|Albuminuria indicates the pressure-associated injury of juxtamedullary nephrons and cerebral strain vessels in spontaneously hypertensive stroke-prone rats.|
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|PMID: 22914555 Owner: NLM Status: MEDLINE|
|Albuminuria is an indicator of renal injury and is closely linked with cardiovascular disease (CVD). However, the mechanism by which albumin is excreted in the urine remains unclear. As the juxtamedullary region of the kidney is highly susceptible to pressure increase, juxtamedullary injury is observed from an early phase in hypertensive rat models. Anatomical similarities are observed between the pre-glomerular vessels of the juxtamedullary nephron and the cerebral vasculature. We previously named these 'strain vessels' for their high vascular tone and exposure to higher pressures. The current studies were designed to determine whether albuminuria is the result of juxtamedullary nephron injury, indicating the presence of pressure injury to the strain vessels in spontaneously hypertensive stroke-prone rats (SHR-SP) fed a high-salt diet. Albuminuria was associated with juxtamedullary nephron injury, and the enhanced expression of monocyte chemotactic protein-1 (MCP-1) and tumor growth factor-beta (TGF-β) in 12-week-old SHR-SP rats fed a 4% high-salt diet from the age of 6 weeks. The wall thickness of the pre-glomerular vessels of the juxtamedullary nephron was also associated with that of the perforating artery of the middle cerebral artery. Reducing the blood pressure with nifedipine reduced the degree of albuminuria and juxtamedullary nephron injury as well as MCP-1 and TGF-β expression in the SHR-SP rats fed an 8% high-salt diet from the age of 9 weeks. Nifedipine inhibited stroke events in these animals until they were 14 weeks old. These results indicate that albuminuria is a result of juxtamedullary nephron injury and a marker of pressure-induced injury of the strain vessels.|
|Tasuku Nagasawa; Takefumi Mori; Yusuke Ohsaki; Yoshimi Yoneki; Qi Guo; Emiko Sato; Ikuko Oba; Sadayoshi Ito|
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|Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2012-08-23|
|Title: Hypertension research : official journal of the Japanese Society of Hypertension Volume: 35 ISSN: 1348-4214 ISO Abbreviation: Hypertens. Res. Publication Date: 2012 Oct|
|Created Date: 2012-10-05 Completed Date: 2013-06-17 Revised Date: 2013-07-12|
Medline Journal Info:
|Nlm Unique ID: 9307690 Medline TA: Hypertens Res Country: England|
|Languages: eng Pagination: 1024-31 Citation Subset: IM|
|Division of Nephrology, Endocrinology and Vascular Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.|
|APA/MLA Format Download EndNote Download BibTex|
Albuminuria / etiology*
Arterioles / pathology
Brain / blood supply
Chemokine CCL2 / analysis
Juxtaglomerular Apparatus / pathology*
Nephrons / pathology*
Rats, Inbred SHR
Stroke / etiology*
Transforming Growth Factor beta / analysis
|0/Actins; 0/Ccl2 protein, rat; 0/Chemokine CCL2; 0/Transforming Growth Factor beta; 0/smooth muscle actin, rat|
Journal ID (nlm-ta): Hypertens Res
Journal ID (iso-abbrev): Hypertens. Res
Publisher: Nature Publishing Group
Copyright © 2012 The Japanese Society of Hypertension
Received Day: 22 Month: 11 Year: 2011
Revision Received Day: 06 Month: 04 Year: 2012
Accepted Day: 12 Month: 04 Year: 2012
Print publication date: Month: 10 Year: 2012
Electronic publication date: Day: 23 Month: 08 Year: 2012
Volume: 35 Issue: 10
First Page: 1024 Last Page: 1031
PubMed Id: 22914555
Publisher Item Identifier: hr2012112
|Albuminuria indicates the pressure-associated injury of juxtamedullary nephrons and cerebral strain vessels in spontaneously hypertensive stroke-prone rats Alternate Title:Albuminuria and injury of strain vessels in SHR-SP rats|
1Division of Nephrology, Endocrinology and Vascular Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan
2Department of Rehabilitation and Sports Medicine, Tianjin Medical University, Tianjin, China
|*Division of Nephrology, Endocrinology and Vascular Medicine, Tohoku University Graduate School of Medicine, 1-1 Seiryocho, Aoba-ku, Sendai 980-8574, Japan. E-mail: email@example.com
