Effects of high-fat diet and the anti-diabetic drug metformin on circulating GLP-1 and the relative number of intestinal L-cells
© Kappe et al.; licensee BioMed Central Ltd. 2014
Received: 23 January 2014
Accepted: 7 May 2014
Published: 2 June 2014
Elevated serum free fatty acids (FFAs) contribute to the pathogenesis of type-2-diabetes (T2D), and lipotoxicity is observed in many cell types. We recently showed that simulated hyperlipidemia induces lipoapoptosis also in GLP-1-secreting L-cells in vitro, while metformin confers lipoprotection.
The aim of this study was to determine if a high fat diet (HFD) reduces the number of enteroendocrine L-cells and/or GLP-1 plasma levels in a rodent model, and potential effects thereupon of metformin treatment.
C57/Bl6 mice received control/HFD for 12-weeks, and oral administration of metformin/saline for the last 14 days. Blood glucose, glycosylated hemoglobin and plasma insulin and GLP-1 were determined before and after treatment with metformin using ELISAs. GLP-1-immunopositive cells in intestinal tissue sections were quantified using immunohistochemistry.
A HFD increased blood glucose, glycosylated hemoglobin, and fasting plasma insulin (33%, 15% and 70% increase, respectively), in conjunction with reduced oral glucose tolerance, indicating the manifestation of insulin resistance. Metformin counteracted these adverse effects, while also reducing prandial plasma FFAs. The number of GLP-1-positive cells was indicated to be reduced (55% reduction of the number of GLP-1-positive cells, p = 0.134), while there was a trend toward increased prandial plasma GLP-1 despite reduced food intake following a HFD.
HFD-fed mice rapidly develop insulin resistance. Metformin exerts beneficial glucose lowering effects, and is indicated to improve the incretin response. Albeit no significant effect, a HFD tends to reduce the number of GLP-1-positive cells. However, considering concurrent normal or increased plasma GLP-1, any reduction in the number of GLP-1-positive cells, probably does not contribute to development of the glucose intolerance, but may contribute to progression of the diabetic state through eventual loss of a functional incretin response.
KeywordsMetformin Glucagon-like peptide-1 Insulinotropic Lipotoxicity L-cell
Glucagon-like peptide-1 (GLP-1) is an incretin hormone with insulinotropic effects, where its release in response to food intake stimulates insulin secretion in a glucose-dependent manner . This incretin response has been suggested to be impaired in type 2 diabetes (T2D), characterized by hyperglycemia resulting from impaired insulin production and insulin resistance in peripheral tissues, as a result of reduced postprandial GLP-1 concentrations .
Administration of GLP-1 to patients restores glucose-induced insulin secretion as well as the β-cells’ sensitivity to glucose and normalizes fasting and postprandial glycemia in T2D patients , but its application as an antidiabetic drug is made difficult by rapid degradation. Native GLP-1 has a half-life of less than 2 minutes, due to degradation by dipeptidyl peptidase-4 (DPP-4) ubiquitously present in plasma. Stable analogs of GLP-1 and DPP-4-blocking agents that inhibit the degradation of active GLP-1 (7–36) amide to its metabolite GLP-1 (9–36) are available as treatments for T2D. Enhancing endogenous GLP-1 production/secretion by direct stimulation of GLP-1 secretion, and promotion of growth and viability, of L-cells may be a novel and more physiological option in incretin-based diabetes therapy. Enteroendocrine L-cells dispersed along the distal intestinal tract are the main source of endogenous GLP-1 secretion. Situated on the villi lining the intestine, the L-cells have apical microvilli facing the gut lumen and secretory vesicles located adjacent to the basolateral membrane. This morphology also enables the L-cells to be regulated by neuronal factors and hormones, as well as by direct nutrient stimulation [4, 5]. Free fatty acids (FFAs) are known to be potent stimulators of GLP-1 secretion, as we and others have demonstrated in vitro. FFAs also acutely stimulate GLP-1 secretion in vivo[7, 8], where unsaturated fatty acids have proven more potent stimulators of incretin secretion than saturated ones .
