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Effect of tolvaptan on renal handling of water and sodium, GFR and central hemodynamics in autosomal dominant polycystic kidney disease during inhibition of the nitric oxide system: a randomized, placebo-controlled, double blind, crossover study
BMC Nephrology volume 18, Article number: 268 (2017)
Tolvaptan slows progression of autosomal dominant polycystic kidney disease (ADPKD) by antagonizing the vasopressin-cAMP axis. Nitric oxide (NO) stimulates natriuresis and diuresis, but its role is unknown during tolvaptan treatment in ADPKD.
Eighteen patients with ADPKD received tolvaptan 60 mg or placebo in a randomized, placebo-controlled, double blind, crossover study. L-NMMA (L-NG-monomethyl-arginine) was given as a bolus followed by continuous infusion during 60 min. We measured: GFR, urine output (UO), free water clearance (CH2O), fractional excretion of sodium (FENa), urinary excretion of aquaporin-2 channels (u-AQP2) and epithelial sodium channels (u-ENaCγ), plasma concentrations of vasopressin (p-AVP), renin (PRC), angiotensinII (p-AngII), aldosterone (p-Aldo), and central blood pressure (cBP).
During tolvaptan with NO-inhibition, a more pronounced decrease was measured in UO, CH2O (61% vs 43%) and FENa (46% vs 41%) after placebo than after tolvaptan; GFR and u-AQP2 decreased to the same extent; p-AVP increased three fold, whereas u-ENaCγ, PRC, p-AngII, and p-Aldo remained unchanged. After NO-inhibition, GFR increased after placebo and remained unchanged after tolvaptan (5% vs −6%). Central diastolic BP (CDBP) increased to a higher level after placebo than tolvaptan. Body weight fell during tolvaptan treatment.
During NO inhibition, tolvaptan antagonized both the antidiuretic and the antinatriuretic effect of L-NMMA, partly via an AVP-dependent mechanism. U-AQP2 was not changed by tolvaptan, presumeably due to a counteracting effect of elevated p-AVP. The reduced GFR during tolvaptan most likely is caused by the reduction in extracellular fluid volume and blood pressure.
Clinical Trial no: NCT02527863. Registered 18 February 2015.
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most frequent hereditary kidney diseases [1, 2]. It is characterized by accelerated cyst growth leading to increased total kidney volume (TKV) and worsening of kidney function . Orthologous ADPKD animal models suggest that vasopressin (AVP) plays a key role in the cytogenesis by promoting cystic epithelial cell proliferation, and by stimulating chloride-driven luminal fluid secretion [4,5,6,7,8]. This response is mediated by the second messenger adenosine 3′,5′- cyclic monophosphate (cAMP) as a consequence of activated vasopressin receptors (V2R). Intracellular aquaporin-2 (AQP2) water channels are in turn translocated to the apical plasma membrane of the collecting duct principal cells [4,5,6,7]. Activation of the V2R may also increase the synthesis of nitric oxide (NO), thereby facilitating renal water absorption by membrane insertion of AQP2 [9,10,11,12,13,14]. NO is synthesized from L-arginine, a NO synthase-catalyzed process competitively inhibited by L-NMMA . Previous clinical studies conducted by our laboratory demonstrated that NO promoted natriuresis and diuresis in healthy subject [15, 16]. Although these results support that NO is involved in the V2R response in the tubular function, it is unknown whether the response is similar in ADPKD patients.
Tolvaptan, a selective V2 receptor antagonist, has recently been approved by the European Medicines Agency (EMA) for the treatment of ADPKD corresponding to chronic kideney disease stages I-III . Tolvaptan reduced cyst growth corresponding to TKV and the decline in GFR by antagonizing the AVP-induced renal cAMP accumulation . The activity in AQP2 water channels and epithelial sodium channels has not previously been investigated in ADPKD patients before and after systemic NO inhibition during tolvaptan treatment. We hypothesized that 1. The function of AQP2- and ENaC channels is abnormal in ADPKD patients; 2. Tolvaptan decreases renal water- and sodium absorption; 3. This response is reduced by systemic NO-inhibition; and 4. Tolvaptan’s effect on renal water and sodium absorption is partially counteracted by increased blood pressure (BP) and vasoactive hormones at baseline and after systemic NO inhibition.
In the present randomized, placebo-controlled, double-blinded, crossover study of ADPKD patients, the aim was to measure tolvaptan’s effect at baseline and during NO inhibition on 1. GFR and tubular handling of water and sodium (GFR (51Cr-EDTA-clearance), urinary output (UO), free water clearance (CH2O), fractional excretion of sodium (FENa), urinary excretion of protein fragments from aquaporin 2 (u-AQP2) and epithelial sodium channels (u-ENaCγ), and urinary nitrate (u-nitrate)); 2. Blood pressure (brachial blood pressure (bBP), central BP (cBP), pulse wave velocity (PW), augmentation index (AI)); and 3. Vasoactive hormones in plasma (vasopressin (p-AVP), renin (PRC), angiotensinII (p-AngII), and aldosterone (p-Aldo)).
ADPKD patients meeting the following inclusion criteria were included:
Caucasian men and women
Age 18–65 yrs.
BMI 18.5–35.5 kg/m2
ADPKD diagnosed by genetic testing for PKD1 (> 85%) and PKD2 mutations, or presence of one of the following ultrasonographic findings in accordance to the classical Ravine criteria : a) patients with a negative family history of ADPKD with more than 10 cysts in each kidney, and exclusion of other causes of extra-renal or renal cyst formations, b) patients with a family history of ADPKD: 15–39 yrs. and 3 cysts or more unilaterally or bilaterally/ 40–59 yrs. and 2 or more cysts in each kidney/ 60 yrs. and at least 4 cysts in each kidney.
Kidney function corresponding to CKD stages 1–3 (eGFR > 30 mL/min/1,73 m2).
