- Open Access
Exendin-4 and sitagliptin protect kidney from ischemia-reperfusion injury through suppressing oxidative stress and inflammatory reaction
Journal of Translational Medicine volume 11, Article number: 270 (2013)
This study tested the hypothesis that exendin-4 and sitagliptin can effectively protect kidney from acute ischemia-reperfusion (IR) injury.
Adult SD-rats (n = 48) equally divided into group 1 (sham control), group 2 (IR injury), group 3 [IR + sitagliptin 600 mg/kg at post-IR 1, 24, 48 hr)], and group 4 [IR + exendin-4 10 μm/kg at 1 hr after procedure] were sacrificed after 24 and 72 hrs (n = 6 at each time from each group) following clamping of bilateral renal pedicles for 60 minutes (groups 2–4).
Serum creatinine level and urine protein to creatinine ratio were highest in group 2 and lowest in group 1 (all p < 0.001) without notable differences between groups 3 and 4. Kidney injury score, expressions of inflammatory biomarkers at mRNA (MMP-9, TNF-α, IL-1β, PAI-1), protein (TNF-α, NF-κB and VCAM-1), and cellular (CD68+) levels in injured kidneys at 24 and 72 hr showed an identical pattern compared to that of creatinine level in all groups (all p < 0.0001). Expressions of oxidized protein, reactive oxygen species (NOX-1, NOX-2), apoptosis (Bax, caspase-3 and PARP), and DNA damage marker (γH2AX+) of IR kidney at 24 and 72 hrs exhibited a pattern similar to that of inflammatory mediators among all groups (all p < 0.01). Renal expression of glucagon-like peptide-1 receptor, and anti-oxidant biomarkers at cellular (GPx, GR) and protein (NQO-1, HO-1, GPx) levels at 24 and 72 hr were lowest in group 1, significantly lower in group 2 than in groups 3 and 4 (all p < 0.01).
Exendin-4 and sitagliptin provided significant protection for the kidneys against acute IR injury.
Acute kidney injury (AKI) is a commonly encountered complication in hospitalized patients and significantly contributes to morbidity and mortality [1–5]. Recent studies have further demonstrated that AKI was evident in around 20% of patients who died in hospitals and up to 50% of patients in the intensive care unit (ICU) [6, 7]. The etiology of AKI is multifactorial [1–12]. Among the various etiologies of hospital-acquired AKI, ischemia-reperfusion (IR) injury is the leading cause of AKI [13–15] that is associated with a high mortality rate [16, 17]. The causes of acute kidney IR injury are divergent, including contrast media-induced nephropathy [9, 18], shock followed by resuscitation in the emergency and intensive care settings [11, 19], kidney transplantation [20, 21], sepsis , and cardiovascular surgery .
Previous studies [11, 15, 23–27] have reported that the underlying mechanisms of acute kidney IR injury are mainly through the generation of oxidative stress and reactive oxygen species (ROS), rigorous inflammatory reaction, and enhancement of cellular apoptosis after prolonged or even transient IR injury [13, 22, 28]. Experimental studies have further revealed that inhibition of inflammatory reaction and suppression of the generations of pro-inflammatory cytokines and oxidative stress using immuno- or pharmaco-modulation significantly protect the kidney from acute IR injury [23–27].
Glucagon-like peptide-1 (GLP-1)-based pharmaceuticals are emerging as potent regimens against type 2 diabetes mellitus (T2DM). Exendin-4 and liraglutide, two GLP-1 analogues, have been reported to have multiple cellular protective effects, including the protection of endothelial cells against senescence mainly through anti-oxidative [29–31] and anti-inflammatory [31–33] processes. Additionally, studies have revealed that GLP-1 mediates in the therapeutic actions of dipeptidyl peptidase (DPP)-IV inhibitors . Interestingly, sitagliptin, currently used for treating type 2 diabetic patients, has been found to be able to enhance circulating GLP-1 levels through inhibition of DPP-IV activity [35, 36] which, in turn, provides cardiovascular protective effect probably through the anti-inflammatory and anti-atherosclerotic actions of GLP-1 . Thus, it is rational to hypothesize that the inflammatory reaction and oxidative stress from acute renal IR injury may be alleviated by either Exendin-4 (i.e., GLP-1 analogue) or sitagliptin treatment through the induction of GLP-1 receptor (GLP-1R) expression.
Materials and methods
All animal experimental procedures were approved by the Institute of Animal Care and Use Committee at Kaohsiung Chang Gung Memorial Hospital (Affidavit of Approval of Animal Use Protocol No. 2008121108) and performed in accordance with the Guide for the Care and Use of Laboratory Animals (NIH publication No. 85–23, National Academy Press, Washington, DC, USA, revised 1996).
Animal grouping and induction of acute kidney ischemia-reperfusion injury
Pathogen-free, adult male Sprague–Dawley (SD) rats (n = 48) weighing 320–350 g (Charles River Technology, BioLASCO Taiwan Co. Ltd., Taiwan) were randomized and equally divided into group 1 (sham controls, n = 12), group 2 (acute kidney IR injury only, n = 12), group 3 (sitagliptin 600 mg/kg orally at post-IR 1, 24, and 48 hr), and group 4 (IR + sitagliptin 600 mg/kg orally + exendin-4 10 μm/kg subcutaneous injection at post-IR 1 hr). The rats were sacrificed at post-IR 24 hr (3 hrs after sitagliptin treatment) and 72 hr (n = 6 each time for each group) for determining the therapeutic effects of sitagliptin and exendin-4 at acute (i.e., 24 hr) and subacute (i.e., 72 hr) phases of IR injury.
