Inhibition of soluble epoxide hydrolase is renoprotective in 5/6 nephrectomized Ren-2 transgenic hypertensive rats

Introduction

Chronic kidney disease (CKD) represents a serious problem of current nephrology and its incidence has been increasing steadily.1 The recognition that CKD tends to progress to end-stage renal disease (ESRD), regardless of the initial cause, has initiated extensive research of the underlying mechanism(s) and of potential therapeutic strategies aimed at interrupting or at least slowing down the progression of CKD to ESRD.2-4 To this end, a model of 5/6 renal mass reduction (5/6 NX), consisting of unilateral nephrectomy combined with surgical removal of two-thirds of the contralateral kidney, has been widely used. Despite extensive investigation conducted over the past 40 years, the mechanism(s) responsible for the progression of CKD to ESRD remain poorly understood. However, it is clear that different renal diseases exhibit common pathomorphological signs, such as tubulointerstitial fibrosis and tubular atrophy, followed by glomerulosclerosis.4-7 The studies using the 5/6 NX model have demonstrated that hypertension and inappropriately activated renin–angiotensin system (RAS) are two critical determinants of the progression rate of CKD to ESRD.3, 8-13 In addition, both experimental and clinical studies have shown that RAS blocking agents, such as angiotensin-converting enzyme inhibitors (ACEI) and angiotensin (Ang) II receptor blockers (ARBs), are highly effective inhibitors of the progression of CKD (renoprotective action).8, 14-17 Therefore, an antihypertensive therapeutic regimen involving direct inhibition of the RAS is currently accepted as a gold standard in therapy.

However, the effectiveness of the renoprotective action of RAS inhibition is limited, especially in advanced CKD.18-20 This points to the need for more complex pharmacological strategies that would possibly also target control systems other than the RAS. Considerable attention has been focused on the role of active metabolites of arachidonic acid (ARA), those generated by cytochrome P450 (CYP)-dependent enzymes. Evidence indicates that ARA is metabolized by CYP epoxygenases to produce epoxyeicosatrienoic acids (EETs), which are important regulators of cardiovascular and renal function.21-23 It has been shown that increasing kidney tissue EETs by preventing their degradation to biologically inactive dihydroxyeicosatrienoic acids (DHETEs), as achieved by blockade of soluble epoxide hydrolase (sEH), exhibits antihypertensive, cardio- and renoprotective actions.24-32 Therefore, increasing the bioavailability of EETs in the kidney could be a new strategy to prevent the progression of CKD to ESRD. However, recent studies addressing this issue have yielded opposing results. A study that used overexpression of CYP2J2, an enzyme that produces EETs, demonstrated important renoprotective effects in 5/6 NX rats,33 whereas another study that inhibited sEH pharmacologically failed to elicit renoprotective actions and increased the rate of progression of CKD in 5/6 NX mice.34

Considering this controversy and in view of the established knowledge that hypertension and increased intrarenal RAS are critical determinants of hypertension-associated end-organ damage and progression of CKD, we examined whether long-term treatment with an sEH inhibitor would retard the progression of CKD in 5/6 NX Ren-2 renin transgenic rats (TGR). In addition, application of this well-defined monogenetic model of AngII-dependent hypertension with endogenous activation of RAS35 appeared well-suited for the purpose.

Results

Series 1: Role of RAS and CYP metabolites in the early phase after 5/6 NX

As shown in Fig. 1a, plasma AngII levels in sham-operated TGR were significantly higher than in sham-operated HanSD (62 ± 5 vs 16 ± 3 fmol/mL, respectively; P < 0.05) and 5/6 NX elicited in the early phase substantial increases in plasma AngII compared with sham-operated TGR (196 ± 15 vs 62 ± 5 fmol/mL, respectively; P < 0.05). Similarly, total kidney AngII concentrations in sham-operated TGR were significantly higher than those in sham-operated HanSD and, in the early phase, 5/6 NX caused a further increase in concentrations that were much higher than those in sham-operated TGR (369 ± 14 vs 87 ± 6 fmol/g, respectively; P < 0.05; Fig. 1b). As shown in Fig. 1c, the intrarenal availability of biologically active epoxygenase metabolites, expressed as the EETs : DHETEs ratio, was significantly lower in sham-operated TGR than in sham-operated HanSD rats and, already in the early phase, 5/6 NX elicited a further profound decrease in the EETs : DHETEs ratio compared with sham-operated TGR (0.72 ± 0.14 vs 1.48 ± 0.17, respectively; P < 0.05).

