Role of Angiotensin-(1-7) on Renal Hypertrophy in Streptozotocin-Induced Diabetes Mellitus

Participation of angiotensin II in chronic kidney diseases including diabetic nephropathy (DN) has been extensively described. Similarly, several studies support a protective role for angiotensin-(1-7). However, other studies suggest that some of the cellular effects of angiotensin-(1-7) may be deleterious. The objective of this study was to determine the role of exogenous angiotensin-(1-7) on renal hypertrophy development in rats with streptozotocin-induced diabetes. A control group and three groups of rats with streptozotocin-induced diabetes: untreated diabetic rats, diabetic rats treated with captopril, and diabetic rats treated with angiotensin-(1-7), were studied. After two weeks of treatment, the kidneys were removed under anesthesia with pentobarbital. The kidneys were weighed and the renal cortex was separated for analysis of AT1R, TGF-β1, MASR, and ACE2 expression by western blot. Rats in the three groups with diabetes had hyperglycemia, increased food and water consumption, and higher urinary volume than control rats. Treatment with captopril or angiotensin-(1-7) reversed streptozotocin-induced renal hypertrophy, measured by kidney weight, protein/DNA ratio in renal cortex, glomerular area, or proximal tubular cells area, proteinuria, and creatinine clearance reduction. AT1R, TGF-β1, and MAS receptor expression in renal cortex of diabetic rats increased significantly as compared to controls (p < 0.05); treatment with captopril or angiotensin-(1-7) reversed such increments. ACE2 in the renal cortex decreased in diabetic rats, but it was increased after treatment with captopril or angiotensin-(1-7). These findings suggest that exogenous administration of angiotensin-(1-7) may be renoprotective in early stages of diabetes mellitus. How to cite this paper: Amato, D., NúñezOrtiz, A.R., del Carmen Benítez-Flores, J., Segura-Cobos, D., López-Sánchez, P. and Vázquez-Cruz, B. (2016) Role of Angiotensin-(1-7) on Renal Hypertrophy in Streptozotocin-Induced Diabetes Mellitus. Pharmacology & Pharmacy, 7, 379-395. http://dx.doi.org/10.4236/pp.2016.79046 Received: August 8, 2016 Accepted: September 23, 2016 Published: September 26, 2016 Copyright © 2016 by authors and Scientific Research Publishing Inc. This work is licensed under the Creative Commons Attribution International License (CC BY 4.0). http://creativecommons.org/licenses/by/4.0/ Open Access


Introduction
The pathophysiological mechanisms related to diabetic nephropathy (DN) development are complex [1] [2]. Initial manifestations of renal injury are hypertrophy and glomerular hyperfiltration [3] [4]. Glomerular hemodynamic dysfunction and the process of kidney growth are interwoven [4] [5]. Early growth of the diabetic kidney depends on the proximal tubule. DNA synthesis is increased in the proximal tubular cells, peaking at day two. Hyperplasia and hypertrophy contribute to kidney enlargement [6]. This is in agreement with in vitro studies reporting that high glucose concentration stimulates proliferation of glomerular mesangial cells, associated initially with increased expression of the early genes c-myc and egr-1, and later to an antiproliferative phase, attributed to the bio-activation of transforming growth factor-β 1 (TGF-β 1 ) [7] [8]. Solute reabsorption increases as a result of proximal tubular cells growth, generating hemodynamic changes such as increased renal plasma flow and glomerular capillary hypertension, due to reduction of pre-glomerular resistance relative to post-glomerular resistance, with consequent hyperfiltration [5] [9], which in turn generates renal injury [10] [11]. Considerable evidence suggests that the renal renin-angiotensin system (RAS) plays an important role in the pathogenesis of DN [12]. Experimental and clinical studies using angiotensin-converting enzyme (ACE) inhibitors and Ang II subtype 1 receptor (AT 1 R) blockers diminish proteinuria and retard progressive glomerulosclerosis [13]- [15]. Ang II promotes systemic and intra-glomerular hypertension, and the aforementioned hypertrophic changes [16]. Ang II also increases TGF-β 1 expression, which in turn mediates mesangial, glomerular, and tubular epithelial cells hypertrophy [17], increases plasminogen activator inhibitor-1 synthesis, resulting in decreased matrix degradation, and inhibits the activity of mesangial cells collagenase [18] [19]. By activating NADPH oxidase, Ang II increases reactive oxygen species (ROS) renal production. ROS may act as signaling molecules and activate protein kinase C with the subsequent activation of mitogen-activated kinases (MAPKs). Redoxdependent activation of Akt/PKB and ERK1/ERK2 contributes to the stimulation of protein synthesis, which is crucial in renal hypertrophy [20].

