International Journal of Hypertension

International Journal of Hypertension / 2013 / Article

Review Article | Open Access

Volume 2013 |Article ID 696598 |

Menno Pruijm, Lucie Hofmann, Bruno Vogt, Marie-Eve Muller, Maciej Piskunowicz, Matthias Stuber, Michel Burnier, "Renal Tissue Oxygenation in Essential Hypertension and Chronic Kidney Disease", International Journal of Hypertension, vol. 2013, Article ID 696598, 7 pages, 2013.

Renal Tissue Oxygenation in Essential Hypertension and Chronic Kidney Disease

Academic Editor: Claudio Borghi
Received25 Aug 2012
Accepted09 Jan 2013
Published20 Feb 2013


Animal studies suggest that renal tissue hypoxia plays an important role in the development of renal damage in hypertension and renal diseases, yet human data were scarce due to the lack of noninvasive methods. Over the last decade, blood oxygenation level-dependent magnetic resonance imaging (BOLD-MRI), detecting deoxyhemoglobin in hypoxic renal tissue, has become a powerful tool to assess kidney oxygenation noninvasively in humans. This paper provides an overview of BOLD-MRI studies performed in patients suffering from essential hypertension or chronic kidney disease (CKD). In line with animal studies, acute changes in cortical and medullary oxygenation have been observed after the administration of medication (furosemide, blockers of the renin-angiotensin system) or alterations in sodium intake in these patient groups, underlining the important role of renal sodium handling in kidney oxygenation. In contrast, no BOLD-MRI studies have convincingly demonstrated that renal oxygenation is chronically reduced in essential hypertension or in CKD or chronically altered after long-term medication intake. More studies are required to clarify this discrepancy and to further unravel the role of renal oxygenation in the development and progression of essential hypertension and CKD in humans.

1. Introduction

Hypertension is a major public health burden and affects about 1 billion people worldwide. Hypertension increases the risk of coronary heart disease and cerebrovascular accidents [1, 2]. Hypertension is also tightly entangled with chronic kidney disease (CKD) [3, 4], defined as “evidence of structural or functional kidney abnormalities that persists for at least three months, or a glomerular filtration rate (GFR) < 60 mL/min/1.73 m², with or without evidence of kidney damage, and irrespective of its cause” [5]. A majority of CKD patients are hypertensive, and hypertension is one of the main causes of CKD, accounting for approximately 30% of cases of end-stage renal disease (ESRD) [6, 7]. Hypertension and CKD cluster in obese and/or diabetic subjects, and both disease states share common underlying pathways, such as chronic low-grade inflammation, increased sodium retention, and an activated renin-angiotensin system [8, 9]. The kidneys are seen by some as the main culprit in the development of hypertension. Transplantation studies have indeed demonstrated that hypertension follows the kidneys [10, 11], and in extreme cases removing both kidneys in transplanted patients can cure resistant hypertension [12].

Animal studies have suggested that renal tissue hypoxia might be another common mechanism of renal damage in hypertension and renal diseases [13]. Indeed, cortical and medullary tissue hypoxia has been documented in both disease states [14, 15]. However, translation of animal studies to humans should be made cautiously and is hampered by the absence of non-invasive techniques allowing the measurement of renal tissue oxygenation in humans. This paper focuses on the determinants of renal tissue oxygenation in humans and on the actual evidence pointing towards a role for renal tissue hypoxia in the development and progression of hypertension and CKD in humans.

2. Determinants of Renal Tissue Oxygenation

Fifty years ago, Aukland and Krog were the first to report the unique oxygenation pattern of kidneys using microelectrodes sensitive to oxygen in dogs and rats. They measured levels of tissue partial pressure of oxygen (pO2) as low as 10–20 mmHg in the medulla and 50 mmHg in the renal cortex [16], despite the fact that renal blood flow, and thus oxygen delivery, is the highest in the body in relation to organ weight. Since then, much has been learned on the mechanisms involved in the regulation of renal medullary tissue oxygenation. As in any organ, the local tissue pO2 is determined by the oxygen delivery (a function of renal perfusion and blood oxygen content) and by the O2 consumption, which is driven essentially by the glomerular filtration rate and the active tubular transport. Renal kidney perfusion is characterized by preglomerular oxygen diffusion shunting, partly explaining the low tissue pO2 levels [17]. In the kidneys, over 90% of all oxygen consumption is used for tubular sodium transport, which differs between cortex and medulla. The well-perfused proximal tubules are mainly located in the renal cortex. Proximal tubular sodium reabsorption is partly based on energy-consuming active transport via basolateral Na+, K+-ATPase and partly on passive transport via paracellular pathways [18]. Hence, despite the fact that the proximal tubules reabsorb 67% of all filtered sodium, they consume only 27% of total O2, resulting in a cortical pO2 around 50 mmHg [1921]. In contrast, Henle’s loops in the medulla receive 10% of RBF and reabsorb 30% of sodium at a relatively high-energy cost. They use 67% of all O2, and local pO2 is as low as 10–15 mmHg under normal circumstances, which renders them highly susceptible to ischemic injury [19, 20].