Chronically elevated levels of circulating FFAs and hyperlipidemia, typically seen in T2D, are correlated to lipotoxicity and cellular dysfunction in many cell types. It has been reported that such lipotoxicity is induced when the capacity of the tissue for triglyceride storage is exceeded and the fatty acids are funneled towards other metabolic fates, such as β-oxidation and increased production of reactive oxygen species (ROS) . In this context, it has also been shown that unsaturated fatty acids protect from saturated fatty acid-induced lipotoxicity through preventing increased β-oxidation and ROS production by promoting triglyceride storage of lipids . This could be a result of increased solubility/stability of lipid droplets containing a higher percentage of unsaturated acyl chains .
Considering the link between obesity and T2D, reduced GLP-1 secretion in T2D, progressively diminished GLP-1 secretory response with increasing BMI , as well as the fact that high levels of FFAs induce apoptosis in a number of different cell types, we investigated if hyperlipidemia could result in increased apoptosis, and thus reduced GLP-1-positive cell number and GLP-1 secretory capacity - using an in vitro model. Our results [6, 13] demonstrate that simulated hyperlipidemia does indeed induce apoptosis of GLP-1-secreting cells, through increased production of ROS. We also found that the most widely prescribed anti-diabetic drug, metformin, confers lipoprotection of GLP-1-secreting cells in vitro[6, 13]. These results may provide an explanation to the increased levels of circulating GLP-1 in obese patients (with or without T2D) receiving metformin .
Leveraging the above findings, the aim of the present study was to determine whether a high fat diet (HFD) can reduce the number of enteroendocrine L-cells in vivo in a rodent model. In addition, we aimed to determine the effects of HFD treatment on GLP-1 plasma levels and possible effects of metformin on these parameters.
Materials and methods
Animals and diet
The use of laboratory animals was performed according to the guidelines of Karolinska Institutet, Sweden, in accordance with national law and approved by the local animal ethics committee (Stockholm South Animal Ethics Committee, permit # S30-12).
C57/Bl6 mice (Nova/Scanbur, Sollentuna, Sweden) arrived 9 weeks old and were housed in our animal department for 1 week prior to initiation of the study. Animals were housed in groups of four in a total of eight cages under standard laboratory conditions of light, temperature and humidity, and received food and water ad libitum. Metformin was purchased from Sigma-Aldrich, St. Louis, MO. At the initiation of the study, the animals were divided into two groups. One group received normal chow (Nova/Scanbur) and the other group received the fat-enriched D12492 diet consisting of 60% kcal% fat (Research Diets, New Brunswick, NJ). Since we aimed to determine not only the effects of a HFD, but also if such effects could be counteracted by metformin treatment, the animals receiving a HFD were divided into two groups (after 10 weeks of dietary treatment) - where eight animals received oral gavage administration of 300 mg/kg/day metformin and the remaining eight animals received oral administration of saline. Volumes administered ranged between 0.128 – 0.235 ml/day. After 14 consecutive days of metformin/saline administration -- 12 weeks after the initiation of the study -- animals were euthanized using carbon dioxide. Throughout the study, weight and food consumption for all animals/cages were recorded once a week.
Blood glucose and HbA1c
Blood samples for glucose measurements were obtained from each mouse by needle puncture of the tail tip vein. Both prandial and fasting glycemia were measured at three time points (before initiation of metformin/saline treatment [time 0], 1 week after initiation [time 1] and 2 weeks after initiation before the end of the study [time 2]). Blood glucose concentrations were determined by means of Bayer’s Elite® Glucometer and compatible blood glucose test strips. Fasting blood samples for HbA1c measurements were obtained at time 0 and time 2 from the same puncture of the tail tip vein. HbA1c was determined using a DCA Vantage® Analyzer (Siemens Healthcare Diagnostics, Tarrytown, NY) and compatible sample cassettes.
