- Open Access
Goettingen Minipigs (GMP): Comparison of Two Different Models for Inducing Diabetes
© Strauss et al; licensee BioMed Central Ltd. 2012
- Received: 30 September 2011
- Accepted: 5 March 2012
- Published: 5 March 2012
Preclinical experiments on large animals are indispensable for evaluating the effectiveness of diabetes therapies. Miniature swine are well suited for such studies due to their physiological and pathophysiological responses.
We compare two methods for inducing diabetes in Goettingen minipigs (GMP), in five with the beta cell toxin streptozotocin (STZ) and in five other GMP by total pancreatectomy (PE). Glucose homeostasis was assessed with the intravenous glucose-tolerance test (IVGTT) and continual monitoring of interstitial glucose levels. At conclusion of the observation period, the pancreata were examined histologically. Three non-diabetic GMP served as control group.
The IVGTT revealed markedly diabetic profiles in both GMP groups. STZ-GMP were found to harbor residual C-peptides and scattered insulin-positive cells in the pancreas. PE-GMP survived the total pancreatectomy only with intensive postoperative care.
Although both methods reliably induced diabetes in GMP, the PE-GMP clearly had more health problems and required a greater expenditure of time and resources. The PE-GMP model, however, was better at eliminating endogenous insulin and C-peptide than the STZ-GMP model.
- pig or swine
- real-time glucose monitoring
- intravenous glucose tolerance test
- total pancreatectomy
Neither the physiology of glucose metabolism [1, 2] nor the pathophysiologies of types 1 and 2 diabetes mellitus [3–8] are fully understood. Among the promising methods for treating type 1 diabetes is the transplantation of isolated microencapsulated islets of Langerhans [9, 10]; metabolic surgery is one of the recently introduced treatment options for type 2 diabetes [11, 12]. Many open questions regarding experimental diabetes treatment modalities have been answered in studies using small animal diabetes models. Such studies, for example, have answered fundamental questions regarding the appropriate transplantation site for islets cells [13, 14], the function of islets cell transplants in vivo [15, 16], the recipient immune response to islets cell transplants , and regarding postoperative glucose homeostasis in the field of diabetes metabolism research . As valuable as such studies are, however, questions regarding the feasibility of such concepts under preclinical conditions can only be answered in large animal models of diabetes.
Although non-human primates are ideally suited for such studies due to their genetic and physiological proximity to humans, ethical considerations and the personnel required and the high associated costs have limited primate studies to a very minimum. For training in the course of transplantation the minipig is a serious alternative because of its physiological resemblance to humans, but also due to its size, ease of handling, and the much lower costs entailed. Because spontaneous diabetes is unknown in swine, the diabetes must be induced. The present study compares two different diabetes models in Goettingen minipigs (GMP), one model inducing diabetes chemically with the beta cell toxin streptozotocin (STZ), the other inducing diabetes surgically by total pancreatectomy (PE).
Both variants have already been described in the literature [19–22]. The results with STZ are largely uniform: the severity of the induced diabetes depends on the STZ dosage. The results with PE are less consistent. Postoperative survival of the animals has been reported as less than 10 days, which would disqualify PE as a diabetes-induction method. But several reports describe diabetic swine and canines that have undergone PE followed by transplantation of islets of Langerhans and remained free of postoperative complications during a long term survival of several months [23, 24]. The present study evaluates and compares the advantages and disadvantages of each of the two models for diabetes induction in GMP. The findings will be used to establish an optimal large animal model for research into specific questions of diabetes therapy.
Ten 11 to 17-month-old female GMP weighing 20-35 kg were studied. The GMP were housed individually under standardized conditions (19-23°C; 40-70% relative humidity; 12:12 hour day/night cycle); they were fed once daily with a standard swine feed (Altromin; Lage, Germany); water was provided ad libitum. All experiments were approved in advance by the government of Lower Franconia.
Diabetes induction with STZ
In 5 GMP, 150 mg/kg body weight (bw) of the beta cell toxin STZ (Sigma-Chemie, Munich, Germany) were infused via a central venous catheter over 10 min (buffered solution: 1 g STZ in 10 mL sodium citrate buffer freshly prepared). To avoid hypoglycemia due to insulin release by the destroyed beta cells, 200 mL 5% glucose solution were given over one hour after STZ application. The observation time in this group was 3-4 months.