Animals and Treatment
In the present study, we used the well-established STZ-induced diabetes model. STZ destroys the pancreatic beta cells causing a state of insulin dependent diabetes. Male Wistar rats were obtained from the rat colony of the Facultad de Estudios Superiores Iztacala. Animals aged 10 weeks, with initial body weight of 250 ± 20 g were studied. Rats had free access to standard rat chow (Rodent Laboratory Chow 5001, Ralston Purina, Richmond Indiana, USA) and tap water, with 12 -12 h light-dark cycles throughout the experiment. Diabetes was induced by a single STZ intraperitoneal (ip) injection (65 mg/kg of body weight) in 10 mM sodium citrate buffer, pH 4.5. Control (C) rats received vehicle (10 mM sodium citrate buffer, pH 4.5) alone. Forty-eight hours after STZ injection, blood glucose concentration was determined in tail vein blood samples using a reflectance meter (One Touch; LifeScan, Milpitas, CA, USA). Only animals with blood glucose levels >300 mg/dL were included in the study. Diabetic rats were randomized into three groups: 1) untreated diabetic rats (DM) receiving vehicle (saline solution), 2) diabetic rats treated with captopril, 10 mg/kg, po (DM + CAP), and 3) diabetic rats treated with Ang-(1-7), 100 µg/kg, ip [DM + Ang-(1-7)]. Once hyperglycemia with serum glucose levels ≥ 300 mg/dl was confirmed, treatment with captopril or Ang-(1-7) was given daily during the 2 weeks of the experiment. Each group consisted of five animals. Two days before STZ injection and two days before the end of the experiment, the animals were placed in metabolic cages to measure food and water consumption, urinary volume, and to obtain urine samples to measure proteins and creatinine.
At the end of the study, the rats were anesthetized with sodium pentobarbital (45 mg/kg, ip). Blood samples were obtained to measure blood glucose and creatinine levels. Both kidneys were quickly removed. The left kidney was decapsulated, weighted, and dissected into cortex and medulla for total DNA and protein extraction, and immunoblot analysis. The right kidney was cannulated, and fixed with 4% formaldehyde. Animal care and procedures were performed in compliance with the Mexican Federal Regulations for Animals Investigation and Care (NOM-062 ZOO-1969, Ministry of Agriculture, Mexico), on care and use of laboratory animals, and the National Institutes of Health guide for the care and use of Laboratory animals (NIH Publications No. 8023, revised 1978). The protocol was approved by the institutional ethics review board.

Measurement of Renal Hypertrophy
Kidney weight/rat body weight ratio was used as a kidney hypertrophy index. The for-maldehyde fixed right kidneys were dehydrated through ethanol graded series, embedded in paraffin, sectioned in 4 µm thick slices, mounted on glass slides and stained with hematoxylin-eosin (HE) and periodic acid-Schiff (PAS). Glomeruli and proximal tubular cells were visualized using an optic microscope and the areas were measured using a computer program (Motic Images Plus 2.0 ML, Richmond, British Columbia, Canada). For glomerular area, 50 consecutive glomeruli per rat were analyzed with 10× magnification. For proximal tubular cells area, 100 cells per field at 40× magnification were counted, and 10 fields per slide were analyzed and averaged. Finally, total DNA and protein from cortex tissue was extracted and quantified by Trizol reagent method (Invitrogen, Grand Island, New York, USA), and the protein/DNA ratio was calculated as an index of relative hypertrophy.