Serum insulin, FFA and GLP-1 determinations
Blood samples were collected from the saphena vein (approx. 50 μl – max. 8 ml/kg/2 weeks) after 6 h fasting at time 0, 1 and 2 (see above), and transferred to centrifuge tubes at room temperature. At time 2, immediately after euthanization, a heart puncture was also performed and a larger volume of prandial blood collected. The blood samples were spun to obtain serum. The serum was stored in a freezer at -70°C for later analysis of insulin, total GLP-1 (7–36 and 9–36), active GLP-1 (7–36) and FFAs. Serum insulin concentrations were determined using a mouse ultrasensitive enzyme-linked immunosorbent assay (ELISA) (Mercodia, Uppsala, Sweden), according to the manufacturer’s instructions. Serum GLP-1 (7–36 and 9–36) and serum GLP-1 (7–36) were determined using specific ELISAs (Millipore, Billerica, MA) according to the manufacturer’s instructions. Serum FFAs were determined using the NEFA-HR(2) assay kit (Wako Chemicals, Richmond, VA) according to its instructions.
Oral glucose tolerance test (OGTT)
Food was removed 6 h prior to oral gavage administration of 1.5 g/kg glucose (50% glucose solution) at the end of the last week of treatment. At 15, 30 and 60 min following administration, blood samples for glucose measurements were obtained from each mouse by needle puncture of the tail tip vein. Blood glucose concentrations were determined by means of Bayer’s Elite® Glucometer and compatible blood glucose test strips.
Immunohistochemistry and quantification of L-cells
After euthanization, intestinal tissue was collected from the animals. The intestine was extracted and carefully removed of all fat. A 4-cm section proximal/distal to the appendix was removed and carefully cut open to have the lumen exposed and facing upward. The intestinal tissue section was then rolled up, starting with the most proximal end and with the lumen facing the center of the roll. The rolls were attached to plastic caps and immediately submerged in a freeze bath of 99% ethanol and dry ice. The rolls were stored in a freezer at -70°C pending sectioning of the intestinal tissue using a cryostat. The intestinal tissue was sectioned using a cryostat in 12 μm thick sections from the top of the roll towards the bottom, leaving each section to expose the lumen and villi of the full length of the intestinal tissue section. These sections were placed in consecutive order on six glass slides starting with position 1 of all slides, followed by position 2 of all slides, etc., leaving each and all slides with 10 sections representing the full cross section of the lumen. Sections were stored at -70°C.
Prior to IHC, sections were washed in PBS and fixed using a 10 min incubation with acetone at -20°C. Sections were then washed 3 × 10 min in PBS-T and incubated overnight at 4°C with a rabbit antibody specific for GLP-1 (Phoenix Europe GmbH, Karlsruhe, Germany. Cat# H-028-11) at 1:500 dilution in PBS-T containing 5% donkey serum. Tissue sections were washed in PBS-T 3 × 10 min and incubated for 2 h at room temperature in the dark with the secondary antibody (ALEXA Fluor 488 conjugated donkey anti-rabbit) (Invitrogen) at 1:200 dilution in PBS-T. Sections were washed in PBS 3 × 10 min and allowed to dry before a cover glass was mounted using Polyvinyl Alcohol mounting medium with DABCO antifading (Fluka Biochemica, Ronkonkoma, NY). For the purpose of quantifying cells after IHC, an advanced stereology platform, which allows unbiased quantification of cell number/volume and structural measurements within the intestinal structure , was used. Suboptimal quality of some of the pictures obtained from immunostaining of intestinal tissue resulted from technical difficulties associated with intestinal side effects of the combination of dietary treatment and metformin, as well as the relatively limited life-span of cryosections due to the formation of ice crystals Cross-sections from the distal intestine were analyzed from each of three animals from the different treatment groups.