Theoretically, worsening of renal tissue oxygenation is the consequence of reduced oxygen delivery or of increased oxygen consumption. Examples of the first category are severe renal artery stenosis, renal hypoperfusion due to septic or cardiogenic shock, or severe anemia. Examples of the second category are energy-consuming glomerular hyperfiltration as seen in obesity and the early stages of diabetes, proinflammatory pathways, and/or enhanced renal sodium reabsorption, as present in essential hypertension.

Whatever the cause, the consequence of renal tissue hypoxia is identical, that is, activation of hypoxia-induced factors (HIF-1) and HIF-1 regulated genes. The activation of these genes will not only lead to an increased erythropoiesis and to neoangiogenesis through activation of vascular endothelial growth factor and inducible nitric oxide synthase, but also to the stimulation of growth factors that cause endothelial dysfunction, activation of inflammatory cells, and oxidative stress, which will lead to tissue injury and interstitial fibrosis [22, 23]. Whereas there is accumulated evidence for a role of hypoxia in the development of acute and chronic renal damage in animals, there is definitively less information on the pathophysiological role of renal hypoxia in humans. This is due essentially to methodological reasons. Indeed, many techniques in animals allow measurement of regional renal oxygen content, such as the insertion of oxygen microelectrodes and the protoporphyrin phosphorescence method [24]. Besides, hypoxia can be measured on dissected kidney tissue using pimonidazole, a molecular “hypoxia probe” which, following injection, binds to tissues with oxygen tension below 10 mm Hg [15] or by tissue dosing of HIF-1 or hypoxia-responsive genes. Unfortunately, these techniques are too invasive or not adapted to be used in humans.

3. Measurement of Renal Tissue Oxygenation in Humans with BOLD-MRI

A relatively new technology called ‘Blood Oxygenation Level-Dependent Magnetic Resonance Imaging (BOLD-MRI), offers now possibilities to assess renal tissue oxygenation non-invasively in humans [25, 26]. The BOLD effect is based upon the different magnetic attributes of hemoglobin. Oxyhemoglobin is diamagnetic, whereas deoxyhemoglobin is paramagnetic. The magnetic field disturbances by paramagnetic molecules result in a loss of phase coherence, leading to signal attenuation on T2*-weighted MR images. Deoxygenated hemoglobin can therefore be used as an endogenous contrast agent. The ratio of deoxyhemoglobin to oxyhemoglobin concentrations is proportional to the pO2 of blood, and blood pO2 is supposed to be in equilibrium with the surrounding tissue. Hence, BOLD signal estimated by transverse relaxation rate R2* (=1/T2*) can be considered as a sensitive indicator of tissue pO2 [26]. The effect of the manipulation of the oxy- to deoxyhemoglobin ratio results in contrast changes in animals [27] and in humans [28]. R2* as measured by BOLD-MRI has been shown to correlate well with tissue pO2 [25, 29]. An example of MR images as obtained using the BOLD-MRI technique in a healthy volunteer is shown in Figure 1(a).

Since 1996, BOLD-MRI has been used in humans to evaluate, amongst others, the effect of water diuresis on renal medulla and cortex in healthy volunteers [34, 35] and diabetic patients [30] and to monitor changes in renal oxygenation after administration of different drugs [36, 37] and after acute renal ischemia [38, 39].

The BOLD-MRI technique itself has been criticized by some [40, 41], arguing that it is difficult to acquire the same anatomical slices in each participant when repeating the BOLD-MRI exams. However, the intraobserver variability of the cortical and medullary R2* values is low when performed by an experienced investigator and when using a standardized breath-hold technique [42]. An identical prehydration protocol and assessment of dietary sodium intake are at least as important, since both factors have been shown to influence the R2* signal (see below).

