This study aimed to investigate the potential of an oral formulation (QV formulation) containing Quercetin and a Dipeptidyl Peptidase-4 Inhibitor (DPP-4 inhibitor), Vildagliptin, in improving metabolic homeostasis in type 1 diabetes model. Female albino Fischer rats were divided into four groups: untreated control animals (C), untreated diabetic animals (D), diabetic animals treated with QV formulation (DQV), and diabetic animals treated with insulin (DI). Diabetes was induced by injection of alloxan (135 mg kg body mass)−1 and confirmed by glycemic test. After the 30-day treatment period, biochemical parameters were analyzed in the pancreas, liver, and serum. Histopathological changes in pancreatic tissue were examined by Hematoxyline & Eosin staining and the insulin content in the islet measured by immunohistochemistry with anti-insulin antibody. The glycogen content in the hepatocytes was quantified by Periodic Schiff Acid staining. The QV formulation reduced the glycemia, preserved the pancreatic architecture, increased insulin levels, furthermore ameliorated lipid profile and to promote higher survival rate of animals. Together, our data suggest that the QV formulation treatment was able to normalize metabolic homeostasis in type 1 diabetic rats.
Type 1 diabetes (T1DM), prevalent in 5 to 10% of the diabetic population, is a result of the immune-mediated destruction of pancreatic beta cells. It manifests earlier than type 2 diabetes (T2DM), and the incidence among children has been increasing in many countries, particularly in individuals under 15 years old1. The individuals affected may find it difficult to perform glycemic control, resulting in less adherence to treatment. This is mainly due to invasive treatment, which consists of the subcutaneous administration of insulin at regular intervals. Conventional treatment generates pain, anxiety, and loss of quality of life, which impacts the life of individuals and their families. In addition, the high financial cost results in medical care and decreased productivity, making this disease burdensome2. Different strategies have been developed to provide greater comfort for patients and to prevent frequent episodes of severe hypoglycemia, such as glucose sensors, oral and dermal insulins3, and oral spray. However, access to these innovations is unfeasible for a large part of the population due to the high cost, considering that 75% of patients with T1DM live in low-income countries. Recently our group demonstrated that drugs indicated for treatment of T2DM have been studied in T1DM and show a variable degree of benefits4. DPP-4 inhibitors participate in numerous biological processes, via glycemic control, weight reduction, and improvement in beta cell function and cardiovascular risk markers5, resulting in additional beneficial effects in metabolic homeostasis. In addition, in T1DM, DPP-4 inhibitors as add-on to insulin therapy can reduce the daily insulin requirements6. Animal studies indicate that Vildagliptin, an oral DPP-4 inhibitor, has a promising effect on T1DM, stimulating the neogenesis of pancreatic beta cells7. Other authors have also reported effects of Vildagliptin on the stimulation of insulin secretion8 and on the maintenance and repair of beta cells9 in animal model. However, no studies to date have demonstrated the effect of Vildagliptin on the regulation of metabolism in the T1DM model. In addition, the use of Quercetin, a flavonoid present in several foods of plant origin, has also been demonstrated to have antidiabetic potential, improving the hyperglycemic state, reducing the incidence of peripheral complications10 and increasing the secretion of insulin and protection of pancreatic cells11. Studies have shown that both Quercetin and Vildagliptin, when administrated alone, have antidiabetic potential, but their combined effect on metabolic homeostasis in the T1DM model is controversial. Considering different mechanisms of action, either by direct effects of Vildagliptin on the inhibition of DPP-4 enzyme, or by the antioxidant activity of Quercetin, we hypothesized that the combination of these two compounds are capable of to generate benefits in biochemical and histological parameters, promoting an improvement in metabolic homeostasis in type 1 diabetic rats.
After 30 days of treatment, the group receiving insulin alone and the group that received the QV formulation had a reduction in the hyperglycemic condition (Fig. 1a). The percentage of blood glucose reduction was 70% in the animals that received the QV formulation, compared to the approximately 55% glycemic reduction in animals receiving insulin alone (Fig. 1b). The serum analysis revealed that QV formulation increased insulin levels to values similar to the control and insulin groups (Fig. 1c), but did not change glucagon levels (Fig. 1d), maintaining a positive insulin/glucagon ratio (Fig. 1e). In the diabetic group that received the QV formulation, all animals survived over the entire period, and the same was observed for the animals in the non-diabetic control group. In contrast, 11.2% of the untreated diabetic animals died within 4 days after confirmation of diabetes, and 33.3% of those treated once daily with insulin died within 7 days (Fig. 1f).
Histological sections of pancreatic islets from the experimental groups reveled positive labeling with anti-insulin antibody (Fig. 2a–f). The QV formulation was able to increase insulin production by pancreatic beta cells (Fig. 2g).