Densitometric analysis revealed no significant differences in CYP2C3 or sEH protein expression in the renal cortex between HanSD rats and TGR (data normalized against β-actin; Fig. 2). In the case of sEH, protein expression tended to be higher in TGR than HanSD rat, although the difference failed to reach statistical significance (Fig. 2b). In the early phase, 5/6 NX did not alter protein expression of CYP2C3, but significantly increased sEH expression.

As shown in Fig. 3, there were no significant differences in CYP4A protein expression and 20-hydroxyeicosatetraenoic acid (20-HETE) concentrations in the renal cortex between HanSD rats and TGR, and 5/6 NX did not alter either value.

Series 2: Effects of RAS blockade and sEH inhibition on survival rate and signs of end-organ damage

All sham-operated TGR and HanSD rats survived until the end of the experiment. As shown in Fig. 4a, untreated 5/6 NX TGR began to die at Week 9 after 5/6 NX, with a final survival rate of 25%. Both therapeutic regimens (i.e. RAS blockade with a combination of 6 mg/L trandolapril and 100 mg/L losartan and sEH inhibition with 3 mg/L cis-4-[4-(3-adamantan-1-yl-ureido)cyclohexyloxy]benzoic acid (c-AUCB)), substantially improved post-5/6 NX survival rates in TGR; however, the former regimen was more effective (88% vs 72%, respectively; P < 0.05).

As shown in Fig. 4b, sham-operated HanSD rats remained normotensive and sham-operated TGR were considerably hypertensive, without any significant changes in systolic blood pressure (SBP) during the experiment. In TGR, 5/6 NX caused further significant increases in SBP above the initial SBP of 179 ± 5 mmHg, with the maximum reached at Week 8 after 5/6 NX (231 ± 4 mmHg; P < 0.05). Treatment with an sEH inhibitor prevented this increase and SBP remained at the same level as observed in sham-operated TGR. In contrast, RAS blockade not only prevented an increase in SBP in TGR after 5/6 NX, but rapidly reduced it, even below the levels observed in sham-operated HanSD rats (115 ± 4 vs 129 ± 4 mmHg, respectively; P < 0.05).

As shown in Fig. 5a, sham-operated HanSD rats exhibited minimal proteinuria throughout the experiment (7.2 ± 0.9 mg/24 h at the end of the experiment). Sham-operated TGR had pronounced proteinuria, more than threefold higher than that observed in sham-operated HanSD rats, throughout the experiment. Untreated 5/6 NX TGR exhibted a marked increase in proteinuria, reaching the maximum 8 weeks after 5/6 NX (161 ± 12 mg/24 h; P < 0.05 vs all other corresponding values). Blockade of the RAS prevented the increase in proteinuria that occurred after 5/6 NX in TGR and, until end of the experiment, the proteinuria was even lower than observed in sham-operated HanSD rats (2.7 ± 1.2 vs 7.2 ± 0.9 mg/24 h, respectively; P < 0.05). Treatment with the sEH inhibitor attenuated the increase in proteinuria in 5/6 NX TGR and, 16 weeks after 5/6 NX, the values observed were similar as those in sham-operated TGR; subsequently (at Week 20 after 5/6 NX) proteinuria was higher than observed in sham-operated TGR, but still significantly lower than that in untreated 5/6 NX TGR (35 ± 3 vs 67 ± 8 mg/24 h, respectively; P < 0.05).

As shown in Fig. 5b, there were no significant differences in creatinine clearance between sham-operated HanSD and sham-operated TGR rats throughout the experimental period, indicating that despite severe hypertension, marked proteinuria and some degree of renal glomerular damage (see below) at the age of 8 months sham-operated TGR did not exhibit significant impairment of renal function. These findings are in accordance with previous studies showing that heterozygous TGR without any intervention (e.g. high salt or 5/6 NX) exhibit high resistance to the development of hypertension-induced renal damage.11, 12 In contrast, untreated 5/6 NX TGR exhibited significantly lower creatinine clearance (especially 8 weeks after 5/6 NX, just before the first rats began to die) compared with sham-operated TGR. Both treatment regimens prevented decreases in creatinine clearance in 5/6 NX TGR.

