Diabetic nephropathy is the leading cause of end-stage renal disease. Dopamine receptors are involved in the regulation of renal hemodynamics and may play a role in diabetes-induced hyperfiltration. To test this hypothesis, we investigated the renal effect of a dopamine D3 receptor antagonist (D3-RA) in hypertensive type II diabetic SHR/N-cp rats. Lean and obese SHR/N-cp rats were randomly assigned to D3-RA, angiotensin-converting enzyme inhibitor (ACE-i), or D3-RA+ACE-i treatment or control conditions. Treated animals were given the D3-RA A-437203 (10 mg/kg/body weight (BW)/day) or the ACE-i trandolapril (0.3 mg/kg BW/day) or a combination of both. At 6 months following perfusion, fixed kidneys were analyzed by morphological and stereological methods. Indices of renal damage (glomerulosclerosis, glomerulosclerosis damage index (GSI), tubulointerstitial and vascular damage), glomerular geometry and functional variables such as urinary albumin excretion, glomerular filtration rate, blood pressure, blood chemistry and BW were determined. The GSI (score 0–4) was significantly higher (P<0.05) in untreated diabetic animals (1.62±0.3) compared to nondiabetic controls (0.4±0.2) and the treatment groups (D3-RA: 0.31±0.12; ACE-i: 0.29±0.1; combination treatment: 0.12±0.01). Urinary albumin excretion (mg/24 h) was higher in untreated diabetic controls (102±19) compared to nondiabetic controls (31±12) and the treatment groups (D3-RA: 44±15; ACE-i: 41±13; combination treatment: 15±8). Mean glomerular volume was higher in untreated diabetic animals compared to nondiabetic controls and to the treatment groups. Desmin expression, a marker of podocyte damage, was elevated in untreated diabetic controls and diminished in all treatment groups. These data suggest that in a model of type II diabetes, the dopamine D3-RA had a beneficial effect on renal morphology and albuminuria, which was comparable in magnitude to that of ACE-i treatment.
Although this intervention is effective, it fails to abrogate progression of renal disease consistently and completely. There is a dire need for additional or alternative interventions. Several innovative strategies have been proposed including blockade of the aldosterone receptor or pharmacological interference with the effects of cytokines and chemokines. We reasoned that one further promising intervention might be blockade of the renal effects of dopamine.
It is well known that dopamine, a central and peripheral neurotransmitter, is synthesized in non-neuronal tissues as well including renal tissue. It could potentially play a role in maintaining sodium balance by direct actions in the kidney and indirect actions mediated via catecholamines or the renin system. In the rat, juxtaglomerular cells are innervated by dopaminergic nerves and express the D1A and D3 receptor subtypes.3, 4, 5 Activation of the D1 receptor was reported to increase renin release.3
It has been shown in several species that dopamine increases the glomerular filtration rate. More recently, selective D2-type antagonists were demonstrated to reverse glomerular hyperfiltration induced by amino acids6, 7 or experimental diabetic hyperglycemia.8 In addition, activation of the D3 receptor in rats caused diuresis, natriuresis and increased glomerular filtration.9
In the present study, we used the SHR/N-cp rat as a hypertensive model of type II diabetes, which develops severe glomerular lesions1 to investigate a potential renoprotective action of a novel D3 receptor antagonist (D3-RA) compared to that of an angiotensin-converting enzyme inhibitor (ACE-i) as the gold standard.
Materials and methods
Animals (Table 1
The SHR/N-cp rat is a novel model of type II diabetes. The animals develop marked renal lesions.10 This strain was generated by mating obese Koletzky rats and hypertensive SHR rats. The resultant progeny are either lean or obese. The diabetic SHR/N-cp inherits obesity as an autosomal recessive trait. As corpulent rats do not reproduce, the rats are bred by mating of heterozygous animals. Mating yields three genotype, but only two phenotypes, that is, the homozygous (cp/cp) corpulent as well as the heterozygous (cp/+) and homozygous (+/+) lean rats, in a ratio of 1:2:1. The development of obesity is linked to reduced metabolic expenditure of energy.10, 11, 12
For the present study, 6-months-old male SHR/N-cp obese rats and their age-matched lean controls were obtained from Vasarr (New York, USA) and were housed at standard light cycle (light 0800–2000 hours daily), 40–70% relative humidity and maintained at 22±1°C in standard box cages. All animals were allowed free access to Standard Purina chow (Na+ content: 0.25%; no. 5012; Purina Mills, St Louis, MO, USA) and water throughout the studies.