Comparisons between groups, treatments and time were made by a one-way ANOVA for repeated measures. Newman-Keul’s post-hoc test was used. Comparisons between control and single treatment groups were done using two-tailed Student’s t test. Correlations were evaluated by determining the Pearson correlation coefficients. P < 0.05 was deemed statistically significant. Power analysis was performed and taken into consideration for all experiments performed.
After 10 weeks, C57/Bl6 mice on a high fat diet display a significant increase in body weight and a diabetic phenotype characterized by hyperglycemia and fasting hyperinsulinemia
Metformin significantly improves glycemia, fasting serum insulin and oral glucose tolerance
A high fat diet significantly increases epididymal fat, serum free fatty acids and reduces the number of GLP-1-positive cells in the distal intestine while upregulating intestinal expression of GLP-1R mRNA
Animals on a HFD develop hyperglycemia in conjunction with hyperlipidemia, indicating the manifestation of insulin resistance. The improved glycemia, fasting serum insulin and oral glucose tolerance observed in response to metformin treatment was expected and in line with the known anti-diabetic properties of metformin [16, 17]. The oral gavage administration did cause nausea and reduced food intake during the 14 days of treatment, where those mice receiving a HFD displayed significantly reduced appetite. Further, metformin treatment initially induced diarrhea. Starting with a lower dosage and increasing up to desired dosage over 3–4 days may have avoided this side-effect of metformin treatment. To detect if the weight loss during treatment was a confounding factor for the beneficial effects of metformin, we evaluated weight as an independent parameter for the improved metabolic state. The fact that weight alone displayed a significant positive correlation with HbA1c, but not fasting serum insulin, indicates that -- although the weight loss most likely contributed to the beneficial effects -- metformin treatment was indeed effective. In contrast to numerous reports of enhanced GLP-1 secretion in response to dietary fat [7, 8], no significant increase in fasting or prandial GLP-1 (7–36 and/or 9–36) could be detected in our animals fed a HFD. This discrepancy may stem from differences in the fatty acid stimuli; lipid load/HFD, as well as the duration of the HFD. In fact, many of the before mentioned studies investigating effects of fatty acids on GLP-1 secretion have focused on acute effects, and it can be hypothesized that toxic effects of chronic hyperlipidemia and reduced L-cell mass at some stage outweigh the stimulatory effect of the enteral fatty acids on GLP-1 secretion, i.e. exceeding the ability of the remaining L-cells to compensate. Extending the duration of the HFD may thus eventually result in a defective postprandial GLP-1 response, while reducing the duration of the HFD may result in observations of increased plasma GLP-1 in this group, as was indeed recently demonstrated . This hypothesis is supported by the trend toward reduced numbers of GLP-1-positive cells detected in the intestinal tissue from HFD-fed mice as compared to intestinal tissue from mice receiving a control diet, and in line with reports of a negative correlation between GLP-1 plasma levels and BMI . Further, metformin was indicated to counteract such effects of a HFD on the number of GLP-1-positive cells. Detrimental effects only after persistent and long term exposure to hyperlipidemia could theoretically be explained by an accumulation of FFAs that eventually exceeds the capacity of the L-cell for triglyceride storage and the subsequent increase in β-oxidation and ROS production [10, 13]. However, measurement of plasma GLP-1 in the different treatment groups following a glucose load would have added to the understanding of potential effects of a high fat diet and metformin treatment on the incretin response, and should be undertaken in future studies.