Exclusion criteria were: 1) clinical signs of diseases in the heart, lungs, endocrine organs, brain or neoplastic disease; 2) clinically significant abnormalities in blood or urine sample at the inclusion; 3) previous cerebrovascular insults; 4) previous clinical evidence of aneurysm; 5) alcohol or drug abuse; 6) smoking; 7) pregnancy or breastfeeding; 8) clinically significant changes in the electrocardiogram; 9) medication except antihypertensive agents and oral contraceptives; and 10) blood pressure > 170/105 mmHg despite treatment with metoprolol and/or amlodipine.
A randomized, double-blinded, placebo-controlled, crossover study was performed in patients with ADPKD before and after NO inhibition using L-NMMA. To test the difference between tolvaptan 60 mg and placebo, each patient participated in two examination days with an intermediate wash-out period of at least 3 weeks to eliminate any carryover effects.
Tolvaptan (SAMSCA®, Otsuka, Tokyo, Japan) 60 mg and placebo were coated in identical gelatine capsules and were orally administered at 8:00 AM. L-NMMA (Bachem, Weil am Rhein, Germany) was dissolved in isotonic saline solution and given intravenously at 11:00 AM.
Number of subjects
CH2O was used as the main effect variable. With a minimal relevant difference of 6 ml/min with an estimated standard deviation (SD) of 4 ml/min, and using a level of significance of 5% and a statistical power of 90%, 12 subjects were needed. To allow for possible drop-outs or incomplete voiding during the examination days, 18 subjects were included.
Eligible ADPKD patients were recruited from the Outpatient Nephrology Clinic of the Department of Medicine at Holstebro Hospital, Denmark.
The primary effect variable was CH2O. The secondary effect variables were 1) renal function (51Cr-EDTA clearance, UO, u-AQP2, u-ENaCγ, FENa, u-nitrate), 2) hemodynamics (bBP, cBP, PWV, AI, and 3) vasoactive hormones (PRC, p-ANG II, p-Aldo, p- AVP).
Antihypertensive medications including diuretics, angiotensin-converting enzyme (ACE) inhibitors, and angiotensin-II inhibitors were discontinued or substituted with metoprolol 50 mg and/or amlodipine 5 mg 14 days prior to each examination day. During the study period, bBP was examined weekly. In addition, 24-h blood pressure was performed 1 week after discontinuation or substitution of the usual antihypertensive treatment prior to the first examination day. Blood pressure of >170/105 mmHg, metoprolol 50 mg, and/or amlodipine 5 mg was given and increased up to metoprolol 150 mg and/or amlodipine 10 mg. Continued blood pressure > 170/105 mmHg despite treatment with metoprolol 150 mg and/or amlodipine 10 mg led to withdrawal from the study. The usual antihypertensive treatment was resumed immediately after the end of the examination day. Patients were given the same dose of metoprolol and/or amlodipine 14 days prior to the second examination day.
Prior to each examination day, ADPKD patients consumed a 4-day standardized diet of 11,000 KJ day−1. The diet was delivered from our facilities, and in conformity with general dietary guidelines, it was composed of 15% proteins, 55% carbohydrates and 30% fat. The sodium content was 150 mmol day−1. No additional sodium or other spices were allowed. The daily fluid intake was also standardized to 2.5 L, including a maximum of two cups of coffee or tea. No alcohol or soft drinks were allowed during the diet period.
The procedures were identical on the two examination days. A 24-h urine sample was collected and a fasting period of 8 h was allowed prior to each examination day. The two examinations were conducted at our facility from 7:45 AM to 1:00 PM.
At 8:00 AM, ADPKD patients were given placebo or tolvaptan 60 mg. An intravenous catheter was placed in each arm to collect blood samples and infuse 51Cr-EDTA. An oral water load of 175 ml was given at 8:00 AM and every 30 min.
BP was measured every 30 min from 8:30 AM to 1:00 PM. At 11:00 AM, a bolus infusion of L-NMMA 4.5 mg/kg was given, followed by continuous infusion (3 mg/kg/h) during 1 h. The dose was based on results from a dose-finding study of healthy subjects conducted by our laboratory . BP was measured every 5 min during infusion of L-NMMA, and every 15 min after infusion of L-NMMA.
From 8:30 AM to 1:00 PM, blood samples were drawn every 30 min and were analyzed for p-Na, p-osm, p-51Cr-EDTA, p-creatinine, and p-albumin. Every 60 min; at 11:00 AM (baseline), at 12:00 AM (after end of L-NMMA infusion), and at 1:00 PM (60 min after end of L-NMMA infusion), blood samples were collected to measure PRC, p-Aldo, p-Ang II, and p-AVP.
From 9:30 AM to 1:00 PM, urine samples were collected by voiding in standing or sitting position every 30 min after collecting BP measurements and blood samples. Otherwise subjects were kept in supine position in a quiet and temperature-controlled room (22–25 °C). Baseline periods were means of the first three clearance periods. The urine samples were analyzed for sodium, osmolality, AQP2, ENaCγ, creatinine, 51Cr-EDTA, and u-nitrate.
Applanation tonometry with SpygmoCor® (CPV System®, AtCor Medical, Sydney, Australia) was performed at 10:10 AM and at 11: 40 AM to measure cBP, PVW, and AI.
51Cr-EDTA clearance was measured using the constant infusion clearance technique with 51Cr-EDTA as a reference substance.
CH2O was determined using the formula CH2O = UO- Cosm, where Cosm is the osmolar clearance.
Clearance (C) of substance X was calculated as CX = UX/ (PX x UO), where UX denotes concentration of x in urine, PX denotes concentration of x in plasma, and UO is urine excretion rate.
Fractional excretion of sodium was determined according to the following formula: FENa = CNa/ 51Cr-EDTA-clearance ×100%, where CNa is sodium clearance.
