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GLP-1 可促进人肾脏皮质和髓质灌注,并在 NaCl 负荷期间维持肾脏氧合。

GLP-1 Promotes Cortical and Medullary Perfusion in the Human Kidney and Maintains Renal Oxygenation During NaCl Loading.

机构信息

Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet Copenhagen University Hospital Copenhagen Denmark.

Sir Peter Mansfield Magnetic Resonance Centre School of Physics and Astronomy University of Nottingham United Kingdom.

出版信息

J Am Heart Assoc. 2023 Feb 7;12(3):e027712. doi: 10.1161/JAHA.122.027712. Epub 2023 Feb 3.

Abstract

Background GLP-1 (glucagon-like peptide-1) receptor agonists exert beneficial long-term effects on cardiovascular and renal outcomes. In humans, the natriuretic effect of GLP-1 depends on GLP-1 receptor interaction, is accompanied by suppression of angiotensin II, and is independent of changes in renal plasma flow. In rodents, angiotensin II constricts vasa recta and lowers medullary perfusion. The current randomized, controlled, crossover study was designed to test the hypothesis that GLP-1 increases renal medullary perfusion in healthy humans. Methods and Results Healthy male participants (n=10, aged 27±4 years) ingested a fixed sodium intake for 4 days and were examined twice during a 1-hour infusion of either GLP-1 (1.5 pmol/kg per minute) or placebo together with infusion of 0.9% NaCl (750 mL/h). Interleaved measurements of renal arterial blood flow, oxygenation (R*), and perfusion were acquired in the renal cortex and medulla during infusions, using magnetic resonance imaging. GLP-1 infusion increased medullary perfusion (32±7%, <0.001) and cortical perfusion (13±4%, <0.001) compared with placebo. Here, NaCl infusion decreased medullary perfusion (-5±2%, =0.007), whereas cortical perfusion remained unchanged. R* values increased by 3±2% (=0.025) in the medulla and 4±1% (=0.008) in the cortex during placebo, indicative of decreased oxygenation, but remained unchanged during GLP-1. Blood flow in the renal artery was not altered significantly by either intervention. Conclusions GLP-1 increases predominantly medullary but also cortical perfusion in the healthy human kidney and maintains renal oxygenation during NaCl loading. In perspective, suppression of angiotensin II by GLP-1 may account for the increase in regional perfusion. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT04337268.

摘要

背景

GLP-1(胰高血糖素样肽-1)受体激动剂对心血管和肾脏结局具有有益的长期作用。在人类中,GLP-1 的利钠作用依赖于 GLP-1 受体相互作用,伴随着血管紧张素 II 的抑制,并且与肾血浆流量的变化无关。在啮齿动物中,血管紧张素 II 收缩直小血管并降低髓质灌注。本项随机、对照、交叉研究旨在检验 GLP-1 可增加健康人体肾脏髓质灌注的假设。

方法和结果

健康男性参与者(n=10,年龄 27±4 岁)摄入固定钠摄入量 4 天,并在 1 小时内输注 GLP-1(1.5 pmol/kg·min)或安慰剂,同时输注 0.9%NaCl(750 mL/h)期间接受两次检查。在输注期间,使用磁共振成像获取肾皮质和髓质中肾动脉血流、氧合(R*)和灌注的交替测量值。与安慰剂相比,GLP-1 输注增加了髓质灌注(32±7%,<0.001)和皮质灌注(13±4%,<0.001)。在这里,NaCl 输注使髓质灌注减少(-5±2%,=0.007),而皮质灌注保持不变。R*值在髓质中增加了 3±2%(=0.025),在皮质中增加了 4±1%(=0.008),表明氧合减少,但在 GLP-1 期间保持不变。肾动脉中的血流在两种干预措施下均未发生显著改变。

结论

GLP-1 主要增加健康人肾脏的髓质灌注,也增加皮质灌注,并在 NaCl 负荷期间维持肾脏氧合。从这个角度来看,GLP-1 对血管紧张素 II 的抑制可能是局部灌注增加的原因。

注册网址

https://www.clinicaltrials.gov;独特标识符:NCT04337268。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2649/9973647/aff19727a68e/JAH3-12-e027712-g001.jpg

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