4. Renal Tissue Oxygenation in Essential Hypertension

Essential hypertension is often characterized by an increased sodium retention, either in the proximal or distal nephron segments, a process requiring active sodium transport which might lead to increased tubular oxygen consumption [43, 44]. Besides, the renin-angiotensin system is in general activated in hypertensive patients, which may affect renal perfusion and oxygen consumption [45]. Therefore, essential hypertension could theoretically lead to cortical and medullary hypoxia.

Indeed, studies in hypertensive rats using oxygen microelectrodes found pronounced medullary and cortical hypoxia in spontaneously hypertensive animals as compared to normotensive controls [14]. Most studies performed in humans so far have focused on renal artery stenosis, as discussed in more detail in another article of this number. Assessment of renal tissue oxygenation in patients with essential hypertension has only been performed in a few studies. In the first study, Textor et al. reported higher medullary R2* levels in 20 African-American hypertensive subjects, as compared to 20 Caucasians suggesting a lower medullary oxygenation in hypertensives [46]. This observation was explained by an increased renal medullary volume (measured by contrast-enhanced multidetector CT) per body surface area (BSA), coupled with increased sodium reabsorption and urinary prostaglandin F2 excretion in African Americans [47]. However, differences in age, body mass index (BMI), and estimated GFR (eGFR) hampered the ability to generalize these results. Besides, the study did not include a normotensive control group.

Schachinger et al. showed that intravenous infusion of angiotensin II to six healthy volunteers leads to an acute rise in blood pressure (BP) and a simultaneous decrease of cortical T2*, suggesting a decrease in cortical oxygenation. Unfortunately, medullary oxygenation was not assessed in this study, and since hypertension was artificially induced, the results cannot be translated to the hypertensive population [48].

Finally, in our research unit, we have investigated ten young normotensive and eight untreated hypertensive men with BOLD-MRI after one week of a high sodium (>200 mmol/day) and again after one week of a low sodium diet (<100 mmol/day). Simultaneously, renal hemodynamics and renal sodium handling were assessed using, respectively, inulin-, PAH-, and endogenous lithium-clearances [47]. The main finding was that a low sodium intake was associated with an increased medullary oxygenation in both normo- and hypertensive individuals, independently of changes in renal perfusion. In our opinion, this is due to a salt depletion-induced shift of the oxygen-consuming sodium transport from the distal to the proximal tubules. Hence, the oxygen consumption in medulla and distal nephron was reduced, whereas oxygen consumption of the cortical proximal tubules increased under low sodium conditions. Cortical oxygenation was not altered, possibly due to the high cortical perfusion, and thus oxygen delivery, opposing the effect of changes in oxygen consumption. Indeed, increased proximal sodium reabsorption under low sodium conditions correlated positively with medullary oxygenation in normotensive individuals, yet not in hypertensive individuals. Hypertensive individuals had increased proximal sodium reabsorption under both low- and high-salt conditions, possibly explaining this lack of correlation and hence further confirming the role of the abnormal proximal reabsorption of sodium in hypertension [44].

Interestingly, at any sodium intake, hypertensive patients had slightly lower medullary R2* values than normotensive subjects, suggesting an increased rather than a decreased medullary oxygenation in young hypertensive men, again possibly due to reduced medullary oxygen consumption as a result of increased proximal sodium reabsorption.

It is important to note that this study was performed in young hypertensive men, under extremely low or high sodium-intake conditions, and the oxygenation pattern might be different in older patients with hypertension-induced organ damage.

Hence, acquired data in humans, so far, are not in line with animal studies and show no clear difference between normotensive and hypertensive subjects or even higher medullary oxygenation in hypertension as compared with normotensive controls. Whether this is due to less active medullar sodium transport, adaptations in medullar microcirculation or altered arterial venous shunting as compared to normal subjects merits further investigations. All presented data should be interpreted with caution, due to the small sample size, and confirmation in larger prospective studies is needed.

