Nephroprotective effects of enalapril after [177Lu]-DOTATATE therapy using serial renal scintigraphies in a murine model of radiation-induced nephropathy
© The Author(s). 2016
Received: 7 May 2016
Accepted: 4 August 2016
Published: 11 August 2016
Radiation-induced nephropathy is still dose limiting in radionuclide therapy of neuroendocrine tumors. We investigated the nephroprotective potential of the angiotensine converting enzyme inhibiting drug enalpril after [177Lu]-DOTATATE therapy in a murine model of radiation-induced nephropathy by renal scintigraphy.
At first, the appropriate therapy activity to induce nephropathy was identified. Baseline scintigraphy (n = 12) entailed 12-min dynamic acquisitions after injection of 25 MBq [99mTc]-MAG3, which was followed by radionuclide therapy at four escalating activities of [177Lu]-DOTATATE: group (Gp) 1: 10 MBq; Gp 2: 20 MBq; Gp 3: 40 MBq; Gp 4: 65 MBq. Follow-up [99mTc]-MAG3 scintigraphy was carried out at days 9, 23, 44, and 65. The treatment activity for the intervention arm was selected on the basis of histological examination and declining renal function. In the second part, daily administration by gavage of 10 mg/kg/d enalapril or water (control group) was initiated on the day of radionuclide therapy. Follow-up scintigraphy was carried out at days 9, 23, 44, 65, and 86. We also created a non-therapy control group to detect therapy-independent changes of renal function over time. For all scintigraphies, mean renogram curves were analyzed and the “fractional uptake rate” (FUR; %I.D./min ± SEM) of the tracer by the kidneys was calculated as an index of renal clearance.
At day 65 of follow-up, no significant change in the FUR relative to baseline (11.0 ± 0.3) was evident in radionuclide therapy groups 1 (11.2 ± 0.5) and 2 (10.1 ± 0.6), but FUR was significantly reduced in groups 3 (8.93 ± 0.6, p < 0.05) and 4 (6.0 ± 0.8, p < 0.01); we chose 40 MBq [177Lu]-DOTATATE (Gp 3) for the intervention study. Here, at the last day of follow-up (day 86), FUR was unaltered in enalapril-treated mice (11.8 ± 0.5) relative to the baseline group (12.4 ± 0.3) and non-therapy group (11.9 ± 0.8), whereas FUR in the control group had undergone a significant decline (9.3 ± 0.5; p < 0.01). Histological examination revealed prevention of kidney damage by enalapril treatment.
Treatment with enalapril is effective for nephroprotection during radionuclide therapy with [177Lu]-DOTATATE in mice. Although these results are only limitedly transferable to human studies, enalapril might serve as a promising drug in the mitigation of nephropathy following treatment with [177Lu]-DOTATATE.
Peptide receptor radionuclide therapy (PRRT) with [Y-90-DOTA0,TYR3]-octreotide ([90Y]-DOTATOC) and [177Lu-DOTA0,TYR3]-octreotate ([177Lu]-DOTATATE) has emerged as a well-established therapy option in the treatment of inoperable or metastasized neuroendocrine tumors (NET) expressing somatostatin receptors [1, 2]. As reported in several studies, PRRT yields encouraging results with respect to favorable response rates and progression-free survival [1–8]. However, an important factor limiting benefits of this therapy is the occurrence of radiation-induced nephropathy, which arises due to renal clearance and megalin-receptor mediated tubular reabsorption of the chelated somatostatin analogues [9, 10]. Significant impairment in renal function has been reported both in clinical and in pre-clinical surveys [11–17]. There are various pharmacological strategies to decrease renal radiation exposure, for instance inhibiting tubular reabsorption. The co-administration of positively charged amino-acids, mainly arginine and lysine, reduces renal uptake of radiolabeled somatostatin analogues both in animal studies [16, 18] and in patient studies [19, 20]. Histopathological findings in kidneys after PRRT present a pattern of tubular and glomerular damage which seems similar to that evoked by external beam radiation .
