Carbonyl stress induces hypertension and cardio-renal vascular injury in Dahl salt-sensitive rats.

One major precursor of carbonyl stress, methylglyoxal (MG), is elevated in the plasma of chronic kidney disease (CKD) patients, and this precursor contributes to the progression of vascular injury, hypertension and renal injury in diabetic nephropathy patients. This molecule induces salt-sensitive hypertension via a reactive oxygen species-mediated pathway. We examined the role of MG in the pathogenesis of hypertension and cardio-renal injury in Dahl salt-sensitive (Dahl S) rats, which is a rat model of CKD. Nine-week-old Dahl S rats were fed a 1% NaCl diet, and 1% MG was added to their drinking water for up to 12 weeks. Blood pressure and cardio-renal injuries were compared with rats treated with tap water alone. The angiotensin II receptor blocker (ARB), candesartan (10 mg kg(-1) day(-1)), was administered to MG Dahl S rats to determine the impact of this drug on the pathogenesis of MG-induced CKD. A progressive increase in systolic blood pressure was observed (123±1-148±5 mm Hg) after 12 weeks of MG administration. MG administration significantly increased urinary albumin excretion, glomerular sclerosis, tubular injury, myocardial collagen content and cardiac perivascular fibrosis. MG also enhanced the renal expression of Nɛ-carboxyethyl-lysine (an advanced glycation end product), 8-hydroxydeoxyguanosine (a marker of oxidative stress), macrophage (ED-1) positive cells (a marker of inflammation) and nicotinamide adenine dinucleotide phosphate (NAD(P)H) oxidase activity. Candesartan treatment for 4 weeks significantly reduced these parameters. These results suggest that MG-induced hypertension and cardio-renal injury and increased inflammation and carbonyl and oxidative stress, which were partially preventable by an ARB.

Introduction

Methylglyoxal (MG) is a highly reactive alpha-dicarbonyl compound that is biosynthesized by the glycolysis pathway. MG modifies the lysine and arginine residues of proteins, including radical scavengers,[1] and it is a potent precursor of advanced glycation end products (AGEs).[2] Plasma MG levels are increased in diabetes patients and in patients with chronic kidney disease (CKD).[3] Therefore, MG and its protein adducts have been implicated in the development of chronic diabetes complications, such as retinopathy and nephropathy, and uremia, which are referred to as carbonyl stress.[2]

We recently demonstrated that increased plasma levels of the carbonyl compound, MG, are associated with vascular and renal complications.[4] MG levels correlated with increases in the intima-media thickness of the carotid artery, systolic blood pressure (SBP), albumin-to-creatinine ratio, pulse-wave velocity and reductions in estimated glomerular filtration rate over a 5-year period. Interestingly, MG was an independent risk factor for intima-media thickness, SBP and pulse-wave velocity after 5 years.

MG reacted with reactive oxygen species, such as hydrogen peroxide (H2O2) in an in vitro study using electron spin resonance, which further exacerbated oxidative stress.[2] We have demonstrated that oral MG administration to Sprague–Dawley (SD) rats induces salt sensitivity and insulin resistance concomitant with enhanced oxidative/carbonyl stress.[5] These features are commonly observed in CKD.[6] Therefore, we hypothesized that MG induces hypertension and vascular injury in the presence of oxidative stress, which results in cardio–renal injury in CKD.

MG was orally administered to Dahl salt-sensitive (Dahl S) rats with a low-salt diet for 4–8 weeks to investigate our hypothesis, and blood pressure and cardio–renal injury were analyzed. The Dahl S rat is an experimental model of salt-sensitive hypertension and progressive kidney disease, a disease progression that is observed in African Americans.[7] Renal oxidative stressors, including superoxide and H2O2, are enhanced in Dahl S rats even without a high-salt diet, and these stressors have a pivotal role in the impaired regulation of blood pressure.[8, 9] Plasma renin activity is reduced in the Dahl S model, but the local renin–angiotensin system- and angiotensin II-induced oxidative stressors are enhanced.[10, 11] Therefore, the cardio–renal benefits of an angiotensin II receptor blocker (ARB), candesartan, was evaluated to determine the role of angiotensin II-mediated oxidative stress and the interaction with MG.