Urinary excretion of AQP2
Urine samples were kept frozen at −20 °C until assayed. U-AQP2 were measured by RIA as previously described [24, 25]. The AQP2 antibody was a gift from Professor Soren Nielsen and Professor Robert Fenton, The Water and Salt Center, Aarhus University. It was raised in rabbits to synthetic peptide corresponding to the 15 COOH-terminal amino acids in human AQP2 to which was added an NH2- terminal cysteine for conjugation and affinity purification. Minimal detection level was 34 pg/tube. The coefficients of variation were 11.7% (inter-assay) and 5.9% (intra-assay).
Urinary excretion of ENaCγ
U-ENaCγ was measured by a modification of the RIA described previously [26, 27]. ENaCγ was synthesized and purchased by Lofstrand, Gaithersburg, Maryland, USA. The ENaCγ antibody was a gift from Professor Soren Nielsen and Professor Robert Fenton, The Water and Salt Center, Aarhus University. It was raised against a synthetic peptide in rabbits, and the affinity purified as described previously . Iodination of ENaCγ was performed by the chloramine T method using 40 μg of ENaCγ and 37 MBq 125I. The reaction was stopped by addition of 20% human serum albumin. 125I–labeled ENaCγ was separated from the iodination mixture by the use of a Sephadex G-25 Fine column. The assay buffer contained 40 mM sodium phosphate (pH = 7.4), 0.2% human albumin, 0.1% Triton X-100, and 0.4% EDTA. A 1.5% solution of bovine gamma globulin (Sigma) and 25% polyethylene glycol 6000 (Merck) also containing 0.625% Tween 20 (Merck) was prepared using the 40 mM phosphate buffer. Urine samples were kept frozen at −20 °C. After thawing out, samples were centrifuged for 10 min at 1.6 × 100 g (3000 rpm). Depending on osmolality of the supernatant, a sample volume was freeze-dried and kept at −20 °C until assayed. The mixture of 300 μl of freeze-dried or standard urine elutes dissolved in 300 μl assay buffer and 50 μl of antibody was incubated for 24 h at 4 °C. Thereafter, 50 μl of the tracer was added, and the mixture was incubated at 4 °C for a further 24 h. Bovine gamma globulin (100 μl) and 2 ml polyethylene glycol 6000 was added. After 30 min, the mixture was centrifuged at 4100 g for 20 min at 4 °C. The precipitate (bound fraction) was counted in a gamma counter after the supernatant (free fraction) was poured off. The unknown content in urine extracts was read from a standard curve. For 6 consecutive standard curves, the zero standard was 49.9 ± 1.6%. For increasing amounts of the ENaCγ standard, the binding inhibition was: 47.5 ± 1.3% (31 pg/tube), 44.0 ± 1.7% (62 pg/tube), 40.6 ± 1.4% (125 pg/tube), 34.6 ± 1.3% (250 pg/tube), 27.0 ± 1.5% (500 pg/tube), 20.4 ± 1.0% (1000 pg/tube), 13.6 ± 0.7% (2000 pg/tube), 8.4 ± 0.5% (4000 pg/tube), and 5.2 ± 0.5% (8000 pg/tube). The ID 50, i.e. the concentration of standard needed for 50% binding inhibition was 626 ± 32 pg/tube (n = 6). The nonspecific binding determined by performing the RIA without antibody was 1.0 ± 0.6% (n = 6). The inter-assay variation was determined by quality controls from the same urine pool spiked with ENaCγ standard. In consecutive assays, the coefficient of variation was as follows: 10% (6 assays) at a mean level of 338 pg/tube, 9% (6 assays) at a mean level of 743 pg/tube. The intra-assay variation was determined using samples from the same urine pool in several assays at different concentration levels. CV was 11% at a mean level of 110 pg/tube (n = 10). CV was 8.3% at a mean level of 118 pg/tube (n = 10). CV was 5.2%at a mean level of 325 pg/tube (n = 10). CV was 5.5% at a mean level of 754 pg/tube (n = 10). CV was 3.4% at a mean level of 942 pg/tube (n = 10). In addition, coefficients of variation were calculated based on duplicate determinations in different assays to 5.0% (n = 6) in the range 125–135 pg/tube, and 5.6% (n = 6) in the range 290–380 pg/ tube. The sensitivity calculated as the smallest detectable difference at the 95% confidence limit was 24 pg/tube in the range 90–130 pg/tube (n = 10), 33 pg/tube in the range 300–350 pg/tube (n = 10), 65 pg/tube in the range 890–1000 pg/tube (n = 10), The lower detectable limit of the assay was 35 pg/tube. It was calculated using the average zero binding for 6 consecutive assays minus 2 SD. The volume of urine used from the same pool varied with 15 different volumes in the range 250–5000 μl, and the mean concentration measured was 151 ± 18 pg/ml. There was a highly significant correlation between the extracted volume of urine and the amount of pg/tube (r = 0.986, n = 15, p < 0.000). When ENaCγ in the range 62.5–1000 pg was added to urine, a highly significant correlation was found between the measured and the expected values (r = 0.903, n = 20, p < 0.000).
Vasoactive hormones in plasma
Blood samples collected to measure vasoactive hormones were centrifuged for 10 min at 2200 G and 4 °C. Plasma was separated from blood cells and kept frozen until assayed. PRC was determined with an immunoradiometric assay from CIS Bio International, Gif-Sur-Yvette Cedex, France. The minimal detection level was 1 pg/tube. The coefficients of variation were 0.9–3.6% for the intra-assay and 3.7–5.0% for the inter-assay in the range of 4–236 pg/ml. Aldo was determined by RIA using a kit from Demeditec Diagnostics GmbH, Kiel, Germany. The minimal detection level was 25 pmol/L. The coefficients of variation were 9.0% for the inter-assay and 8.5% for the intra-assay. Ang II and AVP were extracted from plasma and subsequently determined by radioimmunoassay as previously described [29, 30]. Ang II was obtained from the Department of Clinical Physiology, Glostrup Hospital, Denmark. The minimal detection level was 2 pmol/ L. The coefficients of variation were 12% for the inter-assay and 8% for the intra-assay. The antibody against AVP was a gift from Jacques Dürr, Miami, Fl, USA. The minimal detection level was 0.2 pmol/L. The coefficients of variation were 13% for the inter-assay and 9% for the intra-assay.