The present study shows reduced intestinal proglucagon expression in mice on a HFD following metformin treatment, which aligns well with previously published in vitro data, indicating metformin stimulatory action to be at the level of secretion. However, if metformin treatment increases the number of viable GLP-1-positive cells after a HFD, an increased intestinal proglucagon expression would be expected despite possible counteracting effects of metformin on proglucagon expression at the level of individual L-cells. The interpretation of the available data from this study is made even more difficult due to the adverse gastrointestinal side-effects induced by the metformin treatment, and the relatively short duration of metformin treatment. Therefore, further studies are necessary to confirm whether metformin lipoprotection can be observed in vivo, or is purely an in vitro phenomenon. The upregulation of GLP-1R mRNA in response to a HFD -- and normalization thereof by metformin treatment -- provokes further assessment of the intestinal expression of the GLP-1R under these conditions. Further, the mechanisms behind such effects remain to be investigated. It is, in light of a defective incretin response in diabetic patients improved by metformin treatment, tempting to hypothesize that compensatory mechanisms underlie increased receptor expression in response to reduced levels of the ligand and/or defective GLP-1R signaling in HFD-induced T2D.
In conclusion, our findings provide evidence for rapid development of insulin resistance and diabetes in mice receiving a HFD, with a significant improvement in response to metformin, which also was indicated to improve the prandial incretin response of HFD-fed mice. Further, our data demonstrate a clear trend toward reduced numbers of GLP-1-positive cells in HFD mice. However, considering no significant effect on fasting or prandial levels of GLP-1 in response to HFD, any reduction in the number of GLP-1-positive cells seemingly does not contribute to the development of oral glucose intolerance, hyperinsulinemia and hyperglycemia in this study. It may rather contribute to the progression of the diabetic state as it may lead to decreased prandial GLP-1 secretion when the reduction of GLP-1-positive cell number in response to hyperlipidemia overtakes fatty acid-induced potentiation of GLP-1 secretion.
Reactive oxygen species
High fat diet
Body mass index.
The authors thank Petra Wolbert, Richelle Fall and Diana Rydholm for assistance in maintenance and handling of the animals.
The authors also thank Annika Mehlem and Lars Muhl at the Department of Medical Biochemistry and Biophysics, Karolinska Institutet, for teaching cryostat sectioning techniques and providing the cryostat.
This work was supported by Stiftelsen Sigurd and Elsa Goljes Minne.
- Drucker DJ: The role of gut hormones in glucose homeostasis. J Clin Invest. 2007, 117: 24-32. 10.1172/JCI30076.PubMed CentralView ArticlePubMedGoogle Scholar
- Vilsboll T, Krarup T, Deacon CF, Madsbad S, Holst JJ: Reduced postprandial concentrations of intact biologically active glucagon-like peptide 1 in type 2 diabetic patients. Diabetes. 2001, 50: 609-613. 10.2337/diabetes.50.3.609.View ArticlePubMedGoogle Scholar
- Meier JJ, Nauck MA: Glucagon-like peptide 1(GLP-1) in biology and pathology. Diabetes Metab Res Rev. 2005, 21: 91-117. 10.1002/dmrr.538.View ArticlePubMedGoogle Scholar
- Gribble FM, Williams L, Simpson AK, Reimann F: A novel glucose-sensing mechanism contributing to glucagon-like peptide-1 secretion from the GLUTag cell line. Diabetes. 2003, 52: 1147-1154. 10.2337/diabetes.52.5.1147.View ArticlePubMedGoogle Scholar