Albuminuria has been increasingly recognized as a well-known predictor for cardiovascular disease (CVD) over the last 10 years.1, 2 In 1984, Mogensen first reported that microalbuminuria predicted the eventual onset of clinical proteinuria and early mortality in type 2 diabetes.3 The presence of albuminuria independently increases the risk for CVD, even in the presence of the known risk factors of hypertension, dyslipidemia and diabetes.4, 5 Clinical trials have shown that a reduction in albuminuria significantly improved the CVD outcomes in albuminuric subjects (RENAAL, LIFE PREVENT).6, 7, 8 Surprisingly, albuminuria is recognized as a risk factor not only in diabetic or hypertensive patients but also for the general population.9, 10 Results from these studies suggest that albuminuria is a sensitive surrogate marker for assessing the risk for CVD. Although extensive investigations have been carried out to determine the mechanism of albuminuria, the conclusions that were drawn from these studies have remained controversial.11 In addition, recent clinical studies such as ONTAREGET, TRANSCEND and ACCOMPLISH have failed to demonstrate an association between albuminuria and CVD.12, 13, 14
It was previously demonstrated that juxtamedullary nephron injury is common in early hypertensive renal injury in rats, as well as in humans.15, 16, 17 Mori et al.16 demonstrated in angiotensin II (Ang II)-infused rats that glomerular injury of the juxtamedullary nephron is blood pressure-dependent, while the glomerular integrity of the outer-cortical nephron depends more on Ang II. These results indicate that there is heterogeneity in hypertensive renal injury and that the juxtamedullary nephron may be a source of microalbuminuria in hypertensive subjects. This hypothesis was supported by studies by Ihara et al.,18 who demonstrated the role of Ang II receptor blockers (ARB) in the reduction of proteinuria in elderly diabetic and hypertensive Otsuka Long-Evans Tokushima Fatty rats. In contrast to hydralazine, olmesartan, an ARB, nearly entirely reduced the levels of proteinuria to a normal baseline level, even for blood pressures at which hydralazine had no similar effect. Outer cortical glomerular injury was significantly reduced in the olmesartan group compared with the hydralazine group. However, juxtamedullary glomerular injury was seen in both groups.18 Taken together, these results suggest that the juxtamedullary glomeruli were already injured from sustained hypertension, prior to the administration of the ARB, which could be a source of albuminuria.
Wada et al.19 performed brain magnetic resonance imaging on 651 elderly subjects and found that the level of albuminuria correlated with the degree of cerebral small vessel disease, independent of the presence of other cerebrovascular risk factors such as diabetes, hypertension and dyslipidemia. We paid particular attention to the anatomical characteristics of the pre-glomerular vessels and the cerebrovascular small vessels, especially the perforating arteries. These vessels are strained under the exposure to high blood pressures, because these vessels branch off directly from the larger, high-velocity arteries. In addition, because the perforating arteries are short and small, and exposed to high pressures, they sustain a large pressure gradient over a short distance. We named this type of vessel a ‘strain vessel' and hypothesized that microalbuminuria is a marker of cerebrovascular–renal injury for the strain vessels of these systems.20
To test our hypothesis, we determined the association between albuminuria and injury to the strain vessels of spontaneously hypertensive stroke-prone rats (SHR-SP).
Five-week-old male SHR-SP rats (n=16, Nihon SLC, Hamamatsu, Japan) were fed a 0.5% NaCl standard diet for 1 week at baseline and then a high-salt diet (4% NaCl; Nihon Nosan, Yokohama, Japan) for 6 weeks. The animals were given tap water throughout the experimental period. Systolic blood pressures (SBPs) were measured every week in the conscious rats by the tail-cuff method (Model MK-2000A; Muromachi, Tokyo, Japan) after reaching 9 weeks of age. Twenty-four-hour urine samples were collected under ice-cooled conditions in a metabolic cage in the 12-week-old animals, and 24-h urinary albumin excretion (Ualb) was measured by a standard autoanalyzer (Synchron-CX-3; Beckman Coulter Inc., Fullerton, CA, USA). At 12 weeks of age, the rats were euthanized with an intraperitoneal injection of pentobarbital (100 mg kg−1), and the tissues were harvested. All experiments were approved by the Animal Committee of Tohoku University.