All animals were anesthetized by inhalational 2.0% isoflurane, placed supine on a warming pad at 37°C for midline laparotomies. Sham-operated rats (group 1) received laparotomy only, while acute IR injury of both kidneys were induced in all animals in groups 2 to 4 by clamping the renal pedicles for one hour using non-traumatic vascular clips. The rats were sacrificed at 24 and 72 hrs (n = 6 at each time from each group) after IR procedure. The kidneys were harvested for individual study.
Rationale of drug dosage for the study
To elucidate relatively suitable drug dosages for the present study, acute kidney IR injury in four additional rats was treated by either a low (n = 2) or a high (n = 2) dose of sitagliptin (i.e., 200 or 600 mg/kg/day for three days, respectively). Similarly, four other rats were treated with either a low (n = 2) or a high (n = 2) dose of exendin-4 six (i.e., 5 or 10 μg/kg once, respectively) after renal IR induction. Immunohistochemical (IHC) staining and the protein expressions of GLP-1R in kidney parenchyma were notably higher in the rats treated with a high dose of sitagliptin or exendin-4 compared with those receiving low doses of the two drugs. Thus, 600 mg/kg/day of sitagliptin for three successive days and 10 μg/kg (single dose only) of exendin-4 were utilized in the current study.
To elucidate the possible GLP-1-mediated therapeutic effect of sitagliptin against acute kidney IR injury, the circulating level of GLP-1 was measured in each animal. In addition, eight additional SD rats were equally divided into: 1) sham control, 2) IR only, 3) IR + sitagliptin 600 mg/kg (orally, 1 hr after acute kidney IR), 4) IR + sitagliptin 600 mg/kg + exendin-9-39 (an inhibitor of exendin-4) 10 μm/kg at 1 hr after the procedure. The animals were sacrificed at 24 hr after acute kidney IR. The kidney was collected in each animals for specific study (please see the results of Figure 1).
Assessment of circulating GLP-1 level and renal function before and after IR procedure
Serum GLP-1, creatinine, blood urea nitrogen (BUN), urine protein, and urine creatinine levels were determined in all animals before and after (at 24 and 72 hours) the IR procedure prior to their sacrifice. Quantification of GLP-1 level, BUN, serum and urine creatinine, and urine protein levels was performed using standard methods according to manufacturers’ instructions.
Collection of 24-hour urine before and after (on days 1 and 3) IR procedure
For the collection of 24-hr urine for individual study, each animal was put into the animal's metabolic cage [DXL-D, space: 190 × 290 × 550; shu-sz.com, Mainland China] for 24 hrs with food and water supply. Urine in 24 hr was collected in all animals prior to the IR procedure and at 24 hr and 72 hr after reperfusion prior to their sacrifice to determine the daily urine volume and the ratio of urine protein to urine creatinine.
Histopathology scoring and immunofluorescent (IF) staining at 24 and 72 hr after the IR procedure
Histopathology scoring was determined in a blinded fashion as we previously reported . Briefly, the kidney specimens from all animals were fixed in 10% buffered formalin, embedded in paraffin, sectioned at 5 μm and stained (hematoxylin and eosin; H&E) for light microscopy. The scoring system reflecting the grading of tubular necrosis, loss of brush border, cast formation, and tubular dilatation in 10 randomly chosen, non-overlapping fields (200x) was as follows: 0 (none), 1 (≤10%), 2 (11–25%), 3 (26–45%), 4 (46–75%), and 5 (≥76%) .
The IF methodology used in this study have recently been described in details . The IF staining methodology was used for the examination of CD68+ cells (an indicator of macrophage) using respective primary antibodies.
Western blot analysis of kidney specimens
Equal amounts (10–30 μg) of protein extracts from ischemic kidneys of the animals (n = 10 for each group) were loaded and separated by SDS-PAGE using 7% or 12% acrylamide gradients. The membranes were incubated with monoclonal antibodies against GLP-1R (1:1000, abcam), matrix metalloproteinase (MMP)-9 (1:1000, Millipore), intercellular adhesion molecule (ICAM)-1 (1: 2000, Abcam), NAD(P)H quinone oxidoreductase (NQO) 1 (1: 1000, Abcam), heme oxygenase (HO)-1 (1: 250, Abcam), Glutathione peroxidase (GPx) (1:2000, abcam), and polyclonal antibodies against tumor necrosis factor (TNF)-α (1: 1000, Cell Signaling), nuclear factor (NF)-κB (1:600, Abcam), ADPH oxidase (NOX)-1 (1:1500, Sigma), NOX-2 (1:500, Sigma), Bax (1: 1000, Abcam), caspase 3 (1: 1000, Cell Signaling), poly(ADP-ribose) polymerase (PARP) (1: 1000, Cell Signaling), Bcl-2 (1:250, Abcam), catalase (1:1000, abcam), superoxide dismutase 1 (SOD-1) (1:2000, abcam), γH2AX (1:1000, Cell signaling), and endothelial nitric oxide synthase (eNOS) (1:1000, Abcam) were used. Signals were detected with horseradish peroxidase (HRP)-conjugated goat anti-mouse, goat anti-rat, or goat anti-rabbit IgG.
