Department of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Front Biosci (Landmark Ed). 2023 Mar 28;28(3):62. doi: 10.31083/j.fbl2803062.
Maintaining a balance between the supply and demand of oxygen is vital for proper organ function. Most types of acute kidney injury (AKI) are characterized by hypoxia, a state where the supply of oxygen cannot match the demand for normal cellular activities. Hypoxia results from hypo perfusion and impaired microcirculation in the kidney. It inhibits mitochondrial oxidative phosphorylation, resulting in a decrease in production of adenosine triphosphate (ATP), which is essential to power tubular transport activities, especially reabsorption of Na+, and other vital cellular activities. To ameliorate AKI, the majority of studies have focused on increasing renal oxygen delivery by restoring renal blood flow and altering intra-renal hemodynamics. However, to date these approaches remain inadequate. In addition to augmenting oxygen supply, increasing renal blood flow also increases glomerular filtration rate, leading to increased solute deliver and workload for the renal tubules, causing an increase in oxygen consumption. The relationship between Na+ reabsorption and oxygen expenditure in the kidney is linear. Experimental models have demonstrated that inhibition of Na+ reabsorption can alleviate AKI. Since the proximal tubules reabsorb approximately 65% of filtered Na+, consuming the largest portion of oxygen, many studies focus on examining the effects of inhibiting Na+ reabsorption in this segment. Potential therapeutics that have been examined include acetazolamide, dopamine and its analog, inhibitors of the renin-angiotensin II system, atrial natriuretic peptide, and empagliflozin. The effectiveness of inhibition of Na+ reabsorption in the thick ascending limb of the Loop of Henle by furosemide has been also examined. While these approaches produced impressive results in animal models, their clinical benefits remain mixed. This review summarizes the progress in this area and argues that the combination of increasing oxygen supply with decreasing oxygen consumption or different approaches to reducing oxygen demand will be more efficacious.
维持氧的供需平衡对于器官功能的正常运转至关重要。大多数类型的急性肾损伤(AKI)的特征是缺氧,即氧的供应无法满足正常细胞活动的需求。缺氧是由于肾脏低灌注和微循环受损引起的。它抑制线粒体氧化磷酸化,导致三磷酸腺苷(ATP)的产生减少,而 ATP 是肾小管转运活动(尤其是 Na+的重吸收)和其他重要细胞活动所必需的能量来源。为了改善 AKI,大多数研究都集中在通过恢复肾血流量和改变肾内血液动力学来增加肾氧供应。然而,迄今为止,这些方法仍然不够充分。除了增加氧供应外,增加肾血流量还会增加肾小球滤过率,导致溶质输送和肾小管的工作量增加,从而增加氧消耗。肾脏中 Na+重吸收和氧消耗之间的关系是线性的。实验模型已经证明,抑制 Na+重吸收可以缓解 AKI。由于近端小管吸收了约 65%的滤过 Na+,消耗了大部分的氧,因此许多研究都集中在研究抑制该段 Na+重吸收的效果。已经研究过的潜在治疗方法包括乙酰唑胺、多巴胺及其类似物、肾素-血管紧张素 II 系统抑制剂、心房利钠肽和恩格列净。还研究了通过呋塞米抑制 Henle 袢升支粗段 Na+重吸收的效果。虽然这些方法在动物模型中产生了令人印象深刻的结果,但它们的临床效果仍存在差异。本综述总结了这一领域的进展,并认为增加氧供应与减少氧消耗或采用不同方法降低氧需求相结合将更有效。