As shown in Fig. 6a, sham-operated TGR clearly exhibited cardiac hypertrophy (measured as the ratio of left ventricular weight (LVW) : length (TL)) compared with sham-operated HanSD rats. In TGR, 5/6 NX induced a marked increase in LVW : TL above the values seen in sham-operated TGR (29.6 ± 1.1 vs 24.1 ± 1.2, respectively; P < 0.05). Renin–angiotensin system blockade not only prevented the increase in LVW : TL in 5/6 NX TGR, but even decreased it below values observed in sham-operated HanSD rats (14.4 ± 0.6 vs 16.1 ± 0.8, respectively; P < 0.05). Blockade of sEH prevented the increase in LVW : TL observed in TGR after 5/6 NX.

Sham-operated HanSD rats showed only minimal glomerulosclerosis (measured as the glomerulosclerosis index (GSI); Fig. 6b). After 5/6 NX, TGR showed a substantial increase in GSI (1.71 ± 0.12 vs 0.13 ± 0.02 in sham-operated TGR; P < 0.05). Renin–angiotensin system blockade in 5/6 NX TGR normalized GSI to values observed in sham-operated TGR. Inhibition of sEH substantially attenuated the increase in GSI after 5/6 NX, but it remained markedly higher than in sham-operated TGR. The pattern of kidney tubulointerstitial injury closely resembled that of GSI in all groups (data not shown).

As shown in Fig. 6c, there was no significant difference between glomerular volume in sham-operated HanSD rats and sham-operated TGR. Untreated 5/6 NX TGR exhibited a substantial increase in glomerular volume compared with sham-operated TGR (2.51 ± 0.09 × 10⁶ vs 1.17 ± 0.09 × 10⁶ μm³, respectively; P < 0.05). Each of the two therapeutic regimens significantly reduced glomerular volume in 5/6 NX TGR, but RAS blockade was more effective than sEH inhibition (1.78 ± 0.09 × 10⁶ vs 2.08 ± 0.08 × 10⁶ μm³, respectively; P < 0.05).

Representative slices of renal tissue stained with periodic acid-Schiff (PAS) of sham-operated HanSD rats, untreated 5/6 NX TGR, 5/6 NX TGR treated with RAS blockade and 5/6 NX TGR treated with sEH inhibition are shown in Fig. 7.

As shown in Fig. 8a, plasma AngII levels were significantly higher in sham-operated TGR than in sham-operated HanSD rats and 5/6 NX caused, also in the late phase, further increases in plasma AngII levels in TGR compared with sham-operated TGR (71 ± 6 vs 36 ± 4 fmol/mL, respectively; P < 0.05). Long-term sEH inhibition did not significantly change plasma AngII levels in 5/6 NX TGR. In contrast, RAS blockade caused significant decrease in plasma AngII levels in 5/6 NX TGR to values observed in sham-operated TGR.

Similarly, kidney AngII concentrations were significantly higher in sham-operated TGR than in sham-operated HanSD rats. After 5/6 NX, kidney AngII concenetrations in TGR further increased to levels substantially higher than in sham-operated TGR (212 ± 11 vs 94 ± 6 fmol/g, respectively; P < 0.05). In 5/6 NX TGR, RAS blockade decreased kidney AngII to values that were not significantly different from those in sham-operated HanSD rats (41 ± 6 vs 39 ± 4 fmol/g, respectively). In contrast, sEH blockade did not alter kidney AngII concentrations in 5/6 NX TGR (Fig. 8b). As shown in Fig. 8c, the intrarenal availability of biologically active epoxygenase metabolites, expressed as the EETs : DHETEs ratio, was significantly lower in sham-operated TGR than in sham-operated HanSD rats. The EETs : DHETEs ratio was much lower in untreated 5/6 NX TGR than in sham-operated TGR (0.51 ± 0.09 vs 1.28 ± 0.14, respectively; P < 0.05). Renin–angiotensin system blockade in 5/6 NX TGR did not significantly change the ratio; in contrast, sEH inhibition significantly increased the EETs : DHETEs ratio to levels observed in sham-operated HanSD rats.