Methods

Animals

Nine-week-old male Dahl S rats (Dahl S/Jr Sea, Kyudo, Yoshitomi, Japan) were housed in a temperature- and humidity-controlled room on a 12-h light–dark cycle. The rats were fed with standard 0.5% NaCl rat chow (MR stock, Nihon Nosan, Yokohama, Japan). All procedures were performed in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals, and the animal committee of Tohoku University approved all protocols.

Protocol 1: role of MG in blood pressure, renal injury and myocardial fibrosis

This study used 9-week-old Dahl S rats to examine the effects of MG on hypertension and cardio–renal injury in a model of CKD. Dahl S rats at this age exhibit increased oxidative stress compared with age-matched salt-resistant rats.[8] The rats received either 1% MG in tap water (MG-12W group, n=9) or tap water alone (control group, n=8) for 12 weeks. This oral dose of MG produced plasma levels approximately 10 times higher than the control, which is equivalent to the difference between normal subjects and stage 5 CKD patients. We have used this oral dose of MG in SD rats previously.[5] A preliminary experiment revealed that MG treatment in Dahl S rats decreases food intake for 2–3 days. Therefore, the control group was pair-fed to match the salt intake. SBP was measured every week using a non-invasive tail-cuff blood pressure measurement system (Model MK-2000A, Muromachi, Tokyo, Japan). Blood pressure was monitored in a separate set of rats using a radio-telemetry transmitter (PA-C40 Data Science International, Primetec, Tokyo, Japan) that was implanted in the femoral artery as previously reported.[12] A 24-h urine sample was collected weekly in a metabolic cage, and the samples refrigerated (KN-646, Natume, Tokyo, Japan). Urinary albumin levels were measured using an automatic analyzer (Synchron-CX-3; Beckman Coulter, Fullerton, CA, USA). The rats were anesthetized at the end of the study via intraperitoneal pentobarbital (60 mg kg−1). The right kidneys were removed immediately, weighed, snap frozen in liquid nitrogen and stored at −80 °C for NAD(P)H oxidase assay. The left kidneys were harvested after saline perfusion through the renal artery.

Protocol 2: role of the renin–angiotensin system in MG-mediated hypertension, renal injury and myocardial fibrosis

Age-matched Dahl S rats received 1% MG in tap water (MG-4W group, n=8) or MG plus 10 mg kg−1 day−1 of the ARB, candesartan (Takeda Pharmaceutical, Osaka, Japan), (MG+CAND group, n=12) for 4 weeks. Control rats were pair-fed to ensure equivalent salt intake, as described in protocol 1. SBP, urinary measurements and tissue harvesting were also performed as described in protocol 1.

Histological analysis

Renal and heart tissues were fixed in either 95% ethanol or 10% neutral formalin and embedded in paraffin for histological analysis. Renal sections were stained using the Elastica–Masson method for renal injury and examined under a light microscope. The glomerular sclerosis index was determined by the grading of at least 50 glomeruli per rat, as described previously.[13]

Heart sections were stained with hematoxylin with 0.1% Sirius red F3BA saturated in picric acid.[14] We assessed the total myocardial collagen content (that is, the percentage of Sirius red-stained collagen area to the total myocardial area) in digitalized microscopic images using Image J software.[14] Perivascular adventitial fibrosis was graded as follows: normal (0), mild perivascular fibrosis (1), hypertrophy with fibrosis and some collagen within the media (2) or extensive hypertrophy and perivascular fibrosis with periadventitial mononuclear cell infiltrate (3).[13]