The Oxyblot Oxidized Protein Detection Kit was purchased from Chemicon (S7150). The procedure of 2,4-dinitrophenylhydrazine (DNPH) derivatization was carried out on 6 μg of protein for 15 minutes according to the manufacturer’s instructions. One-dimensional electrophoresis was carried out on 12% SDS/polyacrylamide gel after DNPH derivatization. Proteins were transferred to nitrocellulose membranes which were then incubated in the primary antibody solution (anti-DNP 1: 150) for two hours, followed by incubation with the second antibody solution (1:300) for one hour at room temperature. The washing procedure was repeated eight times within 40 minutes.
Immunoreactive bands were visualized by enhanced chemiluminescence (ECL; Amersham Biosciences), which was then exposed to Biomax L film (Kodak). For quantification, ECL signals were digitized using Labwork software (UVP). For oxyblot protein analysis, a standard control was loaded on each gel.
Real-time quantitative PCR analysis
The mRNA expressions of TNF-α, interleukin (IL)-1β, MMP-9, plasminogen activator inhibitor (PAI), IL-10, and endothelial nitric oxide synthase (eNOS) in each of the four groups of animals were analyzed with RT-qPCR and compared.
Quantitative data are expressed as means ± SD. Statistical analyses were performed using SAS statistical software for Windows version 8.2 (SAS institute, Cary, NC) to conduct ANOVA followed by Bonferroni multiple-comparison post hoc test. A probability value <0.05 was considered statistically significant.
Exendin-9-39 inhibited the effect of sitagliptin on attenuating the acute kidney IR injury (Figure 1)
To assess the effect of sitagliptin therapy on ameliorating acute kidney IR was inhibited by extendin-9-39, an antagonist of exendin-4, 24 hr acute kidney IR injury was done in additional six animals, i.e., IR only (n = 2), IR + sitagliptin (n = 2), and IR + sitagliptin + exendin-9-39. The H. & E. stain showed that as compared with IR only, sitagliptin therapy markedly reduced the kidney injury score. However, this treatment effect was notably reduced by extendin-9-39. Additionally, the expression of GLP-1R in kidney parenchyma was notably higher in sitagliptin-treated animals than in those of IR only animals. However, the treatment effect was remarkably diminished by extendin-9-39 treatment. Moreover, the protein expressions of oxidative stress (oxidized protein), ROS (NOX-1, NOX-2), and inflammatory biomarkers (ICMA-1, TNF-α, NF-κB, MMP-9) were markedly lower in sitagliptin-treated animals than in IR only animals. However, despite of the sitagliptin treatment, these protein expressions were up-regulated again by extendin-9-39 therapy in the acute kidney IR animals. Furthermore, after acute kidney IR injury, the circulating level of GLP-1 was significantly higher animals than in other groups of the animals (Figure 2-L, 2-M). Accordingly, our findings supported that the effect of sitagliptin therapy on attenuating acute kidney IR injury was mainly through regulating the circulating level of GLP-1, a signaling pathway similar to exedinin-4.
Changes in renal functions and circulating levels of GLP-1 at 24 h and 72 h after acute renal IR injury (Figure 2)
Prior to the IR induction, the serum levels of BUN and creatinine were similar among the sham controls (group 1), animals with IR injury only (group 2), IR injury + sitagliptin (group 3), and IR injury + exendin-4 (group 4). However, at 24 hr after reperfusion, the serum levels of BUN and creatinine were significantly higher in group 2 than those in other groups and significantly higher in groups 3 and 4 than those in group 1, but it showed no difference between groups 3 and 4. In addition, at 72 hr after IR procedure, these two parameters showed an identical pattern compared to that of 24 hr among the four groups.
The daily urine amount and the ratio of urine protein to urine creatinine prior to the IR procedure did not differ among the four groups. However, the daily urine amount was significantly less in group 2 than that in other groups and significantly less in group 1 than groups 3 and 4, and significantly less in group 3 as compared to that of the group 4 at 72 hr after reperfusion.
Histopathological scoring of the kidneys at 24 h and 72 after IR injury (Figure 3)
To evaluate the therapeutic impact of sitagliptin and exendin-4 on IR-induced renal injury, histological scoring based on the typical microscopic features of acute tubular damage, including extensive tubular necrosis and dilatation, as well as cast formation and loss of brush border was adopted. The injury was found to be significantly higher in group 2 than in other groups, significantly higher in groups 3 and 4 than in group 1 (Figure 3A-E), and significantly higher in group 3 than group 4 at 24 h or 72 h after IR procedure (Figure 3F-J). These pathological findings might suggest that on dose of exendin-4 was not inferior to sitagliptin therapy for protecting acute kidney IR injury.
Changes in mRNA expression of inflammatory and anti-inflammatory biomarkers in renal parenchyma at 72 h after IR injury (Figure 4)
The mRNA expressions of TNF-1α, MMP-9, and IL-1β, three indicators of inflammation, were remarkably higher in group 2 than those in other groups and significantly higher in groups 3 and 4 than those in group 1, but it showed no difference between group 3 and group 4 (Figure 4A-C). Moreover, the mRNA expression of PAI-1, another indicator of inflammation, was highest in group 2 and lowest in group 1, and significantly higher in group 3 than that in group 4 (Figure 4D). On the other hand, the mRNA expressions of eNOS and IL-10, two anti-inflammatory indexes, were highest in group 1 and lowest in group 2, and significantly higher in group 4 than those in group 3 (Figure 4E-F).