The animals were randomly allotted to the following eight experimental groups:
SHR/N-cp lean untreated control (n=9).
SHR/N-cp lean+dopamine receptor blocker (D3-RA) A-437203 (10 mg/kg BW, n=8).
SHR/N-cp lean+ACE-i trandolapril (0.3 mg/kg BW, n=13).
SHR/N-cp lean+ACE-i-+D3-RA (n=7).
SHR/N-cp obese untreated control (n=7).
SHR/N-cp obese+D3-RA (n=9).
SHR/N-cp obese+ACE-i (n=12).
SHR/N-cp obese+D3-RA+ACE-i (n=7).
The drugs were administered in the drinking fluid at concentrations calculated to deliver the above-mentioned doses. Doses of used drugs were selected based on data provided by ABBOTT from pilot studies in diabetic rats (data not shown). Daily food and water consumption were monitored and the drug doses adjusted. Body weight (BW), blood glucose and blood pressure (by tail plethysmography) were measured at regular intervals. After 6 months, animals were kept in metabolic cages for 1 day to collect 24 h urine. Urinary albumin excretion was measured using a rat-specific sandwich enzyme-linked immunoassay (ELISA) system as described in detail elsewhere.13 Blood samples were taken and the experiment was terminated after 6 months by retrograde perfusion via the abdominal aorta1 under deep anesthesia. Cholesterol and leptin concentrations were measured by Limbach Laboratory (Heidelberg, Germany; courtesy Dr Roth).
One kidney was harvested after perfusion with Rheomacrodex® and ice-cold saline for immunohistological and in situ investigations. The other organs were removed after continuous perfusion with glutaraldehyde for morphometric investigations.1 The glutaraldehyde-perfused kidney was dissected in a plane perpendicular to the interpolar axis, yielding slices of 1 mm width. In all, 10 small pieces of this kidney were selected by area-weighted sampling for embedding in Epon-Araldite. Semi- (1 μm) and ultrathin sections (0.08 μm) were prepared and stained with methylene blue/basic fuchsin or citrate/uranyl acetate, respectively. The remaining tissue slices were embedded in paraffin; 4 μm sections were prepared and stained with hematoxylin/eosin and PAS. For immunohistological investigations, one-half of the NaCl-perfused kidney was fixed in 4% buffered formaldehyde, embedded in paraffin and cut into 2 μm thick sections. For in situ hybridization, the other half of the kidney was snap-frozen in liquid nitrogen-cooled isopentane.
