纳米硒和纳米硒复合材料对大鼠模型组织病理学影响的比较

M. Hajinezhad, A. Jamshidian, Motahareh Abdollahi, Alireza Samzadeh Kermani
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摘要

背景:硒纳米粒子(Se NPs)和硒纳米复合材料(Se NCs)具有不同的生物学效应。本研究旨在比较新合成的硒NPs和硒NCs对大鼠生化和组织病理学参数的影响。采用傅里叶变换红外光谱(FTIR)、x射线衍射(XRD)、能量色散x射线分析(EDAX)和扫描电子显微镜(SEM)对合成的Se NPs进行了表征。材料与方法:将成年雄性Wistar大鼠分为4组,观察Se NPs的生物学效应。对照组大鼠腹腔注射生理盐水,实验组大鼠腹腔注射剂量为(0.4 mg/kg)的硒粉、硒NPs和硒NCs,为期4周。4周后,按常规方法提取血清,然后处死大鼠,分离肝、肾、睾丸组织进行组织病理学检查。结果:腹腔注射硒粉使大鼠血清肝酶水平、血清尿素氮(BUN)脂质过氧化、血清肌酐水平显著升高(P<0.05)。组织病理学检查显示肝脏坏死和脂肪改变。肾脏切片显示细胞质空泡化和透明样铸型,睾丸切片显示精管变性。0.4 mg/kg剂量Se NPs腹腔注射对肝酶、丙二醛(MDA)含量及组织病理学变化无显著影响,但血清BUN和肌酐水平显著升高(P<0.05)。Se NCs组生化指标和组织病理学指标正常(P<0.05)。结论:本研究证实了硒粉的毒性;然而,硒的纳米配方显示出较少的副作用。
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Comparing the Histopathological Effects of Selenium Nanoparticles and Selenium Nanocomposites in Rat Models
Background: Selenium nanoparticles (Se NPs) and selenium nanocomposites (Se NCs) have different biological effects. The current study aimed to compare the effects of newly synthesized Se NPs and Se NCs on biochemical and histopathological parameters of rats. The synthesized Se NPs were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), energy dispersive X-ray analysis (EDAX), and scanning electron microscopy (SEM) techniques. Materials and Methods: Adult male Wistar rats were divided into four equal groups to examine the biological effects of Se NPs. Control rats received saline intraperitoneally while experimental rats were received four-week intraperitoneal injections of Se powder, Se NPs, and Se NCs at the dose of (0.4 mg/kg). After four weeks, serum was obtained by the conventional methods, and then rats were sacrificed to separate liver, kidney, and testis tissues for histopathological examinations. Results: The intraperitoneal injection of Se powder caused significant elevations in serum liver enzyme levels, serum blood urea nitrogen (BUN) lipid peroxidation, and serum creatinine levels (P<0.05). The histopathological investigations showed necrosis and fatty change in liver. Kidney sections showed cytoplasmic vacuolation and hyaline casts, and the testis sections showed degeneration of seminiferous tubules. Se NPs intraperitoneal injections at a dose of 0.4 mg/kg caused no significant effects on liver enzymes, malondialdehyde (MDA) content, and histopathological changes while significantly increased serum BUN and creatinine levels (P<0.05). The group treated with Se NCs showed normal biochemical and histopathological parameters (P<0.05). Conclusion: The current study proved the toxicity of Se powder; however, nano-formulations of Se showed fewer side effects.
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