No inflammatory signs, degenerative or fibrotic areas were found in any of the experimental group animals, either in the acinar components or in the pancreatic islets (Fig. 3a–d). The number of pancreatic islets increased after administration of the QV formulation in the treated animals when compared to the untreated diabetic group, and remained similar in relation to the insulin-treated group (Fig. 3e). Evaluation of the remodeling capacity of the extracellular matrix promoted by the pancreatic MMP-2 (matrix metalloproteinase-2) revealed that treatments with the QV formulation or insulin reduced the MMP-2 activity in relation to the untreated diabetic group, and at levels similar to the control group (Fig. 3f).
None of the treatments showed an effect on the GLUT2 (glucose transporter 2) level present in the pancreas (Fig. 4a). The GLP-1R (glucagon-like peptide-1 receptor) level revealed that the QV formulation enabled an increase the concentration of this receptor (Fig. 4b). The activity of the enzyme pancreatic hexokinase revealed that administration of the QV formulation reestablished the functional capacity of hexokinase in phosphorylating the glucose present in the medium (Fig. 4c).
The activity of hexokinase in hepatocytes of animals that received QV formulation was reestablished (Fig. 5a). Both treatments increased the energetic reserve of glycogen in relation to the untreated diabetic group (Fig. 5b). The representation of hepatic tissues in photomicrography shows glycogen deposits stained by PAS (periodic schiff acid) (Fig. 5c–f).
GLUT2 concentration, as well as GLP-1R concentration present in the liver did not reveal differences between the experimental groups who received the treatments (Fig. 6a,b).
Lipid profile dosages showed that treatment with QV formulation reduced the levels of the non-HDL fraction (particle non high density lipoprotein-cholesterol - atherogenic particles) and increased HDL fraction in relation to the untreated diabetic group. No differences were found between groups in relation to cholesterol total, however the QV formulation exhibited lower triacylglycerol levels in relation to insulin administration. The QV formulation did not exhibit alterations in ALT (alanine aminotransferase), AST (aspartate aminotransferase) and albumin concentrations. Assessment of urea levels showed that treatment with QV formulation was able to promote an improvement in this parameter in comparison to the untreated diabetic group. In contrast, the serum creatinine levels showed no change in any of the groups evaluated (Table 1).
Glucose fluctuation is one of the main risk factors for patients with T1DM. As observed in this research, some prior results reported that DPP-4 inhibitors and Quercetin may reduce glycemic variations in the diabetes model12,13, however clinical trials and other research in T1DM indicate that administration of each of these agents separately is not consistent in altering glycemic parameters8,14, that is, results are conflicting and the final outcomes are inconclusive. The development of the QV formulation was mainly based on previous studies that showed that treatment with Vildagliptin and Quercetin alone did not increase serum insulin levels sufficiently to the extent of reducing glycemia (see Supplementary Table S1). Thus, in this study it was seen that the association of both agents (Vildagliptin and Quercetin) in a formulation was able to improve the hyperglycemic condition and promote a 70% reduction in hyperglycemia in relation to the 54.5% improvement achieved by treatment with insulin. Probably the improvement in glucose homeostasis contributed to a higher survival rate in animals treated with the QV formulation than untreated diabetic rats and diabetic rats treated with a daily dose of insulin, suggesting that the treatment with formulation may be associated with a low risk of the hypoglycemia that sometimes results from insulin administration15.
Glucose homeostasis is directly related to the hormonal balance of insulin and glucagon levels secreted by pancreatic cells. While the inhibitors of DPP-4 regulate glycemia by stimulating the release of insulin by pancreatic beta cells in a glucose-dependent manner, the role of Quercetin in glycemic control occurs mainly due to its antioxidant effects10,11. These inhibitors, by increasing the half-life of GLP-1, increase insulin synthesis and secretion, as well as reducing glucagon secretion by pancreatic alpha cells. Treatment of T1DM rats with Vildagliptin increased insulin secretion, however this increase was not sufficient to promote the lowering of blood glucose7,8. Some findings also revealed that Vildagliptin reduced glucagon during hyperglycemia and maintained its counterregulation during hypoglycemia in T1DM16,17, resulting in reduction in fasting plasma glucose, postprandial plasma glucose, and prevention of hypoglycemia. Glucagon, besides antagonizing the action of insulin, also induces gluconeogenesis and inappropriately raised glucagon secretion in T1DM patients contributed directly to increased hepatic glucose output and worsening of postprandial glucose control as well as variability of glycemia18. In our results, the treatment with the QV formulation was able to increase insulin levels, without altered glucagon levels. GLP-1R are scarce or nonexistent in pancreatic alpha cells, what makes it unlikely that GLP-1 has a direct action in reducing glucagon secretion in this cells19. Based on this finding, we can infer, to some extent, that glucose homeostasis is regulated primarily by insulin and to a lesser extent by glucagon. In addition, our hypothesis is supported since the insulin/glucagon ratio proved to be positive after the treatments, contributing to ameliorate the hyperglycemic state while it also maintains normal glucagon levels, and protects from hypoglycemia.
