In vivo ameliorative effect of cerium oxide nanoparticles in isoproterenol-induced cardiac toxicity

Shereen S. El Shaer , Taher A. Salaheldin , Nashwa M. Saied , Sally M. Abdelazim
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引用次数: 28

Abstract

Background

Cerium oxide nanoparticles have gained much more attention especially in the field of nanomedicine. This work represents cerium oxide nanoparticles as a new prophylactic model for heart failure progression.

Objective

To investigate the potential protective effect of cerium oxide nanoparticles on Isoproterenol (ISO)-induced cardiac toxicity in rats.

Methods

Cerium oxide nanoparticles (5 ± 1 nm) were synthesized by reverse micelle method and characterized using High Resolution Transmission Electron Microscopy, X-Ray Diffraction and particle size analyzer. The experiments were performed on 96 male Wistar rats. The rats were randomly allocated into eight groups. Namely; two Negative and positive control groups, captopril administered group, Nano-ceria (low dose) group, Nano-ceria (high dose) group, Captopril- Isoproterenol group, Nano-ceria (low dose)-Isoproterenol group and Nano-ceria (high dose)-Isoproterenol group. Cardio toxic rat model was induced by subcutaneous administration of Isoproterenol (ISO) (30 mg/kg) for two consecutive days in adult male rats. Two doses (0.5 and 5 μg/kg/week) of cerium oxide nanoparticles were applied for five weeks and 50 mg/kg/day of Captopril was used as a reference drug. Cardiac marker enzymes, Cortisol and Aldosterone hormones were assessed in serum. Oxidant-antioxidant parameters and histopathological examination in heart tissues were also determined.

Results

These dose of nano-ceria, showed a promising ameliorative and prophylactic effect against cardiac toxicity compared to Captopril reference drug. Serum cardiac markers were decreased by noticeable percentage, CK-MB (50% and 57%), LDH (47% and 57.7%), AST (38% and 36.5%) and ALT (33.5% and 30.6%) for both doses respectively, while increased tissues level of the antioxidant enzymes, catalase (48% − 26%) and superoxide dismutase (64%, 143%).

Conclusion

These consistent biochemical and histopathological results suggest that, nano-ceria could be used as effective antioxidant in prophylactic protocols for management of cardiac disorders associated with oxidative stress.

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氧化铈纳米颗粒对异丙肾上腺素引起的心脏毒性的体内改善作用
氧化铈纳米颗粒尤其在纳米医学领域受到越来越多的关注。这项工作代表了氧化铈纳米颗粒作为一种新的预防心力衰竭进展的模型。目的探讨氧化铈纳米颗粒对异丙肾上腺素(ISO)致大鼠心脏毒性的潜在保护作用。方法采用反胶束法合成氧化铈纳米颗粒(5±1 nm),采用高分辨透射电镜、x射线衍射和粒度分析仪对其进行表征。实验对象为96只雄性Wistar大鼠。大鼠被随机分为8组。即;阴性和阳性对照组:卡托普利给药组、纳米铈(低剂量)组、纳米铈(高剂量)组、卡托普利-异丙肾上腺素组、纳米铈(低剂量)-异丙肾上腺素组和纳米铈(高剂量)-异丙肾上腺素组。采用30 mg/kg异丙肾上腺素(iso30 mg/kg)连续2 d皮下注射的方法建立成年雄性大鼠心脏毒性模型。以卡托普利50 mg/kg/d为对照药,分别给药0.5和5 μg/kg/周,连续5周。测定血清中心脏标志物酶、皮质醇和醛固酮激素。测定心脏组织的氧化-抗氧化参数和组织病理学检查。结果与卡托普利对照药相比,纳米二氧化铈对心脏毒性有较好的改善和预防作用。两组血清心脏标志物CK-MB(50%和57%)、LDH(47%和57.7%)、AST(38%和36.5%)和ALT(33.5%和30.6%)分别显著降低,组织中抗氧化酶、过氧化氢酶(48% ~ 26%)和超氧化物歧化酶(64%,143%)水平升高。结论这些一致的生化和组织病理学结果表明,纳米二氧化铈可作为有效的抗氧化剂用于氧化应激相关心脏疾病的预防治疗方案。
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来源期刊
CiteScore
2.08
自引率
0.00%
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0
审稿时长
5.3 weeks
期刊介绍: Cessation. The international multidisciplinary journal is devoted to the publication of studies covering the whole range of experimental research on disease processes and toxicology including cell biological investigations. Its aim is to support progress in the interdisciplinary cooperation of researchers working in pathobiology, toxicology, and cell biology independent of the methods applied. During the past decades increasing attention has been paid to the importance of toxic influence in the pathogenesis of human and animal diseases. This is why Experimental and Toxicologic Pathology meets the urgent need for an interdisciplinary journal felt by a wide variety of experts in medicine and biology, including pathologists, toxicologists, biologists, physicians, veterinary surgeons, pharmacists, and pharmacologists working in academic, industrial or clinical institutions.
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