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脂肪组织的炎症过程。

The inflammatory process of adipose tissue.

作者信息

Blüher Matthias

机构信息

Department of Medicine, University of Leipzig, Leipzig, Germany.

出版信息

Pediatr Endocrinol Rev. 2008 Sep;6(1):24-31.

Abstract

Obesity and inflammation are highly integrated processes in the pathogenesis of insulin resistance, diabetes, atherosclerosis, and non-alcoholic fatty liver disease. The evidence that obesity can be regarded as an inflammatory disease comes from numerous studies showing a moderate increase of circulating inflammatory factors in obese patients and the identification of different types of immune cells infiltrating the human adipose tissue. Obesity may induce a pro-inflammatory state, which can cause or worsen insulin resistance in adipose tissue, skeletal muscle, and liver. The causative factors of this inflammation process in obesity are not entirely understood, but adipose tissue seems to play an important role in the relationship between obesity and chronic inflammation. Increased infiltration of adipose tissue with immune cells could cause adipose tissue insulin resistance via autocrine and paracrine cytokine/adipokine signalling, which contributes to systemically decreased insulin sensitivity via endocrine signalling. On the other hand, obesity-induced inflammation could represent a compensatory mechanism for increased adipose tissue turnover in obese states, which might protect obese individuals against deleterious effects of fat accumulation. A better understanding of the mechanisms and molecular components of obesity induced inflammatory response might lead to identifying novel therapeutic targets to prevent obesity-related complications.

摘要

肥胖与炎症在胰岛素抵抗、糖尿病、动脉粥样硬化和非酒精性脂肪性肝病的发病机制中是高度整合的过程。肥胖可被视为一种炎症性疾病,这一证据来自众多研究,这些研究表明肥胖患者循环炎症因子适度增加,以及鉴定出浸润人体脂肪组织的不同类型免疫细胞。肥胖可能诱导促炎状态,这可导致或加重脂肪组织、骨骼肌和肝脏中的胰岛素抵抗。肥胖中这种炎症过程的致病因素尚未完全了解,但脂肪组织似乎在肥胖与慢性炎症的关系中起重要作用。免疫细胞对脂肪组织的浸润增加可通过自分泌和旁分泌细胞因子/脂肪因子信号传导导致脂肪组织胰岛素抵抗,这通过内分泌信号传导导致全身胰岛素敏感性降低。另一方面,肥胖诱导的炎症可能代表肥胖状态下脂肪组织更新增加的一种代偿机制,这可能保护肥胖个体免受脂肪堆积的有害影响。更好地理解肥胖诱导的炎症反应的机制和分子成分可能会导致确定预防肥胖相关并发症的新治疗靶点。

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