Other biochemical measurements
Plasma osmolality was determined by using freeze-point depression (Multi-Sample Osmometer, Model 3900, Advanced Instruments, MA, USA). Urinary excretion rate of nitrate was determined by using a colorimetric assay using a kit from R&D Systems (Minneapolis, MN, USA) as previously decribed . Sodium, albumin, hemoglobin, and glucose were measured by routine methods in Department of Clinical Biochemistry, Holstebro Hospital, Denmark.
Brachial and central blood pressure
Brachial BP was measured using an oscillometer (Omron 705IT) and recorded in accordance with recommendations from the European Society of Hypertension. Brachial systolic and diastolic blood pressures were recorded as the average of duplicate measures. Central BP was measured using applanation tonometry. Recordings of carotid-femoral PWV and PWA were obtained by applanation tonometry (SphygmoCor® CPV System®, AtCor Medical, Sydney, Australia) as previously described .
Statistical analyses were performed using IBM SPSS statistics version 23.0.0 (SPSS Inc., Chicago, IL, USA). General Linear Model Repeated Measures were used for comparison between and within subjects to test differences between placebo and tolvaptan treatment at baseline and during and after L-NMMA infusion. Paired sample t-test or Wilcoxon’s signed rank test was performed to compare tolvaptan and placebo treatment at baseline and during and after L-NMMA infusion. Post-hoc Bonferoni test was performed to compare differences between baseline versus during and after L-NMMA infusion. Statistical significance was at <0.05 in all analyses. Data with normal distribution are presented as means ± SD/SEM or medians with 25th and 75th percentiles. Non-parametric test was performed for data with non-normal distribution, and such data are reported as medians with 25th and 75th percentiles.
Twenty-one ADPKD patients with CDK stage I-III were included in the study. Three of the patients were excluded due to withdrawal of consent. Eighteen patients completed the study; 6 males and 12 females. Their mean age was 47 years (range 21–62 years), weight 85.2 ± 12.7 kg, BMI 28 ± 5 kgm2, p-sodium 141 ± 1.7 mmol/L, p-potassium 3.8 ± 0.2 mmol/L, p-creatinine 84.2 ± 23.8 μmol/L, systolic brachial blood pressure (SBP) 137 ± 13 mmHg, diastolic brachial blood pressure (DBP) 88 ± 7 mmHg.
Urine collection before the examination day
24-h urine samples were collected prior to each examination day. Values are shown in Table 1. No differences were measured in UO, CH2O, u-AQP2, u-Na, and u-K between the treatment periods.
Body weight during the examination day
No difference was measured in body weight at the beginning and at the end of the examination day after placebo (83.2 ± 12,8 kg vs 83.4 ± 12.8 kg). After tolvaptan 60 mg, body weight decreased significantly at the end of the examination day compared with the beginning of the examination day (83.1 ± 12.1 kg vs 82.1 ± 12.1 kg, p = 0.001).
During baseline, 51Cr-EDTA clearance was the same after placebo and tolvaptan 60 mg (Table 2). During L-NMMA infusion, 51Cr-EDTA clearance decreased significantly and similarily after both treatments during the first 30 min of L-NMMA infusion (paired t-test: placebo p = 0.028 and tolvaptan p = 0.001). There was no difference in the relative changes in 51Cr-EDTA clearance between groups (Fig. 1a).
During the post infusion period, 51Cr-EDTA clearance was unchanged after placebo and decreased after tolvaptan during the entire post infusion period (paired t-test: during the post infusion period 150–180 min p = 0.008 and during the post infusion period 180–210 min p = 0.001). The relative changes in 51Cr-EDTA clearance were only differed during the first 30 min of the post-infusion period (p = 0.012).
Tubular water excretion
During baseline, UO and CH2O were significantly lower after placebo than after tolvaptan treatment. During L-NMMA infusion 90–120 min, UO and CH2O decreased after both treatments. The relative decrease in UO and CH2O from baseline to NO inhibition was significantly higher after placebo than after tolvaptan (p = 0.035 and 0.003). However, CH2O also decreased relatively more during the last 30 min of the L-NMMA infusion period (120–150 min), unlike UO.
During the post infusion period 180–210 min, UO and CH2O increased towards baseline level after placebo, but remained suppressed after tolvaptan at the level that was measured during NO inhibition.
Tubular sodium excretion
During baseline, no difference was measured in FENa during placebo and tolvaptan treatment.
During L-NMMA infusion 120 min, FENa significantly decreased after placebo, but remained unchanged after tolvaptan (placebo: 0.48% (corresponding to a percentage decrease of 35%) compared with tolvaptan: 0.32% (26%)). The relative changes from baseline to NO inhibition showed a tendency to lower level of FENa after placebo (p = 0.055). During the remaining L-NMMA infusion period 180–210 min, FENa decreased significantly more after placebo than after tolvaptan.
During the post-infusion period, FENa remained relatively lower after placebo. During the last 30 min of the post-infusion period, FENa increased to baseline level after tolvaptan and remained 26% lower compared with baseline level after placebo.
U-AQP2 and u-ENaCγ
During baseline, we saw a tendency towards a higher level of u-AQP2 after placebo treatment (p = 0.075). During L-NMMA infusion, u-AQP2 decreased to the same extent in both absolute and relative values. During the post-infusion period (180–210 min), u-AQP2 returned to baseline level after placebo, but remained lower after tolvaptan treatment (p = 0.015). However, no difference was measured in the relative values between treatments, despite a considerable difference in u-AQP2 which may be due to a large variation in u-AQP2.
During baseline, u- ENaCγ was alike in the two treatment groups (0.78 ng/min vs 0.75 ng/min). During L-NMMA infusion, no difference in either absolute or relative measures existed between treatments. The same result was measured in the post-infusion period.