The renin-angiotensin-aldosterone-system (RAAS) is also decisively implicated in the pathogenesis of radiation-induced nephropathy [21, 22]. RAAS-modifying pharmacotherapies have been ascertained for the reduction of renal damage after radiation in animal models. The nephroprotective potential of angiotensin-converting-enzyme (ACE) inhibitors after external beam radiation of the kidneys in rats was first reported by Cohen et al. in 1992 . The mitigative effects of ACE inhibitors were confirmed in further pre-clinical experiments by the same and other research groups [24, 25], as well as in humans by Moll et al. .
Given the similar pathologies and histopathological changes, we hypothesized that the pharmacological treatments effective in nephrotoxity induced by external beam radiation might also mitigate [177Lu]-DOTATATE induced nephrotoxicity.
Animals and experimental design
All animal experiments were conducted in accordance with institutional guidelines and approved by the ethics committee and Administrative Panel on Laboratory Animal Care (Government of Upper Bavaria, Germany; reference number 55.2-1-54-2531-136-09). We used female Balb C mice, aged 10 weeks and weighing 20 to 24 g (Charles River Laboratories, Sulzfeld, Germany), which were fed a standard diet and given free access to water.
No-carrier added lutetium-177 was obtained from Isotope Technologies Garching GmbH (Garching, Germany). DOTA0,TYR3-octreotate was obtained from ABX advanced biochemical compounds (Dresden, Germany). Radiolabeling was performed according to a previously described protocol [26, 27]. Other pharmaceuticals were obtained from Sigma-Aldrich (Taufkirchen, Germany).
The study consisted of two parts. In the first part, we investigated the activity-dependent impairment of renal function in mice treated with four activities of [177Lu]-DOTATATE: group 1 (n = 6), 10 MBq; group 2 (n = 8), 20 MBq; group 3 (n = 7), 40 MBq, and group 4 (n = 7), 65 MBq. PRRT was carried out at day 2. [177Lu]-DOTATATE was injected via the tail vein. Follow-up scintigraphies to assess renal function were carried out at days 9, 23, 44, and 65.
In the second part of the study, the nephroprotective properties of enalapril were evaluated in mice (n = 7) treated with 40 MBq [177Lu]-DOTATATE, as selected in part one. PRRT was performed under anesthesia as described above. Enalapril was administered by gavage on the day of radionuclide therapy, and daily thereafter until the end of the study. The pharmaceutical dose (10 mg/kg) was chosen in accordance with previously published studies . Control mice (n = 7) received daily gavage with sterile water. Furthermore, we created a third group of (n = 7) mice, which served as a non-therapy control. In this group, no PRRT was carried out and mice received MAG3 scintigraphy to identify therapy-independent changes in renal function over 3 months in healthy mice.
MAG3 scintigraphy was obtained at baseline in order to determine the renal function prior to PRRT. Follow-up renal scintigraphies to assess renal function were carried out in all mice at days 9, 23, 44, 65, and 86.
MAG3 scintigraphy (Technescan MAG3, Covidien, Neustadt/Donau, Germany) was performed as previously described [29–31]. After the induction of anesthesia with a combination of ketamine (75 mg/kg, i.p.) and medetomidine (1 mg/kg, i.p.), mice were placed on a thermostatically heated pad to maintain body temperature close to 37 °C. Mice received a standard activity of 25 MBq [99mTc]-MAG3 administered in 150 μl saline as a bolus via a tail vein. Whole body scintigraphic recordings using one head of a triple-headed gamma camera (Philips—former Picker—Prism 3000 XP, Cleveland, USA) equipped with a LEHR collimator were initiated upon tracer administration. The dynamic planar acquisitions consisted of 144 frames of 5 s each, to a total of 12 min. The image magnification was set to four times.
Histological assessment criteria for renal damage (adapted from Rolleman et. al, EJNMMI 2007 )
More or less normal aspect
Apoptosis of endothelium cells
High glomerular cell count
Rough protein staining
Normal basal membrane
No proteine cylinders
Same as grade 1
More apoptotic cells
Tubular cell damage
More pronounced dilation
Thickened basal membrane
Little tubular protein cylinders
Regenerating cells (mitotic activity)
Stronger tubular dilation
Smaller vascular lumina, few erythrocytes
Partly, complete loss of epithelium
More thickened basal membrane
Severe tubular dilation
Same as grade 3
Same as grade 3, but more empty cylinders
More optical empty space due to glomerular shrinkage
Data are expressed as mean ± SEM. Normality was tested with the Shapiro-Wilk test. The paired or unpaired t test (two-sided) was used to test statistical significant differences of normally distributed results, and the Mann-Whitney-U-test was used when normality requirements were not met, with p < 0.05 considered in both cases as statistically significant.