Glucose metabolism is influenced by a complex regulatory network that involves pancreatic and hepatic hexokinase enzyme activity. These enzymes are responsible for the phosphorylation of glucose and its entrapment in the intracellular environment. In pancreatic beta cells, hexokinase acts as a glucose sensor that activates insulin secretion. In hepatocytes, hexokinase activity is dependent on the insulin/glucagon ratio for the removal of excess glucose from the blood and its targeting to the glycolytic or glycogenesis pathway, through stimulation of glucose-induced glycogen synthesis20,21. In the absence of insulin, as occurs in individuals T1DM, hexokinase activity is reduced. Alloxan is a substance used as diabetogenic agent to induce T1DM in experimental animals and promotes selective inhibition of glucose-induced insulin secretion by inhibiting hexokinase22. This corroborates our findings regarding the inhibition of hexokinase activity in the group of untreated diabetic animals. Our results showed that, by preserving the pancreatic enzyme activity, the QV formulation increased insulin secretion and activated the liver enzyme to store glycogen in the hepatocytes, even after induction with alloxan. This effect probably occurred due to the action of Vildagliptin, which inhibits the DPP-4 enzyme and increases GLP-1 half-life, triggering exocytosis of insulin granules23 by activation of hexokinase after binding to its receptor. The GLP-1R are expressed in tissues other than pancreatic islets24, as in hepatocytes, but studies suggest that certain actions of GLP-1 in hepatic glucose metabolism occur through mechanisms that are independent of GLP-1R, and no alternative route seems to have been fully elucidated25. Administration of the QV formulation increased the pancreatic GLP-1R level, indicating a possible increase in the availability of GLP-1, whereas in the liver these levels did not change. Based on this, our results suggest that the sequence of modulatory effects on glucose metabolic homeostasis exhibited by the binding of GLP-1 to its receptor are possibly influenced, to a greater extent, by the interaction of GLP-1 with its pancreatic receptor and are less dependent on interaction with hepatic GLP-1R. Still regarding the signaling cascade, it should be noted that incretin-based treatment is able to increase the regulation of the GLUT222,26. Vildagliptin is capable of preserving the expression of this transporter in the membrane of pancreatic beta cells27, while Quercetin reduces glucose absorption by inhibiting GLUT2 in intestinal cells28. However, even though alloxan did not inhibit the GLUT2 transporter function29, in this study, no alteration in GLUT2 levels was seen after administration of the QV formulation.
The QV formulation also had a positive effect on the lipid profile of diabetic rats, reducing non-HDL fraction and increasing HDL fraction, which is of particular significance because lipidic metabolism is directly related to dyslipidemia as well as microvascular and cardiovascular complications are typical of diabetes30. Atherosclerosis is a pathological condition resulting from lipid deposition and atheromatous plaque formation in the subendothelial layer of blood vessels, and oxidative stress and inflammatory responses are among the major triggers31. A study with patients with uncontrolled T2DM showed that Vildagliptin as an add-on to insulin therapy did not alter the lipid profile32, while Vildagliptin treatment ameliorated this parameter in diabetic mice33. The QV formulation had a beneficial effect in reducing atherogenic cholesterol fractions (decrease in non-HDL fraction accompanied by increase HDL fraction), while daily administration of insulin was responsible for increasing triacylglycerol levels when compared to treatment with the QV formulation. Although we did not observe improvement in triacylglycerol levels, some authors report that increased incretin plasma concentration is related to the reduction of intestinal absorption of triacylglycerol in animal studies34, besides Vildagliptin be able to lowers triacylglycerol-rich lipoprotein postprandial levels in T2DM, suggesting that DPP-4 inhibitors mobilize and burn fat during meals, and thus the fat that is associated with cardiovascular risk is not accumulated35. Our research group has previously suggested that treatment with Vildagliptin for 30 days improved the lipid profile in chronic T1DM model. Treatment with Vildagliptin alone reduced total cholesterol levels, and this reduction was due to decrease in the concentration of atherogenic fractions, since there was no change in the HDL fraction. Additionally, there was reduction of triacylglycerol levels7. Nath et al. also showed that Vildagliptin ameliorated lipid profile in diabetic mice33. In contrast, Maeda et al. did not observe alterations in total cholesterol, HDL fraction, and triacylglycerol levels in T1DM rats after treatment with Vildagliptin36. The effect of Quercetin has also been reported in the prevention and treatment of chronic non-infectious diseases, such as diabetes, obesity, and hyperlipidemia, mainly for its antioxidant effects. Studies have shown that Quercetin was able to improve the regulation of lipid metabolism37 and suppress the formation of atheromatous plaques in an atherosclerosis mouse model31. Therefore, supported by literature, our results reveal that 30-day treatment with QV formulation was effective in improving the lipid profile of animals.