Discussion

The present study evaluated the effectiveness of chronic EET activity, achieved by blockade of soluble sEH using c-AUCB, on the progression of CKD induced by 5/6 NX in TGR rats, a unique monogenetic model of RAS-dependent hypertension. This was compared with the effectiveness of a thorough two-level RAS blockade, which is currently accepted as the gold standard therapy used to retard the progression of CKD to ESRD.8, 11, 12, 14-17, 36

The first important finding of the present study was that the 5/6 NX in TGR not only increased circulating and kidney concentrations of AngII, as reported previously,12 but it aslo elicited a profound decrease in the intrarenal availability of biologically active epoxygenase metabolites, as evidenced by the decrease in the EETs : DHETEs ratio in the early and late phase after 5/6 NX. Because the renal generation of EETs in TGR after 5/6 NX is apparently in normal range, as indicated by unaltered protein expression of the CYP2C23 enzyme, the reduced intrarenal availability of biologically active epoxygenase metabolites is likely the result of increased conversion of EETs to DHETEs, as indicated by the distinctly increased renal expression of sEH protein in 5/6 NX TGR. Furthermore, our data show that intrarenal formation of 20-HETE was unaltered in 5/6 NX TGR compared with both sham-operated HanSD rats and sham-operated TGR. This finding is of particular importance because it is now well recognized that abnormalities in the CYP hydroxylase pathway play an important role in the pathophysiology of hypertension and hypertension-associated end-organ damage in various experimental models.37, 38 In addition, sEH inhibition with c-AUCB in TGR subjected to 5/6 NX substantially improved the rats’ survival rate, prevented blood pressure increases, retarded the progression of cardiac hypertrophy, reduced proteinuria and the degree of glomerular and tubulointerstitial injury, prevented decreases in the clearance of endogenous creatinine and reduced glomerular volume. All these organ-protective actions were associated with normalization of the intrarenal EETs : DHETEs ratio to levels observed in sham-operated HanSD rats, but no significant change in increased intrarenal AngII. Remarkably, our finding that the dose of c-AUCB used in the present study (3 mg/L) substantially increased tissue concentrations of EETs without altering intrarenal AngII levels in the remnant kidney indicates that all the beneficial effects of long-term treatment with sEH inhibition in 5/6 NX TGR should be ascribed to increased intrarenal EETs bioavailability.

Together, the findings support the notion that the deficiency in the intrarenal availability of biologically active epoxygenase metabolites contributes to the progression of CKD and development of ESRD in 5/6 NX TGR. This view is in accordance with previous studies reporting that net intrarenal deficiency of EETs contributes to the pathophysiology of certain forms of AngII-dependent hypertension.22, 24-32 It is of particular note that c-AUCB treatment with a dose that increased the intrarenal EETs : DHETEs ratio but did not alter the elevated circulating and renal RAS activity was still able to attenuate the development of AngII-dependent malignant hypertension and of hypertension-induced end-organ damage.29, 31, 32

Nevertheless, it is important to note that in a recent study with 5/6 NX mice, Jung et al.34 demonstrated that long-term c-AUCB treatment at an almost identical dosage to that used in the present study did not prevent the progression of CKD (no effect on SBP, no improvement in survival rate and no attenuation of renal glomerular and tubulointerstitial injury) and tended to accelerate rather than retard (vide augmented albuminuria) the course of CKD. There is no satisfactory explanation for these results, which contradict those of the present study, as well as earlier findings showing beneficial effects of sEH inhibitor treatment on the progression of end-organ damage.25, 26, 29, 31 However, it should be noted that in the study of Jung et al.34 the 5/6 NX mice exhibited suppression of sEH expression and elevated EETs levels, the opposite to findings in AngII-dependent hypertension models in rats, in which increased expression and activity of sEH with consequent reduction of biologically active EETs were found.29, 31, 39, 40 Apparently, blockade of sEH is antihypertensive and renoprotective only under conditions of increased sEH activity and reduced EETs bioavailability.22-24 The reasons for the suppression of sEH expression in 5/6 NX mice remain unclear; a species difference between rats and mice possibly involving different regulation of sEH expression and/or activity should be considered.