- Tolhurst G, Reimann F, Gribble FM: Nutritional regulation of glucagon-like peptide-1 secretion. J Physiol. 2009, 587: 27-32. 10.1113/jphysiol.2008.164012.PubMed CentralView ArticlePubMedGoogle Scholar
- Kappe C, Patrone C, Holst JJ, Zhang Q, Sjoholm A: Metformin protects against lipoapoptosis and enhances GLP-1 secretion from GLP-1-producing cells. J Gastroenterol. 2013, 48: 322-332. 10.1007/s00535-012-0637-5.View ArticlePubMedGoogle Scholar
- Beglinger S, Drewe J, Schirra J, Goke B, D’Amato M, Beglinger C: Role of fat hydrolysis in regulating glucagon-like Peptide-1 secretion. J Clin Endocrinol Metab. 2010, 95: 879-886. 10.1210/jc.2009-1062.View ArticlePubMedGoogle Scholar
- Tolhurst G, Heffron H, Lam YS, Parker HE, Habib AM, Diakogiannaki E, Cameron J, Grosse J, Reimann F, Gribble FM: Short-chain fatty acids stimulate glucagon-like peptide-1 secretion via the G-protein-coupled receptor FFAR2. Diabetes. 2012, 61: 364-371. 10.2337/db11-1019.PubMed CentralView ArticlePubMedGoogle Scholar
- Reimann F: Molecular mechanisms underlying nutrient detection by incretin-secreting cells. Int Dairy J. 2010, 20: 236-242. 10.1016/j.idairyj.2009.11.014.PubMed CentralView ArticlePubMedGoogle Scholar
- Listenberger LL, Han X, Lewis SE, Cases S, Farese RV, Ory DS, Schaffer JE: Triglyceride accumulation protects against fatty acid-induced lipotoxicity. Proc Natl Acad Sci U S A. 2003, 100: 3077-3082. 10.1073/pnas.0630588100.PubMed CentralView ArticlePubMedGoogle Scholar
- Cnop M, Hannaert JC, Hoorens A, Eizirik DL, Pipeleers DG: Inverse relationship between cytotoxicity of free fatty acids in pancreatic islet cells and cellular triglyceride accumulation. Diabetes. 2001, 50: 1771-1777. 10.2337/diabetes.50.8.1771.View ArticlePubMedGoogle Scholar
- Muscelli E, Mari A, Casolaro A, Camastra S, Seghieri G, Gastaldelli A, Holst JJ, Ferrannini E: Separate impact of obesity and glucose tolerance on the incretin effect in normal subjects and type 2 diabetic patients. Diabetes. 2008, 57: 1340-1348. 10.2337/db07-1315.View ArticlePubMedGoogle Scholar
- Kappe C, Holst JJ, Zhang Q, Sjoholm A: Molecular mechanisms of lipoapoptosis and metformin protection in GLP-1 secreting cells. Biochem Biophys Res Commun. 2012, 427: 91-95. 10.1016/j.bbrc.2012.09.010.View ArticlePubMedGoogle Scholar
- Mannucci E, Ognibene A, Cremasco F, Bardini G, Mencucci A, Pierazzuoli E, Ciani S, Messeri G, Rotella CM: Effect of metformin on glucagon-like peptide 1 (GLP-1) and leptin levels in obese nondiabetic subjects. Diabetes Care. 2001, 24: 489-494. 10.2337/diacare.24.3.489.View ArticlePubMedGoogle Scholar
- Gundersen HJ, Bendtsen TF, Korbo L, Marcussen N, Moller A, Nielsen K, Nyengaard JR, Pakkenberg B, Sorensen FB, Vesterby A, West MJ: Some new, simple and efficient stereological methods and their use in pathological research and diagnosis. APMIS. 1988, 96: 379-394. 10.1111/j.1699-0463.1988.tb05320.x.View ArticlePubMedGoogle Scholar
- Giannarelli R, Aragona M, Coppelli A, Del Prato S: Reducing insulin resistance with metformin: the evidence today. Diabetes Metab. 2003, 29: 6S28-6S35. 10.1016/S1262-3636(07)70079-4.View ArticlePubMedGoogle Scholar
- Matsui Y, Hirasawa Y, Sugiura T, Toyoshi T, Kyuki K, Ito M: Metformin reduces body weight gain and improves glucose intolerance in high-fat diet-fed C57BL/6 J mice. Biol Pharm Bull. 2010, 33: 963-970. 10.1248/bpb.33.963.View ArticlePubMedGoogle Scholar
- Ahlkvist L, Brown K, Ahren B: Upregulated insulin secretion in insulin-resistant mice: evidence of increased islet GLP1 receptor levels and GPR119-activated GLP1 secretion. Endocr Connect. 2013, 2: 69-78. 10.1530/EC-12-0079.PubMed CentralView ArticlePubMedGoogle Scholar
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