Diabetes is responsible for causing damage to various organs including the liver and kidney. Assessment of liver function parameters revealed that QV formulation treatment did not reduce serum levels of ALT and AST enzymes. In contrast, treatment with insulin increased AST levels and since this enzyme is found in other compartments such as the heart, muscles, kidneys, and the brain and is released into the blood after some type of damage, it suggests the presence of some extrahepatic injury. Differently, the ALT enzyme is found largely in the liver, being released into the circulation as a result of liver damage. Alloxan hepatic metabolism may have been responsible for the increase in ALT/AST levels in diabetic animals, since the structural similarity with the glucose molecule allows its absorption by the cell through the GLUT2 transporter38, occasioning possible damage to cells which express this carrier. Treatment with the QV formulation also did not normalize the serum levels of albumin, a protein produced in the liver. Diabetes is responsible for reducing blood levels of albumin, which is also indicative of liver failure. Vildagliptin add-on insulin therapy in T2DM also did not alter the level of liver enzymes32, whereas in a hepatic fibrosis model the administration of Quercetin resulted in maintenance of ALT/AST levels and increased serum albumin levels, suggesting a possible hepatoprotective effect39. Diabetes is characterized by redox imbalance in the kidneys that can lead to nephropathy40. In addition, alloxan toxicity may also affect this organ due to the presence of the GLUT2 transporter in renal tubular cells38. Based on this, in relation to renal function, urea levels increased in diabetic animals, which may be justified by the higher protein catabolism and higher excretion of this metabolite. The QV formulation treatment, unlike the insulin treatment, promoted an improvement in this parameter to values similar to the control group, characterizing a possible renoprotective effect. Some studies indicate possible beneficial effects of DPP-4 inhibitors on renal complications caused by diabetes. In addition to providing protective effects against tubular damage and slowing the progression of chronic kidney disease, it has been suggested that the renoprotective effects of DPP-4 inhibitors may be due to increased levels of GLP-141. Although our study showed no difference in creatinine levels, research using an experimental model of diabetic nephropathy showed that Quercetin treatment reduced serum creatinine, restored clearance, and reduced glomerular hyperplasia and oxidative stress40.
Metalloproteinases are extracellular matrix remodeling enzymes, and any change in their regulatory mechanism may contribute to complications in T1DM42. In this study, both the QV formulation and insulin reduced the MMP-2 activity, which was increased in untreated diabetic animals. Besides, we also confirmed that there is a strongly positive correlation between glycemic values and MMP-2 activity (see Supplementary Fig. S1). The hyperglycemic state, characteristic of T1DM, is responsible for the increase of MMP-243. Peeters et al. in recent studies also associated higher MMP-2 plasma levels with higher incidence of cardiovascular events and diabetic nephropathy in T1DM patients42. Thus, the improvement in glycemic levels after the pharmacological treatments may justify the reduction in the activity of this enzyme.
Evaluation of pancreatic histology revealed that QV formulation was able to increase not only the number of pancreatic islets, but also the stored insulin content in the beta cells. These results allow us to infer that the QV formulation exerted a protective effect on the pancreatic tissue even after the alloxan induction. Progressive damage in beta cell function is the primary basis of diabetic manifestations44. In this sense, several authors have already reported a positive influence of DPP-4 inhibitors and GLP-1 on pancreatic tissue in the T2DM model, either by proliferation/maintenance of functional beta cells, inhibition of apoptosis or pancreatic islet neogenesis9,45. The islets express DPP-4 enzyme and can produce GLP-1. Thus, it is possible that the improvement in islet function it also results from inhibiting the local DPP-4 enzyme while the pancreatic GLP-1 is preserved46. This class of drugs improves pancreatic islet dysfunction, however are restricted the studies that verified these same effects in T1DM model, whether in the presence or absence of detectable beta cell function47. The close relationship involving hyperglycemia-mediated oxidative damage in T1DM has suggested that agents that improve the glycemic index and/or oxidative stress may have beneficial effects in the treatment of diabetes. This is the first study that demonstrates the effects of a formulation containing a DPP-4 inhibitor together with a Flavonoid, both with antidiabetic properties, in promoting the improvement of metabolic homeostasis in a T1DM model.
Thus, the present findings suggest a potential benefit of formulation QV in improves of metabolic homeostasis in rats (Fig. 7).
Alloxan is used to induce the characteristic symptoms of type 1 diabetes, however, should be emphasized that the etiogenesis of type 1 diabetes in an animal model is distinct from autoimmune type 1 diabetes observed in humans. The effects observed in this study with the treatment of diabetic animals with the QV formulation may be different from that observed in autoimmune diabetes. Therefore, future studies should be conducted to evaluate the effect of QV formulation in the treatment of autoimmune diabetes.
Vildagliptin (Novartis Pharma Stein AG, Stein, Switzerland) was commercially acquired in the pharmacy (Ouro Preto, Brazil). Quercetin and Alloxan (2, 4, 5, 6-tetraoxypyrimidine; 5, 6-dioxyuracil) was purchased from Sigma-Aldrich (St. Louis, MO, USA).