To determine whether blood pressure is responsible for the strain vessel injury and the cerebrovascular–renal connection, a number of follow-up protocols were followed. As the timing of albuminuria onset in Protocol 1 was heterogeneous, we decided to shorten the duration of exposure but increase the salt content of the diet, which resulted in a uniform timing of albuminuria onset. Beginning at 9 weeks of age, the SHR-SP rats (n=16) were fed a standard 0.5% NaCl diet for 1 week at baseline and then a high-salt diet (8% NaCl; Nihon Nosan) for 2 weeks. The rats were given tap water throughout the experimental period. The animals were randomly divided into two groups. One group served as the control group (n=8), and the other received nifedipine (n=8). Medication administration was started on the day the diets were switched from normal to high salt, and the nifedipine was mixed into the food (Sigma-Aldrich, St Louis, MO, USA, 1.1 g kg−1 diet) and administered orally. The rats took in 80–100 mg kg−1 per day of nifedipine on average, as calculated by their food consumption. The SBP and Ualb were measured every week by the same method used for Protocol 1. After a 2-week observation period, the rats were euthanized with an intraperitoneal injection of pentobarbital (100 mg kg−1), and their tissues were harvested.
At the end of the Protocol 1 experiment, a saline wash was introduced through the renal artery, and the left kidney was then removed and fixed for 48 h (24 h in 10% formalin, followed by 24 h in 100% ethanol). The tissue was paraffin embedded and sectioned at a thickness of 2 μm. The renal sections were stained using the periodic acid-Schiff method for renal injury and captured by an optical microscope connected to a CCD video camera (BX51, DP70; Olympus Optical Co., Tokyo, Japan). The glomerular sclerosis index for each sample was determined by grading at least 50 glomeruli per rat, as previously described.21
For alpha-smooth muscle actin (α-SMA), TGF-β, monocyte chemotactic protein-1 (MCP-1), ED-1 and desmin staining, the residual fixed sample of kidney was retrieved after histological analysis by microwaving the deparaffinized sections in 10 mmol l−1 of citrate buffer (pH 7.0) for 5 min. Immunohistochemical analysis was performed using antibodies against α-SMA (diluted 1:100; Dako Cytomation, Glostrup, Denmark), TGF-β (diluted 1 : 20, Santa Cruz, CA, USA), MCP-1 (diluted 1 : 300, Abcam, Cambridge, UK), ED-1 (diluted 1 : 400, Serotec, Oxford, UK) and desmin (diluted 1:1000, Abcam), and the samples were processed according to previously described methods.22 Immunopositive areas were analyzed from 20 randomly captured images with Image J software (NIH software, Ver. 1.37, NIH, Bethesda, MD, USA). The results were reported as the percent of positively stained areas, except for the ED-1 results, which were expressed as the number of immunopositive cells per slide.
At the end of the experiment in Protocol 1, the brains were removed after being perfused, via the left ventricle, with 4% para-formaldehyde for 5 min. The samples were fixed for 48 h before they were embedded in paraffin (24 h in 10% formalin, then 6 h in 70% ethanol, 6 h in 80% ethanol, 6 h in 90% ethanol and finally 6 h in 100% ethanol). The tissue was embedded in paraffin and sectioned at a thickness of 2 μm. Following the same method mentioned above, the immunohistochemical analysis was performed using antibodies against α-SMA.
Arterioles in the juxtamedullary and/or outer cortical region of the kidney and with an external diameter of 20–30 μm were analyzed. For the brain tissue analysis, any arterioles that were present on the sagittal plane at the level of the optic chiasm were analyzed. Arterioles with a long-axis-to-short-axis ratio <1.3 were chosen as suitable for cross-sectional analysis. The medial and luminal cross-sectional areas were quantitatively analyzed and expressed as the percentage of the α-SMA-positive arteriolar wall relative to the entire circumferential area of the arteriole, which was determined from the sections that were immunostained for α-SMA, using Image J software. With the use of light microscopy and a × 400 magnification, the average wall thickness for each rat was derived as the arithmetic mean of the results for eight arterioles.