Expression of glucagon-like peptide-1 receptor (GLP-1R) in kidney at 24 hr and 72 hr after reperfusion (Figure 5)
IHC staining showed that renal GLP-1R expression was highest in group 4 and lowest in group 1, and significantly higher in group 3 than that in group 2 at 24 h (Figure 5A-E) and 72 h (Figure 5F-I) after the procedure. Additionally, the protein expression of GLP-1R in the renal parenchyma showed an identical pattern of IHC staining. These findings suggest that GLP-1R had an intrinsic ability of an auto-regulating expression after acute kidney IR injury and an inversed correlation between the severity of renal IR injury and GLP-1R expression in renal parenchyma (Figure 5K-L).
Renal infiltration of CD68+ cells at 24 and 72 hr after reperfusion
IF staining demonstrated that the number of CD68+ cells (i.e., macrophages), an index of inflammation, was highest in group 2 and lowest in group 1, and significantly higher in group 3 than that in group 4 at 24 hr or 72 hr after reperfusion (Figure 6).
The protein expressions of inflammatory, oxidative-stress biomarkers, and reactive oxygen species (ROS) at 24 and 72 hr after IR injury (Figures 7, 8 and 9).
The protein expressions of TNF-α, NF-κB, and ICAM-1, three indicators of inflammation, were significantly higher in group 2 than those in other groups, significantly higher in groups 3 and 4 than those in group 1 at both 24 h and 72 h after IR procedure. No significant difference in the expressions of the three parameters, however, was noted between group 3 and group 4 (Figure 7). Besides, the protein expressions of NOX-1 and NOX-2, two indices of ROS, exhibited an identical pattern compared to that of inflammatory biomarker expressions (Figure 8) among the four groups at the two time points. Furthermore, the expression of oxidized protein, an index of oxidative stress, displayed a pattern similar to that of ROS among the four groups at the two time points (Figure 9).
The protein expressions of apoptotic, anti-apoptotic, and DNA damage markers at 24 and 72 hr after reperfusion (Figures 10 and 11)
The protein expressions of mitochondrial Bax and cleaved (i.e., active form) caspase 3 and PARP, three indices of apoptosis, were significantly higher in group 2 than those in other groups, and significantly higher in groups 3 and 4 than those in group 1, but it showed no difference between groups 3 and 4 at 24 hr and 72 hr after reperfusion (Figure 10A-F). Conversely, the protein expression of Bcl-2 showed an opposite pattern compared to that of apoptotic biomarkers after the two intervals of reperfusion (Figure 11). Furthermore, the protein expression of γ-H2AX, an indicator of DNA damage, was significantly higher in group 2 than that in other groups, and significantly higher in groups 3 and 4 than that in group 1, but no difference was noted between groups 3 and 4 at these two time points (Figure 11A-D).
The protein expressions of anti-oxidative and anti-inflammatory biomarkers at 24 and 72 hr after reperfusion (Figures 12 and 13)
The protein expressions of HO-1, NQO-1, and GPx, three indicators of anti-oxidative activities, were not lowest in group 2, and significantly lower in group 1 than that in groups 3 and 4, but it displayed no difference between groups 3 and 4 at 24 h and 72 after IR procedure (Figure 12A-F).
The protein expressions of catalase and SOD-1, two scavengers of superoxide, were lowest in group 1 and highest in group 4, and significantly higher in group 3 than that in group 2 after the two intervals of reperfusion (Figure 13). In addition, the protein expression of eNOS, an indicator of anti-inflammation, was significantly higher in group 1 than that in other groups, significantly higher in groups 3 and 4 than that in group 2, but it showed no difference between groups 3 and 4 after these two time intervals (Figure 13A-F).
The present study, which investigated the therapeutic effect of sitagliptin and exendin-4 against acute renal IR injury, yielded several conspicuous implications.
First, exendin-4 was comparable to sitagliptin in attenuating the architectural integrity of renal parenchyma and arresting the deterioration of renal function after IR injury. Second, either drug remarkably suppressed IR-induced acute kidney injury via inhibiting IR-triggered macrophage recruitment, DNA damage, inflammation, oxidative-stress and ROS generation, as well as through attenuating cellular apoptotic signaling pathway and enhancing GLP-1R expression and anti-oxidant factors in renal parenchyma. Third, to the best of our knowledge, this is the first study to demonstrate the benefits of sitagliptin and exendin-4 in protecting the kidneys from acute IR injury other than their therapeutic actions against hyperglycemia. Of importance is the fact that the results were promising.
Benefits of sitagliptin and exendin-4 therapy in attenuating IR-induced acute kidney injury---- functional assay and pathological findings
The most distinctive finding in the current study is that the serum BUN and creatinine levels, two important indices of kidney function, were remarkably elevated in animals after acute renal IR injury than those in sham controls. The increases of these parameters were significantly suppressed after sitagliptin or exendin-4 treatment. One important finding is that the ratio of urine protein to creatinine, a useful indicator of impaired renal function, was markedly increased in animals after acute kidney IR compared to that in the sham controls at 24 hr and 72 hr after the procedure. IR-induced elevation of this parameter was significantly suppressed by either sitagliptin or exendin-4 treatment. Another noteworthy finding in the present study is that the histopathological renal injury scores were significantly higher in animals after renal IR than those in sham controls at the two time points, but were significantly reduced by either sitagliptin or exendin-4 therapy. Importantly, this study is the first to demonstrate the therapeutic actions of sitagliptin and exendin-4 in protecting the kidney against acute IR injury other than their roles as hypoglycemic agents. Moreover, the results of the present study also demonstrated comparable protection offered by the two drugs.