Identification of nephrotoxic activity of [177Lu]-DOTATATE
The synopsis of renogram, FUR analysis, and histopathological changes illustrated comprehensive renal damage at the two highest activities. We selected group 3 [177Lu]-DOTATATE activity (40 MBq) for the evaluation of pharmaceutical nephroprotection after enalapril treatment as a trade-off between producing a measureable defect and potentially excessive kidney failure.
Evaluation of pharmaceutical nephroprotection
Non-therapy control group
No relevant changes in mean renograms were observable during the follow-up period of 3 months (data not shown). Mean FUR values at the final day of follow-up revealed significant differences as compared to the water-treated control group, whereas no significant differences were measured in comparison to enalapril-treated mice underlining the nephroprotective effect of these treatment options (mean FUR after 3 months: 11.9 ± 0.8 %IA/min; p < 0.05 vs. water; p = n.s. vs. enalapril) (see Fig. 6). Histological sections did not reveal any renal damage in this group.
In clinical practice, the acceptable limit for kidney radiation during PRRT (23 Gy) is based upon findings with external beam radiation . Mitigation of nephrotoxicity would offer the possibility to increase the radioactivity per cycle of PRRT and/or increase the number of cycles, to the benefit of NET patients. With this in mind, we investigated the nephroprotective characteristics of enalapril treatment in a mouse model of [177Lu]-DOTATATE therapy-induced nephropathy based upon encouraging results in studies based on external beam radiation [12, 24, 25].
Renal laboratory parameters such as blood urea nitrogen (BUN) and creatinine were unaffected in rats 6 weeks after PRRT, despite the occurrence of histological proven nephrotoxicity . However, other studies are contradictory and describe an accordance of blood urea nitrogen and creatinine levels with kidney damage in mice, which was, however, true only in pronounced radiation-induced kidney damage [35, 36]. Therefore, we implemented MAG3 scintigraphy in order to quantify renal function in the course of treatments. MAG3 scintigraphy offers a non-invasive and individual evaluation of renal function in the course of radiation nephropathy . Firstly, we determined the activity of [177Lu]-DOTATATE-induced nephrotoxic effects measured with MAG3 scintigraphy in mice. The establishment of a mouse model is of great importance, as the availability of diverse immune-deficient mouse models could deliver more insight into immunological processes of radiation nephropathy in prospective studies. Renograms proved to be highly variable in mice, such that we decided to test the FUR quantitative approach, which provided a more sensitive index of the extent of renal failure at day 65. The FUR approach also showed clearly the temporal dynamics of altered renal function, which included a transient decline at day 9 irrespective of the [177Lu]-DOTATATE activity, subsequent recovery at days 23 and 44, and the emergence of a clearly activity-dependent nephrotoxic effect at day 65. However, the transient decline evident at day 9 even in the present group of mice receiving only 10 MBq [177Lu]-DOTATATE suggests the occurrence of acute toxicity at an activity far below that required to provoke chronic renal failure, which takes several months to develop.
The superiority of FUR to renograms is substantiated by the findings of our group in a mouse model of ischemia-reperfusion injury . We settled upon 40 MBq [177Lu]-DOTATATE, so as to obtain a distinct and reproducible impairment of renal function in the subsequent nephroprotection treatment arm of the study, without risking morbidity due to complete renal failure.
As noted above, the most common intervention for reducing kidney irradiation from radiolabeled somatostatin analogues is to competitively block their tubular reabsorption by co-infusion of basic amino-acids. Alternately, it might be possible to interfere with radiation-induced pathological processes leading to fibrosis and apoptosis. For example, the anti-oxidant amifostine attenuated renal damage in rats by the reduction of oxidative stress arising from [177Lu]-DOTATATE treatment . Dual therapy with amino acids and anti-oxidants might have an additive or super-additive (synergistic) effect in rescuing renal function following internal irradiation, but this approach has yet to be investigated. Given that the RAAS pathway seems to play a central role in the pathophysiology of radiation-induced nephropathy , pharmaceutical intervention and modification of the RAAS should also present avenues for the mitigation of renal damage during PRRT. Enalapril is of proven efficacy in reducing injury in therapies leading to comparable patterns of renal damage as are provoked by [177Lu]-DOTATATE therapy. In particular, enalapril prevented radiation nephritis and fibrosis in rats after external beam radiation [24, 38]. The underlying mechanism of this effect of enalapril is uncertain; however, changes in glomerular capillary pressure and a reduction of circulating angiotensin II are discussed to be responsible for the mitigation of renal damage .
