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下丘脑在癌症恶病质发展中的作用。

The role of the hypothalamus in the development of cancer cachexia.

作者信息

Stagikas Dimitrios, Simos Yannis Vasileios, Lakkas Lampros, Filis Panagiotis, Peschos Dimitrios, Tsamis Konstantinos Ioannis

机构信息

Laboratory of Physiology, Faculty of Medicine, School of Health Sciences, University of Ioannina, 45110, Ioannina, Greece.

Department of Medical Oncology, School of Medicine, University of Ioannina, 45110, Ioannina, Greece; Department of Hygiene and Epidemiology, School of Medicine, University of Ioannina, 45110, Ioannina, Greece.

出版信息

Physiol Behav. 2025 Jun 1;295:114909. doi: 10.1016/j.physbeh.2025.114909. Epub 2025 Apr 5.

Abstract

Cachexia is a complex multiorgan syndrome associated with various chronic diseases, characterized by anorexia and increased tissue wasting in the context of chronic inflammation. A specific form of this syndrome, known as cancer cachexia (CC), occurs alongside different types of tumors. The pathogenesis of CC is multifactorial. Inflammatory mediators and hormones released by both tumor and host cells have a relevant role in driving the peripheral catabolic process through several direct mechanisms. Accumulating evidence indicates that the central nervous system (CNS) plays an integral role in the pathogenesis of CC. The hypothalamus has emerged as a critical brain region that senses and amplifies peripheral stimuli, generating inappropriate neuronal signaling and leading to the dysregulation of energy homeostasis under cachexia conditions. Circulating cytokines may act in concert with hormones and neurotransmitters and perturb critical hypothalamic neurocircuits shifting their activity towards the anorexigenic pathway and increase of energy expenditure. This review discusses the mechanisms mediating the hypothalamic homeostatic imbalance in the context of anorexia and cachexia associated with cancer.

摘要

恶病质是一种与多种慢性疾病相关的复杂多器官综合征,其特征为在慢性炎症背景下出现厌食和组织消耗增加。这种综合征的一种特定形式,即癌症恶病质(CC),伴随不同类型的肿瘤出现。CC的发病机制是多因素的。肿瘤细胞和宿主细胞释放的炎症介质和激素通过多种直接机制在驱动外周分解代谢过程中发挥相关作用。越来越多的证据表明,中枢神经系统(CNS)在CC的发病机制中起不可或缺的作用。下丘脑已成为一个关键的脑区,它感知并放大外周刺激,产生不适当的神经元信号,导致恶病质状态下能量稳态失调。循环细胞因子可能与激素和神经递质协同作用,扰乱关键的下丘脑神经回路,使其活动转向厌食途径并增加能量消耗。本综述讨论了在与癌症相关的厌食和恶病质背景下介导下丘脑稳态失衡的机制。

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