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Metformin (MET) is a first-line drug for type 2 diabetes mellitus (DM); its effect on new-onset diabetes after transplantation caused by immunosuppressant therapy is unclear. We compared the effects of MET on DM caused by tacrolimus (TAC) or sirolimus (SRL).
DM was induced by injection of TAC (1.5 mg/kg) or SRL (0.3 mg/kg) for 2 weeks in rats, and MET (200 mg/kg) was injected for 2 more weeks. The effects of MET on DM caused by TAC or SRL were evaluated using an intraperitoneal glucose tolerance test (IPGTT) and by measuring plasma insulin concentration, islet size, and glucose-stimulated insulin secretion (GSIS). The effects of MET on the expression of adenosine monophosphate-activated protein kinase (AMPK), a pharmacological target of MET, were compared between TAC- and SRL-treated islets.
IPGTT showed that both TAC and SRL induced hyperglycemia and reduced plasma insulin concentration compared with vehicle. These changes were reversed by addition of MET to SRL but not to TAC. Pancreatic islet cell size was decreased by TAC but not by SRL, but addition of MET did not affect pancreatic islet cell size in either group. MET significantly increased GSIS in SRL- but not in TAC-treated rats. AMPK expression was not affected by TAC but was significantly decreased in SRL-treated islets. Addition of MET restored AMPK expression in SRL-treated islets but not in TAC-treated islets.
MET has different effects on hyperglycemia caused by TAC and SRL. The discrepancy between these drugs is related to their different mechanisms causing DM.
New-onset diabetes after transplantation (NODAT) is a serious complication after kidney transplantation (KT) and is associated with worse patient and graft survival [1-3]. The causes of NODAT are multifactorial. Among them, the relationship between NODAT and immunosuppressive medications used after transplantation has been well documented , and immunosuppressive drugs account for up to 74% of the risk of NODAT development [5,6].
Tacrolimus (TAC) and cyclosporine are the mainstay of immunosuppressive therapy in transplantation . However, long-term treatment with calcineurin inhibitors (CNIs) causes both irreversible and chronic renal dysfunction as well as diabetes and cardiovascular disease in KT recipients . Sirolimus (SRL), a mammalian target of rapamycin inhibitor, is a promising immunosuppressant for reducing or replacing CNIs . However, more recent data from the US Renal Data System suggest that SRL is also independently associated with an increased risk of NODAT in KT recipients [10,11].
Metformin (MET), an oral hypoglycemic agent, is often prescribed to prevent or treat type 2 diabetes in people who have not undergone transplantation . There is increasing interest in the use of MET after solid organ transplantation . The safety and efficacy of MET in patients with preexisting diabetes who undergo transplantation or who develop NODAT have been demonstrated . However, the effects of MET on controlling NODAT in KT recipients receiving CNIs or SRL have not been well studied. Therefore, we aimed to study whether MET can effectively control hyperglycemia caused by immunosuppressant therapy, specifically TAC and SRL.
The Animal Care Committee at the Catholic University of Korea approved the experimental protocol (CUMC-2013-0131-03). Male Sprague Dawley rats (Charles River Technology, Seoul, Korea) weighing 200 to 220 g were housed in individual cases in a temperature- and light-controlled environment and allowed free access to a low-salt diet (0.05% sodium; Teklad Premier, Madison, WI, USA) and tap water.
The experimental design is shown in Fig. 1. Rats were randomized to five groups (n = 9 per group) as follows. (1) The vehicle group (VH) received olive oil (Sigma, St. Louis, MO, USA) daily via oral gavage for 4 weeks; (2) the TAC group received TAC (1.5 mg/kg; Prograf, Astellas Pharma, Ibaraki, Japan) injected daily subcutaneously for 4 weeks; (3) the SRL group received SRL (0.3 mg/kg; Wyeth-Ayerst Research, Princeton, NJ, USA) injected daily subcutaneously for 4 weeks; (4) the TAC + MET group received TAC injected daily for 4 weeks and MET (200 mg/kg; Dongwha Pharmaceutical Co., Seoul, Korea) daily via oral gavage from day 14; and (5) the SRL + MET group received SRL injected daily for 4 weeks and MET daily via oral gavage from day 14. An intraperitoneal glucose tolerance test (IPGTT) was performed at the end of the 4-week treatment period.
