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氧化铈纳米粒子可改善神经病理性大鼠的氧化应激、炎症和痛行为。

Cerium Oxide Nanoparticles Ameliorate Oxidative Stress, Inflammation, and Pain Behavior in Neuropathic Rats.

机构信息

Neuroscience Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Department of Neuroscience, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

出版信息

Curr Neurovasc Res. 2023;20(1):54-61. doi: 10.2174/1567202620666230125104604.

Abstract

BACKGROUND

Neuropathic pain originating from a dysfunction in the nervous system is often intractable and chronic. Recently, several studies using nanoparticles suggested a new way to control neuropathic pain. This study intended to explore the potential neuroprotective effect of Cerium Oxide Nanoparticles (CNPs) synthesized by pullulan in neuropathic pain in rats.

METHODS

On the right common sciatic nerve of male Wistar rats, the chronic constriction injury (CCI) procedure was used to establish a neuropathic pain model. CNPs were injected into the caudal vein of the rat. Behavioral methods were used to detect mechanical allodynia, cold allodynia, and thermal hyperalgesia in rats. Besides, inflammation factors, including tumor necrosis factor (TNF)-α, interleukin (IL)-1β, nitric oxide (NO), and markers of oxidative stress, including Malondialdehyde (MDA) and total thiol, were measured in the spinal cord segment of rats.

RESULTS

In rats with CCI, mechanical allodynia, cold allodynia, and thermal hyperalgesia developed, which improved when the rats were administered CNPs. Spinal cord specimens of CCI rats had elevated inflammation and oxidative stress status (↑IL-1β, ↑TNF-α, ↑NO, ↑MDA) and decreased antioxidative levels (↓total thiol). As a result of CNPs treatment, these changes were reversed in the spinal cord specimens.

CONCLUSION

CNPs alleviate neuropathic pain by exhibiting antioxidative and anti-inflammatory activities.

摘要

背景

源于神经系统功能障碍的神经性疼痛通常是难治性和慢性的。最近,一些使用纳米粒子的研究为控制神经性疼痛提供了一种新方法。本研究旨在探索由普鲁兰合成的氧化铈纳米粒子(CNPs)在大鼠神经性疼痛中的潜在神经保护作用。

方法

在雄性 Wistar 大鼠的右侧坐骨神经总干上,采用慢性缩窄性损伤(CCI)程序建立神经性疼痛模型。将 CNPs 注入大鼠尾静脉。采用行为学方法检测大鼠的机械性痛觉过敏、冷觉过敏和热痛觉过敏。此外,还测量了大鼠脊髓节段中的炎症因子,包括肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β、一氧化氮(NO)和氧化应激标志物,包括丙二醛(MDA)和总巯基。

结果

在 CCI 大鼠中,出现了机械性痛觉过敏、冷觉过敏和热痛觉过敏,而给予 CNPs 后这些症状得到改善。CCI 大鼠的脊髓标本中炎症和氧化应激状态升高(↑IL-1β、↑TNF-α、↑NO、↑MDA),抗氧化水平降低(↓总巯基)。CNPs 治疗后,这些变化在脊髓标本中得到逆转。

结论

CNPs 通过发挥抗氧化和抗炎作用缓解神经性疼痛。

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