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大鼠体内化学修饰纳米纤维素的肝毒性。

In vivo hepatotoxicity of chemically modified nanocellulose in rats.

机构信息

Division of Biochemistry, Department of Chemical Sciences, Redeemer's University, Ede, Osun State, Nigeria.

Division of Industrial Chemistry, Department of Chemical Sciences, Redeemer's University, Ede, Osun State, Nigeria.

出版信息

Hum Exp Toxicol. 2020 Feb;39(2):212-223. doi: 10.1177/0960327119881672. Epub 2019 Oct 13.

Abstract

Chemical modification of cellulose is currently attracting attention as researchers attempt to take advantage of the abundance of hydroxyl groups on its surface to introduce extra biological functionality. However, the possible deleterious effect of exposure to functionalized nanocellulose (CSN) remains a concern. Therefore, this study aims to explore the potential mechanisms of hepatotoxicity of CSN modified with oxalate ester (NCD) in rats. A 7-day repeated oral toxicity study of NCD at the doses of 50 and 100 mg kg body weight was conducted, and plasma and liver tissue samples were assayed using biochemical analysis, liver histopathology, and protein expression. NCD, at both doses, did not significantly ( > 0.05) alter the relative weight of liver, alkaline phosphatase activity, and lipid peroxidation levels of the animals. However, NCD at the dose of 100 mg kg body weight significantly elevated aspartate aminotransferase, alanine aminotransferase, and myeloperoxidase activities. NCD also enhanced the immunohistochemical expression of inducible nitric oxide synthase and Bcl-2-associated X protein in the liver of rats. Histological observations revealed necrosis and severe cellular infiltration at the high-dose treatment. Our study provides an experimental basis for the safe application of NCDs.

摘要

纤维素的化学修饰目前引起了人们的关注,研究人员试图利用其表面丰富的羟基,引入额外的生物功能。然而,暴露于功能化纳米纤维素(CSN)可能产生的有害影响仍然令人担忧。因此,本研究旨在探讨草酸酯(NCD)修饰的 CSN 在大鼠中产生肝毒性的潜在机制。我们进行了为期 7 天的 NCD(剂量为 50 和 100 mg kg 体重)重复口服毒性研究,并使用生化分析、肝组织病理学和蛋白质表达检测了血浆和肝组织样本。在两个剂量下,NCD 均未显著(>0.05)改变动物的肝相对重量、碱性磷酸酶活性和脂质过氧化水平。然而,在 100 mg kg 体重的剂量下,NCD 显著提高了天冬氨酸转氨酶、丙氨酸转氨酶和髓过氧化物酶的活性。NCD 还增强了大鼠肝中诱导型一氧化氮合酶和 Bcl-2 相关 X 蛋白的免疫组织化学表达。组织学观察显示,在高剂量处理下发生了坏死和严重的细胞浸润。我们的研究为 NCD 的安全应用提供了实验依据。

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