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过度减肥的抗炎作用:强烈抑制脂肪组织中白细胞介素 6 和肿瘤坏死因子 α 的表达。

Anti-inflammatory effects of excessive weight loss: potent suppression of adipose interleukin 6 and tumour necrosis factor alpha expression.

机构信息

Christian Doppler Research Laboratory for Gut Inflammation and Department of Internal Medicine II, Medical University Innsbruck, 6020 Innsbruck, Austria.

出版信息

Gut. 2010 Sep;59(9):1259-64. doi: 10.1136/gut.2010.214577. Epub 2010 Jul 21.

Abstract

OBJECTIVE

Severe obesity is a chronic inflammatory disease where various cytokines/adipocytokines play a key role. Pro-inflammatory cytokines such as interleukin 6 (IL-6) and tumour necrosis factor-alpha (TNFalpha) are produced by human adipose tissue dependent on the degree of obesity. Mouse studies suggest a key role of adipose tissue-derived IL-6 in hepatic insulin resistance via modification of liver suppressor of cytokine signalling 3 (SOCS-3) expression.

DESIGN AND METHODS

We examined the effect of excessive weight loss on systemic levels, subcutaneous and visceral adipose tissue and liver expression of IL-6 and TNFalpha in 20 severely obese patients undergoing laparoscopic adjustable gastric banding (LAGB). Furthermore, we studied liver expression of SOCS3, an important regulator of insulin resistance, and fat tissue expression of the anti-inflammatory adipocytokine adiponectin and its receptors. Serum and tissue samples were collected before and 6 months after LAGB surgery.

RESULTS

IL-6/TNFalpha mRNA expression before weight loss were similar in subcutaneous and visceral adipose tissue and much higher compared to hepatic expression. Subcutaneous adipose tissue mRNA expression of both pro-inflammatory cytokines, but especially of IL-6 decreased dramatically after extensive weight loss whereas expression of adiponectin and its receptors increased. Weight loss also led to a significant reduction in liver IL-6 expression, whereas liver TNFalpha mRNA expression did not change. IL-6 and C-reactive protein serum levels decreased after weight loss whereas TNFalpha serum levels were below the detection limit before and after surgery. These effects were paralleled by reduced hepatic SOCS3 expression and improved insulin resistance 6 months after LAGB surgery.

CONCLUSION

Expression of IL-6 and TNFalpha mRNA is more pronounced in adipose compared to liver tissue in patients with severe obesity. Our results highlight excessive weight loss as a successful anti-inflammatory strategy.

摘要

目的

重度肥胖是一种慢性炎症性疾病,其中各种细胞因子/脂肪细胞因子起着关键作用。依赖肥胖程度,人脂肪组织产生促炎细胞因子如白细胞介素 6(IL-6)和肿瘤坏死因子-α(TNFalpha)。小鼠研究表明,脂肪组织来源的 IL-6 通过改变肝脏细胞因子信号转导抑制因子 3(SOCS-3)表达在肝胰岛素抵抗中起关键作用。

设计和方法

我们检查了 20 例接受腹腔镜可调节胃束带术(LAGB)的重度肥胖患者体重过度减轻对全身水平、皮下和内脏脂肪组织及肝脏中 IL-6 和 TNFalpha 表达的影响。此外,我们研究了 SOCS3 的肝脏表达,SOCS3 是胰岛素抵抗的重要调节剂,以及脂肪组织中抗炎脂肪细胞因子脂联素及其受体的表达。在 LAGB 手术前和手术后 6 个月收集血清和组织样本。

结果

减肥前,IL-6/TNFalpha mRNA 表达在皮下和内脏脂肪组织中相似,且明显高于肝脏表达。经过广泛减肥后,两种促炎细胞因子,特别是 IL-6 的皮下脂肪组织 mRNA 表达急剧下降,而脂联素及其受体的表达增加。体重减轻还导致肝脏 IL-6 表达显著降低,而肝脏 TNFalpha mRNA 表达不变。减肥后,IL-6 和 C-反应蛋白血清水平降低,而 TNFalpha 血清水平在手术前后均低于检测限。这些影响与术后 6 个月 SOCS3 表达降低和胰岛素抵抗改善相平行。

结论

在重度肥胖患者中,与肝脏组织相比,IL-6 和 TNFalpha mRNA 的表达在脂肪组织中更为明显。我们的结果强调了体重过度减轻是一种成功的抗炎策略。

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