Exploring the potential hypothalamic role in mediating cisplatin-induced negative energy balance

IF 4.7 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yang Tae Kim , Byong Seo Park , Hye Rim Yang , Seon Yi , Il Seong Nam-Goong , Jae Geun Kim
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引用次数: 0

Abstract

Cisplatin is a chemotherapeutic drug commonly used for treating different types of cancer. However, long-term use can lead to side effects, including anorexia, nausea, vomiting, and weight loss, which negatively affect the patient's quality of life and ability to undergo chemotherapy. This study aimed to investigate the mechanisms underlying the development of a negative energy balance during cisplatin treatment. Mice treated with cisplatin exhibit reduced food intake, body weight, and energy expenditure. We observed altered neuronal activity in the hypothalamic nuclei involved in the regulation of energy metabolism in cisplatin-treated mice. In addition, we observed activation of microglia and inflammation in the hypothalamus following treatment with cisplatin. Consistent with this finding, inhibition of microglial activation effectively rescued cisplatin-induced anorexia and body weight loss. The present study identified the role of hypothalamic neurons and inflammation linked to microglial activation in the anorexia and body weight loss observed during cisplatin treatment. These findings provide insight into the mechanisms underlying the development of metabolic abnormalities during cisplatin treatment and suggest new strategies for managing these side effects.

Abstract Image

探讨下丘脑在介导顺铂诱导的负能量平衡中的潜在作用。
顺铂是一种常用于治疗不同类型癌症的化疗药物。然而,长期使用会导致副作用,包括厌食、恶心、呕吐和体重减轻,对患者的生活质量和接受化疗的能力产生负面影响。本研究旨在探讨顺铂治疗过程中负能量平衡发展的潜在机制。用顺铂治疗的小鼠表现出食物摄入、体重和能量消耗减少。我们观察到,在顺铂治疗的小鼠中,参与能量代谢调节的下丘脑细胞核中的神经元活性发生了改变。此外,我们观察到顺铂治疗后小胶质细胞的激活和下丘脑的炎症。与这一发现一致的是,抑制小胶质细胞活化有效地挽救了顺铂诱导的厌食症和体重减轻。本研究确定了下丘脑神经元和与小胶质细胞激活相关的炎症在顺铂治疗期间观察到的厌食症和体重减轻中的作用。这些发现深入了解了顺铂治疗过程中代谢异常发生的机制,并为控制这些副作用提出了新的策略。
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来源期刊
CiteScore
7.70
自引率
3.90%
发文量
410
审稿时长
36 days
期刊介绍: Chemico-Biological Interactions publishes research reports and review articles that examine the molecular, cellular, and/or biochemical basis of toxicologically relevant outcomes. Special emphasis is placed on toxicological mechanisms associated with interactions between chemicals and biological systems. Outcomes may include all traditional endpoints caused by synthetic or naturally occurring chemicals, both in vivo and in vitro. Endpoints of interest include, but are not limited to carcinogenesis, mutagenesis, respiratory toxicology, neurotoxicology, reproductive and developmental toxicology, and immunotoxicology.
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