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通过抑制化疗诱导的神经病理性疼痛动物模型中的 NADPH 氧化酶 2,来研究柚子皮乙醇提取物的神经保护特性。

Neuroprotective properties of ethanolic extract of Citrus unshiu Markovich peel through NADPH oxidase 2 inhibition in chemotherapy-induced neuropathic pain animal model.

机构信息

Department of Nursing, University of Ulsan, Ulsan, Republic of Korea.

Department of Clinical Laboratory Science, Catholic University of Pusan, Busan, Republic of Korea.

出版信息

Phytother Res. 2021 Dec;35(12):6918-6931. doi: 10.1002/ptr.7304. Epub 2021 Nov 24.

Abstract

The present study aimed to determine the antioxidant effect of Citrus unshiu Markovich (CUM) extract in neuronal cell lines under oxidative stress and to investigate the effect of chemotherapy-induced peripheral neuropathy (CIPN) on the nociceptive response in a preclinical mice model. We tested the inhibition of H O in Neuro2A cells treated with CUM. Experimental animals were treated with oxaliplatin to induce CINP, and then administered oral CUM for 4 weeks in order to observe the effect of CUM. Animals were evaluated weekly for thermal hyperalgesia and digital motor nerve conduction velocity (NCV). Lumbar dorsal root ganglia (DRG) isolated from each animal were evaluated through immunochemical and western blot analysis for nerve damage, inflammatory response, and expression of redox signaling factors. The main mechanisms were determined to be decreased inducible nitric oxide synthase (iNOS) production due to the inhibition of NADPH oxidase 2 (NOX2). To determine the functional role of NOX2 in CINP, we administrated CUM into NOX2-deficient mice with neuropathic pain. Therefore, we suggest that CUM controls the expression levels of inflammatory factors in CINP via NOX2 inactivation. This study demonstrated that a complementary medicine such as CUM might be a potential novel therapeutic agent for the treatment of CINP.

摘要

本研究旨在确定柚子(Citrus unshiu Markovich,CUM)提取物在氧化应激下对神经元细胞系的抗氧化作用,并研究化疗诱导的周围神经病变(CIPN)对临床前小鼠模型痛觉反应的影响。我们测试了 CUM 对经 CUM 处理的 Neuro2A 细胞中 H O 的抑制作用。实验动物用奥沙利铂处理以诱导 CINP,然后口服 CUM 治疗 4 周,以观察 CUM 的效果。每周评估动物的热痛觉和数字运动神经传导速度(NCV)。从每个动物分离的腰椎背根神经节(DRG)通过免疫化学和 Western blot 分析评估神经损伤、炎症反应和氧化还原信号因子的表达。主要机制被确定为由于 NADPH 氧化酶 2(NOX2)的抑制导致诱导型一氧化氮合酶(iNOS)的产生减少。为了确定 NOX2 在 CINP 中的功能作用,我们将 CUM 给予有神经痛的 NOX2 缺陷型小鼠。因此,我们认为 CUM 通过 NOX2 失活来控制 CINP 中炎症因子的表达水平。本研究表明,补充医学如 CUM 可能是治疗 CIPN 的一种有潜力的新型治疗剂。

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