Total RNA from the renal cortex and outer medulla was extracted using ISOGEN (Nippon Gene, Tokyo, Japan) according to the manufacturer's protocol. Two micrograms of total RNA was used as a template for cDNA synthesis. Complementary DNA was synthesized using SuperScript III First-Strand Synthesis SuperMix (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's protocol. An aliquot of synthesized cDNA was used as a template for quantitative PCR, using an Applied Biosystems StepOnePlus (Life Technologies Co, Carlsbad, CA, USA). The target cDNAs were amplified by specific primers, using the SYBR Premix Ex Taq solution (Takara Bio, Otsu, Japan) (TGF-β1: forward: 5′-TGCGCCTGCAGAGATTCAAG-3′, reverse: 5′-AGGTAACGCCAGGAATTGTTGCTA-3′; osteopontin: forward: 5′-TCCTGCGGCAAGCATTCTC-3′, reverse: 5′-CTGCCAAACTCAGCCACTTTCA-3′; MCP-1: forward: 5′-CTATGCAGGTCTCTGTCACGCTTC-3′, reverse: 5′-CAGCCGACTCATTGGGATCA-3′; glyceraldehyde-3-phosphate dehydrogenase (GAPDH): forward: 5′-GGCACAGTCAAGGCTGAGAATG-3′, reverse: 5′-ATGGTGGTGAAGACGCCAGTA-3′). The relative levels of mRNA expression were normalized against the level of GAPDH mRNA expression.
To further evaluate the effects of blood pressure on the small vessels in the brain, we followed the survival rate of salt-loaded SHR-SP rats for up to 5 weeks. This protocol is the same as Protocol 2, except that the rats were immediately euthanized and their organs harvested if a stroke event (seizure, palsy) was observed. Once strokes were observed in all rats in the control group, all rats in the nifedipine group were euthanized, and their organs were harvested.
The data are presented as the mean±s.e.m. Inter-group comparisons of SBP and Ualb measurements taken over the study period were analyzed by repeated-measures ANOVA and the Holm-Sidak post-hoc test. All other data analyses were performed using the Bonferroni/Dunn test for multiple comparisons, following a one-way analysis of variance. All analyses were performed using the raw data. A P-value of <0.05 was considered statistically significant.
Heterogeneity existed among the rats in their daily Ualb concentrations. Thus, we divided up them according to their Ualb concentrations (cutoff level: Ualb=5 mg per day), into a high-excretion group (HIGH: Ualb=21.1±3.6 mg per day, n=8) and a low-excretion group (LOW: Ualb=1.2±0.6 mg per day, n=8). We compared the physiological and histological parameters of the two groups, as shown below. As shown in Table 1, the mean body weights and the mean heart and kidney masses were not different between the groups. No differences were observed in the 24-h urine volume produced or in the amount of food and water consumed between the groups (data are not shown).
We separately analyzed the arterioles of the brain cortex and medulla. As shown in Figures 1a and b, the wall thicknesses of the arterioles in the brain medulla were considerably thicker in the HIGH group than in the LOW group (82.5±4.3% vs. 62.8±4.2%, P<0.05). By comparison, the wall thicknesseses of the arterioles in the brain cortex were not significantly different between the two groups (65.5±5.6% vs. 56.0±3.8%, P<0.05). We also assessed the arterioles of the renal juxtamedullary region and found that the arteriolar thickness was considerably greater in the HIGH group than in the LOW group (86±0.5% vs. 82±0.5%, P<0.05, Figure 1c). These results indicate that albuminuria is associated not only with pre-glomerular arteriolar injury but also with cerebrovascular arteriolar injury.
We hypothesized that albuminuria is a marker of juxtamedullary nephron injury. We separately analyzed the glomeruli of the outer cortical and juxtamedullary nephrons. As shown in Figure 2a, the glomerular sclerosis index scores showed an increased level of glomerulosclerosis in the juxtamedullary glomeruli of the HIGH group compared with the LOW group (1.4±0.1 vs. 0.9±0.2, P<0.05). In contrast, the degree of glomerulosclerosis in the outer cortical glomeruli did not differ significantly between the groups (0.9±0.2 vs. 0.6±0.2, NS). Overall, the level of glomerulosclerosis was significantly higher in the juxtamedullary glomeruli than in the outer cortical glomeruli of the HIGH group, while no significant differences were observed in the LOW group. To determine whether albuminuria is associated with juxtaglomerular injury, the tissue slides were immunostained with desmin antibodies. As shown in Figure 2f, desmin immunostaining was enhanced in the region of the juxtamedullary nephrons compared with the outer cortical nephrons, indicating that podocyte injury is taking place in the juxtamedullary glomeruli.