Indices of renal damage (glomerulosclerosis, tubulointerstitial and vascular damage)
The degree of sclerosis within the glomerular tuft as an index of progression (glomerulosclerosis damage index, GSI) was determined on PAS-stained paraffin sections adopting the semiquantitative scoring system proposed by El Nahas et al.14 Using light microscopy at a magnification of × 400, the glomerular score of each animal was derived as the mean of 100 glomeruli. The severity of glomerulosclerosis was expressed on an arbitrary scale from 0 to 4 as described elsewhere.14, 15
Tubulointerstitial damage index (TBI) and vascular damage index (VDI) were assessed on PAS-stained paraffin sections at a magnification of × 100 using a similar scoring systems with scores 0–4.16
Area (AA) and volume density (VV) of the renal cortex and medulla as well as the number of intact glomeruli per area (NA) were measured using a Zeiss eyepiece (Integrationsplatte II; Zeiss Co., Oberkochen, Germany) and the point counting method (PP=AA=VV) at a magnification of × 400, described in detail.17, 18
Analysis of glomerular capillarization and cellularity on semithin sections
On five semithin sections per animal, glomerular capillarization and cellularity were analyzed using the point counting method and a 100-point eyepiece (Integrationsplatte II; Zeiss Co.) at a magnification of × 1000 (oil immersion) as described previously.19 Briefly, the length density (Lv) of glomerular capillaries was determined according to the standard stereological formula, Lv=2QA (with QA being the number of capillary transects per area of the capillary tuft). Total length of glomerular capillaries per one kidney (Ltotal) was then derived from Lv and the total glomerular volume (Vglom) with Vglom=Vvglom × Vcortex. Glomerular cellularity (podocytes, mesangial cell and endothelial cells) was assessed by stereological techniques in at least 30 glomeruli per animal from cell density per volume (Ncv) and volume density of the cell type (Vcv) according to the equation: Ncv=k/β × NcA1.5/Vcv0.5, with β for podocytes=1.5 and for mesangial and endothelial cell=1.4 and k=1.20 The respective cell volume was calculated with Vc=Vcv × Vglom.
Paraffin sections were reacted with antibodies using the avidin–biotin method:13, 21 PCNA (proliferating cell nuclear antigen; α-PCNA monoclonal mouse; Immunotech, Marseille, France; 1:150), TGF-β1 (anti-TGF-β1, rabbit polyclonal IgG; Santa Cruz Biotechnology, Santa Cruz, CA, USA; 1:300), fibronectin (α-fibronectin polyclonal rabbit; Sigma-Aldrich Chemie GmbH, Steinheim, Germany; 1:10), collagen IV (polyclonal rabbit; Biotrend, Cologne, Germany), nephrin (pan to nephrin; Flaunders, NJ, USA; 1:100) and desmin (α-desmin monoclonal mouse; DAKO, Hamburg, Germany; 1:400). Cryostat sections (5 μm) were prepared and were reacted with antibodies using the avidin–biotin method: PDGF-AB (platelet-derived growth factor; α-PDGF-AB polyclonal goat; Upstate Biotechnology Inc., Waltham, USA; 1:50), collagen I (polyclonal rabbit; Chemicon, Tenecula, CA, USA; 1:2000) and endothelin (α-ET-1 polyclonal rabbit; Biotrend, Cologne, Germany; 1:20). PCNA immunohistochemistry was examined using light microscopy at a magnification of × 400. In 50 glomeruli per kidney, the number of PCNA-positive cells per glomerulus as well as per glomerular and per tubulointerstitial area were counted.
The immunohistological stains were analyzed by two investigators masked to the allocation of the animals to treatment groups; scoring was performed as described in detail earlier.13
Semiquantitative RT-PCR for Renal ET-1 and TGF-β mRNA Expression
The methods used have been described in detail elsewhere.18, 19 Briefly, total RNA (1 μg) was dissolved in 20 μl of a reaction mixture containing 4 mM dATP, dCTP, dTTP and dGTP; 10 U RNAsin (Life Technologies BLR, Grand island, NY, USA); 100 pmol random hexamers (Boehringer Mannheim GmbH, Mannheim, Germany); PCR buffer (final concentrations: 1.6 mM (NH4)2SO4, 2.0 mM Tris-HCl (pH 8.4), 1.5 mM MgCl2); and 100 U Superscript reverse transcriptase (Life Technologies BLR). After incubation at 42°C for 45 min, the enzyme was denatured for 5 min at 94°C. Semiquantification of ET-1 and TGF-β mRNA was carried out using deletion mutants of the ET-1 and TGF-β cDNA as internal standard. The amplifications of the mutants resulted in PCR products of 300 bp for ET-1 and 302 bp for the TGF-β. The mutant cDNAs were added to the PCR mixture after RT to complete with the endogenous ET-1 0.4 pg (respectively TGF-β 0.05 pg) of the plasmid was added to the PCR mixture per sample. The PCR products were separated in a 3% metaphorgel and scanned as TIF data. The quotient of measured endogenous sample and equivalent mutant was calculated by Scion-Image-program (National Institute of Health, MD, USA).
