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探究二甲双胍对化疗脑的影响:从细胞到临床的报告

Investigating the effect of metformin on chemobrain: Reports from cells to bedside.

作者信息

Leddy Evelyn, Attachaipanich Tanawat, Chattipakorn Nipon, Chattipakorn Siriporn C

机构信息

School of Biological Sciences, The University of Manchester, Greater Manchester M13 9PL, United Kingdom; Cardiac Electrophysiology Research and Training Center, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand; Center of Excellence in Cardiac Electrophysiology Research, Chiang Mai University, Chiang Mai 50200, Thailand; Neurophysiology Unit, Cardiac Electrophysiology Research and Training Center, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.

Cardiac Electrophysiology Research and Training Center, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand; Center of Excellence in Cardiac Electrophysiology Research, Chiang Mai University, Chiang Mai 50200, Thailand; Neurophysiology Unit, Cardiac Electrophysiology Research and Training Center, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.

出版信息

Exp Neurol. 2025 Mar;385:115129. doi: 10.1016/j.expneurol.2024.115129. Epub 2024 Dec 27.

Abstract

Chemobrain can be defined as the development of cognitive side effects following chemotherapy, which is increasingly reported in cancer survivor patients. Chemobrain leads to reduced patients' quality of life by causing different symptoms ranging from strokes and seizures to memory loss and mood disorders. Metformin, an antidiabetic drug, has been proposed as a potential treatment to improve the symptoms of chemotherapy-induced cognitive dysfunction. Several benefits of metformin on chemobrain have been suggested, including anti-inflammation, anti-oxidative stress, restoring impaired mitochondrial function, stabilizing apoptosis, ameliorating impairments to dendritic spine density, normalizing brain senescence protein levels, and attenuating reductions in cell viability, along with reversing learning and memory deficits. These benefits occur through various pathways of metformin, including adenosine monophosphate-activated protein kinase (AMPK), TAp73, and phosphatidylinositol 3-kinase/protein kinase B (Akt) pathways. In addition, metformin can exert neuroprotective effects and restore deficits in brain homeostasis caused by chemotherapy. Furthermore, activation of AMPK following metformin therapy promotes autophagy, stimulates energy production, and improves cell survival. Metformin's interaction with Tap73 and Akt pathways allows for regulated cell proliferation in adult neural precursor cells and cell growth, respectively. Although the negative effects on cerebral function induced by chemotherapeutics have been alleviated by metformin in several instances, further studies are required to confirm its beneficial effects. This research is essential as it addresses the pressing issue of chemobrain, which is on the rise alongside global increases in cancer. Exploring metformin's potential as a neuroprotective agent offers a promising avenue for mitigating these cognitive impairments and highlights the need for further studies to validate its therapeutic mechanisms. This review comprehensively summarises evidence from both in vitro and in vivo studies to demonstrate metformin's effects on cognitive function when co-administered with chemotherapy and identifies gaps in knowledge for further investigation.

摘要

化疗脑可定义为化疗后出现的认知副作用,癌症幸存者患者中对此的报道日益增多。化疗脑通过引发从中风、癫痫到记忆丧失和情绪障碍等不同症状,导致患者生活质量下降。二甲双胍,一种抗糖尿病药物,已被提议作为改善化疗诱导的认知功能障碍症状的潜在治疗方法。已提出二甲双胍对化疗脑有多种益处,包括抗炎、抗氧化应激、恢复受损的线粒体功能、稳定细胞凋亡、改善树突棘密度损伤、使脑衰老蛋白水平正常化、减轻细胞活力降低,以及逆转学习和记忆缺陷。这些益处通过二甲双胍的各种途径实现,包括腺苷单磷酸激活蛋白激酶(AMPK)、TAp73和磷脂酰肌醇3激酶/蛋白激酶B(Akt)途径。此外,二甲双胍可发挥神经保护作用,并恢复化疗引起的脑内稳态缺陷。此外,二甲双胍治疗后AMPK的激活促进自噬、刺激能量产生并改善细胞存活。二甲双胍与Tap73和Akt途径的相互作用分别允许成年神经前体细胞中细胞增殖的调节和细胞生长。尽管在一些情况下二甲双胍减轻了化疗药物对脑功能的负面影响,但仍需要进一步研究来证实其有益效果。这项研究至关重要,因为它解决了化疗脑这一紧迫问题,随着全球癌症发病率的上升,化疗脑也在增加。探索二甲双胍作为神经保护剂的潜力为减轻这些认知障碍提供了一条有前景的途径,并突出了进一步研究以验证其治疗机制的必要性。本综述全面总结了体外和体内研究的证据,以证明二甲双胍与化疗联合使用时对认知功能的影响,并确定了有待进一步研究的知识空白。

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