In this study, we chose 1.5 mg/kg of TAC and 0.3 mg/kg of SRL based on our previous study which showed dose-dependent increase of blood glucose level by IPGTT [15,16]. MET dose (200 mg/kg) was chosen based on previous reports that the MET doses of 100 and 200 mg/kg are effective in glucose control [17-19] and MET at doses ≥ 600 mg/kg/day shows clinical signs of toxicity . Thus, the dose of MET used in this study is suitable for blood glucose control without MET toxicity.
Rats were pair-fed and their body weight was monitored daily. After the 4-week treatment period, animals were housed individually in metabolic cages (Tecniplast, Gazzada, Italy), and their water intake and urine volume were measured over 24 hours. On the following day, animals were anesthetized, and blood samples and tissue specimens were obtained for further analysis.
The IPGTT was performed at the end of the 4-week treatment period as previously described . Briefly, after 1 day of fasting, 25% dextrose (2 g/kg) was injected, and the blood glucose concentration was measured just before and 30, 60, 90, and 120 minutes after the injection using a glucose analyzer (Accu-Chek, Roche Diagnostics, Basel, Switzerland). The area under the curve for glucose (AUCg) was calculated by trapezoidal estimation from the values obtained in the IPGTT.
Serum creatinine concentration was measured using a quantitative enzyme colorimetric method (Stanbio Laboratory, Boerne, TX, USA). The whole-blood TAC and SRL concentrations were quantified using liquid chromatography-mass spectrometry with an API3000 LC/MS/MS system (Applied Biosystems, Foster City, CA, USA) equipped with an electrospray ionization interface used to generate negative ions [22,23].
Insulin concentration was measured in plasma from experimental animals and in culture media from islet cells subjected to a glucose-stimulated insulin secretion (GSIS) test. Insulin concentration was measured using a rat insulin sandwich enzyme-linked immunosorbent assay (ELISA) kit according to the manufacturer’s protocol (Millipore Corp., St. Charles, MO, USA). Absorbance was measured at 450 nm using a Versa Max ELISA Microplate Reader (Molecular Devices, Sunnyvale, CA, USA).
To detect insulin, mounted tissue sections were incubated overnight at 4°C with polyclonal guinea pig anti-insulin antibody (1:3,000; Invitrogen, Carlsbad, CA, USA) as the primary antibody. The sections were incubated with donkey antiguinea pig antibody (1:200; Jackson ImmunoResearch Laboratories, West Grove, PA, USA) as the secondary antibody. The area per pancreas section occupied by insulin staining was calculated for each pancreas using an image analyzer (TDI Scope Eye version 3.5, Olympus, Seoul, Korea).
To measure glucose-stimulated insulin release, isolated islets were treated initially with TAC (30 ng/mL) or SRL (90 ng/mL) for 12 hours, followed by treatment with MET (165 ng/mL) for a further 12 hours. The islets were washed with Krebs-Ringer Modified Buffer (KRB; 130 mmol/L NaCl, 3.6 mmol/L KCl, 1.5 mmol/L CaCl2, 0.5 mmol/L MgSO4, 0.5 mmol/L KH2PO4, 2.0 mmol/L NaHCO3, and 10 mmol/L HEPES), and the supernatant was collected (basal) and replaced with KRB containing 25 mM glucose for an additional 30 minutes. The supernatant was sampled to measure the insulin level. Fig. 2 shows the workflow for the isolation of islets from rats.