In Situ Hybridization for Renal TGF-β mRNA and Collagen IV Expression
Non radioactive in situ hybridization using TGF-β sense and antisense probes was performed in five animals per group as described briefly: cryostat sections (10 μm) were fixed with 3% paraformaldehyde/phosphate-buffered saline (5 min, 4°C, pH 7.0). Subsequently, the sections were dehydrated, air-dried and stored at −20°C.
Probe preparation and labelling
A 340 bp cDNA fragment of the TGF-β cDNA was obtained from a PCR product using rat TGF-β-specific primers after RT of rat kidney total RNA.20 The segment encoding the TGF-β gene was inserted into the pGEM-T vector system (Promega Biotech., Madison, WI, USA). For preparation of the antisense RNA probe, the plasmid was linearized with SpeI and transcribed using T7 bacteriophage RNA polymerase. Linearization of the plasmid with NcoI and transcription with SP6 RNA polymerase generated the sense RNA probe. Digoxigenin-labelled RNA probes were synthesized using a DIG RNA labelling mix (Roche, Mannheim, Germany). The sections were hybridized with 4 ng of labelled probe in buffer in a moist chamber. Hybridization of the probe with native mRNA was allowed for 18 h at 50°C. Afterwards, several posthybridization steps were performed. After posthybridization washes, the sections were equilibrated in buffer I. Nonspecific background staining was blocked by incubation for 1 h with 0.5% blocking reagent/buffer I (Roche, Mannheim, Germany). The hybridization products were visualized by ELISA using alkaline phosphatase-conjugated sheep anti-digoxigenin-Fab fragments (750 U/ml; Roche Mannheim, Germany). Following incubation at 4°C overnight, unbound conjugate was removed by two washes in buffer I followed by equilibration of the sections in buffer II. Nitroblue tetrazolium and 5-bromo-4-chloro-3-indolylphosphate served as chromogens. Negative controls included hybridization with the sense RNA probe, incubation without probe for detection of unspecific binding of the primary antibody and omission of both probe and primary antibody. Staining intensity was analyzed using the previously described semiquantitative scoring system (scores 0–4).20
Collagen IV sense and antisense probes were generously prevented by Professor J Floege and T Ostendorf (Aachen, Germany).22
Data are given as mean±s.d. After testing for normal distribution, the Kruskal–Wallis test or one-way ANOVA were chosen for analysis of variance, followed by Duncan's multiple-range test to test for differences between groups. The results were considered significant when the probability of error (P) was less than 0.05.
Nondiabetic control rats (lean) weighed significantly less than untreated diabetic animals (obese). Treatment with ACE-i or D3-RA had no influence on BW. Blood glucose was significantly higher in obese diabetic rats compared to both lean controls and treated animals. Systolic blood pressure was significantly higher in untreated obese animals compared to lean controls and all treatment groups. D3-RA treatment lowered blood pressure significantly in obese, but not in lean animals. Urinary albumin excretion was significantly lower in nondiabetic lean compared to obese diabetic rats. ACE-i and D3-RA reduced albuminuria in diabetic rats to a similar extent. The combination of both interventions in diabetic rats resulted in a significant additive beneficial effect.
In untreated diabetic rats, the glomerular filtration rate was significantly decreased; in contrast, sodium excretion rate was increased compared to nondiabetic controls. Both parameters were normalized in treated groups. Plasma leptin levels were significantly higher in diabetic animals compared to lean animals and were significantly lowered by all interventions. Triglycerides and cholesterol were significantly elevated in diabetic animals compared to lean controls and were lowered by ACE-i and combination treatment only.
Diabetes was associated with a significantly increased GSI in untreated rats (Table 3, Figure 1). In lean and obese rats, all pharmacological interventions reduced the GSI significantly and comparably. The TBI was higher in diabetic rats compared to nondiabetic animals. In treated animals, all interventions lowered tubulointerstitial lesions, but ACE-i and the combination treatment were much more effective than D3-RA. The VDI was higher in diabetic compared to nondiabetic rats and all interventions.
