Antigen Presenting Cell Isolevuglandins Link Salt-Sensitivity of Blood Pressure to Insulin Resistance.

IF 5.1
Lale A Ertuglu, Mert Demirci, Ashley L Mutchler, Cheryl L Laffer, Mohammad Saleem, T Alp Ikizler, Annet Kirabo
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Abstract

Background: Insulin resistance has been associated with salt sensitivity and low sodium intake; however, the mechanisms remain elusive. Our previous studies showed that sodium-induced isolevuglandin (IsoLG) formation in antigen-presenting cells (APCs) leads to systemic inflammation and salt-sensitive hypertension and IsoLG formation in APCs is affected by acute alterations in salt intake in salt-sensitive but not salt-resistant people. In this clinical study, we investigated how acute salt loading and depletion change insulin resistance markers and whether these changes are linked with changes in IsoLGs in APCs.

Methods: 20 participants with hypertension underwent an inpatient protocol of salt loading and depletion for assessment of salt sensitivity. Plasma glucose and insulin levels were measured after 24 hours of salt loading and depletion and insulin resistance was measured by the homeostasis model assessment index (HOMA-IR). IsoLG-adduct accumulation in APCs (dendritic cells, classical, intermediate and non-classical monocytes) was assessed by flow cytometry.

Results: Baseline insulin resistance correlated with higher salt sensitivity. Insulin resistance significantly increased from salt loading to salt depletion. Salt-depletion induced changes in IsoLG+ APCs significantly correlated with changes in HOMA-IR. This correlation was significant only in participants who were insulin resistant at baseline.

Conclusion: Within 24 hours of acute salt depletion, markers of insulin resistance exhibit a significant increase, which strongly correlates with change in IsoLG formation in APCs. This finding implies that oxidative stress in APCs may be implicated in the salt-sensitive modulation of glucose metabolism.

抗原呈递细胞内的异戊糖甙将血压的盐敏感性与胰岛素抵抗联系起来。
背景:胰岛素抵抗与盐敏感性和低钠摄入有关;然而,其机制仍然难以捉摸。我们之前的研究表明,钠诱导的抗原呈递细胞(apc)中IsoLG的形成导致全身炎症和盐敏感性高血压,而在盐敏感而非耐盐人群中,apc中IsoLG的形成受盐摄入量的急性改变的影响。在这项临床研究中,我们研究了急性盐负荷和消耗如何改变胰岛素抵抗标志物,以及这些变化是否与apc中isolg的变化有关。方法:20名高血压患者接受了盐负荷和消耗的住院治疗方案,以评估盐敏感性。在盐负荷和耗竭24小时后测定血浆葡萄糖和胰岛素水平,并采用稳态模型评估指数(HOMA-IR)测定胰岛素抵抗。通过流式细胞术评估apc(树突状细胞、经典、中间和非经典单核细胞)中isolg加合物的积累。结果:基线胰岛素抵抗与较高的盐敏感性相关。从盐负荷到盐耗尽,胰岛素抵抗显著增加。盐枯竭诱导的IsoLG+ apc的变化与HOMA-IR的变化显著相关。这种相关性仅在基线时胰岛素抵抗的参与者中有意义。结论:急性缺盐24小时内,胰岛素抵抗标志物显著升高,这与apc中IsoLG形成的变化密切相关。这一发现表明,APCs中的氧化应激可能与糖代谢的盐敏感调节有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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