Analytical Methods
A 24 h urine sample was collected placing the animals in metabolic cages. Samples were immediately frozen and stored at −80˚C to measure proteins and creatinine. Protein concentration in urine was measured by the Bradford method (Bio-Rad), we used bovine serum albumin (BSA) (Sigma Chemical Co.) as standard, and creatinine was measured with Cayman reagents (Cayman Chemical, Ann Arbor, Michigan, USA). The protein/creatinine urinary excretion ratio was calculated.

Western Blotting
Renal tissue was homogenized in 100 mM Tris (hydroxymethyl-aminomethane-trishydrochloride, Sigma, St Louis, MO, USA), pH 7.4, incubated with a protease-inhibitor cocktail (Mini Complete EDTA-free protease inhibitor cocktail, Roche, Germany) and centrifuged at 10,000 g for ten min to remove insoluble debris. The protein concentration of the supernatant was quantified using the Bradford method. 50 µg of protein were loaded into a 10 % SDS-PAGE mini-gel under reducing conditions and transferred to polyvinylidene fluoride (PVDF) membranes (Amersham Hybond-ECL, GE Health Care, Buckinghamshire, UK). The membranes were blocked with 5% nonfat milk in Tris buffered saline (pH 7.6) containing 0.05% Tween 20 (TBST) for two hours at room temperature. Membranes were incubated for 16 h at 4˚C with a 1:400 dilution of a rabbit polyclonal antibody to AT 1 R, TGF-β 1 , ACE2 (Santa Cruz Biotechnology Inc., Santa Cruz, California, USA) and MASR respectively (Novus Biological, Littleton CO, USA). After incubation with the primary antibody, the membranes were washed with TBST buffer and incubated with a 1:1000 dilution of horseradish-peroxidase-labeled goat anti rabbit IgG secondary antibody (Zymed, Invitrogen, Grand Island, New York, USA) at room temperature for 2 hours. Visualization was performed with an enhanced chemiluminiscence (ECL) western blotting kit (Luminol, Santa Cruz Biotechnology Inc., Santa Cruz, California, USA). The obtained films were scanned and digitalized using a flatbed scanner. Band intensity was measured by computer analysis using Multi Gauge, Fuji Film Science, Lab2003 (Fuji Photo Film Co., LTD). All membranes were stripped, re-blocked and incubated with goat β-actin antibody (Santa Cruz Biotechnol-ogy Inc., Santa Cruz, California, USA) used as housekeeping protein with the same protocol.

Statistical Analysis
All values are presented as mean ± SEM, and compared by ANOVA followed by Newman-Keuls test. Differences were considered statistically significant with p values ≤0.05. Table 1 shows whole animal data for C, DM, DM+CAP, and DM+Ang-(1-7) rats: glycemia, body weight, consumption of food and water and urinary volume. All STZ-induced diabetic rat groups had significant hyperglycemia (plasma glucose: DM, 450 ± 17.6 mg/dLvs control 115 ± 4.03 mg/dL, p < 0.05) at the time of experiment. In DM+ Ang-(1-7) and DM+CAP groups, glycemia did not differ from the DM group. Body weight was lower than that of the control group. Conversely, food and water consumption, and urinary volume were markedly increased in the 3 groups of diabetic animals.