The number of glomeruli per kidney was lower in untreated lean and obese animals as compared to the treatment groups. All three pharmacological interventions resulted in a significantly higher number of glomeruli per kidney both in the lean and the diabetic SHR/N-cp. Mean glomerular volume was higher in untreated diabetic compared to nondiabetic animals and compared to the three intervention arms in lean and diabetic SHR/N-cp.
The length density is an acknowledged indicator of capillary obliteration and was lower in untreated diabetic compared to nondiabetic rats and all treatment groups.
In untreated diabetic compared to nondiabetic rats, the mean number of podocytes per glomerulus was lower and mean podocyte volume higher. In diabetic rats, all interventions prevented loss and hypertrophy of podocytes.
In diabetic rats, the endothelial cell number, the mesangial cell number and the mesangial matrix volume per glomerulus were higher compared to nondiabetic lean animals and all intervention groups.
PCNA: Untreated diabetic animals had more PCNA-positive glomerular cells (mostly podocytes) per glomerular profile than nondiabetic lean controls. In lean animals, treatment had no effect on the number of PCNA+cells. ACE-i and combination treatment lowered the number of glomerular PCNA+cells. The D3-RA was less effective in this respect (see Table 4).
The number of PCNA-positive tubulointerstitial cells per view field was higher in untreated diabetic compared to nondiabetic lean rats. The number was lower in the ACE-i group and also combination treatment led to lower numbers of PCNA+glomerular cells in obese and lean rats. Again, the D3-RA was less effective in this respect (Table 5).
ET-1: ET-1 protein expression was higher in podocytes and mesangial cells of untreated diabetic rats compared to nondiabetic lean controls. In nondiabetic rats, the pharmacological interventions showed no significant effect, but in diabetic rats, all three treatments lowered the expression of ET-1 significantly. Tubulointerstitial staining with ET-1 was significantly more pronounced in diabetic compared to nondiabetic rats. In diabetic rats, the expression of ET-1 on the protein level was lower in the ACE-i and combination treatment groups only (see Figure 2).
Fibronectin: Fibronectin staining (score 0–4) was higher in glomeruli and tubulointerstitium of untreated diabetic (glomerular: 2.74±0.18; tubulointerstitial: 2.95±0.16) compared to nondiabetic lean rats (glomerular: 1.18±0.15; tubulointerstitial: 2.15±0.12). None of the interventions showed a significant influence on glomerular and tubulointerstitial expression of fibronectin in lean rats. In diabetic rats, all pharmacological treatments lowered glomerular and tubulointerstitial expression of fibronectin (ACE-i—glomerular: 2.02±0.08, tubulointerstitial: 1.93±0.07; D3-RA—glomerular: 2.29±0.12, tubulointerstitial: 2.49±0.15; combination—glomerular: 2.18±0.09, tubulointerstitial: 2.12±0.19).
PDGF: Glomerular expression of PDGF-AB on the protein level showed no significant difference between the study groups. Tubulointerstitial expression of PDGF-AB was significantly (P<0.05) higher in diabetic rats (0.89±0.11) compared to lean nondiabetic animals (0.32±0.12). Interventions had no influence in non-diabetic lean rats, but tubulointerstitial PDGF-AB expression was lower in diabetic rats after treatment with ACE-i (0.31±0.09) and combination (0.29±0.04), but not with D3-RA (0.67±0.14).
TGF-β1: Glomerular and tubulointerstitial expression of TGF-β1 was higher in diabetic compared to nondiabetic lean rats. In lean rats, the treatments had no significant effect. In diabetic rats, all intervention groups had significantly lower glomerular and tubulointerstitial expression (P<0.05; see Figure 4).
