDs) has received much attention because of increasing biomedical applications. However, little has been known about how cadmium telluride (CdTe) QDs influence the gut microbiota and lipid metabolism. In this study, mice were exposed orally to CdTe QDs (200 μL of 0.2, 2, 20 or 200 μm; twice per week) for 4 weeks. The oral experiments showed CdTe QD exposure led to a decrease of the Firmicutes/Bacteroidetes (F/B) ratio of gut microbiota, which highly negatively correlated with the low-density lipoprotein (LDL), triglyceride (TG) and total cholesterol (TC) levels in serum. In addition, the low-dose (0.2 and 2 μm) CdTe QDs significantly increased the diversity of gut microbiota, and did not elevate the LDL, TG and TC levels in serum. The medium dose (20 μm) of CdTe QDs caused the biggest decrease of the F/B ratio, so it significantly increased the LDL, TG and TC levels compared with the control. Furthermore, high-dose (200 μm) CdTe QDs caused various toxicities in the histopathology of liver and intestine, liver function and intestinal immunity, but did not significantly lead to changes of the LDL, TG and TC levels in serum. This study demonstrates that high-dose oral CdTe QDs mainly lead to tissue damage of the liver and intestine, while the medium and low doses of oral CdTe QDs induce shifts of gut microbiota structure, which are associated with blood lipid levels.
由于生物医学应用的增加,含镉量子点(QD)的潜在毒性受到了广泛关注。然而,人们对于碲化镉(CdTe)QD 如何影响肠道微生物群和脂质代谢知之甚少。在这项研究中,小鼠经口暴露于 CdTe QD(200 μL 的 0.2、2、20 或 200 μm;每周两次)4 周。口服实验表明,CdTe QD 暴露导致肠道微生物群的厚壁菌门/拟杆菌门(F/B)比值下降,这与血清中低密度脂蛋白(LDL)、甘油三酯(TG)和总胆固醇(TC)水平呈高度负相关。此外,低剂量(0.2 和 2 μm)CdTe QD 显著增加了肠道微生物群的多样性,而不会升高血清中的 LDL、TG 和 TC 水平。中剂量(20 μm)的 CdTe QD 导致 F/B 比值下降最大,因此与对照组相比,它显著增加了 LDL、TG 和 TC 水平。此外,高剂量(200 μm)CdTe QD 对肝脏和肠道的组织病理学、肝功能和肠道免疫造成了各种毒性,但不会导致血清中 LDL、TG 和 TC 水平的显著变化。本研究表明,高剂量口服 CdTe QD 主要导致肝脏和肠道的组织损伤,而中低剂量口服 CdTe QD 则导致肠道微生物群结构的改变,这与血液脂质水平有关。