To determine the localization of interstitial injury, the expression of α-SMA in the outer renal medulla and cortical region was analyzed. As shown in Figure 2b, the expression of α-SMA was significantly higher in the outer medullary interstitium of the HIGH group than in the LOW group (8.3±1.5% vs. 4.5±1.5%, P<0.05). However, no significant difference existed between the groups in their outer cortical interstitial α-SMA expression (1.7±0.4% vs. 1.0±0.1%, NS), indicating that albuminuria is associated with juxtamedullary nephron injury.
As shown in Figure 2c, the percentage of TGF-β-positive tubules, most prominent in the thick ascending limb and proximal straight tubules of the juxtamedullary region, was significantly higher in the HIGH group than in the LOW group (30.5±2.6% vs. 22.1±1.6%, P<0.05). The percentage of MCP-1-positive tubules (Figure 2d), most prominent in the proximal straight tubules of the juxtamedullary region, was also significantly higher in the HIGH group than in the LOW group (39.8±5.1% vs. 22.3±1.3%, P<0.05). The number of ED-1-positive cells, infiltrating cells of the interstitium, in the juxtamedullary region (excluding the glomerular tuft, Figure 2e), was significantly greater in the HIGH group compared with the LOW group (15.4±2.4 per field vs. 8.9±0.7 per field, P<0.05).
To determine whether elevated blood pressures are responsible for the juxtamedullary nephron injury in SHR-SP rats, the blood pressures were reduced by administering nifedipine, an L-type Ca2+-channel blocker. Because the timing of albuminuria onset was heterogeneous between the rats in Protocol 1, the animals were fed a high-salt diet over a shortened period time to achieve a uniform increase in albuminuria among the animals. As shown in Figure 3a, the nifedipine-treated rats maintained significantly decreased SBPs throughout the experimental period (235±4 vs. 191±2, 221±10 vs. 166±6 and 240±9 vs. 190±3 mmHg on days 6, 15 and 20, respectively, all P<0.05). The mean Ualb for the nifedipine-treated rats was significantly reduced compared with the control rats (0.4±0.01 vs. 10.4±3.8, 0.4±0.03 vs. 46.5±6.1 mg per day at 1 and 2 weeks, P<0.05 and P<0.01, respectively, Figure 3b). We measured the mRNA levels of inflammatory markers related in the outer renal medulla by the quantitative reverse transcription-PCR method. The nifedipine-treated rats demonstrated significantly decreased mRNA levels of inflammatory markers, cytokines and markers of tubular injury, such as osteopontin, MCP-1 and TGF-β, respectively. As shown in Figure 4, the nifedipine group showed reduced levels of mRNA expression for osteopontin, MCP-1, and TGF-β, all of which co-localized to the tubules in the outer medulla, indicating the involvement of not only the glomeruli but also the tubules of the juxtamedullary nephrons. This occurred because a large portion of the tubules in the outer medulla are from the juxtamedullary nephrons, which was demonstrated in Protocol 1. No major vascular injuries in the brain were observed in either group (data are not shown).
As shown in Figure 5, desmin immunostaining is enhanced in the juxtamedullary nephrons compared with the outer cortical nephrons. This enhancement of desmin immunostaining is attenuated in response to nifedipine treatment, indicating that the reduction of blood pressure is effective in preventing podocyte injury in the juxtamedullary glomeruli.
To better delineate the role of the pre-glomerular arterioles, the wall thickness of the juxtamedullary and outer cortical arterioles was determined. As shown in Figure 6, the mean wall thickness of the pre-glomerular juxtamedullary arterioles was greater than that of the outer cortical arterioles. However, nifedipine reduced the mean juxtamedullary arteriolar wall thickness, indicating that the wall thickness is dependent on blood pressure.
To determine whether blood pressure is responsible for cerebrovascular events, the incidence of stroke events was determined. Figure 7 shows the 35-day, event-free survival curves. The survival analysis showed that the nifedipine group had 35 days of event-free survival, while all of those in the control group suffered an event within the same 35 days (log-rank test, 15.1; P<0.01).