Desmin: Expression was virtually absent in podocytes of nondiabetic lean rats (0.2±0.05) and was higher in podocytes of untreated diabetic rats (1.5±0.4), indicating early podocyte damage. Desmin expression of podocytes was lower after treatment with ACE-i (0.4±0.2), D3-RA (0.5±0.3) and combination treatment (0.4±0.2).
Nephrin: Expression was visible in podocytes of nondiabetic lean rats (0.94±0.4) and was lower in obese rats (0.41±0.2). Nephrin expression was higher in dopamine (1.13±0.4), ACE-i (1.21±0.2) and combination treated animals (1.45±0.3).
Collagen I: Glomerular expression of collagen I was increased in diabetic obese rats (2.4±0.12) compared to lean nondiabetic rats (1.27±0.3). There was no significantly effect of treatment in nondiabetic lean rats, but in diabetic animals, all three pharmacological interventions lowered collagen I expression to a similar extent (ACE-i: 1.3±0.1; D3-RA: 1.43±0.4; combination: 1.5±0.4). Tubulointerstitial staining was also increased in obese rats (2.28±0.47) compared to nondiabetic lean animals (1.77±0.6). In lean animals, only ACE-i and combination treatment lowered expression (ACE-i: 1.19±0.1; combination: 1.26±0.4), but not D3-RA (1.71±0.4). In obese animals, all interventions led to comparably lower tubulointerstitial expression for collagen I (ACE-i: 1.26±0.15; D3-RA: 1.22±0.4; combination: 1.21±0.5).
Collagen IV (see Figure 3): Expression of glomerular collagen IV was significantly higher in diabetic animals compared to lean controls. There was no effect of treatment in nondiabetic lean rats. In contrast, in diabetic animals, all interventions lowered collagen IV staining to a similar extent. Tubulointerstitial collagen IV expression was significantly higher in diabetic animals compared to lean rats. Again, there was no significant effect of treatment in nondiabetic lean animals. In diabetic rats, ACE-i and combination treatment, but not treatment with D3-RA lowered collagen IV expression significantly.
RT-PCR for TGF-β mRNA and ET-1 mRNA
TGF-β1 mRNA expression was increased in untreated diabetic rats (83.8±23.7) compared to nondiabetic untreated rats (39.7±17.8). In nondiabetic animals, there was no significant effect of treatment. In diabetic rats, TGF-β1 mRNA expression was lower in animals treated with ACE-i (35.9±22), in animals treated with D3-RA (32.2±14.8) and combination treatment (33.8±18.7).
ET-1 mRNA was increased in obese untreated animals (116±37.1) compared to nondiabetic lean controls (53.4±18). In nondiabetic animals, there was no significant effect of treatment. In obese diabetic rats, all three pharmacological interventions reduced ET-1 expression, but ACE-i and combination treatment were significantly (P<0.05) more effective than therapy with the D3-RA alone (ACE-i: 50.6±13.4; D3-RA: 88.5±20.1; combination: 54.3±23.5).
In situ hybridization for TGF-β mRNA and collagen IV mRNA
The expression of TGF-β mRNA was higher in podocytes and mesangial cells of untreated diabetic rats compared to nondiabetic controls (score: 0.62±0.03 vs 0.07±0.02) or diabetic rats treated with ACE-i (score: 0.21±0.08), D3-RA (score: 0.2±0.11) or combination treatment (score: 0.18±0.1). In the tubulointerstitial space expression of collagen IV, mRNA was stronger in untreated diabetic than in nondiabetic control rats (score: 0.97±0.44 vs 0.124±0.14) and in diabetic rats treated with ACE-i or the combination or ACEi+D3-RA (ACE-i: 0.14±0.02; combination: 0.26±0.16). Treatment with D3-RA alone had no significant effect on expression of TGF-β mRNA in the tubulointerstitial space: 0.61±0.2.