Plasma sodium and plasma osmolarity
During baseline, p-sodium and p-osm were significantly lower after placebo than after tolvaptan (Table 3). During L-NMMA infusion, p-sodium and p-osm remained lower after placebo and this response was sustained throughout the examination day.
Urinary excretion rate of nitrate
During baseline, a significantly higher urinary excretion rate of NO3 (u-NO3) was measured after placebo treatment (placebo 0.61 ± 0.23 μmol/min vs tolvaptan: 0.50 ± 0.14 μmol/min, p = 0.027).
During L-NMMA infusion, u-NO3 decreased significantly from the baseline level after both treatments (placebo: 0.39 ± 0.16 μmol/min and tolvaptan: 0.35 ± 0.11 μmol/min, p = 0.001). However, the decrease in u-NO3 was identical (p = 0.185). The same response was measured during the post-infusion period (placebo: 0.36 ± 0.15 μmol/min and tolvaptan: 0.35 ± 0.10 μmol/min).
During L-NMMA infusion, the response measured during baseline conditions was sustained throughout the NO-inhibition period and also in the post-infusion period.
Brachial and central blood pressure
During baseline, no significant difference was measured in SPB, DBP, and pulse rate (Table 5). The values were unaffected both during L-NMMA infusion, and the post-infusion period.
During baseline, no change was measured in PWV, AI, CSPB, or CDBP (Table 6).
During L-NMMA infusion, PWV increased identically after both treatments. AI also increased, but only after placebo and to the same level as that measured after tolvaptan. Central SBP (CSBP) increased alike after both treatments. Although CDBP increased after placebo and tolvaptan treatment, CDBP remained significantly higher after placebo (p = 0.004).
The present paper reports short-term effects of tolvaptan on renal water and sodium excretion, vasoactive hormones, and brachial and central blood pressures during baseline and after systemic inhibition of the NO system in ADPKD patients.
The major results of the study were: During baseline, tolvaptan increased renal water excretion with no effect on sodium excretion. During NO-inhibition, tolvaptan decreased both water and sodium excretion to a lesser extent compared with placebo. During the post-infusion period, the reduced water excretion remained after tolvaptan, whereas sodium excretion returned towards baseline level. After NO-inhibition, GFR increased after placebo and remained unchanged after tolvaptan (5% vs −6%). Central diastolic BP increased to a higher level after placebo than tolvaptan. Body weight fell during tolvaptan treatment.
51 Cr-EDTA clearance
GFR fell after tolvaptan treatment in the post-infusion period 150–180 min, whereas51Cr-EDTA clearance was unchanged after placebo. This reduction may be attributed to changes in renal hemodynamics induced by tolvaptan . Alternatively, the fall in GFR could be caused by dehydration due to increased renal water excretion after tolvaptan. However, it cannot be excluded that the elevated p-AVP level led to V1a receptor-mediated mesangial cell contraction and thus reduced GFR [33, 34]. Most likely, mild dehydration and extracellular fluid volume reduction is - at least partly - the explanation, since our patients lost approximately 1 kg in body weight after tolvaptan treatment, in contrast to an unchanged body weight during placebo. This is in good agreement with the significantly lower CDBP and the higher urinary output during tolvaptan treatment compared with placebo. The increase in p-AVP was very pronounced during tolvaptan, i. e. threefold larger than during placebo, and might have inhibited further blood pressure fall by a stimulation of the V1a receptor in the vascular bed. No increase was measured in the components in the renin-angiotensin-aldosterone system, which could have been expected after mild dehydration, but the very large increase in p-AVP seemed to have been a sufficient vasoconstrictor response during tolvaptan treatment. In our previous RCTs with tolvaptan, we did not measure a decrease in 51Cr-EDTA clearance [15, 16]. However, in these trials, we studied healthy control subjects, and the dosis of tolvaptan used was 15–45 mg in contrast to a dosis of 60 mg in the present study. Our results during baseline condition are in good agreement with those reported by Boertien et al. , where tolvaptan did not change renal hemodynamics in ADPKD with chronic kidney disease stages I-III. However, minor reduction in GFR occurred and was explained as related to acute, reversible inhibition by the tubulo-glomerular feedback mechanism [35, 36]. The TEMPO 3:4 trial and post hoc analysis of the TEMPO 3:4 trial showed that tolvaptan reduced the annual eGFR decline in ADPKD by 26% (from 3.70 to 2.72 mL/min/1.73 m2) . Tolvaptan induced an acute decrease in eGFR during initiation of treatment. However, after discontinuation of tolvaptan, eGFR increased again. This is in good agreement with the results from the present acute study, in which GFR decreased after tolvaptan and remained lower throughout the post infusion. During NO-inhibition, we clearly demasked a reduction in 51Cr-EDTA clearance by tolvaptan. Thus, tolvaptan in a dose of 60 mg reduced glomerular filtration rate in ADPKD both with and without blockade of the nitric oxide synthesis.
Tubular water excretion
As expected, tolvaptan increased renal water excretion during baseline conditions. This result is in accordance with our previous RCT in healthy subjects [15, 16]. Both studies proved increased renal water excretion following tolvaptan administration. Also, the results from the dose-response study showed that the increased renal water excretion was dose-dependent up to tolvaptan 30 mg. However, the levels of CH2O and UO after tolvaptan 60 mg in ADPKD were approximately the same as after tolvaptan 30 and 45 mg in healthy subjects, which is compatible with a dysfunctional urine concentration ability in ADPKD kidneys. Thus, a higher dose of tolvaptan was necessary to induce a diuretic response in ADPKD patients. This agrees well with previous ADPKD studies [3, 21, 35, 36].
During NO inhibition, tolvaptan antagonized the antidiuretic action of L-NMMA, at least partly by an AVP-dependent mechanism. In our single-dose study, tolvaptan 15 mg promoted renal water excretion . In the dose-response study, tolvaptan antagonized the antidiuretic action of L-NMMA, in part via an AVP-dependent mechanism consistent with the present study . This apparent discrepancy could be explained by a difference in the administration time of the study drug, since tolvaptan was given at 6:00 AM in the single-dose study compared with 8:00 AM in the dose-response study and the present study. Thus tolvaptan antagonized the antidiuretic effect of NO-inhibition in ADPKD.