To identify the expression of adenosine monophosphate-activated protein kinase (AMPK), isolated rat islets were treated initially with TAC (30 ng/mL) or SRL (90 ng/mL) for 12 hours, followed by treatment with MET (165 ng/mL) for a further 12 hours. After washing with KRB, the islets were pelleted by centrifugation, and lysis buffer was added (10 mM Tris, pH 7.5, 1% SDS, 1 mM NaVO4). The blots which transferred equal amount of protein resolves were incubated with blocking solution containing 5% nonfat milk (BD Difco, Sparks, MD, USA) in phosphate buffered saline, followed by an overnight incubation at 4°C with polyclonal rabbit antitotal AMPK antibody (1:1000; Cell Signaling Technology, Danvers, MA, USA) or polyclonal rabbit antiphosphorylated AMPK (p-AMPK, 1:1000; Cell Signaling Technology) diluted in SignalBoost immunoreaction enhancer (Millipore Corp.) as the primary antibody. The next day, the blots were incubated for 1 hour with peroxidase-conjugated goat antirabbit antibody (Cell Signaling Technology) diluted in SignalBoost immunoreaction enhancer. Antibody binding was detected using a commercial chemiluminescence kit (ATTO Corp., Tokyo, Japan). Quantification was performed using relative density, in which the VH group was assigned a density of 100% and the densities were normalized by each total AMPK band from the same gel (Quantity One version 4.4.0, Bio-Rad, Hercules, CA, USA).
Data are presented as mean ± standard error. Significance between groups was determined using a one-way analysis of variance with the Bonferroni post hoc test (SPSS version 19.0, IBM Co., Armonk, NY, USA). Significance was accepted at p< 0.05.
Table 1 shows the effect of MET with TAC or SRL on basic parameters in the experimental groups. The TAC and SRL groups had significantly lower body weight and higher 24-hour water intake and urine volume compared with the VH group. These changes were restored by treatment with MET. Serum creatinine concentration was higher in the TAC group, and lower in the TAC + MET group compared with the VH group. MET treatment did not affect the trough level of TAC or SRL in whole blood.
The IPGTT showed that TAC or SRL treatment for 4 weeks increased blood glucose concentration and decreased plasma insulin concentration (Fig. 3). The AUCg calculated from the IPGTT graph was higher in the TAC and SRL groups compared with the VH group. The combined treatment of MET for 2 weeks following induction of diabetes did not improve these changes in the TAC group. The AUCg was 244 ± 7 mg/dL/min in the TAC group and 270 ± 19 mg/dL/min in the TAC + MET group (p< 0.05). The insulin concentration was 0.30 ± 0.01 ng/mL in the TAC group and 0.28 ± 0.02 ng/mL in the TAC + MET group (p> 0.05). SRL induced hyperglycemia and reduced the plasma insulin concentration, but these effects were reversed by MET treatment. The AUCg was 216 ± 8 mg/dL/min in the SRL group and 160 ± 4 mg/dL/min in the SRL + MET group (p< 0.05). The insulin concentration was 0.31 ± 0.01 in the SRL group and 0.34 ± 0.01 in the SRL + MET group (p< 0.05).
Immunostaining for insulin showed a strong and uniform pattern of staining in a large proportion of the islet β-cells in the VH group (Fig. 4A). However, a lower intensity of insulin staining, irregularity in islet boundaries, and evidence of vacuolization in islets were observed in β-cells from the TAC group. The SRL group showed similar insulin immunoreactivity to the VH group. Addition of MET did not change the staining intensity compared with TAC or SRL alone. Quantification of these results by measuring the insulin-positive areas (Fig. 4B) showed that the islet size was significantly smaller in the TAC and TAC + MET groups compared with the VH group (9.2 ± 0.9 μm2 × 103 in the TAC group and 11.4 ± 0.9 μm2 × 103 in the TAC + MET group vs. 20.7 ± 3.2 μm2 × 103 in the VH group; p< 0.05 compared with the VH group). The islet size did not differ significantly between the TAC and TAC + MET groups. Consistent with the insulin-staining results, islet size did not differ significantly between the VH, SRL, and SRL + MET groups (14.1 ± 2.2 μm2 × 103 in the SRL group and 18.4 ± 2.5 μm2 × 103 in the SRL + MET group).