The results of this study indicate that albuminuria is associated with glomerular injury, pre-glomerular vascular injury and inflammation of the juxtamedullary nephrons in SHR-SP rats. Lowering the blood pressure in susceptible animals with the L-type Ca2+ antagonist nifedipine inhibited albuminuria and the other indications of glomerular and arteriolar injury. Juxtamedullary nephron injury and albuminuria were associated with injury to the perforating arteries in the cerebral medulla and the incidence of stroke events. To our knowledge, this is the first evidence demonstrating the relationship between albuminuria and juxtamedullary nephron and cerebrovascular injury. We have also demonstrated that the incidence and extent of these injuries was attenuated by using nifedipine to lower the blood pressure, indicating the potential role of blood pressure in explaining the cerebrovascular-renal connection.
The juxtamedullary nephrons extend deep into the renal medulla and branch off either directly from an arcuate artery or from the basal portion of an interlobular artery. Because of the anatomical configuration of the urinary system, the afferent arteriole of a juxtamedullary nephron is exposed to high blood pressures. Glomerular capillary pressure is normally maintained at a constant of approximately 50 mmHg in both the outer-cortical and juxtamedullary glomeruli.20 The pre-glomerular vessels, and especially the afferent arterioles, are responsible for regulating the glomerular capillary pressure. The outer-cortical glomeruli can reduce the effective blood pressure from approximately 90 mmHg in the arcuate artery to 50 mmHg, over a relatively long distance. By comparison, the juxtamedullary nephron must accomplish this reduction in blood pressure over a much shorter distance. Consequently, the afferent arteriole of the juxtamedullary artery is susceptible to chronic strain from exposure to high pressures and is sensitive to early elevations in blood pressure.
In fact, tissue injury is most obvious in the juxtamedullary region and the outer medulla in spontaneously hypertensive rats (SHR), Dahl salt-sensitive hypertensive rats, renovascular hypertension and Ang II-induced hypertension.15, 16, 23, 24 In addition, it has been shown in SHR rats that glomerular lesions first appear predominantly in the juxtamedullary nephrons and then later extend to involve the more superficial nephrons.23 This is consistent with the present study's findings of juxtamedullary nephron injury in the absence of any significant injury in the outer cortex. Albuminuria was associated with juxtamedullary nephron injury but not cortical nephron injury, indicating that albumin excretion is predominantly occurring in injured juxtamedullary nephrons.
The wall thickness of the pre-glomerular arteriole of the juxtamedullary nephron is increased when albuminuria is present. In addition, increased wall thickness of the pre-glomerular arteriole is observed in the juxtamedullary nephron without comparable increases in arteriolar wall thickness in the outer cortical nephron. Reducing the blood pressure with nifedipine reduced the wall thickness of these arterioles. Kimura et al.25 have demonstrated that the afferent arteriole is constricted and the efferent arteriole is dilated in SHR rats, while glomerular sclerosis is obvious in the juxtamedullary nephron. Our study corroborates these histological findings. Similar to nifedipine in the present study, treatment with captopril or trichlormethiazide plus hydralazine reduced glomerular sclerosis and resulted in the dilatation of the afferent arteriole and constriction of the efferent arteriole. Taken together, the pre- and post-glomerular arterioles have an important role in the development of glomerular sclerosis.
Our previous studies involved the use of a servo-controlled renal perfusion pressure technique in Ang II-infused hypertensive rats and demonstrated that Ang II-dependent renal injury occurred mostly in the outer-cortical glomeruli; by comparison, high blood pressure-mediated injury occurred primarily in the juxtamedullary glomeruli.16 Interestingly, when this technique was applied to Dahl salt-sensitive rats, which are known to have a lesser capacity to regulate glomerular capillary pressure, they had higher levels of proteinuria after a trial of salt-induced hypertension, and the incidence of glomerular injury depended primarily on the increase in blood pressure, even in the outer cortical glomeruli. These results indicate that the pre-glomerular vessels are mostly responsible for regulating the glomerular capillary pressure and limiting the damage from continuous exposure to high blood pressures. To determine whether the renin–angiotensin system and/or blood pressure is responsible for the relationship between albuminuria and strain vessel injury, the servo-control technique should be used in future studies with WKY, SHR and SHR-SP rats, both with and without the use of an ARB.