ADPKD cysts arise primarily from AVP-sensitive tubular segments and they have overexpression of V2R and AQP2 [37, 38]. Several studies have shown that tolvaptan’s diuretic action is caused by preventing AVP to bind to the V2 receptors, and thus to activate AQP2 by the second messenger cAMP. In the present study, we measured a similar level of u-AQP2 after placebo and tolvaptan, which is in agreement with our previous studies [15, 16]. This response could be explained by the 3-fold increase in p-AVP after tolvaptan. U-AQP2 reflects the action of AVP on the collecting ducts [25, 39]. Even modest changes in p-AVP have been shown to change the activity in AQP2 water channels within a few hours [40,41,42]. Since AQP2 is the only known apical water channel in the plasma membrane and the density of AQP2 in the plasma membrane is a rate-limiting barrier for tubular water transport , the compensatory and very pronounced increase in p-AVP may have counteracted tolvaptan’s effect on the V2-receptors. The very large increase in p-AVP after tolvaptan corresponds very well with our previous RCTs [15, 16].
Tubular sodium excretion
In the present study of ADPKD, FENa decreased more after placebo than after tolvaptan during NO-inhibition. This response differs from our previous RCTs of healthy subjects [15, 16]. In both studies, FENa decreased after placebo and tolvaptan during NO-inhibition. However, in the dose-response study, FENa decreased most pronouncedly after tolvaptan . Thus, in ADPKD, urinary sodium excretion seems to be lower after tolvaptan than in healthy control subjects, most likely due to an abnormal tubular function in CKD stages 1–3. In the present study, u-ENaC was the same after tolvaptan and placebo, which is in agreement with our results from a previous study in ADPKD . In accordance with the present study, it showed that ADPKD patients have an abnormal tubular sodium absorption unrelated to the activity in the epithelial sodium channels .
Vasoactive hormones and brachial and central blood pressure
We measured no significant changes in the components of the renin-angiotensin-aldosterone system during tolvaptan treatment, which is in agreement with our previous study in healthy subjects [15, 16]. CDBP was higher after placebo than after tolvaptan during the post-infusion period. Dehydration may have contributed to the lower level in CDBP as evidenced by body weight reduction in the tolvaptan group. These results are in good agreement with our previous studies [15, 16]. AVP has been suggested to contribute to the development of hypertension through the V2R by different ways. On one hand, AVP promotes function and expression of ENaC, and potentiates the effect of aldosterone on the collecting ducts [44, 45]. On the other hand, activation of V2R also exerts an antihypertensive effect by increasing the synthesis of NO in the collecting ducts and by increasing renal plasma flow [46,47,48]. However, u-ENaC was unchanged, and the NO-system was blocked in the present study. Apparently, these mechanisms were not involved in the blood pressure regulation in the present study. The very high level of AVP during tolvaptan treatment might have stimulated VR1 receptors in the vascular bed, and it cannot be excluded that this stimulation has compensated for further blood pressure decrease during tolvaptan treatment.
Urinary excretion rate of nitrate
We found a lower baseline u-NO3 after tolvaptan. However, the difference was minimal and further studies with larger population are necessary to reveal any difference. During NO-inhibition u-NO3 decreased after both treatments confirming proper inhibition of NO-synthesis.
Tolvaptan treatment has been associated with common adverse events including polyuria, nocturia and hepatotoxicity . In the present study, none of these adverse events were observed. Howerver, the observation time was relatively short and our patients had normal liver function at the inclusion. Tolvaptan dose was administered according to the ERA-EDTA recommendations, namely CKD stages 1–3 and independent of body weight .
Strengths and limitations
The study design as a randomized, placebo-controlled, double-blinded, crossover is one of the major strengths of the present study. Another major strength is the use of standardized diet and fluid intake to avoid any confounding of the results. Furthermore, urinary nitrate measurement has been performed to directly document inhibition of the NO system.
The methods used to analyze u-AQP2 and u-ENaC have limitations. Emerging data suggest that the regulated fractions of these channels are excreted as urinary exosomes. These fractions were not isolated and therefore not analyzed in the present study. However, our laboratory and others have previously shown positive correlation to the function reflected by the methods used in this study.
A proportion of the patients was treated with antihypertensives during the examination period, since withdrawal of antihypertensive treatment was not ethically justified, but the treatment was the same during both placebo and tolvaptan treatment, thus a possible difference due to use of antihypertensive therapy would be expected to be minimal.
During NO inhibition, tolvaptan antagonized both the antidiuretic and the antinatriuretic effect of L-NMMA, partly via an AVP-dependent mechanism. U-AQP2 was not changed by tolvaptan, presumably due to a counteracting effect of elevated p-AVP. The reduced GFR during tolvaptan most likely is caused by the reduction in extracellular fluid volume and blood pressure.
Our findings express short-term effects of tolvaptan before and during inhibition of NO. Therefore, studies with longer treatment periods are needed to clarify long-term effects of tolvaptan.
Autosomal Dominant Polycystic Kidney Disease
Brachial blood pressure
Central blood pressure
Central diastolic blood pressure
- CH2O :
Free water clearance
Central systolic blood pressure
Diastolic blood pressure
European Medicines Agency
- FENa :
Fractional excretion of sodium
- GFR (51Cr-EDTA-clearance):
Glomerular filtration rate
Plasma angiotensin II
Plasma concentrations of rennin
Pulse wave velocity
Systolic blood pressure
Urinary aquaporin-2 channels
Urinary epithelial sodium channels
- u-NO3 :
Urinary excretion rate of nitrate
Steinman TI. Polycystic kidney disease: a 2011 update. Curr Opin Nephrol Hypertens. 2012;21(2):189–94.