Protection against acute renal IR injury through attenuation of inflammation
Previous studies have shown that ischemia or IR elicits tremendous inflammatory response [20, 22, 38]. In addition, the initiation and propagation of inflammatory reaction are major contributors to tissue/organ damage after acute IR injury [20, 22, 38]. One essential finding in the present study is the augmentation the expressions of inflammatory biomarkers at cellular (i.e., macrophage), gene (i.e., MMP-9, IL-1β, TNF-α, PAI-1), and protein (i.e., TNF-α, NF-κB, ICAM-1) levels in kidney parenchyma in the IR animals compared to those in the sham controls not only occurred at 24 hr, but also at 72 hr after reperfusion. Accordingly, our findings are consistent with those of previous studies [20, 22, 38]. Of importance is the fact that these inflammatory biomarkers were markedly suppressed in the IR animals after receiving sitagliptin or exendin-4 treatment. In this way, our findings further reinforce those of previous studies that also reported the link between the reduction of inflammatory reaction and the preservation of functional integrity of the kidney after ischemia/IR injury [20, 38]. Fascinatingly, the expressions of anti-inflammatory biomarkers at gene (IL-10, eNOS) and protein (eNOS) levels were notably enhanced in IR animals after sitagliptin and exendin-4 treatment, highlighting the intrinsic anti-inflammatory properties of the two agents other than their hypoglycemic actions. Therefore, our findings could, at least in part, explain the notably aggravated renal histological distortion and dysfunction in the setting of acute kidney IR and also the mechanisms by which sitagliptin and exendin-4 suppressed the renal IR-induced damage.
Protection against acute renal IR injury through reduction of oxidative stress
The generation of oxidative stress and ROS have also been shown to play a crucial role in acute kidney IR injury [11, 15, 20, 23–27, 39]. The principal finding in the present study is the markedly enhanced protein expressions of oxidative stress (i.e., oxidized protein) and ROS (i.e., NOX-1, NOX-2) in renal parenchyma of animals following acute kidney IR compared to those in the sham controls at both 24 hr and 72 hr after reperfusion. However, the expressions of these biomarkers were notably suppressed in IR animals after receiving either sitagliptin or exendin-4 treatment. Of importance is that the expressions of the anti-oxidative markers at protein level (HO-1, NQO-1, GPx-1, catalase, SOD) was significantly upregulated in the IR animals with either sitagliptin or exendin-4 treatment compared to those without. Beside their well-known roles as hypoglycemic agents, GLP-1 analogues (including exendin-4) have been reported to possess both anti-oxidative properties [29–31] and anti-inflammatory [31–33] properties. Moreover, sitagliptin, an oral hyperglycemic agent, has been found to be capable of enhancing circulating GLP-1 levels via suppressing DPP-IV activity [35, 36], thereby contributing to its anti-inflammatory and anti-atherosclerotic cardiovascular protective effect . Our findings, therefore, in addition to being supported by the previous studies [29–37], could further explain the protective effects of sitagliptin and exendin-4 against acute renal IR injury.
Protection against acute renal ir injury through suppression of cellular apoptosis and DNA damage
Inevitably, cellular apoptosis always takes place after acute ischemia/IR injury [21, 38, 39]. An association between cellular apoptosis and organ dysfunction has long been identified by experimental studies [21, 38, 39]. An important finding in the present study is the significantly elevated protein expressions of apoptotic (i.e., cleaved caspase 3 and PARP, mitochondrial Bax) and DNA damage (i.e., γ-H2AX) biomarkers in renal parenchyma of IR animals compared to those in the sham controls at both 24 hr and 72 hr following reperfusion. In this way, our findings corroborated those of previous studies [21, 38, 39]. However, these biomarkers were substantially reduced in the kidney parenchyma of IR animals after receiving either sitagliptin or exendin-4 treatment. Besides, the protein expression of the anti-apoptotic biomarker, i.e., Bcl-2, was notably augmented after treatment with either agent. Our findings could partially account for the suppressed IR-induced renal histopathological damage after treatment with sitagliptin and extendin-4.
Protection against acute renal IR injury through enhancing circulating GLP-1 level and GLP-1R expression in renal parenchyma
Although the distribution of GLP-1 binding sites (i.e., GLP-1R) in the central nervous system and the peripheral autonomic nervous system has been extensively investigated in previous studies [40–45], the expression of GLP-1R in renal parenchyma has not been reported. One interesting finding in the current study is the significantly higher circulating GLP-1 level in IR animals with and without exendin-4 treatment than that in the sham controls and also the highest level in IR animals receiving sitagliptin treatment. This may be the result of stress stimulation from IR injury that enhanced the generation of GLP-1 from the digestive system. Additionally, the highest circulating level of GLP-1 after sitagliptin treatment could be due to the inhibitory effect of sitagliptin on the enzymatic activity of DDP-IV which has been found to cleave GLP-1 in the circulation [35, 36]. The novel finding in the present study is that, under normal situation, GLP-1 binding sites were rare in the kidney parenchyma as shown in immunohistochemical staining and western blotting. However, during acute kidney IR injury, the expression of GLP-1 binding sites (i.e., through western blot) was markedly enhanced in the kidney parenchyma. The other novel and interesting finding (i.e., IHC staining result) is the predominant distribution of GLP-1 binding sites in the both glomeruli and renal tubules.