5. Renal Tissue Oxygenation in Chronic Kidney Disease

In clinical practice, renal ischemia has become a well-accepted cause of acute renal failure in situations of circulatory shock, accounting for almost 50% of cases of acute renal insufficiency [49]. However, the role of renal hypoxia in the pathophysiology of chronic kidney diseases remained largely underreported. Recently, Fine and Norman proposed that kidney injury leads to a vicious circle of tissue fibrosis, pursuant obliteration of the renal microvasculature, and further hypoxia [50]. Their statement was based on the fact that the extent of renal dysfunction is poorly associated with changes in glomerular morphology as seen in kidney biopsies of patients with chronic renal disease, whereas it correlates well with chronic tubulointerstitial fibrosis, a known consequence of renal hypoxia [51]. Once installed, the reduction of functional renal mass in CKD results in a number of common functional, structural, and metabolic adaptations that lead to further kidney damage, whatever the underlying cause [52]. Amongst these mechanisms are the activation of the renin-angiotensin system, glomerular hyperfiltration in residual glomeruli, the upregulation of inflammatory cytokines such as TGF-β which on his turn stimulates the formation of interstitial fibrosis, the development of proteinuria, and worsening of tissue hypoxia [52, 53].

Accumulating data from animal studies supports indeed, a pathogenic role of tissue hypoxia in the chronic deterioration of kidney function. The most convincing evidence probably comes from Manotham et al., who have shown in a remnant kidney model (which is a representative model of CKD) that the number of hypoxic tubules was markedly increased 4 and 7 days after subtotal (5/6) nephrectomy, as compared to a sham-operated control group [15]. Hypoxia was measured on kidney biopsies using immunostaining for pimonidazole. Of interest, these findings occurred in parallel with disturbed peritubular capillary perfusion and antedated any histologic evidence of tubulointerstitial damage. Hypoxia persisted until the development of interstitial fibrosis; in a subgroup treated with olmesartan, an angiotensin II type 1 receptor blocker, blockade of the renin-angiotensin system ameliorated peritubular capillary perfusion and tubular hypoxia and led to less interstitial fibrosis. Studies by Johnson et al. have also demonstrated that chronic systemic hypoxia causes renal interstitial damage and predisposes animals to persistent hypertension and its renal damages [54]. Medullary hypoxia has been documented in animal studies examining the development of diabetic nephropathy [55, 56].

BOLD-MRI can also be used to estimate renal tissue oxygenation in CKD patients (Figure 1(b)), and several studies have used BOLD-MRI in humans to investigate renal oxygenation in different forms of CKD. Diabetic nephropathy has been most frequently studied, and a summary of the results is shown in Table 1. Only one study reported lower medullary oxygenation in diabetics as compared with controls; two found no differences, whereas one even reported higher medullary oxygenation in diabetics. Concerning the cortex, again only the study of Yin et al. reported a lower cortical oxygenation (higher R2* levels) in diabetics as compared with controls [31]; the other studies found no differences. However, large differences existed in eGFR of the diabetics included in these studies. Moreover, different standardization procedures were followed (sober versus prehydration, medication withdrawal versus none), further hampering direct comparisons. In the study of Yin et al., diabetics were divided into four groups of increasing kidney damage (stage I–IV, according to Mogensen). Although medullary oxygenation was slightly lower in all diabetic groups as compared with controls, medullary oxygenation increased with worsening kidney function, despite the fact that hemoglobin levels strongly decreased, and age increased from stage I to IV. This unexpected finding was explained by the authors as a possible sign of decreased oxygen consumption due to reduced GFR and active tubular transport. This could suggest that in advanced CKD, reduced tubular oxygen consumption outlevels reduced medullary perfusion and oxygen diffusion and that progressive interstitial fibrosis merely increases rather than decreases medullary oxygenation.

StudyPatient Age (y)eGFR
(mL/min/1.73 m²)

Epstein et al. (2002) [30] DM2948 ± 3119 ± 61.517 ± 0.513 ± 0.2
Control951 ± 2133 ± 71.517 ± 0.813 ± 0.2
Yin et al. (2012) [31] DM24838–708–1103HigherHigher
Control6751 ± 14n.m.3LowerLower
Wang et al. (2011) [32]DM22065 (49–77)47 (14–71)1.514 ± 211 ± 1
Control735 (30–45)n.m.1.519 ± 112 ± 1
Inoue et al. (2011) [33] DM24359 ± 1144 ± 281.5n.m. 74 ± 8a
Control1036n.m.1.559 ± 574 ± 5a

value instead of value reported; n.m.: not mentioned.