Devuyst O, Knoers NV, Remuzzi G, Schaefer F. Board of the Working Group for inherited kidney diseases of the European Renal Association and European dialysis and transplant association. Rare inherited kidney diseases: challenges, opportunities, and perspectives. Lancet. 2014;383(9931):1844–59.
Torres VE, Chapman AB, Devuyst O, et al. Tolvaptan in patients with autosomal dominant polycystic kidney disease. N Engl J Med. 2012;367(25):2407–18.
Wang X, Wu Y, Ward CJ, Harris PC, Torres VE. Vasopressin directly regulates cyst growth in polycystic kidney disease. J Am Soc Nephrol. 2008;19(1):102–8.
Gattone VH 2nd, Wang X, Harris PC, Torres VE. Inhibition of renal cystic disease development and progression by a vasopressin V2 receptor antagonist. Nat Med. 2003;9(10):1323–6.
Torres VE, Wang X, Qian Q, Somlo S, Harris PC, Gattone VH 2nd. Effective treatment of an orthologous model of autosomal dominant polycystic kidney disease. Nat Med. 2004;10(4):363–4.
Wang X, Gattone V 2nd, Harris PC, Torres VE. Effectiveness of vasopressin V2 receptor antagonists OPC-31260 and OPC-41061 on polycystic kidney disease development in the PCK rat. J Am Soc Nephrol. 2005;16(4):846–51.
Reif GA, Yamaguchi T, Nivens E, Fujiki H, Pinto CS, Wallace DP. Tolvaptan inhibits ERK-dependent cell proliferation, cl(−) secretion, and in vitro cyst growth of human ADPKD cells stimulated by vasopressin. Am J Physiol Renal Physiol. 2011;301(5):F1005–13.
Klokkers J, Langehanenberg P, Kemper B, Kosmeier S, von Bally G, Riethmuller C, Wunder F, Sindic A, Pavenstadt H, Schlatter E, Edemir B. Atrial natriuretic peptide and nitric oxide signaling antagonizes vasopressin-mediated water permeability in inner medullary collecting duct cells. Am J Physiol Renal Physiol. 2009;297:F693–703.
Bouley R, Breton S, Sun T, McLaughlin M, Nsumu NN, Lin HY, Ausiello DA, Brown D. Nitric oxide and atrial natriuretic factor stimulate cGMP-dependent membrane insertion of aquaporin 2 in renal epithelial cells. J Clin Invest. 2000;106:1115–26.
Kurtz A, Wagner C. Role of nitric oxide in the control of renin secretion. AmJ Physiol. 1998;275:F849–62.
Ortiz PA, Garvin JL. Role of nitric oxide in the regulation of nephron transport. Am.J. Physiol Renal Physiol. 2002;282:F777–84.
Forstermann U, Sessa WC. Nitric oxide synthases: regulation and function. European heart journal. 2012;33(7):829–837, 837a–837d.
Baylis C. Nitric oxide deficiency in chronic kidney disease. Am.J. Physiol Renal Physiol. 2008;294:F1–9.
Al Therwani S, Mose FH, Jensen JM, Bech JN, Pedersen EB. Effect of vasopressin antagonism on renal handling of sodium and water and central and brachial blood pressure during inhibition of the nitric oxide system in healthy subjects. BMC Nephrol. 2014;15:100. doi:10.1186/1471-2369-15-100.
Al Therwani S, Rosenbaek JB, Mose FH, Bech JN, Pedersen EB. Effect of tolvaptan on renal water and sodium excretion and blood pressure during nitric oxide inhibition: a dose-response study in healthy subjects. BMC Nephrol. 2017;18(1):86. doi:10.1186/s12882-017-0501-1.
Schafer JA. Abnormal regulation of ENaC: syndromes of salt retention and salt wasting by the collecting duct. Am J Physiol Renal Physiol. 2002;283(2):F221–35.
Schafer JA, Hawk CT. Regulation of na+ channels in the cortical collecting duct by AVP and mineralocorticoids. Kidney Int. 1992;41(2):255–68.
Butterworth MB, Edinger RS, Johnson JP, Frizzell RA. Acute ENaC stimulation by cAMP in a kidney cell line is mediated by exocytic insertion from a recycling channel pool. J Gen Physiol. 2005;125(1):81–101.
Graffe CC, Bech JN, Lauridsen TG, Pedersen EB. Urinary excretion of AQP2 and ENaC in autosomal dominant polycystic kidney disease during basal conditions and after a hypertonic saline infusion. AmJ Physiol Renal Physiol. 2012;302:F917–27.
Gansevoort RT, Arici M, Benzing T, et al. Recommendations for the use of tolvaptan in autosomal dominant polycystic kidney disease: a position statement on behalf of the ERA-EDTA working groups on inherited kidney disorders and european renal best practice. Nephrol Dial Transplant. 2016;31(3):337–48.
Ravine D, Gibson RN, Walker RG, Sheffield LJ, Kincaid-Smith P, Danks DM. Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1. Lancet. 1994;343(8901):824–7.
Larsen T, Mose FH, Bech JN, Pedersen EB. Effect of nitric oxide inhibition on blood pressure and renal sodium handling: a dose-response study in healthy man. Clin Exp Hypertens. 2012;34(8):567–74.
Graffe CC, Bech JN, Pedersen EB. Effect of high and low sodium intake on urinary aquaporin-2 excretion in healthy humans. AM J Physiol Renal Physiol. 2012;302(2):F264–75.
Pedersen RS, Bentzen H, Bech JN, Pedersen EB. Effect of water deprivation and hypertonic saline infusion on urinary AQP2 excretion in healthy humans. Am J Physiol Renal Physiol. 2001;280(5):F860–7.
Matthesen SK, Larsen T, Lauridsen TG, Vase H, Gjorup PH, Nykjaer KM, Nielsen S, Pedersen EB. Effect of amiloride and spironolactone on renal tubular function, ambulatory blood pressure, and pulse wave velocity in healthy participants in a double-blinded, randomized, placebo-controlled, crossover trial. Clin Exp Hypertens. 2012;34(8):588–600.