Another distinctive finding is that the protein expression of GLP-1 binding sites in kidney parenchyma was rare in normal condition that was only markedly augmented after acute IR injury. Of particularly distinctive finding was that the expression of this biomarker in renal parenchyma was significantly higher in IR animals with sitagliptin treatment than in IR animals without treatment and further significantly higher in IR animals after receiving exendin-4 treatment. These findings suggest an automatic up-regulating expression of GLP-1 binding sites in IR animals after both drug treatment. Of importance is that these findings (i.e., circulating GLP-1 and GLP-1 binding sites in kidney parenchyma) not only were consistent with our hypothesis, but also provided a good positive correlation between the up-regulated expression of GLP-1 binding sites and suppressing the generations of inflammation, oxidative stress, and ROS in the present study.
This study has several limitations. First, we remain uncertain regarding the explanation of the finding that exendin-4 had relatively higher potency than that of sitagliptin in suppressing kidney injury score and inflammatory cells (CD68+) and in up-regulating the expressions of GLP-1R and anti-oxidants (SOD, catalase). This is perhaps due to the fact that exendin-4, a GLP-1 analogue, possess stronger anti-oxidative [29–31] and anti-inflammatory [31–33] properties compared to those of sitagliptin. Second, despite extensive investigation in the current study, the precise signaling pathway(s) through which sitagliptin and exendin-4 exert their therapeutic effects have not been elucidated. We have, however, proposed the mechanisms based on the findings of the current study as summarized in Figure 14. Third, although the rationale of using sitagliptin and exendin-4 was elucidated in the present study, we did not test the potential toxicity of these two drugs in the setting of acute renal injury. In fact, the dosage of sitagliptin has been recommended to be reduced by half if the patient's estimated glomerular filtration rate (eGFR) is < 30 mL/min/1.73 m2. Therefore, the regimen dosage of this study is not recommended to extrapolate to humankind in critical settings such as contrast media-induced nephropathy, shock followed by resuscitation in the emergency and intensive care, kidney transplantation, sepsis or cardiovascular surgery.
In conclusion, acute kidney IR injury significantly augmented GLP-1R expression in kidney parenchyma that were further augmented after sitagliptin or exendin-4 therapy. Either sitagliptin or exendin-4 treatment effectively protected the kidney from IR injury through the suppression of inflammatory reaction, apoptosis, oxidative stress in a rodent model of renal IR injury.
Yen-Ta Chen and Tzu-Hsien Tsai equal contribute to first authors.
Yung-Lung Chen and Hon-Kan Yip equal contribute to corresponding authors.
Uchino S, Kellum JA, Bellomo R, Doig GS, Morimatsu H, Morgera S, Schetz M, Tan I, Bouman C, Macedo E: Acute renal failure in critically ill patients: a multinational, multicenter study. JAMA. 2005, 294: 813-818. 10.1001/jama.294.7.813.
Hoste EA, Clermont G, Kersten A, Venkataraman R, Angus DC, De Bacquer D, Kellum JA: RIFLE criteria for acute kidney injury are associated with hospital mortality in critically ill patients: a cohort analysis. Crit Care. 2006, 10: R73-10.1186/cc4915.
Bagshaw SM, George C, Dinu I, Bellomo R: A multi-centre evaluation of the RIFLE criteria for early acute kidney injury in critically ill patients. Nephrol Dial Transplant. 2008, 23: 1203-1210.
Clec'h C, Gonzalez F, Lautrette A, Nguile-Makao M, Garrouste-Orgeas M, Jamali S, Golgran-Toledano D, Descorps-Declere A, Chemouni F, Hamidfar-Roy R: Multiple-center evaluation of mortality associated with acute kidney injury in critically ill patients: a competing risks analysis. Crit Care. 2011, 15: R128-10.1186/cc10241.
Dennen P, Douglas IS, Anderson R: Acute kidney injury in the intensive care unit: an update and primer for the intensivist. Crit Care Med. 2010, 38: 261-275. 10.1097/CCM.0b013e3181bfb0b5.
Fang Y, Ding X, Zhong Y, Zou J, Teng J, Tang Y, Lin J, Lin P: Acute kidney injury in a Chinese hospitalized population. Blood Purif. 2010, 30: 120-126. 10.1159/000319972.
Lafrance JP, Miller DR: Acute kidney injury associates with increased long-term mortality. J Am Soc Nephrol. 2010, 21: 345-352. 10.1681/ASN.2009060636.
Li PK, Burdmann EA, Mehta RL: World Kdney Day 2013: acute kidney injury-global health alert. Am J Kidney Dis. 2013, 61: 359-363. 10.1053/j.ajkd.2013.01.002.
Lameire N, Kellum JA: Contrast-induced acute kidney injury and renal support for acute kidney injury: a KDIGO summary (Part 2). Crit Care. 2013, 17: 205-10.1186/cc11455.
Gueler F, Gwinner W, Schwarz A, Haller H: Long-term effects of acute ischemia and reperfusion injury. Kidney Int. 2004, 66: 523-527. 10.1111/j.1523-1755.2004.761_11.x.
Di Nardo M, Ficarella A, Ricci Z, Luciano R, Stoppa F, Picardo S, Picca S, Muraca M, Cogo P: Impact of severe sepsis on serum and urinary biomarkers of acute kidney injury in critically ill children: an observational study. Blood Purif. 2013, 35: 172-176. 10.1159/000346629.
Alsabbagh MM, Asmar A, Ejaz NI, Aiyer RK, Kambhampati G, Ejaz AA: Update on clinical trials for the prevention of acute kidney injury in patients undergoing cardiac surgery. Am J Surg. 2013, 206: 86-95. 10.1016/j.amjsurg.2012.08.007.