What are the mechanisms underlying the renoprotective actions of sEH inhhibitor treatment in 5/6 NX TGR? It will be recalled that the first theory explaining the mechanism of the progression of CKD, truly a milestone in nephrological research, was formulated by Brenner.2 On the basis of micropuncture studies with remnant kidneys of 5/6 NX rats,5 Brenner2 proposed that glomerular hyperfiltration and hypertension represented a compensatory response to a reduction in nephron number that results in damage to the healthy remnant glomeruli. The compensation is, in fact, maladaptive and, within the vicious circle, glomerulosclerosis progresses, ultimately leading to ESRD. According to this ‘haemodynamic’ theory, all renoprotective measures applied in CKD should focus on the correction of abnormal glomerular haemodynamics.2, 4, 5 However, subsequent studies using a serial micropuncture technique in remnant kidneys of 5/6 NX rats revealed that, on the one hand, haemodynamic abnormalities that developed in the remnant glomeruli had no correlation with the degree of sclerosis subsequently developing in the same glomerulus41, 42 and, on the other hand, an unequivocal correlation between glomerular hypertrophy and glomerulosclerosis.43, 44 Based on these studies, it had to be recognized that glomerular hypertrophy is an additional independent risk factor for the development of glomerulosclerosis, which, in accordance with Laplace's law (tension = radius × pressure), leads to an increase in wall tension and glomerular capillary damage, as well as to podocyte injury and depletion, the latter also identified as one of the major causes of glomerulosclerosis.7, 43-45 Considering this ‘hypertrophy’ theory, of particular interest is our finding that sEH inhibitor treatment significantly reduced the glomerular volume in 5/6 NX TGR.

When the findings of the present study are considered in the context of the earlier studies and theories, we suggest that the mechanism underlying the renoprotective effects of long-term sEH inhibitor treatment in 5/6 NX TGR is related to attenuation of maladaptive compensatory glomerular growth, which in these animals is mediated through antiproliferative effects of normalized intrarenal EETs levels. Nevertheless, it is known that renal fibrosis is an important factor in the progression of CKD,7, 46 and it has been documented that increased renal expression of fibronectin and collagen is a characteristic feature of 5/6 NX rats.47 Therefore, the lack of measurement of expression of these factors is an obvious limitation of the present study. Another limitation becomes apparent with the current evidence that oxidative stress is an important contributor to the pathogenesis of renal fibrosis.48 Because TGR, an AngII-dependent model of hypertension, exhibits increased generation of superoxide (),49 the role of oxidative stress in the progression of CKD in this model should also be considered and investigated. These two limitations inevitably narrow our insight into the complex mechanisms responsible for the renoprotective actions of sEH inhibitor treatment in 5/6 NX TGR.

Another important finding of the present study is that in 5/6 NX TGR, the antihypertensive regimen based on combined RAS blockade markedly improved survival rate and normalized blood pressure, cardiac hypertrophy and proteinuria; moreover, the treatment prevented the development of renal glomerular and tubulointerstitial injury and decreases in the clearance of endogenous creatinine. Furthermore, combined RAS blockade not only prevented the rise in kidney AngII concentration, but even decreased it to levels observed in sham-operated HanSD rats. All these findings are in good agreement with our recent study showing that hypertension and increased intrarenal RAS are two critical determinants of the rate of progression of CKD in 5/6 NX TGR,12 as well as with studies suggesting the crucial role of the intrarenal RAS in the pathophysiology of hypertension-associated end-organ damage.50-53 Nevertheless, the results of the present study indicate that the effectiveness of the renoprotective action of RAS blockade is limited during the late stage of CKD. Even though hypertension and intrarenal RAS activity were effectively controlled, some 5/6 NX TGR under RAS blockade started Week 18 (two of 17 rats), which was was preceded by a transient exacerbation of proteinuria. Together, these findings further support the notion that even if an antihypertensive regimen based on RAS blockade is a key component of the treatment strategy aimed at slowing-down the progression of CKD,8, 11, 12, 14-17, 36, 54, 55 there is a need to target vasoactive systems other than the RAS.