Immunohistochemical staining

The left kidney tissue was immediately fixed with 95% ethanol (for staining osteopontin (OPN) and ED-1 antibody) or 10% formalin (for staining Nɛ-carboxyethyl-lysine (CEL), 8-hydroxydeoxyguanosine (8-OHdG), and receptor for AGEs (RAGE)) and embedded in paraffin. For OPN, CEL and 8-OHdG staining, deparaffinized sections were retrieved by microwaving in 10 mmol l−1 citrate buffer (pH 7.0) for 5 min. Immunohistochemical analysis was performed using antibodies against OPN (diluted 1:100, Santa Cruz Biotechnology, Santa Cruz, CA, USA, sc-10591), ED-1 (diluted 1:100, Serotec, Oxford, UK, MCA341F), CEL (diluted 1:50, TransGenic, Kobe, Japan, KH-025), 8-OHdG (5 μg ml−1, Japan Institute for the Control of Aging, Shizuoka, Japan, MOG-020P) and RAGE (diluted 1:1000, Millipore, Carrigtwohill, Ireland, AB5484) and processed according to previously reported methods.[5] Immunopositive areas were analyzed from 20 randomly captured images using Image J software. The results are expressed as the percentage of positively stained areas, except for ED-1, which is expressed as the number of immunopositive cells per slide.

NAD(P)H oxidase activity

NAD(P)H oxidase-derived superoxide anion generation was analyzed using lucigenin-enhanced chemiluminescence as described previously.[12] The activity of NAD(P)H oxidase is expressed as c.p.m. per 200 mg protein.

Statistical analysis

Data are expressed as means±s.e.m. The data were analyzed using the t-test and two-way analysis of variance for statistical comparisons of the means of all groups. Differences between the two groups were considered significant when P<0.05.

Results

MG induces hypertension and renal injury in Dahl S rats

No significant changes in SBPs were observed in the control group throughout the 12-week experimental period (Figure 1a). However, SBP in the MG-12W group significantly increased from week 2 (P<0.05 vs. week 0 in the MG-12W group) to the end of the experiment, and this increase was significant compared with the control group (P<0.05). Candesartan treatment significantly attenuated the MG-induced increase in SBP (Figure 1b, P<0.05).

Figure 1

Sequential systolic blood pressure (SBP) values measured using the tail-cuff method during the 12-week experimental period in protocol 1 (a); and during the 4-week experimental period in protocol 2 (b). Twenty-four-hour SBP values from the femoral artery measured using a radio-telemetry transmitter system (c). Protocol 1: control (n=8), treatment with tap water; MG-12W (n=9), treatment with 1% methylglyoxal (MG) in drinking water for 12 weeks. Protocol 2: MG-4W (n=8), treatment with 1% MG in drinking water; MG+CAND (n=12), co-treatment with MG and candesartan for 4 weeks. Data are presented as means±s.e. *P<0.05 vs. control group and data of MG-12W at 0 week; †P<0.05 vs. MG+CAND group and data of MG-4W at 0 week. ‡P<0.05 vs. control group.

We monitored blood pressure using radio-telemetry to confirm MG-induced hypertension and determine the diurnal variations in blood pressure. The mean blood pressure was significantly increased in the MG group compared with the control group during the active phase but not the inactive phase (Figure 1c).

Urinary albumin excretion, glomerular sclerosis index and OPN expression were significantly increased in the MG-12W group compared with the control group (Figure 2 and Table 1, P<0.05). We examined treatment with candesartan for 4 weeks in protocol 2 because SBP was increased from week 2 in MG-12W group. Candesartan treatment for 4 weeks decreased urinary albumin excretion, glomerular sclerosis index and OPN expression in the MG+CAND group compared with the MG group (P<0.05).

Figure 2

Twenty-four-hour urinary albumin excretion during the 12-week experimental period in protocol 1 (a), and during the 4-week experimental period in protocol 2 (b). Protocol 1: control (n=8), treatment with tap water; MG-12W (n=9), treatment with 1% methylglyoxal (MG) in drinking water for 12 weeks. Protocol 2: MG-4W (n=8), treatment with 1% MG in drinking water; MG+CAND (n=12), co-treatment with MG and candesartan for 4 weeks. Data are presented as means±s.e. *P<0.05 vs. control or MG+CAND group; †P<0.05 vs. data of MG-12W or MG-4W group at 0 week.

