金、银纳米颗粒对大鼠附睾和前列腺形态功能状态的影响

V. Kalynovskyi, A. Pustovalov, G. Grodzyuk, N. Andriushyna, M. Dzerzhynsky
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引用次数: 1

摘要

金属在现代医学中被广泛使用:铁、铜、锌、钒、钛——它们都对治疗不同的疾病至关重要。最近出现了一个新的医疗技术领域,其重点是金属纳米粒子的生物医学应用,特别是对金和银基材料的兴趣。这些结构已经用于光热抗癌治疗、药物输送、生物成像、放射增敏剂和药物本身。尽管纳米粒子被广泛使用,但我们对纳米材料的毒性仍然知之甚少。纳米毒理学研究主要是在体外进行的,但在体内的影响仍然难以捉摸。因此,我们重点研究了金和银纳米颗粒的生殖毒性。在聚磷酸钠作为包衣和稳定剂的情况下,用抗坏血酸分别还原四氯酸钠(III)和硝酸银,合成了10-15 nm的球形金纳米粒子和银纳米粒子。接下来,这些颗粒以1 mg/kg的剂量腹腔注射给幼龄和成年动物(分别为1个月和6个月),持续10天。我们用附睾小管的直径、附睾上皮细胞的高度和核截面以及前列腺上皮的相对体积作为功能活性的定量标记。我们发现,尽管我们发现附睾上皮细胞的核横截面积减少,但幼年动物腹腔注射纳米金没有引起明显的组织学改变。同时,纳米金在成年动物中引起了更多的形态变化。纳米银组也得到了类似的结果。银纳米颗粒引起幼鼠附睾小管腔内精子数量明显减少,同时附睾外细胞数量增加。附睾和前列腺的形态测量参数也下降。给成年动物注射纳米银也会下调这两个器官的形态功能状态,尽管没有发现组织学变化。我们发现纳米金和纳米银对大鼠附睾和前列腺的功能活性都有不良影响。值得一提的是,银纳米颗粒通常比金纳米颗粒毒性更大,这与它们已知的细胞作用机制有关。虽然金和银作用的确切机制需要进一步研究,但我们的研究结果对于纳米材料在生物医学和临床实践中的实际应用是有用的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of gold and silver nanoparticles on the morpho-functional state of the epididymis and prostate gland in rats
Metals are widely used in modern medicine: iron, copper, zinc, vanadium, titanium – all of them are vital for treatment of different diseases. Recently a new field of medical technology has emerged, which focuses on the biomedical application of metallic nanoparticles, with a particular interest in a gold and silver-based materials. These structures are already used for photothermal anticancer therapy, drug delivery, bioimaging, radiosensitizers and as drugs themselves. Despite the wide usage of nanoparticles, we still don’t know much about the toxicity of nanomaterials. Nanotoxicological studies are mainly carried out in vitro , but in vivo effects are still elusive. Hence, we focused on the reproductive toxicity of gold and silver nanosized particles. Spherical 10–15 nm gold and silver nanoparticles were synthesized through the reduction of sodium tetrachloroaurate (III) and silver nitrate respectively with ascorbic acid in the presence of sodium polyphosphate as a coating and stabilizing agent. Next, these particles were administered intraperitoneally to the young and adult animals (1- and 6-months old respectively) at 1 mg/kg dose for 10 days. As quantitative markers of functional activity, we used the diameter of epididymal tubules, height and the nuclear cross-section of epididymal epitheliocytes and relative volume of the prostatic epithelium. We showed that intraperitoneal administrations of nanogold to young animals caused no significant histological changes, although we found a decrease in the nuclear cross-sectional area of epididymal epitheliocytes. At the same time, nanogold caused more morphometric changes in adult animals. Similar results were obtained from the nanosilver groups. Silver nanoparticles caused an observable decrease of sperm quantity in the lumen of epididymal tubules with a simultaneous increase in the number of extraepididymal cells in young animals. Morphometric parameters of the epididymis and prostate also decreased. Administration of nanosilver to adult animals also downregulated the morpho-functional state of both organs, although no histological changes were found. We showed that both nanogold and nanosilver can cause adverse effects on the functional activity of the epididymis and prostate of rats. It is worth mentioning that silver nanoparticles were generally more toxic than the gold ones, which correlates with their known mechanism of cellular action. Although the exact mechanisms of gold and silver action require further study, our results are useful for practical usage of nanomaterials in biomedical and clinical practice.
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