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辅酶 Q10 可改善小鼠化疗引起的认知障碍:一项临床前研究。

Coenzyme Q10 ameliorates chemotherapy-induced cognitive impairment in mice: a preclinical study.

机构信息

Department of Pharmacology, ISF College of Pharmacy Affiliated to I.K Gujral Punjab Technical University, Jalandhar, Moga, Punjab, 142001, India.

Department of Pharmaceutical Sciences, School of Health Sciences & Technology, UPES, Dehradun, Uttarakhand, 248007, India.

出版信息

Mol Biol Rep. 2024 Aug 22;51(1):930. doi: 10.1007/s11033-024-09872-0.

Abstract

BACKGROUND

Among the three most used anticancer drugs, cyclophosphamide, Adriamycin, and 5-Fluorouracil (CAF), the most significant outcome is chemobrain, caused by increased oxidative stress, inflammatory insult, and mitochondrial dysfunction.

OBJECTIVE

In this study, endogenous antioxidant coenzyme Q10 (CoQ10) was evaluated for its neuroprotective effects in CICI.

MATERIALS AND METHODS

The chemobrain was induced in Swiss albino female mice by administering CAF (40 + 4 + 25 mg/kg) intraperitoneal (i.p.) in three cycles (single injection per week) followed by treatment with CoQ10 (40 mg/kg; p.o.) for up to 3 weeks followed by behavioral, biochemical, molecular and histopathological analysis.

RESULTS

Treatment with CoQ10 significantly improved cognition by improving exploring time in novel objects recognition test followed by increasing the time spent in the target quadrant in MWM test as compared to CAF-treated animals. Moreover, CoQ10 demonstrated antioxidant properties by reducing the expression of LPO while increasing levels of GSH, SOD, and catalase as compared to CAF-treated animals. While the levels of AChEs were significantly reduced after CoQ10 treatment in CAF-treated animals. In terms of its mechanism, it effectively counteracted the pro-inflammatory substances (TNF-α and IL-1β) triggered by CAF while also enhancing the levels of anti-inflammatory markers (IL-10 and Nrf2). Moreover, CoQ10 showed mitochondrial enhancers and it improved the level of Complex (I, II, and IV). Besides that, mitochondrial morphological analysis was done by TEM, and neuronal morphology along with quantification analysis was performed by H&E staining using Image J software to confirm the neuroprotective effect of CoQ10 over CAF-induced cognitive impairment.

CONCLUSION

This study suggests CoQ10 can protect the mitochondria by imposing antioxidant, and anti-inflammatory properties, which could be a potential therapy for CICI.

摘要

背景

在三种最常用的抗癌药物中,环磷酰胺、阿霉素和 5-氟尿嘧啶(CAF)中,最显著的后果是化学性脑损伤,这是由氧化应激增加、炎症损伤和线粒体功能障碍引起的。

目的

在这项研究中,内源性抗氧化辅酶 Q10(CoQ10)被评估用于 CAF 诱导的化学性脑损伤的神经保护作用。

材料和方法

通过腹腔内(i.p.)给予 CAF(40+4+25mg/kg)三次循环(每周单次注射),在瑞士白化雌性小鼠中诱导化学性脑损伤,随后用 CoQ10(40mg/kg;p.o.)治疗长达 3 周,随后进行行为、生化、分子和组织病理学分析。

结果

与 CAF 处理的动物相比,CoQ10 治疗显著改善了认知,提高了新物体识别试验中的探索时间,增加了 MWM 试验中在目标象限中的时间。此外,CoQ10 通过降低 LPO 的表达,同时增加 GSH、SOD 和过氧化氢酶的水平,表现出抗氧化特性,与 CAF 处理的动物相比。而 CAF 处理的动物用 CoQ10 治疗后,AChE 的水平显著降低。就其机制而言,它有效地对抗了 CAF 触发的促炎物质(TNF-α 和 IL-1β),同时也提高了抗炎标志物(IL-10 和 Nrf2)的水平。此外,CoQ10 表现出线粒体增强剂,并改善了复合物(I、II 和 IV)的水平。此外,通过 TEM 进行线粒体形态分析,并用 H&E 染色通过 Image J 软件进行神经元形态学及其定量分析,以确认 CoQ10 对 CAF 诱导的认知障碍的神经保护作用。

结论

本研究表明,CoQ10 可以通过施加抗氧化和抗炎特性来保护线粒体,这可能是 CAF 诱导的化学性脑损伤的一种潜在治疗方法。

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