Ihara et al.,18 using 55-week-old diabetic, hypertensive Otsuka Long-Evans Tokushima Fatty rats, demonstrated that using an ARB significantly reduced the levels of proteinuria, compared with hydralazine, in rats who had previously been hypertensive and proteinuric and even though similar reductions in blood pressure were achieved with both the antihypertensive medications. The presence and/or extent of outer cortical glomerular injury was determined by desmin staining, as a marker of podocyte injury, and was reduced by ARB use, while no effect was observed in those animals taking hydralazine. However, the severity of juxtamedullary glomerular injury was not altered with either of the treatments. Why did these antihypertensives fail to prevent juxtamedullary glomerular injury?
When the hydralazine and ARB group of rats were started on the antihypertensive drug, their juxtamedullary glomeruli had already been exposed to high blood pressures, and the animals had already demonstrated significant levels of proteinuria. Concurrently, it was expected that the outer-cortical glomeruli were protected from glomerular hypertension. Because outer cortical glomerular injury is dependent on Ang II, as we observed in a previous study, we hypothesized that ARB administration would protect the outer cortical glomeruli.16 These results from our current study support our previous finding that juxtamedullary injury is mostly blood pressure-dependent. Our current study achieved a reduction in the mean SBP by approximately 30 mmHg, and this degree of reduction succeeded in preventing stroke and renal juxtamedullary injury in the nifedipine-treated animals. These results strengthen the evidence that elevated blood pressure affects arterioles not only in the brain but also in kidney. In other words, blood pressure-lowering therapy protects ‘strain vessels'.
Recent studies have demonstrated that the severity of albuminuria is also dependent on the process of reabsorption in the proximal tubules.26 Two basic mechanisms contribute to Ualb. First, there is an uptake of any filtered albumin from the luminal side of the proximal tubule and reabsorption into the surrounding network of peritubular capillaries.11 Second, a relatively small amount of albumin is excreted in the urine as a result of peptide metabolism.11 In the present study, the renal tubules in the outer medulla, including the proximal straight tubules, were injured in the rats with frank albuminuria. This is because the medullary circulation is derived from the efferent arteriole of the juxtamedullary nephron. The relevant mechanisms can be identified by detecting the expression of tubular-injury markers, such as 𝒩-acetyl-beta-𝒟-glucosaminidase, beta-2 microglobulin or megalin, which has a key role in the reabsorption of albumin in the proximal tubules.11 This was not the focus of the present study, however, and further studies are required. It has been shown that an increase in the renal perfusion pressure increases the renal medullary blood flow, which in turn, increases the renal medullary and cortical interstitial hydrostatic pressures and the peritubular capillary pressure, which together may inhibit Na reabsorption in the proximal tubules.27, 28 This mechanism of pressure natriuresis may be impaired when albuminuria is present.
The findings from the present study indicate that albuminuria is the result of juxtamedullary injury. The number of juxtamedullary nephrons is <10% the number of cortical nephrons, which supports the findings that albuminuria is limited to a very small amount in the early phase of hypertensive renal injury. However we must acknowledge the possibility that the sclerotic juxtamedullary glomeruli are not the source of albuminuria but rather intact outer cortical glomeruli with increased filtration.
We sought to delineate the mechanism of strain vessel injury, which occurs through a cytokine-mediated inflammatory process. An increase in the renal perfusion pressure has been shown to increase inflammation, which is indicated by the increased number of ED-1-positive cells and greater α-SMA immunostaining on immunohistochemistry.29, 30 Although a large portion of its renoprotective effects are attributed to lower blood pressures, nifedipine may function directly as an antioxidant and anti-inflammatory agent.31, 32 The potentially pleiotropic effects of nifedipine is a limitation of the present study and its mechanism of action in mitigating renal injury requires further study in the future. Because bardoxolone, which is a first-in-class drug being touted as an antioxidant inflammation modulator, has been shown to exert a renoprotective effect, it is possible that nifedipine reduced juxtamedullary injury not only by reducing the blood pressure, but also by exerting an anti-inflammatory effect.33
In conclusion, the results of this study indicate that albuminuria is a marker for juxtamedullary nephron and pre-glomerular injury in SHR-SP rats. Albuminuria and renal injury were also associated with cerebrovascular injury and the risk for stroke events. The pressure-induced injury of strain vessels may explain the cerebrovascular-renal connection.
This study was supported by the Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan (Nos. 21390259 and 20590970). In addition, we thank Kiyomi Kisu and Hiroko Ito for their expert technical assistance.
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Keywords: albuminuria, brain, renal juxtamedullary nephron, SHR-SP, strain vessel.
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