Immunobloting
AT 1 R, TGF-β 1 , ACE2, and MASR protein expression in renal cortex homogenates were determined by western blot analysis and standardized with β-actin. AT 1 R protein expression in renal cortex of diabetic rats increased significantly as compared to control group; treatment with captopril or Ang-(1-7) reversed AT 1 R protein expression increment, but only treatment with Ang-(1-7) showed significant differences from that of diabetic rats (Figure 5(a)). Levels of TGF-β 1 protein expression in the renal cortex of diabetic rats increased three-fold as compared to the control group. Treatments with Ang-(1-7) and captopril reversed this effect. Ang-(1-7) treatment reduced TGF-β 1 protein expression to control values ( Figure 5(b)). MAS receptor protein expression in renal cortex from diabetic rats was higher than that of the control group; treatment with captopril or Ang-(1-7) reversed this increment. Both treatments reduced MASR expression in renal cortex of diabetic rats, as compared to control group. This latter effect was more notorious in the DM+Ang-(1-7) group ( Figure 6(a)). Finally, ACE2 protein expression in the renal cortex of control rats was not different from that of diabetic rats. Captopril increased ACE2 protein expression in the renal cortex. However, Ang-(1-7) did not modify the expression of the enzyme (Figure 6(b)).

Discussion
The earlier manifestations of renal injury produced by DM are structural changes consisting of tubuloepithelial and glomerular hypertrophy, followed by thickening of glomerular and tubular basement membranes and progressive accumulation of extracellular matrix proteins in the mesangium and interstitium. The structural changes start before any other measurable clinical changes are detectable (1-3). Among many factors reported to be involved in early diabetes renal hypertrophy, the RAS, through Ang II, participates in the generation of renal disturbances preceding the development of DN [29] [30]. Ang-(1-7) is synthetized directly by cleavage of Ang II by ACE2. Ang-(1-7) is produced in proximal tubular cells. Several studies have shown that Ang-(1-7) may limit the pressor and proliferative effects of Ang II in the progression of chronic kidney disease. Ang-(1-7) has a protective role in this setting, counterbalancing the effects of Ang II. Reportedly, Ang-(1-7) has an important role in cardiovascular alterations acting as an antiarrhythmic agent and protecting the myocardium from the consequences of cardiac injury-reperfusion [21] [31]. However, the effects of Ang-(1-7) on renal hypertrophy and DN [27] [32] are controversial. For that reason, the objective of this study was to examine whether exogenous Ang-(1-7) is capable of modifying the early renal hypertrophy development in STZ-induced diabetes in rats. STZ selectively destroys the β cells of the pancreatic islets of Langerhans trough DNA alkylation [33]. In this study, diabetes was induced by a single ip injection of STZ to create a diabetes model with pathological features similar to human diabetes [34]. The results showed that the ip daily administration of Ang-(1-7), 100 µg/kg for 2 weeks to rats after STZ-induced diabetes, attenuated the early renal damage associated to DN, evidenced by reduction of renal hypertrophy and proteinuria, and creatinine clearance improvement. The anti-hypertrophic effect of Ang-(1-7) on rats with STZ-induced diabetes and renal injury was reflected by the reduction of kidney weight/body weight ratio, protein/DNA ratio, glomerular area, and proximal tubular cells area, occurring only 2 weeks after treatment with the heptapeptide. Moreover, the treatment with Ang-(1-7) improved the renal function since the urinary protein/creatinine ratio was reduced, and creatinine clearance increased. This was associated with less body weight reduction than that of untreated diabetic rats. In accordance with our results, it has been recently reported that treatment with Ang-(1-7) for a longer period (4 weeks) to rats with STZ-induced diabetes, reduced kidney hypertrophy, and improved renal function [28]. It has been demonstrated in LLC-PK1 proximal tubular cells incubated with high glucose that Ang-(1-7) activates tyrosine phosphatases, which in turn inhibit the mitogen-activated protein kinases (p38 MAPK) stimulated by high-glucose, thereby suppressing highglucose-induced protein synthesis and hypertrophy [35]. Furthermore, treatment with Ang-(1-7) reduced AT 1 R, TGF-β 1 , and MASR expression in renal cortex. Similar effects were produced by treatment with captopril. Treatment with Ang-(1-7) did not modify the expression of ACE2, and captopril produced a significant increment of the enzyme.