We used the GSIS test to confirm the in vivo results (Fig. 2). Exposure of isolated islets to TAC or SRL significantly reduced GSIS (19.8 ± 0.1 ng/mL in the TAC group and 20.2 ± 0.1 ng/mL in the SRL group vs. 21.8 ± 0.1 ng/mL in the VH group; p< 0.05 vs. VH). Insulin concentration did not differ between the TAC + MET and TAC groups, whereas GSIS was restored in the SRL + MET group. GSIS was 20 ± 0.1 ng/mL in the TAC+MET group (p> 0.05 vs. the TAC group) and 21.1 ± 0.2 ng/mL in the SRL + MET group (p< 0.05 vs. the SRL group) (Fig. 5).
To evaluate the effects of MET on the expression of AMPK, a pharmacological target of MET, in TAC- and SRL-treated pancreatic islet cells, immunoblot analysis of p-AMPK was conducted using the samples from the basal condition in the GSIS test (Fig. 6). The p-AMPK protein abundance relative to total AMPK abundance did not differ between the TAC + MET group compared with the TAC group. p-AMPK abundance was 1.6-fold lower in the SRL group compared with the VH group. By contrast, p-AMPK abundance was 2.4-fold higher in the SRL + MET group compared with the SRL group (165% ± 9% in the SRL + MET group vs. 67% ± 2% in the SRL group, p< 0.05).
The present study was undertaken to investigate whether MET, the first-line drug in the management of type 2 diabetes, is also effective in treating diabetes caused by immunosuppressant therapy. The results of the in vivo and in vitro experiments showed that MET was effective in altering the effects of SRL-induced diabetes but not those of TAC-induced diabetes. The differences in the effects of MET on diabetes seem to relate to the different causal mechanisms of diabetes. These results may be useful for understanding NODAT and when choosing antidiabetic drugs for patients with NODAT.
The most important finding of this study is that MET caused different glucose-lowering effects when combined with TAC- or SRL-induced hyperglycemia. Both drugs caused hyperglycemia and decreased plasma insulin concentration. However, the response to MET treatment differed between the TAC- and SRL-treated groups. In the SRL group, adding MET to SRL attenuated hyperglycemia and increased the plasma insulin concentration; this effect was not observed in the TAC group (Fig. 3). The results of our study are consistent with those of previous reports, which showed that MET treatment significantly reduced mean random glucose concentration in SRL-treated animals but not in TAC-treated animals .
It is generally accepted that insulin resistance is a main component to SRL-induced hyperglycemia. Therefore, it is expected that SRL induces hyperinsulinemia and adding MET to SRL decreases blood glucose and subsequent decline of serum insulin concentrations. On the contrary, our study showed that SRL treatment decreased plasma insulin level and adding MET to SRL increased plasma insulin level. This opposite result seems to related to the our model which is based on SRL-induced pancreatic islet cell injury, Thus, main pathogenesis of SRL-induced diabetes mellitus in our model is reduced insulin secretion rather than insulin resistance. This may explain why SRL treatment decreased plasma insulin level and adding MET to SRL increased plasma insulin level in our study.
In our study, immunohistochemical analysis of pancreatic islet cells showed that TAC decreased islet size, but SRL did not, and that MET treatment did not affect islet size in either group. This finding suggests that the decrease in plasma insulin concentration observed in the TAC and SRL groups is related to differences in the causal mechanisms of diabetes. In the TAC group, plasma insulin concentration decreased because of the reduced pancreatic β-cell mass, whereas in the SRL group, it decreased because of impaired insulin secretion. This conclusion is consistent with previous reports showing that the predominant mechanism of hyperglycemia induced by TAC is reduced β-cell mass through direct TAC-induced pancreatic β-cell injury and that hyperglycemia caused by SRL is closely associated with impaired insulin signaling .