In view of our current encouraging findings indicating renoprotective effects of normalization of intrarenal EETs bioavailability on the progression of CKD, it seems logical and desirable to investigate whether combined sEH inhibition and RAS blockade may have additive beneficial effects in this model of CKD. However, it this regard it is important to emphasize that the renoprotective action of RAS blockade was much less successful in the late phase of CKD18-20 and, in agreement with the present results, we have found previously that in TGR the two-level RAS inhibition provides complete renoprotection when applied no later than 16 weeks after 5/6 NX.11, 12 Therefore, it is reasonable to assume that potentially superior renoprotection of combined sEH inhibition and RAS blockade can possibly be demonstrated in very long-term studies only. Therefore, a relevant research project would require a follow-up period substantially longer than is routinely used in studies with 5/6 NX rats.11, 12, 55

In addition, we recently demonstrated in HanSD rats, which are originally normotensive and have normal plasma and kidney AngII levels, 5/6 NX led to the development of hypertension and marked activation of the intrarenal RAS in the remnant kidney and that these factors were dominant determinants of the rate of progression of CKD.12 Therefore, one could reasonably assume that 5/6 NX HanSD rats would also exhibit decreased EETs availability in the remnant kidney and that sEH inhibition could also exhibit renoprotective actions and retard the progression of CKD in initially normotensive HanSD rats subjected to renal mass reduction. However, the present study was designed to address first the role of intrarenal biologically active epoxygenase metabolites in the progression of CKD in hypertensive animals with already augmented RAS activity; the reason for this was that previous studies22-24, 27-32 provided a good rationale for the use of sEH inhibition as a new therapeutic strategy to slow the progression of CKD in an AngII-dependent hypertensive model. Nevertheless, the findings of the present study highlight the need to establish whether the renoprotective effects of long-term treatment with an sEH inhibitor would also be demonstrable in 5/6 NX animals with originally normal blood pressure and without inappropriate activation of the RAS. This would make a desirable target of a future, hopefully more conclusive, study.

In conclusion, the results of the present study show that hypertensive TGR subjected to 5/6 renal mass reduction exhibit a profound decrease in the intrarenal EETs : DHETEs ratio, which strongly suggests that the deficiency of intrarenal active epoxygenase metabolites accelerates the progression of CKD in this AngII-dependent hypertensive model. In addition, long-term restoration of intrarenal biologically active EETs, achieved by pharmacological sEH inhibition, provided an important renoprotective effect. The finding that normalization of the intrarenal availability of active epoxygenase products substantially attenuates the progression of CKD in 5/6 NX TGR should be considered in attempts to develop new pharmacological strategies aimed at slowing down the progression of CKD to ESRD.

Methods

Experimental design

Series 1: Role of RAS and CYP metabolites in the early phase after 5/6 NX

The aim of this series of experiments was to evaluate the degree of activation of the RAS system and of the rate of synthesis within the two CYP-dependent enzymatic pathways, namely epoxygenase and ω-hydroxylase.

Male HanSD rats and TGR (9 weeks old) were anaesthetized with a mixture of tiletamine + zolazepam (8 mg/kg; Virbac, Carros, France) and xylazine (4 mg/kg, i.m.; Spofa, Prague, Czech Republic) and 5/6 NX was performed as described previously.11, 12 Sham-operated HanSD rats served as healthy normotensive controls. It is well recognized that AngII is the major active product of the RAS and a reliable marker of the activity of the system.50 Therefore, at the end of the experiments, unaesthetised rats were decapitated and plasma and tissue AngII concentrations were determined by radioimmuassay. This approach was used because we have recently demonstrated that measured AngII levels are altered by anaesthesia.56, 57 Moreover, we were able to compare the results of the present study with those of our earlier studies into the role of the RAS in the pathophysiology of hypertension.11, 12, 51-53, 56, 57 In addition, we determined EETs and DHETEs concentrations in the kidney cortex. Samples were extracted and the extracts separated by reverse-phase HPLC being being analysed by negative-mode electrospray ionization and tandem mass spectroscopy as described previously.27-32, 58 Specifically, 8,9-EETs, 11,12-EETs and 14,15-EETs were measured separately and then presented as a total. These metabolites are the most active products formed in the CYP epoxygenase enzymatic pathway.22, 23 The EETs : DHETES ratio was obtained using total concentrations of EETs and DHETEs. Western blot analysis of the protein expression of CYP2C23, the enzyme predominantly responsible for the formation of EETs in the kidney, and sEH, the enzyme responsible for the conversion of EETs to DHETEs, in the renal cortex was performed as described previously,29, 58 with levels normalized against β-actin. In addition, 20-HETE and protein expression of CYP4A, the enzyme responsible for the formation of 20-HETE, were analysed in the renal cortex as described previously.28

The following experimental groups were investigated: (i) sham-operated HanSD + vehicle (water) treated (n = 7); (ii) sham-operated TGR + vehicle (water) treated (n = 7); and (iii) 5/6 NX TGR + vehicle (water) treated (n = 9).