Table 1

Parameters of kidney and heart tissue in protocols 1 and 2

	Protocol 1		Protocol 2
Group	Control	MG-12W	MG-4W	MG+CAND
GSI	1.86±0.06	2.08±0.07*	1.69±0.05	1.35±0.03†
OPN-positive area (% of cortex and outer medulla)	0.50±0.10	1.49±0.12*	1.18±0.28	0.36±0.08†
ED-1 in glomerulus (cells per glomerulus)	0.55±0.09	1.34±0.15*	1.26±0.09	0.97±0.09†
ED-1 in interstitial area (cells per × 400 field)	1.47±0.25	3.37±0.17*	2.15±0.06	1.16±0.13†
CEL-positive area (% of cortex and outer medulla)	2.8±0.5	17.7±5.5*	7.1±0.9	2.8±0.3†
8-OhdG-positive area (% of cortex and outer medulla)	2.91±0.12	4.10±0.22*	2.10±0.25	1.17±0.21†
NADPH oxidase activity (c.p.m. per 200 mg protein)	86±3	121±10*	143±6	124±4†
Total collagen content (%)	3.5±0.3	6.9±0.6*	4.4±0.4	1.4±0.1†
Perivascular fibrosis score	1.8±0.1	2.5±0.2*	1.7±0.1	1.2±0.2†

Abbreviations: CEL, Nɛ-carboxyethyl-lysine; ED-1, macrophage; GSI, glomerular sclerosis index; MG, methylglyoxal; NADPH, nicotinamide adenine dinucleotide phosphate; OPN, osteopontin; 8-OHdG, 8-hydroxydeoxyguanosine.

Protocol 1: control (n=8), tap water; MG-12W (n=9), treatment with 1% MG in drinking water for 12 weeks. Protocol 2: MG-4W (n=8), treatment with 1% MG in drinking water; MG+CAND (n=12), co-treatment with MG and candesartan for 4 weeks. Data are presented as means±s.e. *P<0.01 vs. control group; †P<0.05 vs. MG-4W group.

Role of MG in renal inflammation and carbonyl/oxidative stress in Dahl S rats

The number of ED-1-positive cells in the glomerulus and interstitial areas increased significantly in the MG-12W group compared with the control group (Figure 3 and Table 1, P<0.05). The number of ED-1-positive cells in the glomerulus and interstitial areas decreased significantly in the MG+CAND group compared with the MG-4W group (Figure 3 and Table 1).

Figure 3

Images of glomerular sclerosis stained with the Elastica–Masson method and immunostained with Nɛ-carboxyethyl-lysine (CEL), 8-hydroxydeoxyguanosine (8-OhdG), osteopontin (OPN), ED-1 antibodies (black arrowheads) and receptor for advanced glycation end products (RAGEs) in the kidney (a), and collagen deposition in the myocardial interstitial space and cardiac perivascular fibrosis in the heart (b), in protocol 1 (control and MG-12W groups treated for 12 weeks), and protocol 2 (MG-4W, MG+CAND, and CAND groups treated for 4 weeks).

Strong CEL positivity was observed in the juxtamedullary and outer medullary regions (Figure 3). The percentage of the CEL-positive area was significantly higher in the MG-12W group than the control group (Table 1, P<0.05). MG+CAND treatment significantly reduced the percentage of CEL-positive regions compared with MG alone (P<0.01). A significant increase in 8-OHdG expression was observed in the kidney following MG treatment for 12 weeks (Figure 3 and Table 1). A clear decrease in 8-OHdG expression was observed in the MG+CAND compared with the MG-4W group (P<0.05).

NAD(P)H oxidase activity in kidney tissue increased significantly in the MG-12W group compared with the control group (Table 1, P<0.05). Renal NAD(P)H oxidase activity was reduced significantly in the MG+CAND group compared with the MG group (P<0.01).

RAGE expression was prominent in podocytes, the distal tubules and collecting ducts and some areas of positive CEL and 8-OHdG staining. These results suggest that the AGE–RAGE axis is partially present in MG-induced renal injury (Figure 3).

MG induces cardiovascular injury in Dahl S rats

The total myocardial collagen content and perivascular adventitial fibrosis scores were significantly higher in the MG-12W group compared with the control group, and these factors were significantly lower in the MG+CAND group compared with the MG-4W group (Table 1).

Discussion

This study demonstrated that MG-induced hypertension and cardio–renal injury in a non-diabetic rat CKD model. Cardio–renal tissue damage was partially dependent on the angiotensin II type-1 receptor-mediated pathway, and it was associated with enhanced carbonyl and oxidative stress.