In our study, enalapril treatment likewise substantially rescued renal function, which was restored to baseline levels at day 86, as measured by FUR, and as also seen by renogram analysis. Furthermore, renal histology was entirely normal in the enalapril-treatment group, providing further support for the potential clinical use of enalapril in reducing functional and histopathological changes in the kidney after PRRT with [177Lu]-DOTATATE.
We consistently found that kidney function was reduced in the acute phase 1 week after [177Lu]-DOTATATE therapy, for the entire range of activities as depicted in significantly decreased FUR values. This seems to be the first such report after PRRT in mice. We did not obtain histological sections at day 9, and so we are unable to ascertain if this initial decline in renal function is associated with structural alterations. The functional impairment evoked by 40 MBq at day 9 was not reduced by enalapril treatment and persisted in the water-treated control group until day 86. However, mean FUR scores had normalized by day 86 in enalapril-treated mice. As data on pharmacological nephroprotection in mice after PRRT is still missing, the applied dose of enalapril was based upon results of previously published studies dealing with other scientific questions. A dose-response analysis would have been more accurate and will be performed in upcoming studies.
Functional data was based on MAG3 scintigraphy within a period of almost 3 months. A rat study has shown that MAG3 is a highly sensitive marker for the detection of renal damage after [177Lu]-DOTATATE therapy within a follow-up period of almost 4 months . However, in a study dealing with folate-receptor-targeted therapy kidney damage was accurately measured using [99 m]-DMSA SPECT. This enabled an analysis of the correlation of kidney dose and kidney damage, which might offer an even more enhanced monitoring of kidney damage . A previous study of our workgroup demonstrated that MAG3 scintigraphy with one single head of a triple-headed camera was accurate enough to depict renal function. However, there are several studies using a dedicated dynamic animal-SPECT [39, 40]. Studies comparing these different methods are missing, but, e. g., in terms of ROI vs. VOI analysis and thus accuracy SPECT is likely to be superior. Nevertheless, with the aid of renogram analysis and the calculation of the FUR, persistent impairment of renal function in mice after [177Lu]-DOTATATE therapy activity of at least 40 MBq is measurable by scintigraphy and was verified by histology.
Treatment with enalapril for 3 months after radiotherapy with [177Lu]-DOTATATE mitigated renal damage in mice. Enalapril treatment could be an additional option for ameliorating the dose-limiting effects of radiation-induced kidney damage, thus allowing application of more effective therapy activities. Due to a moderate side effect profile and the applicability in patients with renal risk factors like hypertension and diabetes, which aggravate the nephrotoxicity of PRRT , enalapril treatment might be a promising therapy.
ACE, angiotensin-converting-enzyme; FUR, fractional uptake rate; HE, hematoxylin-eosin; MAG3, [99mTc]-mercaptoacetyltriglycine; NET, neuroendocrine tumor; PAS, periodic acid-Schiff reagent; PRRT, peptide receptor radionuclide therapy; RAAS, renin-angiotensin-aldosterone-system; ROI, region of interest
This study was funded by the FöFoLe program of the medical faculty of the Ludwig-Maximilians-University of Munich.
HI and AH contributed to the study design, preparation of the study, conducting of the measurements, analyzing of the data, drafting of the manuscript, and critical revision of the manuscript. HW, FG, CW, TH, AT, JS, and PC contributed to the preparation of the study, conducting of the measurements, and analyzing of the data. MH and PB contributed to the study design, drafting of the manuscript, and critical revision of the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
All animal experiments were conducted in accordance with institutional guidelines and approved by the ethics committee and Administrative Panel on Laboratory Animal Care (Government of Upper Bavaria, Germany; reference number 55.2-1-54-2531-136-09).
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