首页> 美国卫生研究院文献>Frontiers in Behavioral Neuroscience >The High Costs of Low-Grade Inflammation: Persistent Fatigue as a Consequence of Reduced Cellular-Energy Availability and Non-adaptive Energy Expenditure
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The High Costs of Low-Grade Inflammation: Persistent Fatigue as a Consequence of Reduced Cellular-Energy Availability and Non-adaptive Energy Expenditure

机译:低度炎症的高昂代价:持续疲劳是细胞能量利用率降低和非适应性能量消耗的结果

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摘要

Chronic or persistent fatigue is a common, debilitating symptom of several diseases. Persistent fatigue has been associated with low-grade inflammation in several models of fatigue, including cancer-related fatigue and chronic fatigue syndrome. However, it is unclear how low-grade inflammation leads to the experience of fatigue. We here propose a model of an imbalance in energy availability and energy expenditure as a consequence of low-grade inflammation. In this narrative review, we discuss how chronic low-grade inflammation can lead to reduced cellular-energy availability. Low-grade inflammation induces a metabolic switch from energy-efficient oxidative phosphorylation to fast-acting, but less efficient, aerobic glycolytic energy production; increases reactive oxygen species; and reduces insulin sensitivity. These effects result in reduced glucose availability and, thereby, reduced cellular energy. In addition, emerging evidence suggests that chronic low-grade inflammation is associated with increased willingness to exert effort under specific circumstances. Circadian-rhythm changes and sleep disturbances might mediate the effects of inflammation on cellular-energy availability and non-adaptive energy expenditure. In the second part of the review, we present evidence for these metabolic pathways in models of persistent fatigue, focusing on chronic fatigue syndrome and cancer-related fatigue. Most evidence for reduced cellular-energy availability in relation to fatigue comes from studies on chronic fatigue syndrome. While the mechanistic evidence from the cancer-related fatigue literature is still limited, the sparse results point to reduced cellular-energy availability as well. There is also mounting evidence that behavioral-energy expenditure exceeds the reduced cellular-energy availability in patients with persistent fatigue. This suggests that an inability to adjust energy expenditure to available resources might be one mechanism underlying persistent fatigue.
机译:慢性或持续性疲劳是几种疾病的常见,令人衰弱的症状。在几种疲劳模型中,持久疲劳与低度炎症相关,包括癌症相关的疲劳和慢性疲劳综合症。然而,目前尚不清楚低度炎症如何导致疲劳。我们在这里提出了一种由于低度炎症导致的能量供应和能量消耗失衡的模型。在这篇叙述性综述中,我们讨论了慢性低度炎症如何导致细胞能量利用率降低。低度炎症引起新陈代谢的转变,从高能效的氧化磷酸化转变为速效但效率较低的有氧糖酵解能量的产生。增加活性氧种类;并降低胰岛素敏感性。这些作用导致葡萄糖的利用率降低,从而降低了细胞能量。此外,越来越多的证据表明,慢性低度炎症与在特定情况下付出努力的意愿增强有关。昼夜节律的变化和睡眠障碍可能会介导炎症对细胞能量可用性和非自适应能量消耗的影响。在本综述的第二部分中,我们为持久性疲劳模型中的这些代谢途径提供了证据,重点是慢性疲劳综合症和与癌症相关的疲劳。关于与疲劳有关的细胞能量利用率降低的大多数证据来自对慢性疲劳综合症的研究。尽管来自癌症相关疲劳文献的机理证据仍然有限,但稀疏的结果也表明细胞能量的利用率也会降低。越来越多的证据表明,持续性疲劳患者的行为能量支出超过了降低的细胞能量利用率。这表明无法将能量消耗调整为可用资源可能是持续疲劳的一种机制。

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