Role of MG in hypertension development

A link between MG accumulation and hypertension has been demonstrated previously in experimental animals.[5, 15, 16] Aortic and renal MG levels increase in spontaneously hypertensive rats compared with Wistar Kyoto rats.[15, 16] SBP significantly increases after the oral administration of MG for 1 week in Wistar Kyoto rats.[17] A diet high in fructose, which is a precursor of MG, induces hypertension and renal injury.[18, 19] This study confirmed that MG-induced hypertension and renal injury in Dahl S rats that were fed a normal diet and further elucidated the underlying mechanisms. Vasdev et al.[17] demonstrated that MG binds to the sulfhydryl groups of vascular Ca2+ channels, which increases cytosolic [Ca2+] and vascular retention and leads to hypertension. We demonstrated that renal oxidative stress is another mechanism for MG-induced hypertension.

Taylor et al.[9] demonstrated that renal medullary H2O2 concentrations are higher in Dahl S rats than salt-resistant (SS13BN) control rats, and H2O2 contributes to hypertension development in Dahl S rats. The reduction of renal medullary oxidative stress by an NAD(P)H oxidase inhibitor, apocynin, reduces salt sensitivity in Dahl S rats.[9] In contrast, the renal medullary interstitial infusion of H2O2 in SS13BN rats induces hypertension.[20] These results indicate that enhanced renal oxidative stress underlies the hypertension development. However, an 8% salt diet does not produce hypertension in SD rats despite enhanced renal oxidative stress,[12] and 1% MG in drinking water does not produce hypertension in SD rats.[5] A high-salt diet in SD rats treated with the same dose of MG surprisingly produces hypertension and enhances renal oxidative stress, which suggests that MG induces salt sensitivity in these rats.[5] These previous results and this study suggest that MG causes hypertension in rats with enhanced renal oxidative stress. This hypothesis explains an oral dose of MG that does not induce hypertension in SD rats produces hypertension in Dahl S rats, which exhibit high renal H2O2 levels even in the absence of a high-salt diet.[20]

MG-induced oxidative stress and inflammation

Several mechanisms may be involved in MG-induced renal oxidative stress. First, this study demonstrated that MG-enhanced renal NAD(P)H oxidase activity. This result is consistent with a previous study that demonstrated an MG-induced increase in NAD(P)H oxidase expression.[21] Second, MG stimulates mitochondrial oxidative stress.[22] Mitochondria and NAD(P)H oxidase are two primary sources of superoxide production in the kidney, in particular the renal medulla.[23] Therefore, these pathways may also be involved in MG-induced enhancement of renal oxidative stress. Third, the MG-induced impairment of glutathione peroxidase (GSH-Px) and glutathione reductase (GSSG-Red)[15] would also increase oxidative stress because GSSG-Red has an important antioxidant defense role by reducing GSSG to GSH. In contrast, GSH-Px scavenges peroxides, which can be converted to very reactive free radicals using GSH as the electron donor.[24] Fourth, RAGE contributes to the pathogenesis of renal injury, and NAD(P)H oxidase is enhanced by the RAGE-mediated pathway.[25] These results are consistent with this study of enhanced renal NAD(P)H oxidase in MG-treated Dahl S rats. However, further investigation is required to determine RAGE pathway-mediated alterations in blood pressure. Fifth, we recently demonstrated that an increase in renal perfusion pressure induces renal oxidative stress.[26] Therefore, we cannot exclude the possibility that enhanced oxidative stress was partially due to MG-mediated hypertension. Finally, MG reacts with H2O2 and induces further reactive oxygen species in vitro.[27] Therefore, the high renal H2O2 levels in Dahl S rats may have interacted with MG to further enhance renal oxidative stress and elevate blood pressure.

The precise mechanism was not determined in this study, but the results suggest that MG-enhanced renal inflammation.[28] Oxidative stress is an initiator of inflammation and vice versa, and MG may have induced an inflammatory reaction via the oxidative stress pathway. We previously demonstrated that reductions in renal perfusion pressure reduces the number of renal ED-1-positive cells in Dahl S rats.[29] Therefore, MG-induced hypertension was partially responsible for the induction of the inflammatory changes in this study.