Expression of collagen IV mRNA was higher in podocytes and mesangial cells of untreated diabetic rats than in nondiabetic controls (score: 0.83±0.08 vs 0.06±0.08; Figure 4). In diabetic rats treated with ACE-i (score: 0.04±0.08), D3-RA (score: 0.17±0.11) or their combination (score: 0.05±0.1), it was significantly less as well. In the tubulointerstitial space expression of collagen IV, mRNA was stronger in untreated diabetic animals than in nondiabetic controls (score: 1.33±0.18 vs 0.12±0.14; Figure 4) or treated diabetic rats (ACE-i: 0.14±0.02; D3-RA: 0.61±0.2; combination: 0.26±0.16).
The salient feature of the present study is the observation that the D3-RA proved to be a remarkably effective renoprotective agent in a type II diabetes animal model. Treatment with D3-RA had a beneficial effect on glomerular filtration rate, albuminuria, morphological indices of renal damage (GSI, TBI and VDI) as well as on the number of PCNA-positive cells in glomeruli and tubulointerstitium and finally on the expression of mediators of renal damage (ET-1, collagen IV, TGF-β). Treatment with the combination of an ACE-i with D3-RA had an even significantly greater effect than monotherapy.
Beneficial effects of a D3-RA are remarkable in view of the known actions mediated by the D3 dopaminergic receptor. Disruption of the D3 receptor increased renal renin production, and caused renal sodium retention as well as renin-dependent hypertension in one study.23 The ability of dopamine to stimulate renin secretion is enhanced by a low sodium diet and blunted by a high sodium diet.24 A defective renal dopaminergic system seems to be a major cause of renal malfunction in Dahl salt-sensitive and spontaneously hypertensive rats: their kidneys produce less dopamine. The natriuretic and diuretic response to a sodium load is attenuated.25, 26, 27
In previous studies, D3-RA failed to change blood pressure values. In the present study, we found an antihypertensive effect of D3-RA, which was comparable in magnitude to the effect of an ACE-i. This effect may contribute to the renoprotective action. We believe, however, that the opposite is more probable, that is, that the effect of D3-RA on renal hemodynamics might have beneficially influenced systemic blood pressure.
The effect of the D3-RA on albuminuria was comparable in magnitude to that of monotherapy with an ACE-i, while the combination showed additive efficacy. This finding in diabetic animals cannot be solely explained by blood pressure effects, since in lean animals the D3-RA also reduced albuminuria to a similar extent, although no change in blood pressure was observed. Such an antiproteinuric effect is remarkable, since albuminuria induced by high altitude hypoxia is increased by dopamine. There is increasing interest in hypoxia as a mediator of progressive renal damage.28, 29 Studies of Norman et al30 documented that hypoxia increases matrix synthesis and decreases matrix breakdown in the renal interstitium.
Diabetic patients have an impaired ability to excrete sodium. It has been hypothesized that defective renal tubular dopamine mobilization may be responsible.31 A defective renal dopamine system has been documented early in type I diabetic patients and in individuals with familial hypertension.32
Glomerular hypertension/hyperfiltration plays a major role in the development of diabetic nephropathy.33 A D3 agonist caused a dose-related increase of glomerular filtration rate by up to 20%.34 Conversely, D3-RAs decrease glomerular hyperfiltration in experimental diabetes in rats.35
The D3-RA had remarkable effects on the renal structure. The glomerular volume was significantly increased in the diabetic SHR/N-cp and decreased in all pharmacological intervention groups. Since perfusion pressure during fixation was rigorously controlled, it is unlikely that the difference in glomerular volume was an artifact. It is very interesting that the D3-RA prevented not only the decrease of glomerular number in untreated diabetic animals compared to diabetic animals treated with ACE-i alone or combined with the DR3-RA. The latter prevented loss and hypertrophy of podocytes as well. The hypothesis had been advanced that dopamine D3 receptors are important modulators of glomerular filtration and contribute to hyperfiltration in diabetes.35 Our results are in agreement with this concept. In the glomerulus, strong D3 receptor immunoreactivity was demonstrated in podocytes36 and less pronounced in mesangial cells.37 The latter is relevant to the in vitro observation that angiotensin II induces a shape change of mesangial cells, which is abrogated by dopamine.38 The expression of D3 receptors on podocytes and mesangial cells is also relevant with respect to our observation that D3-RA prevented podocyte loss and mesangial cell growth in diabetic animals.