Series 2: Effects of RAS blockade and sEH inhibition on survival rate and signs of end-organ damage

Male HanSD rats and TGR (8 weeks old) derived from several litters were randomly assigned to experimental groups to make sure that the animals from a single litter did not prevail in any group. To detect intergroup differences in SBP over time, SBP was measured in accordance with recommendations for blood pressure measurements in conscious animals by tail plethysmography using a tail-cuff apparatus (MC 4000 (Hatteras Instruments, Cary, NC, USA) and RTBP 1007 (Kent Scientific, Torrington, CT, USA)).59 Three days before starting actual measurements, rats were accustomed to the indirect tail-cuff SBP measurement procedure. This method, regularly used in our laboratory,11, 12 was previously validated and a close correlation found between these values and those yielded by direct blood pressure measurements in conscious rats using an indwelling aortic catheter. Measurements of SBP were started 14 days before 5/6 NX and performed at 3 day intervals until the end of the experiment. On Day 0 (9 weeks of age), 5/6 NX was performed as described above. After 72 h recovery, rats were either started on treatment or left untreated. The following experimental groups were investigated: (i) sham-operated HanSD + water (initial n = 10); (ii) sham-operated TGR + water (initial n = 10); (iii) 5/6 NX TGR + water (initial n = 24); (iv) 5/6 NX TGR + RAS blockade (initial n = 17); and (v) 5/6 NX TGR + sEH inhibitor (initial n = 18).

The follow-up period was 20 weeks. At Weeks 4, 8, 16 and 20 after Day 0, after appropriate habituation training, rats were placed in individual metabolic cages and 24 h urine was collected for determination of protein and creatinine. Blood samples were taken from the tail vein and plasma creatinine concentrations were measured by the picric acid colorimetric method using a commercially available kit (Lachema, Brno, Czech Republic). This approach was validated previously and is regularly used in our studies.11, 12 At the end of the experiments, unaesthetised rats were decapitated and AngII, EETs and DHETEs concentrations were assessed as described for Series 1.

Samples from the second half of the kidney were used to assess renal glomerular damage. Kidneys were fixed in 4% formaldehyde, dehydrated and embedded in paraffin. Sections were stained with haematoxylin–eosin and PAS and were examined and evaluated in a blinded manner. Fifty glomeruli in each kidney were examined on a semiquantitative scale as follows:60 Grade 0, all glomeruli normal; Grade 1, sclerotic area up to 25% (minimal sclerosis); Grade 2, sclerotic area 25–50% (moderate sclerosis); Grade 3, sclerotic area 50–75% (moderate-to-severe sclerosis); and Grade 4, sclerotic area 75–100% (severe sclerosis). The GSI was calculated as follows:

where n_x is the number of glomeruli in Grade x of glomerulosclerosis.

Renal cortical tubulointerstitial injury was evaluated as described by Nakano et al.60 and as used in our recent studies11, 12 to determine inflammatory cell infiltration, tubular dilatation, atrophy or interstitial fibrosis. Injury was graded semiquantitatively using the following scale of lesions: Grade 0, no abnormal findings; Grade 1, mild (< 25% of the cortex); Grade 2, moderate (25–50% of the cortex); and Grade 3, severe (> 50% of the cortex). Lesions were assessed in at least 30 random and non-overlapping fields in the renal cortex.

Morphometric evaluation of the glomerular volume was made in the same kidney sections that were examined for morphological changes using the method validated by Lane et al.60 and used in our recent studies11, 12, 61 using the Nikon NIS-Elements AR 3.1 morphometric program (Nikon, Tokyo, Japan).

Based on previous experience,51, 52 we used the the ratio of LVW : to determine the degree of cardiac hypertrophy.

Disclosure

The authors declare no conflicts of interest.