Animals and Experimental Design
Forty-three female albino Fischer healthy rats (Laboratory of Experimental Nutrition of the University Federal of Ouro Preto), approximately 120 days of age and weighing 200 g, were used for this study. During the experimental period, the rats were maintained in well-ventilated cages with controlled temperature, ventilation, and humidity. They had access to water and commercial rat chow ad libitum. The animals were randomly divided into four experimental groups: untreated control animals (C) received 1 mL of the formulation containing the vehicle (n = 6); untreated diabetic animals (D) received 1 mL of the formulation containing the vehicle (n = 11); diabetic animals treated with QV formulation (DQV) received 1 mL of the formulation containing Vildagliptin8,48,49 (10 mg kg body mass)−1 and Quercetin (50 mg kg body mass)−1 (n = 14); and the diabetic animals treated with insulin (DI) received 2UI of insulin intraperitoneal injection* (n = 12). The animals of C, D, DQV and DI groups were submitted to orogastric treatment (oral gavage) daily, and in this order, for 30 consecutive days (Fig. 8). Animals were anesthetized by isoflurane inhalation and then euthanized. This work was conducted in accordance with the international standards of animal protection and the ethical principles of the National Council of Animal Experimentation and was approved by the Ethics Committee on Animal Use of the University Federal of Ouro Preto (#2014/17).
*Daily and for 30 consecutive days, at 9:00 AM, 2UI of exogenous insulin (NPH recombinant human insulin −10 mL suspension/100UI/mL concentration) were administered intraperitoneally and with the aid of a syringe. The insulin flask was kept under refrigeration (2–8 °C).
Induction of Type 1 Diabetes
‘T1DM was induced by a single intraperitoneal injection of 135 mg alloxan (kg body mass)−1 dissolved in 0.2 mL sterile saline22. Control animals received only 0.2 mL of sterile saline solution. Three days after alloxan administration, animals were considered to be diabetic when after-fasting tail-vein blood glucose concentrations of ≥16 mmol/L, measured by an AccuChek Glucometer (Accu-Chek® Active, Roche).
For biochemical analysis, the blood samples collected at the end of the experiment were used to measure glucose, triacylglycerol, total cholesterol, and high-density lipoprotein-cholesterol (HDL), alanine aminotransferase (ALT), aspartate aminotransferase (AST), urea and albumin levels all by Labtest Kits (Lagoa Santa, MG, Brazil). The serum insulin and glucagon levels were determined using a commercial Rat/Mouse Insulin enzyme-linked immunosorbent assay (ELISA) kit Merck Millipore (Kenilworth, NJ, USA) and by competitive inhibition enzyme immunoassay technique for quantitative measurement, using the enzyme-linked immunosorbent assay kit from Cloud-Clone Corp. (Katy, TX, USA), respectively.
The pancreas and liver were also collected at the end of the experiment. For determination of Hexokinase activity in pancreas and liver, 10 mg of tissues were rapidly homogenize with 200 µl ice cold HK Assay Buffer* for 10 minutes on ice. The homogenates were centrifuged at 12.000 rpm for 5 minutes e the supernatant was collect and store at −80 °C for further analysis. (Hexokinase Colorimetric Assay Kit – BioVision/Milpitas, CA, USA).
*HK Assay Buffer: Hexokinase Colorimetric Assay Kit (Catalog # K789-100).
For determination of GLUT2 (Glucose transporter 2) and GLP-1R (glucagon-like peptide 1 receptor) concentrations in pancreas and liver, tissues were rinsed in ice-cold PBS (0.01 mol.L−1, pH 7.0–7.2) to remove excess blood thoroughly and weighed before homogenization. Minced the tissues to small pieces (20 mg) and homogenized them in 1 mL lysis buffer* with a homogenizer on ice. The resulting suspension was sonicated with an ultrasonic cell disrupter to further break the cell membranes. After that, the homogenate was centrifuged for 5 minutes at 5.000 × g, for GLP-1R, and centrifuged for 5 minutes at 10.000 × g, for GLUT2. The respective supernatants were collected in aliquot and store at −80 °C for further analysis. Evaluated by sandwich enzyme immunoassay, using the Enzyme-linked Immunosorbent Assay Kit from Cloud-Clone Corp. (Katy, TX, USA).
*Lysis buffer: 50 mM.L−1 Tris-HCl pH 8,0; 1 mM.L−1 EDTA; 1% NP40; 150 mM.L−1 NaCl; 4 mL DTT.sample−1; 10 mL protease inhibitor/sample.
For histological evaluation, the pancreas and liver fragments were fixed in 10% formaldehyde solution, dehydrated, diaphanized, and embedded in paraffin. The pancreas slides were stained with Hematoxylin and Eosin (H&E) to differentiate the architecture of pancreatic islets, and stained with anti-insulin antibody (1:5000 dilution) (Monoclonal Anti-Insulin, I2018-2mL, lot:084M4769, Sigma-Aldrich) for immunohistochemical staining of insulin in pancreatic tissue. (NOTE: Antibody Validation: positive and negative control of histological section of pancreatic islet immunolabeled with anti-insulin antibody). To quantify glycogen, the liver slides were stained with Periodic Schiff Acid (PAS). Photomicrographs were obtained using Leica Application Suite analysis software, magnification x440, and quantification was performed on Leica QWin Plus software version 3.0 (Leica Microsystems Inc., Buffalo Grove, IL, USA).