In diabetic animals, monotherapy with the D3-RA reduced glomerulosclerosis and vascular damage and also prevented mesangial cell growth and endothelial cell loss as effectively as an ACE-i.
The TBI was also somewhat lowered by the D3-RA; howeverm far less than with an ACE-i. These differences of the effect of a D3-RA were paralleled by the known differences in the expression of D3 receptors. They are found in glomerular cells and in proximal tubular epithelial cells, but not in cells of the tubulointerstitial space. Presumably under the stimulating influence of angiotensin II, cells in the tubulointertitium express TGF-β and ET-1. This finding explains the expected effect of ACE-i on the expression of TGF-β and ET-1 confirmed in the present study by immunohistochemistry, RT-PCR and in situ hybridization. Combination treatment led to numerically lower values of these parameters, but this was not statistically significant.
Podocyte damage was documented in our study by expression of desmin, which is known to be a sensitive marker of podocyte injury.39 All pharmacological interventions lowered podocyte damage. Podocytes possess receptors for a variety of hormones, including adrenergic beta (2) and dopamine D(1) receptors, stimulation of which increases cAMP,40 a potent regulator of actin assembly, cell morphology and matrix production.40 D3 receptors are expressed by podocytes as well, but not by mesangial cells as documented by O’Connell et al36 using immunohistochemistry. This is one further argument to assume that the beneficial effect of the D3-RA on GSI and desmin staining is a direct action of the antagonist and not an indirect result of altered hemodynamics.
It has been suggested that filtration slit structure injury and, in particular, podocyte loss contribute to the progressive development of glomerulosclerosis and albuminuria in diabetic nephropathy.41 Nephrin is located in the slit diaphragm of the glomerular podocyte barrier. Interestingly, ACE-i and D3-RB increased the expression of nephrin to a similar extent. It remains undecided, however, whether increased expression of nephrin and decreased expression of desmin in treated diabetic rats results from lower blood pressure and less proteinuria or whether it reflects a primary action of the D3-RA.
The SHR/N-cp rat is a model of type II diabetes, with modest hyperglycemia, but marked obesity. There is increasing evidence that obesity is a potent risk factor for progression.42, 43, 44 In the present study, obese SHR/N-cp rats had significantly higher plasma leptin concentrations. Leptin is a potential progression promoter45 and enhances the effect of TGF-β.46, 47 The action of leptin in some cells is mediated by norepinephrine, a leptin-inducible neurotransmitter. Against this background, it is of interest that both ACE-i and D3-RA reduced leptin concentrations in the present study.
In conclusion, the present experiments show a beneficial action of D3-RA treatment on renal changes in experimental type II diabetes, characterized by a lower albumin excretion and less structural damage. These effects were comparable to those achieved by ACE-i treatment. Since ACE inhibitors fail to completely prevent progression in patients with diabetic nephropathy, it would be of interest to evaluate whether the combination of an ACE-i with a D3-RA has superior efficacy in humans as well.
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M Adamczak has been supported by a Marie Curie Fellowship of the European Community programme: Improving the Human Research Potential and the Socio-economic knowledge base under Contract Number: HPMF-CT-2001-01501. The skilful technical assistance of Z Antoni, P Rieger and S Söllner is gratefully acknowledged. We thank Dr V Henschel, Department of Biostatistics, University of Heidelberg for statistical advice. Special thanks to H Derks and U Burkhardt for organizing photographs and the layout.
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Gross, ML., Koch, A., Mühlbauer, B. et al. Renoprotective effect of a dopamine D3 receptor antagonist in experimental type II diabetes. Lab Invest 86, 262–274 (2006). https://doi.org/10.1038/labinvest.3700383
- type II diabetes
- dopamine receptor antagonist
- glomerular cells
- dopamine D3 receptor
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