To confirm the in vivo results showing different glucose-lowering effects of MET when combined with TAC or SRL, we performed the GSIS test (Fig. 2). Exposure of isolated islets to TAC or SRL significantly reduced GSIS. Combined SRL and MET treatment of islets restored GSIS (Fig. 5), whereas combined TAC and MET treatment did not. This finding suggests that MET improves insulin secretion in SRL-treated islets but not in TAC-treated islets and that the glucose-lowering effect of MET is mediated by increased insulin secretion in the SRL group. AMPK is a key metabolic sensor in both insulin-sensitive and -insensitive tissues. It is well-known that antidiabetic properties of MET are mediated by activating the AMPK pathway in hepatocyte . In our study, we found that MET also activates the AMPK expression in pancreatic islet cells, and this finding was consistent with previous reports that AMPK activator increase insulin release in isolated islets and the perfused pancreas  and activation of AMPK improves insulin sensitivity and increases insulin secretion in β-cells . Taken together, our results suggests that MET may exert its glucose-lowering effect by activating the AMPK pathway in pancreatic islet cell, but further study will be needed to define a role of pancreatic islet compared to the hepatocyte in evaluating antidiabetic effect of MET.
The results of our study clearly demonstrate that SRL but not TAC treatment significantly decreased p-AMPK expression, and MET treatment significantly increased p-AMPK expression in SRL-treated but not in TAC-treated pancreatic islet cells. This finding suggests that SRL-induced diabetes is mediated by the AMPK pathway and that MET exerts its glucose-lowering effect by activating the AMPK pathway. It is interesting that that MET did not increase AMPK expression in TAC-treated pancreatic islet cells. We expected that MET increase AMPK expression because MET is a well known AMPK activator, but the effect of MET on AMPK activation was not significant in TAC-treated pancreatic islet cells. The reason for no increase of AMPK by MET is unclear, but we speculate two possibilities. First, AMPK signaling pathway may not be involved in TAC-induced pancreatic islet injury . Second, MET dose may not be enough to activate AMPK in a setting of TAC-induced pancreatic islet injury.
The results of our study may have clinical applications. The current guideline for the management of NODAT is based on the treatment of type 2 diabetes, but the results of our study suggest that the choice of antidiabetic drugs in patients with NODAT should be made based on the type of immunosuppressant causing NODAT. In patients with TAC-induced diabetes, MET is not suitable as an antidiabetic drug for the control of hyperglycemia. Rather, dipeptidyl peptidase 4 inhibitors may be beneficial considering their protective effect against various injuries . Our results also suggest that MET may be recommended for patients with SRL-induced diabetes. This approach may provide a better rationale for the management of NODAT in KT recipients.
Our study has some limitations. First, 2 weeks of TAC or SRL treatment is too short to evaluate the long-term effect of each drug. Second, the trough level of TAC (around 10 ng/mL) was higher and that of SRL (around 3.0 ng/mL) was lower than the clinically recommended trough level. Third, we did not observe other beneficial effects of MET such as anti-inflammatory and antineoplastic effects [30,31].
In conclusion, the results of our study suggest that the development of NODAT differs according to the immunosuppressant used. The choice of antidiabetic drugs for NODAT should be made based on the mechanism through which immunosuppressant drugs cause diabetes.
1. The pathogenesis of new-onset diabetes after transplantation (NODAT) differs according to the type of immunosuppressant.
2. Antidiabetic drugs for NODAT should be chosen in accordance with the causal mechanism of NODAT.
This study was supported by a grant of the Korean Health Technology R&D Project, Ministry for Health and Welfare, Republic of Korea (HI14C3417).
No potential conflict of interest relevant to this article was reported.