MMP-2 activity was detected using gelatin zymography, as previously described by Sung et al.50.
The normality of the data was tested by the Kolmogorov-Smirnov test and followed normal distribution (parametric data). The results were expressed as mean ± standard error and statistical analysis was performed using One-Way Analysis of Variance (ANOVA), followed by Bonferroni post-test for multiple comparisons. Differences were considered statistically significant when p < 0.05. All analyses were performed using GraphPad Prism software version 6.01 for Windows (San Diego, California, USA).
All procedures followed were in accordance with the international standards of animal protection and the ethical principles of the National Council of Animal Experimentation and was approved by the Ethics Committee on Animal Use of the University Federal of Ouro Preto (#2014/17).
The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.
IDF. International Diabetes Federation: Diabetes Atlas. 8th edn, (International Federation Of Diabetes, 2017).
GILMER, T. P. et al. Predictors of health care costs in adults with diabetes. Diabetes Care 28, 59–64 (2005).
Yu, J. et al. Microneedle-array patches loaded with hypoxia-sensitive vesicles provide fast glucose-responsive insulin delivery. Proc Natl Acad Sci USA 112, 8260–8265, https://doi.org/10.1073/pnas.1505405112 (2015).
Frandsen, C. S., Dejgaard, T. F. & Madsbad, S. Non-insulin drugs to treat hyperglycaemia in type 1 diabetes mellitus. Lancet Diabetes Endocrinol 4, 766–780, https://doi.org/10.1016/s2213-8587(16)00039-5 (2016).
Nauck, M. Incretin therapies: highlighting common features and differences in the modes of action of glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors. Diabetes Obes Metab 18, 203–216, https://doi.org/10.1111/dom.12591 (2016).
Guo, H. et al. The efficacy and safety of DPP4 inhibitors in patients with type 1 diabetes: A systematic review and meta-analysis. Diabetes Res Clin Pract 121, 184–191, https://doi.org/10.1016/j.diabres.2016.08.022 (2016).
Miranda, P. H. A. et al. Vildagliptin induces β-cell neogenesis and improves the lipid profile in a later phase of type 1 diabetes. Curr Pharm Biotechnol 16, 60–65 (2015).
Ávila, De. L. et al. Vildagliptin ameliorates oxidative stress and pancreatic beta cell destruction in type 1 diabetic rats. Arch Med Res 44, 194–202, https://doi.org/10.1016/j.arcmed.2013.03.004 (2013).
Hamamoto, S. et al. Vildagliptin preserves the mass and function of pancreatic β cells via the developmental regulation and suppression of oxidative and endoplasmic reticulum stress in a mouse model of diabetes. Diabetes Obes Metab 15, 153–163, https://doi.org/10.1111/dom.12005 (2013).
Jeong, S. M., Kang, M. J., Choi, H. N., Kim, J. H. & Kim, J. I. Quercetin ameliorates hyperglycemia and dyslipidemia and improves antioxidant status in type 2 diabetic db/db mice. Nutr Res Pract 6, 201–207, https://doi.org/10.4162/nrp.2012.6.3.201 (2012).
Coskun, O., Kanter, M., Korkmaz, A. & Oter, S. Quercetin, a flavonoid antioxidant, prevents and protects streptozotocin-induced oxidative stress and beta-cell damage in rat pancreas. Pharmacol Res 51, 117–123, https://doi.org/10.1016/j.phrs.2004.06.002 (2005).
Awata, T. et al. Possible Long-Term Efficacy of Sitagliptin, a Dipeptidyl Peptidase-4 Inhibitor, for Slowly Progressive Type 1 Diabetes (SPIDDM) in the Stage of Non-Insulin-Dependency: An Open-Label Randomized Controlled Pilot Trial (SPAN-S). Diabetes Ther 8, 1123–1134, https://doi.org/10.1007/s13300-017-0299-7 (2017).
Kim, J. H. et al. Quercetin attenuates fasting and postprandial hyperglycemia in animal models of diabetes mellitus. Nutr Res Pract 5, 107–111, https://doi.org/10.4162/nrp.2011.5.2.107 (2011).
George, P. S. & McCrimmon, R. J. Saxagliptin co-therapy in C-peptide negative Type 1 diabetes does not improve counter-regulatory responses to hypoglycaemia. Diabet Med 33, 1283–1290, https://doi.org/10.1111/dme.13046 (2016).
Gooßen, K. & Gräber, S. Longer term safety of dipeptidyl peptidase-4 inhibitors in patients with type 2 diabetes mellitus: systematic review and meta-analysis. Diabetes Obes Metab 14, 1061–1072, https://doi.org/10.1111/j.1463-1326.2012.01610.x (2012).