Chertow GM, Burdick E, Honour M, Bonventre JV, Bates DW: Acute kidney injury, mortality, length of stay, and costs in hospitalized patients. J Am Soc Nephrol. 2005, 16: 3365-3370. 10.1681/ASN.2004090740.
Lameire N, Van Biesen W, Vanholder R: Acute renal failure. Lancet. 2005, 365: 417-430.
Boros P, Bromberg JS: New cellular and molecular immune pathways in ischemia/reperfusion injury. Am J Transplant. 2006, 6: 652-658. 10.1111/j.1600-6143.2005.01228.x.
Santos WJ, Zanetta DM, Pires AC, Lobo SM, Lima EQ, Burdmann EA: Patients with ischaemic, mixed and nephrotoxic acute tubular necrosis in the intensive care unit–a homogeneous population?. Crit Care. 2006, 10: R68-10.1186/cc4904.
Levy EM, Viscoli CM, Horwitz RI: The effect of acute renal failure on mortality. A cohort analysis. JAMA. 1996, 275: 1489-1494. 10.1001/jama.1996.03530430033035.
Parikh CR, Coca SG, Wang Y, Masoudi FA, Krumholz HM: Long-term prognosis of acute kidney injury after acute myocardial infarction. Arch Intern Med. 2008, 168: 987-995. 10.1001/archinte.168.9.987.
Friedericksen DV, Van der Merwe L, Hattingh TL, Nel DG, Moosa MR: Acute renal failure in the medical ICU still predictive of high mortality. S Afr Med J. 2009, 99: 873-875.
Sementilli A, Franco M: Renal acute cellular rejection: correlation between the immunophenotype and cytokine expression of the inflammatory cells in acute glomerulitis, arterial intimitis, and tubulointerstitial nephritis. Transplant Proc. 2010, 42: 1671-1676. 10.1016/j.transproceed.2009.11.042.
Jang HR, Ko GJ, Wasowska BA, Rabb H: The interaction between ischemia-reperfusion and immune responses in the kidney. J Mol Med (Berl). 2009, 87: 859-864. 10.1007/s00109-009-0491-y.
Bagshaw SM, Bennett M, Haase M, Haase-Fielitz A, Egi M, Morimatsu H, D'Amico G, Goldsmith D, Devarajan P, Bellomo R: Plasma and urine neutrophil gelatinase-associated lipocalin in septic versus non-septic acute kidney injury in critical illness. Intensive Care Med. 2010, 36: 452-461. 10.1007/s00134-009-1724-9.
Morgan CJ, Gill PJ, Lam S, Joffe AR: Peri-operative interventions, but not inflammatory mediators, increase risk of acute kidney injury after cardiac surgery: a prospective cohort study. Intensive Care Med. 2013, 39: 934-941. 10.1007/s00134-013-2849-4.
Chen YT, Sun CK, Lin YC, Chang LT, Chen YL, Tsai TH, Chung SY, Chua S, Kao YH, Yen CH: Adipose-derived mesenchymal stem cell protects kidneys against ischemia-reperfusion injury through suppressing oxidative stress and inflammatory reaction. J Transl Med. 2011, 9: 51-10.1186/1479-5876-9-51.
Grossini E, Molinari C, Pollesello P, Bellomo G, Valente G, Mary D, Vacca G, Caimmi P: Levosimendan protection against kidney ischemia/reperfusion injuries in anesthetized pigs. J Pharmacol Exp Ther. 2012, 342: 376-388. 10.1124/jpet.112.193961.
Canacankatan N, Sucu N, Aytacoglu B, Gul OE, Gorur A, Korkmaz B, Sahan-Firat S, Antmen ES, Tamer L, Ayaz L: Affirmative effects of iloprost on apoptosis during ischemia-reperfusion injury in kidney as a distant organ. Ren Fail. 2012, 34: 111-118. 10.3109/0886022X.2011.633446.
El Eter E, Aldrees A: Inhibition of Pro-inflammatory Cytokines by SCH79797, a Selective PAR1 Antagonist, Protects Rat Kidney Against Ischemia Reperfusion Injury. Shock. 2012, (In press)
Hamilton A, Holscher C: Receptors for the incretin glucagon-like peptide-1 are expressed on neurons in the central nervous system. Neuroreport. 2009, 20: 1161-1166. 10.1097/WNR.0b013e32832fbf14.
Oeseburg H, de Boer RA, Buikema H, van der Harst P, van Gilst WH, Sillje HH: Glucagon-like peptide 1 prevents reactive oxygen species-induced endothelial cell senescence through the activation of protein kinase A. Arterioscler Thromb Vasc Biol. 2010, 30: 1407-1414. 10.1161/ATVBAHA.110.206425.
Shimoda M, Kanda Y, Hamamoto S, Tawaramoto K, Hashiramoto M, Matsuki M, Kaku K: The human glucagon-like peptide-1 analogue liraglutide preserves pancreatic beta cells via regulation of cell kinetics and suppression of oxidative and endoplasmic reticulum stress in a mouse model of diabetes. Diabetologia. 2011, 54: 1098-1108. 10.1007/s00125-011-2069-9.
Iwai T, Ito S, Tanimitsu K, Udagawa S, Oka J: Glucagon-like peptide-1 inhibits LPS-induced IL-1beta production in cultured rat astrocytes. Neurosci Res. 2006, 55: 352-360. 10.1016/j.neures.2006.04.008.
