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肥胖和胰岛素抵抗儿童的胰岛素分泌动力学改变与氧化应激和炎症小体激活有关。

Altered insulin secretion dynamics relate to oxidative stress and inflammasome activation in children with obesity and insulin resistance.

机构信息

Grupo de Inflamación, Nutrición, Metabolismo y estrés Oxidativo, Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), c/Doctor Marañón, 3 - Edificio Andrés Segovia, 11002, Cádiz, Spain.

Translational Research in Respiratory Medicine, University Hospital Arnau de Vilanova and Santa Maria, IRBLleida, Lleida, Spain.

出版信息

J Transl Med. 2023 Aug 20;21(1):559. doi: 10.1186/s12967-023-04337-7.

Abstract

BACKGROUND

Insulin resistance (IR) is considered the main driver of obesity related metabolic complications, and is related to oxidative stress and inflammation, which in turn promote each other. There is currently no specific definition of IR in children, rather, that for adult population is used by pediatric endocrinologists instead. Altered insulin secretion dynamics are associated with worse metabolic profiles and type 2 diabetes mellitus development, thus we aimed to test whether insulin response relates to oxidative stress and inflammation in children.

METHODS

We conducted a case-control study, including 132 children classified as follows: 33 children without obesity (Lean); 42 with obesity but no IR according to the American Diabetes Association criteria for adults (OBIR-); 25 with obesity and IR and an early insulin response to an oral glucose tolerance test (OGTT) (EP-OBIR +); 32 with obesity, IR, and a late insulin peak (LP-OBIR +); and studied variables associated with lipid and carbohydrate metabolism, oxidative stress, inflammation and inflammasome activation.

RESULTS

The measured parameters of children with obesity, IR, and an early insulin response were similar to those of children with obesity but without IR. It was late responders who presented an impaired antioxidant system and elevated oxidative damage in erythrocytes and plasma, and inflammasome activation at their white blood cells, despite lower classical inflammation markers. Increased uric acid levels seems to be one of the underlying mechanisms for inflammasome activation.

CONCLUSIONS

It is insulin response to an OGTT that identifies children with obesity suffering oxidative stress and inflammasome activation more specifically. Uric acid could be mediating this pathological inflammatory response by activating NLRP3 in peripheral blood mononuclear cells.

摘要

背景

胰岛素抵抗(IR)被认为是肥胖相关代谢并发症的主要驱动因素,与氧化应激和炎症有关,而氧化应激和炎症又相互促进。目前,儿科内分泌医生在儿童中使用的是针对成人的 IR 定义,而不是儿童特有的定义。胰岛素分泌动力学的改变与更差的代谢特征和 2 型糖尿病的发展有关,因此,我们旨在测试儿童的胰岛素反应是否与氧化应激和炎症有关。

方法

我们进行了一项病例对照研究,纳入了 132 名儿童,分为以下几类:33 名非肥胖儿童(Lean);42 名根据美国糖尿病协会成人标准无肥胖但无 IR(OBIR-)的儿童;25 名肥胖且有 IR,口服葡萄糖耐量试验(OGTT)胰岛素早期反应良好的儿童(EP-OBIR+);32 名肥胖、IR 和胰岛素晚期峰(LP-OBIR+)的儿童;并研究了与脂质和碳水化合物代谢、氧化应激、炎症和炎症小体激活相关的变量。

结果

肥胖、IR 和早期胰岛素反应的儿童的测量参数与肥胖但无 IR 的儿童相似。只有晚期反应者表现出抗氧化系统受损,红细胞和血浆中的氧化损伤增加,白细胞中的炎症小体激活,尽管经典炎症标志物较低。尿酸水平升高似乎是炎症小体激活的潜在机制之一。

结论

OGTT 对胰岛素的反应更能准确地识别出肥胖且遭受氧化应激和炎症小体激活的儿童。尿酸可能通过激活外周血单核细胞中的 NLRP3 来介导这种病理性炎症反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7010/10440893/4fd1f24b9033/12967_2023_4337_Fig1_HTML.jpg

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