Farngren, J., Persson, M., Schweizer, A., Foley, J. E. & Ahrén, B. Vildagliptin reduces glucagon during hyperglycemia and sustains glucagon counterregulation during hypoglycemia in type 1 diabetes. J Clin Endocrinol Metab 97, 3799–3806, https://doi.org/10.1210/jc.2012-2332 (2012).
Malmgren, S. & Ahren, B. DPP-4 inhibition contributes to the prevention of hypoglycaemia through a GIP-glucagon counterregulatory axis in mice. Diabetologia 58, 1091–1099, https://doi.org/10.1007/s00125-015-3518-7 (2015).
Salehi, A., Vieira, E. & Gylfe, E. Paradoxical stimulation of glucagon secretion by high glucose concentrations. Diabetes 55, 2318–2323, https://doi.org/10.2337/db06-0080 (2006).
Ahren, B. et al. Mechanisms of action of the dipeptidyl peptidase-4 inhibitor vildagliptin in humans. Diabetes Obes Metab 13, 775–783, https://doi.org/10.1111/j.1463-1326.2011.01414.x (2011).
Aukrust, I. et al. SUMOylation of pancreatic glucokinase regulates its cellular stability and activity. J Biol Chem 288, 5951–5962, https://doi.org/10.1074/jbc.M112.393769 (2013).
Hers, H. G. The control of glycogen metabolism in the liver. Annu Rev Biochem 45, 167–189, https://doi.org/10.1146/annurev.bi.45.070176.001123 (1976).
Lenzen, S. The mechanisms of alloxan- and streptozotocin-induced diabetes. Diabetologia 51, 216–226, https://doi.org/10.1007/s00125-007-0886-7 (2008).
Papaetis, G. S. Incretin-based therapies in prediabetes: Current evidence and future perspectives. World J Diabetes 5, 817–834, https://doi.org/10.4239/wjd.v5.i6.817 (2014).
Richards, P. et al. Identification and characterization of GLP-1 receptor-expressing cells using a new transgenic mouse model. Diabetes 63, 1224–1233, https://doi.org/10.2337/db13-1440 (2014).
Tomas, E. & Habener, J. F. Insulin-like actions of glucagon-like peptide-1: a dual receptor hypothesis. Trends Endocrinol Metab 21, 59–67, https://doi.org/10.1016/j.tem.2009.11.007 (2010).
Wang, X. et al. Glucagon-like peptide-1 regulates the beta cell transcription factor, PDX-1, in insulinoma cells. Endocrinology 140, 4904–4907, https://doi.org/10.1210/endo.140.10.7158 (1999).
Ishibashi, K. et al. Beneficial effects of vildagliptin combined with miglitol on glucose tolerance and islet morphology in diet-controlled db/db mice. Biochemical and biophysical research communications 440, 570–575, https://doi.org/10.1016/j.bbrc.2013.09.110 (2013).
Kwon, O. et al. Inhibition of the intestinal glucose transporter GLUT2 by flavonoids. FASEB J 21, 366–377, https://doi.org/10.1096/fj.06-6620com (2007).
Elsner, M., Tiedge, M., Guldbakke, B., Munday, R. & Lenzen, S. Importance of the GLUT2 glucose transporter for pancreatic beta cell toxicity of alloxan. Diabetologia 45, 1542–1549, https://doi.org/10.1007/s00125-002-0955-x (2002).
Soedamah-Muthu, S. S. et al. High risk of cardiovascular disease in patients with type 1 diabetes in the U.K.: a cohort study using the general practice research database. Diabetes Care 29, 798–804 (2006).
Kawabata, K., Mukai, R. & Ishisaka, A. Quercetin and related polyphenols: new insights and implications for their bioactivity and bioavailability. Food Funct 6, 1399–1417, https://doi.org/10.1039/c4fo01178c (2015).
Li, F. F. et al. Effects of Vildagliptin Add-on Insulin Therapy on Nocturnal Glycemic Variations in Uncontrolled Type 2 Diabetes. Diabetes Ther 8, 1111–1122, https://doi.org/10.1007/s13300-017-0303-2 (2017).
Nath, S., Ghosh, S. K. & Choudhury, Y. A murine model of type 2 diabetes mellitus developed using a combination of high fat diet and multiple low doses of streptozotocin treatment mimics the metabolic characteristics of type 2 diabetes mellitus in humans. J Pharmacol Toxicol Methods 84, 20–30, https://doi.org/10.1016/j.vascn.2016.10.007 (2017).
Qin, X. et al. GLP-1 reduces intestinal lymph flow, triglyceride absorption, and apolipoprotein production in rats. Am J Physiol Gastrointest Liver Physiol 288, G943–949, https://doi.org/10.1152/ajpgi.00303.2004 (2005).
Matikainen, N. et al. Vildagliptin therapy reduces postprandial intestinal triglyceride-rich lipoprotein particles in patients with type 2 diabetes. Diabetologia 49, 2049–2057, https://doi.org/10.1007/s00125-006-0340-2 (2006).