The largest study so far assessing renal oxygenation at different degrees of kidney dysfunction was recently reported by Michaely et al. [57]. This study included 400 patients who underwent MR imaging for nonspecific reasons, including staging of abdominal tumors and MR angiographies of intra-abdominal vessels. Of them, 280 patients had available serum creatinine values, and all KDOQI stages of CKD were represented. No correlation was found between R2* values and eGFR (according to the MDRD formula [58]), and R2* values were not affected by age and gender. Hence, despite some shortcomings of this study (no information on medication or dietary sodium intake, no standardization of BOLD and creatinine measurement), it seems that renal oxygenation is kept constant over a broad range of physiological and pathological conditions. As such, the findings of Michaely et al. put into question whether “chronic renal hypoxia” truly exists in humans or whether acute episodes of hypoxia are “corrected” by, for example, alterations in renal microcirculation and HIF-induced interstitial fibrosis. In line with this hypothesis, Juillard et al. have described acute increases in cortical and medullary R2* levels the first days after subtotal clipping of the renal artery [38]. Yet, four weeks after clipping, renal hypoxia could no longer be detected [59].

6. Antihypertensive Drugs and Renal Oxygenation

The use of blockers of the renin-angiotensin system (RAS blockers) as antihypertensive and antiproteinuric medication has been particularly effective in slowing the progression of renal disease in type 2 diabetics [60], and all existing guidelines advise to introduce an angiotensin converting enzymes inhibitor (ACEI) or an angiotensin II receptor blocker (ARB) in diabetic patients with CKD, as soon as microalbuminuria is detected or in case of hypertension [61].

Animal studies have suggested that administration of RAS blockers leads to an acute increase in renal tissue oxygenation [24, 53]. In humans, Djamali et al. reported a decrease in cortical R2* levels, suggesting increased oxygenation, in nine healthy volunteers two hours after the intake of 50 mg of losartan [62].

We recently performed a cross-over pilot study in twelve patients with type 2 diabetes and CKD (mean age 60 y, eGFR 62 mL ± 22 min/1.73 m²). Patients were either already on treatment with an ACEI or ARB or had a formal indication to start one (hypertension, (micro)albuminuria, or both). In this study, cortical and medullary R2* levels were not altered after one month of enalapril (20 mg qd) nor after one month of candesartan (16 mg qd) as compared with baseline (data presented at the 5th International meeting of the French Society of Hypertension, Paris, France, December 2011). Acute changes in R2* levels were not assessed in this study. However, in combination with the study of Djamali et al., one might conclude that RAS blockers induce acute yet not chronic increases in renal oxygenation.

The administration of furosemide has been shown to induce in an acute drop of medullary and to a lesser degree cortical R2* levels in healthy volunteers, in diabetics, and in patients with renal artery stenosis suggesting a diuretic-induced increase in renal oxygenation [21, 46]. The effect of furosemide on renal oxygenation has been attributed to a reduction of the active oxygen-consuming sodium transport in the ascending loop of Henle [46]. To the best of our knowledge, no studies have assessed the effect of chronic furosemide intake on renal oxygenation.

7. Conclusions and Perspectives

Taken together, the BOLD-MRI technique has opened an exciting new field of research that allows for the first time the assessment of renal oxygenation non-invasively in humans. The changes in renal oxygenation observed in response to furosemide or in association with dietary sodium intake suggest that renal sodium handling is one of the main determinants of renal tissue oxygenation.

So far, no studies have convincingly demonstrated that renal oxygenation is reduced in essential hypertension, diabetes, or CKD. These findings are in contrast with most animal studies. First of all, it might be that BOLD-MRI is not sensitive enough or simply not as good a tool to assess renal oxygenation. Indeed, the assumption that tissue oxygenation varies with blood oxygenation might not always hold in kidneys that are characterized by profound arteriovenous oxygen shunting. Nonetheless, several animal studies have validated this technique. Another possibility is that animal studies provide excellent models to study short-term changes in oxygenation but that they are suboptimal in simulating the long-term changes and adaptations in the kidney that might have occurred after several decades of exposure to chronic disease states such as diabetes or hypertension. Whatever the truth may be, BOLD-MRI and other new radiological techniques that study renal functioning non-invasively merit the full attention of clinicians, and their development will certainly help to further unravel the role of renal oxygenation in the development and progression of essential hypertension and CKD in humans.


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