MG induces hypertension and renal injury through the renin–angiotensin system

Angiotensin II produces renal oxidative stress via NAD(P)H oxidase.[30] Angiotensin II-induced oxidative stress is enhanced in Dahl S rats compared with control salt-resistant SS13BN rats, and it is responsible for blood pressure control. Fructose, which is a precursor of carbonyl stress, induces hypertension and insulin resistance, which is inhibited by losartan treatment.[18] These results suggest that the renin–angiotensin system is responsible for carbonyl stress-induced hypertension and insulin resistance.[5] The ARB, candesartan, reduced MG-induced renal injury and AGE accumulation in this study. This result is consistent with previous reports that candesartan reduces renal AGE accumulation in diabetic mice.[31] The superoxide response to angiotensin II is enhanced in tissues that are isolated from the renal outer medulla of Dahl S rats compared with SS-13BN rats.[32] These studies suggest that oxidative stress contributes to the salt sensitivity of Dahl S rats, which is partially mediated through the renin–angiotensin system. The activation of angiotensin II type-1 receptors stimulates the generation of superoxide by NAD(P)H oxidase.[30] In addition, MG increases angiotensinogen.[23] However, a 4-week candesartan treatment did not significantly alter plasma MG levels, despite the reduction in AGE accumulation (data not shown). The results of this study suggest that MG-enhanced NAD(P)H oxidase activity via an angiotensin II-mediated pathway, which enhanced renal oxidative stress and induced hypertension and renal injury.

Role of MG in myocardial fibrosis

MG also induced myocardial and perivascular fibrosis in Dahl S rats. Candesartan treatment improved the MG-induced myocardial and perivascular fibrosis that was associated with the decrease in blood pressure. These results suggest that MG-induced hypertension produced myocardial and perivascular fibrosis via a RAS-mediated pathway. However, further investigation is required to determine whether the fibrosis was mediated via the blood pressure or the direct action of MG. This study also provides evidence that MG-induced carbonyl stress in CKD contributed to cardio–renal injury.

This study suffers one notable limitation. We assessed the maximum blood pressure response and used the highest possible concentration of MG because of the limited sensitivity in the detection of hypertension. We selected 1% MG because this dose is the highest dosage that has been used in previous rat studies.[5] However, 4 weeks of 1% MG treatment in the drinking water increased plasma MG levels in Dahl S rats <10-fold compared with control rats in this study (3367±307 nmol l−1, n=8 vs. 253±5 nmol l−1, n=6). Plasma MG levels were assayed using derivatization with o-phenylenediamine and electrospray ionization liquid chromatography-mass spectrometry of the resulting quinoxalines, as reported previously.[4] The increase in rat serum MG levels was equivalent to the increase in patients with stage 5 CKD compared with healthy controls.[3] Blood pressure responses to this dose of MG in this study were within physiological limits because the response was completely inhibited with candesartan. We could not determine whether the effects of MG on hypertension were dose dependent because of the technical limitations of measurements and the control of plasma and/or tissue concentration of MG.

The kidney injury and oxidative stress levels in the Dahl S rat model of CKD are affected by a high-salt diet and aging.[8, 33] Our results showed that the absolute value of 24-h urinary albumin excretion was higher (but no significantly) in 21-week-old control rats in protocol 1 than 13-week-old MG-4W rats in protocol 2 (Figure 2), which is consistent with previous studies. Therefore, the reasons that the glomerular sclerosis index and 8-OHdG-positive areas in the controls in protocol 1 were greater than the MG-4W in protocol 2 may include the older age of the rats in protocol 1 than protocol 2, despite MG administration.

Perspectives

Carbonyl stress contributes to the pathogenesis of CKD and cardiovascular disease, and it is concomitant with salt-sensitive hypertension and insulin resistance. Enhanced oxidative stress and inflammatory markers are often observed in CKD patients, and ARB can reduce these factors, which is consistent with this study. Therefore, carbonyl compounds, such as MG, may be a target for the treatment of CKD and cardiovascular disease and a marker of disease pathogenesis.