Maeda, S., Matsui, T. & Yamagishi, S. Vildagliptin inhibits oxidative stress and vascular damage in streptozotocin-induced diabetic rats. Int J Cardiol 158, 171–173, https://doi.org/10.1016/j.ijcard.2012.04.087 (2012).
Yan, S. X., Li, X., Sun, C. D. & Chen, K. S. [Hypoglycemic and hypolipidemic effects of quercetin and its glycosides]. Zhongguo Zhong Yao Za Zhi 40, 4560–4567 (2015).
Thorens, B., Sarkar, H. K., Kaback, H. R. & Lodish, H. F. Cloning and functional expression in bacteria of a novel glucose transporter present in liver, intestine, kidney, and beta-pancreatic islet cells. Cell 55, 281–290 (1988).
Lee, C. C., Shen, S. R., Lai, Y. J. & Wu, S. C. Rutin and quercetin, bioactive compounds from tartary buckwheat, prevent liver inflammatory injury. Food Funct 4, 794–802, https://doi.org/10.1039/c3fo30389f (2013).
Gomes, I. B. et al. Renoprotective, anti-oxidative and anti-apoptotic effects of oral low-dose quercetin in the C57BL/6J model of diabetic nephropathy. Lipids Health Dis 13, 184, https://doi.org/10.1186/1476-511x-13-184 (2014).
Hasan, A. A. & Hocher, B. Role of soluble and membrane-bound dipeptidyl peptidase-4 in diabetic nephropathy. J Mol Endocrinol 59, R1–R10, https://doi.org/10.1530/jme-17-0005 (2017).
Peeters, S. A. et al. Plasma matrix metalloproteinases are associated with incident cardiovascular disease and all-cause mortality in patients with type 1 diabetes: a 12-year follow-up study. Cardiovasc Diabetol 16, 55, https://doi.org/10.1186/s12933-017-0539-1 (2017).
Zheng, D. et al. Exogenous Hydrogen Sulfide Attenuates Cardiac Fibrosis Through Reactive Oxygen Species Signal Pathways in Experimental Diabetes Mellitus Models. Cell Physiol Biochem 36, 917–929, https://doi.org/10.1159/000430266 (2015).
Prentki, M. & Nolan, C. J. Islet beta cell failure in type 2 diabetes. J Clin Invest 116, 1802–1812, https://doi.org/10.1172/jci29103 (2006).
Cho, J. M. et al. A novel dipeptidyl peptidase IV inhibitor DA-1229 ameliorates streptozotocin-induced diabetes by increasing β-cell replication and neogenesis. Diabetes Res Clin Pract 91, 72–79, https://doi.org/10.1016/j.diabres.2010.10.012 (2011).
Ahren, B. & Foley, J. E. Improved glucose regulation in type 2 diabetic patients with DPP-4 inhibitors: focus on alpha and beta cell function and lipid metabolism. Diabetologia 59, 907–917, https://doi.org/10.1007/s00125-016-3899-2 (2016).
George, P. & McCrimmon, R. J. Potential role of non-insulin adjunct therapy in Type 1 diabetes. Diabet Med 30, 179–188, https://doi.org/10.1111/j.1464-5491.2012.03744.x (2013).
Hamidi Shishavan, M. et al. Metformin Improves Endothelial Function and Reduces Blood Pressure in Diabetic Spontaneously Hypertensive Rats Independent from GlycemiaControl: Comparison to Vildagliptin. Scientific reports 7, 10975, https://doi.org/10.1038/s41598-017-11430-7 (2017).
Akarte, A. S., Srinivasan, B. P. & Gandhi, S. Relationships between the islets blood flow, nitric oxide, insulin, and cytosolic calcium in rat pancreatic islets: effects of DPP-IV inhibitor vildagliptin. European journal of pharmaceutical sciences: official journal of the European Federation for Pharmaceutical Sciences 45, 546–551, https://doi.org/10.1016/j.ejps.2011.11.016 (2012).
Sung, M. M. et al. Matrix metalloproteinase-2 degrades the cytoskeletal protein alpha-actinin in peroxynitrite mediated myocardial injury. Journal of molecular and cellular cardiology 43, 429–436, https://doi.org/10.1016/j.yjmcc.2007.07.055 (2007).
This research was supported by the Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG) (Grant Number: APQ 01453-15 and PPM 00282-11); Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (Grant Number: 454472/2014-5); Coordenação de Aperfeiçoamento de Pessoal de Nível superior (CAPES) and Universidade Federal de Ouro Preto, Brazil, allowing the purchase of reagents and kits for the development of the project.
The authors declare no competing interests.
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Miranda, P.H.d.A., Lacerda, K.C.D., Araújo, C.M. et al. Oral formulation of DPP-4 inhibitor plus Quercetin improves metabolic homeostasis in type 1 diabetic rats. Sci Rep 8, 15310 (2018). https://doi.org/10.1038/s41598-018-33727-x
- Untreated Diabetic Group
- Anti-insulin Antibodies