Lauridsen TG, Vase H, Bech JN, Nielsen S, Pedersen EB. Direct effect of methylprednisolone on renal sodium and water transport via the principal cells in the kidney. Eur J Endocrinol. 2010;162:961–9.
Hager H, Kwon TH, Vinnikova AK, et al. Immunocytochemical andimmunoelectron microscopic localization of alpha-, beta-, and gamma-ENaC in rat kidney. Am J Physiol Renal Physiol. 2001;280:F1093–106.
Pedersen EB, Danielsen H, Spencer ES. Effect of indapamide on renal plasma flow, glomerular filtration rate and arginine vasopressin in plasma in essential hypertension. Eur J Clin Pharmacol. 1984;26(5):543–7.
Pedersen EB, Eiskjaer H, Madsen B, Danielsen H, Egeblad M, Nielsen CB. Effect of captopril on renal extraction of renin, angiotensin II, atrial natriuretic peptide and vasopressin, and renal vein renin ratio in patients with arterial hypertension and unilateral renal artery disease. Nephrol Dial Transplant. 1993;8(10):1064–70.
Mose FH, Jensen JM, Therwani S, et al. Effect of nebivolol on renal nitric oxide availability and tubular function in patients with essential hypertension. Br J Clin Pharmacol. 2015;80(3):425–35.
Boberg U, Persson AE. Tubuloglomerular feedback during elevated renal venous pressure. Am J Phys. 1985;249(4 Pt 2):F524–31.
Bichet DG, Razi M, Arthus MF, et al. Epinephrine and dDAVP administration in patients with congenital nephrogenic diabetes insipidus. Evidence for a pre-cyclic AMP V2 receptor defective mechanism. Kidney Int. 1989;36(5):859–66.
Irazabal MV, Torres VE, Hogan MC, et al. Short-term effects of tolvaptan on renal function and volume in patients with autosomal dominant polycystic kidney disease. Kidney Int. 2011;80(3):295–301.
Boertien WE, Meijer E, de Jong PE, et al. Short-term renal hemodynamic effects of tolvaptan in subjects with autosomal dominant polycystic kidney disease at various stages of chronic kidney disease. Kidney Int. 2013;84(6):1278–86.
Torres VE. Vasopressin in chronic kidney disease: an elephant in the room? Kidney Int. 2009;76(9):925–8.
Wallace DP. Cyclic AMP-mediated cyst expansion. Biochim Biophys Acta. 2011;1812(10):1291–300.
Bachinsky DR, Sabolic I, Emmanouel DS, et al. Water channel expression in human ADPKD kidneys. Am J Phys. 1995;268(3 Pt 2):F398.
Nielsen S, Chou CL, Marples D, Christensen EI, Kishore BK, Knepper MA. Vasopressin increases water permeability of kidney collecting duct by inducing translocation of aquaporin-CD water channels to plasma membrane. Proc Natl Acad Sci U S A. 1995;92(4):1013–7.
Nielsen S, Kwon TH, Christensen BM, Promeneur D, Frokiaer J, Marples D. Physiology and pathophysiology of renal aquaporins. JAm Soc Nephrol. 1999;10:647–63.
Nielsen S, Knepper MA. Vasopressin activates collecting duct urea transporters and water channels by distinct physical processes. Am J Phys. 1993;265(2 Pt 2):F204–13.
Bankir L. Antidiuretic action of vasopressin: quantitative aspects and interaction between V1a and V2 receptor-mediated effects. Cardiovasc Res. 2001;51(3):372–90.
Flamion B, Spring KR. Water permeability of apical and basolateral cell membranes of rat inner medullary collecting duct. Am J Phys. 1990;259(6 Pt 2):F986–99.
Djelidi S, Fay M, Cluzeaud F, et al. Transcriptional regulation of sodium transport by vasopressin in renal cells. J Biol Chem. 1997;272(52):32919–24.
Loffing J, Korbmacher C. Regulated sodium transport in the renal connecting tubule (CNT) via the epithelial sodium channel (ENaC). Pflugers Arch. 2009;458(1):111–35.
Ahn KY, Mohaupt MG, Madsen KM, Kone BC. In situ hybridization localization of mRNA encoding inducible nitric oxide synthase in rat kidney. Am J Physiol Renal Fluid Electrolyte Physiol. 1994;267:F748–57.
Stoos BA, Garcia NH, Garvin JL. Nitric oxide inhibits sodium reabsorption in the isolated perfused cortical collecting duct. J Am Soc Nephrol. 1995;6(1):89–94.
Koshimizu TA, Nasa Y, Tanoue A, et al. V1a vasopressin receptors maintain normal blood pressure by regulating circulating blood volume and baroreflex sensitivity. Proc Natl Acad Sci U S A. 2006;103(20):7807–12.
The authors thank Otsuka for a research grant to the study.
We thank our laboratory technicians, including Anne Mette Ravn, Henriette Vorup Simonsen and Kirsten Nygaard for their skillful assistance.
The study was supported by grants from The Research Foundation of Central Denmark Region and Otsuka.
Availability of data and materials
The datasets used/or analyzed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
This study was approved by The Central Denmark Region Committees on Health Research Ethics (Clinical Trial no: NCT02527863). The study was conducted in conformity with the principles of the declaration of Helsinki. Written informed consent was obtained from all subjects.
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Al Therwani, S., Malmberg, M.E.S., Rosenbaek, J.B. et al. Effect of tolvaptan on renal handling of water and sodium, GFR and central hemodynamics in autosomal dominant polycystic kidney disease during inhibition of the nitric oxide system: a randomized, placebo-controlled, double blind, crossover study. BMC Nephrol 18, 268 (2017) doi:10.1186/s12882-017-0686-3
- Nitric oxide
- Blood pressure
- Vasoactive hormones