Hattori Y, Jojima T, Tomizawa A, Satoh H, Hattori S, Kasai K, Hayashi T: A glucagon-like peptide-1 (GLP-1) analogue, liraglutide, upregulates nitric oxide production and exerts anti-inflammatory action in endothelial cells. Diabetologia. 2010, 53: 2256-2263. 10.1007/s00125-010-1831-8.
Kim S, Moon M, Park S: Exendin-4 protects dopaminergic neurons by inhibition of microglial activation and matrix metalloproteinase-3 expression in an animal model of Parkinson's disease. J Endocrinol. 2009, 202: 431-439. 10.1677/JOE-09-0132.
Holst JJ, Deacon CF: Glucagon-like peptide-1 mediates the therapeutic actions of DPP-IV inhibitors. Diabetologia. 2005, 48: 612-615. 10.1007/s00125-005-1705-7.
Zerilli T, Pyon EY: Sitagliptin phosphate: a DPP-4 inhibitor for the treatment of type 2 diabetes mellitus. Clin Ther. 2007, 29: 2614-2634. 10.1016/j.clinthera.2007.12.034.
Scheen AJ: Dipeptidylpeptidase-4 inhibitors (gliptins): focus on drug-drug interactions. Clin Pharmacokinet. 2010, 49: 573-588. 10.2165/11532980-000000000-00000.
Matsubara J, Sugiyama S, Sugamura K, Nakamura T, Fujiwara Y, Akiyama E, Kurokawa H, Nozaki T, Ohba K, Konishi M: A dipeptidyl peptidase-4 inhibitor, des-fluoro-sitagliptin, improves endothelial function and reduces atherosclerotic lesion formation in apolipoprotein E-deficient mice. J Am Coll Cardiol. 2012, 59: 265-276. 10.1016/j.jacc.2011.07.053.
Sheu JJ, Chua S, Sun CK, Chang LT, Yen CH, Wu CJ, Fu M, Yip HK: Intra-coronary administration of cyclosporine limits infarct size, attenuates remodeling and preserves left ventricular function in porcine acute anterior infarction. Int J Cardiol. 2011, 147: 79-87. 10.1016/j.ijcard.2009.08.008.
Yip HK, Chang YC, Wallace CG, Chang LT, Tsai TH, Chen YL, Chang HW, Leu S, Zhen YY, Tsai CY: Melatonin treatment improves adipose-derived mesenchymal stem cell therapy for acute lung ischemia-reperfusion injury. J Pineal Res. 2013, 54: 207-221. 10.1111/jpi.12020.
Leu S, Kao YH, Sun CK, Lin YC, Tsai TH, Chang LT, Chua S, Yeh KH, Wu CJ, Fu M, Yip HK: Myocardium-derived conditioned medium improves left ventricular function in rodent acute myocardial infarction. J Transl Med. 2011, 9: 11-10.1186/1479-5876-9-11.
Goke R, Larsen PJ, Mikkelsen JD, Sheikh SP: Distribution of GLP-1 binding sites in the rat brain: evidence that exendin-4 is a ligand of brain GLP-1 binding sites. Eur J Neurosci. 1995, 7: 2294-2300. 10.1111/j.1460-9568.1995.tb00650.x.
Kinzig KP, D'Alessio DA, Seeley RJ: The diverse roles of specific GLP-1 receptors in the control of food intake and the response to visceral illness. J Neurosci. 2002, 22: 10470-10476.
Vahl TP, Tauchi M, Durler TS, Elfers EE, Fernandes TM, Bitner RD, Ellis KS, Woods SC, Seeley RJ, Herman JP, D’Alessio DA: Glucagon-like peptide-1 (GLP-1) receptors expressed on nerve terminals in the portal vein mediate the effects of endogenous GLP-1 on glucose tolerance in rats. Endocrinology. 2007, 148: 4965-4973. 10.1210/en.2006-0153.
Bucinskaite V, Tolessa T, Pedersen J, Rydqvist B, Zerihun L, Holst JJ, Hellstrom PM: Receptor-mediated activation of gastric vagal afferents by glucagon-like peptide-1 in the rat. Neurogastroenterol Motil. 2009, 21: 978–e978-
Baraboi ED, Smith P, Ferguson AV, Richard D: Lesions of area postrema and subfornical organ alter exendin-4-induced brain activation without preventing the hypophagic effect of the GLP-1 receptor agonist. Am J Physiol Regul Integr Comp Physiol. 2010, 298: R1098-R1110. 10.1152/ajpregu.00326.2009.
This study was supported by a program grant from Chang Gung Memorial Hospital, Chang Gung University (CMRPG8B0231). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
The authors declare that they have no competing interests of any sort, including commercial association, such as consultancies, stock ownership or other equity interests or patent-licensing arrangements.
CYT, TTH, and HKY participated in the design of the study, data acquisition and analysis as well as drafting the manuscript. CKS, SL, YCC, and CLT were responsible for the laboratory assay and troubleshooting. LTC, THT,SCK, YLC, CCL, CHH and HWC participated in data acquisition, analysis, and interpretation. ZYY, HWC, SL, and HKY conceived of the study, and participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
Rights and permissions
Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/2.0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
About this article
Cite this article
Chen, YT., Tsai, TH., Yang, CC. et al. Exendin-4 and sitagliptin protect kidney from ischemia-reperfusion injury through suppressing oxidative stress and inflammatory reaction. J Transl Med 11, 270 (2013). https://doi.org/10.1186/1479-5876-11-270
- Acute ischemia-reperfusion injury
- Oxidative stress