Numerous studies have demonstrated that Ang II induces renal hypertrophy and glomerulosclerosis by activation of its specific receptor AT 1 R [36]- [38]. High glucose concentration on cultured mesangial cells induces matrix protein synthesis and inhibition of proteolytic enzymes activity, such as plasmin and collagenase. These effects are similar to those produced by addition of Ang II to the culture medium [39]. High glucose concentration activates angiotensinogen gene expression in renal tubular cells, increasing Ang II production [40]. Moreover, administration of AT I R blockers or ACE inhibitors attenuates renal injury. Our results showed augmented expression of AT 1 R in diabetic rats, suggesting that induced diabetes stimulated its expression. It is described that 12-lipooxigenase (12-LO) pathway in glomerular cells in vitro and glomeruli in vivo, is activated in diabetes, and up-regulates AT 1 R, thus magnifying Ang II effects and leading to DN [41]. Treatment with captopril and/or Ang-(1-7) decreased AT I R expression and also its hypertrophic effect.
Reportedly, TGF-β 1 promotes the progression of renal fibrosis and acts as a major mediator of hypertrophic and prosclerotic changes in DN [20]. It interferes with the normal cell cycle regulation by inducing cyclin-dependent kinase inhibitors. The cell enters in a period of protein synthesis without DNA replication and undergoes hypertrophy [42]. It is also known that Ang II-induced hypertrophy may be mediated by stimulation, production and secretion of TGF-β 1 [7] [38]. In this study we observed a positive correlation between the increment of the AT 1  Our results suggest that treatment with Ang-(1-7) may exert a beneficial effect on the progression of DN, beyond reducing proteinuria and increasing creatinine clearance. In db/db mice Ang II induced oxidative stress and kidney inflammation through AT 1 R.
The synthesis of Ang-(1-9) from Ang I and the catabolism of Ang II to produce Ang-(1-7). Classic ACE inhibitors do not inhibit this effect. Ang-(1-7) binds to the MASR and counteracts the effects of Ang II in DN [47]. Previous studies have shown high levels of both enzymes, ACE and ACE2, in proximal tubule cells, they have also shown that ACE2 expression is reduced in experimental DN [47] [48]. It has been reported that ACE2 loss accelerates glomerular and tubulointerstitial damage in STZ-induced diabetic mice [49]. Moreover, in NRK-52E renal cells incubated with high glucose, ACE2 expression increased at 8 -24 h and decreased at 72 h [49]. ACE2 kidney expression is down-regulated in models of diabetic mice and in diabetic patients [51] [52].
Treatment with the ACE2 inhibitor, MLN-4760, in db/db diabetic mice caused increased proteinuria, effect reverted by AT 1 R blockers [51]. We found that ACE2 expression decreased in diabetic rats as compared to control rats, showing an opposite correlation between the TGF-β 1 expression and the ACE2 expression. The mechanism of ACE2 deficiency in DN is not well known, however, is likely that an interaction between ACE2 and TGF-β 1 could exist.
These results are similar with those found in NRK-52E cells incubated with high glucose for 24 -72 h. ACE2 and MASR expression were decreased while TGF-β 1 expression was increased [50]. In this work, Ang-(1-7) administration did not modify ACE2 expression, however, captopril significantly increased it, which is in accordance with several reports, where administration of ACE inhibitors and AT 1 R blockers causes substantial increases in plasma Ang-(1-7) levels and ACE2 expression [53] [54].

Conclusion
The results suggest that early exogenous administration of Ang-(1-7) may reduce renal hypertrophy by regulating the activity of TGF-β 1 in the proximal tubule, indicating the importance of the ACE2-Ang-(1-7)-MAS receptor axis, and its potential renoprotective effect in early stages of DN.