Diabetes induction with total pancreatectomy
Five GMP underwent total pancreatectomy under general anesthesia. After transverse upper abdominal laparotomy, the pancreas tail was carefully detached from the surrounding tissue. Small vessels originating in the spleen and the V. portae were ligated and cut. The spleen was always left intact. Next the corpus and caput were detached from the surrounding tissue while sparing the pancreaticoduodenal vessels and the vessels supplying the duodenum. Lastly the pancreatic duct was exposed, double ligated and cut. The abdomen was closed and once the anesthetic wore off the animal was returned to its pen where it received intensive medical care. Over the next 5 days the PE-GMP were given analgesia with 1 g Novalgin® (Aventis Pharma; Frankfurt am Main, Germany) and 3 × 50 mg Tramal® (Ratiopharm; Ulm, Germany) daily. Prophylactic antimicrobial therapy was also administered with Tazobac® EF4 g/0.5 g (Wyeth Pharma GmbH; Muenster, Germany). When feeding was begun on the 6th to 8th postoperative day, the GMP received an exogenous pancreas enzyme (Creon® 25,000 IE/Tag) (Solvay Arzneimittel; Hanover, Germany) at every feeding. The observation time for this group was 28 days.
Real time glucose monitoring
The CGMS® (Medtronic MiniMed; Northridge, USA) continuous glucose monitoring system was used as described by us previously .
Blood sugar monitoring
All blood sugar readings were done on capillary blood from the ears. The first drop was discarded; the second was placed on a test strip of the Ascensia Contour® blood glucose monitoring system (Bayer Health Care; Mishawaka, USA).
Intravenous glucose tolerance test and hyperglycemic clamp
The intravenous glucose tolerance test (IVGTT) was performed between the 20th and 28th days after diabetes induction. The values of the diabetic GMP were compared with those of the normoglycemic control GMP. Feeding and insulin treatment were discontinued 12-16 h before IVGTT was performed. At time point t = 0 0.5 g/kg bw glucose was injected. At time points t = -20 min; -10; 0; +1; +3; +5; +7; +10; +20; +30; +40; and +60 min blood samples were taken and the serum insulin and C-peptide levels measured. At the same time blood glucose levels were determined. For the subsequent hyperglycemic clamp in normoglycemic animals, 0.6 g glucose pro kg bw were given at t = +60 min to raise the blood glucose level above 500 mg/dL, followed by continuous glucose infusion (2 g/kg bw/hour) to maintain blood glucose levels at over 500 mg/dL till t = +100 min, then the infusion was stopped. At t = +90 min 67 mg arginine/kg bw was administered. Blood samples for monitoring insulin and C-peptide as well as blood glucose values were taken at time points t = +60 min, +61, +63, +65, +67, +70, +80, +90, +91, +93, +95, +97, +100 and +110 min. In diabetic GMP there was no renewed application of glucose solution or continuous glucose infusion. Arginine was given at t = +60 min. Blood glucose levels were measured and blood samples taken at t = +60 min, +61, +63, +65, +67, +70, +80 and +90 min.
C-peptide was determined in GMP serum samples using the RIA-Kit (PCP-22K, Linco Research; Missouri, USA). The resulting radioactivity was measured with a Gamma counter (Berthold; Bad Wildbad, Germany) in counts per minute ( cpm). C-peptide in ng/mL was calculated using a standard curve.
Serum insulin levels were measured with a commercial ELISA-Kit (Biosource; Nivelles, Belgium). The samples were analyzed at two wavelengths (450 nm and 490 nm) against a reference filter (650 nm) with the aid of an ELISA reader (Thermo Max Microplate Reader, MWG Biotech; Ebersberg, Germany). Insulin levels were measured on a standard curve and shown in μU/mL.
At conclusion of the observation time, the pancreata of the STZ-GMP were removed and 1 cm3 tissue blocks from the head, corpus and tail were cryoconserved in liquid nitrogen. Sections from the different sites of the pancreas were prepared from these blocks. The sections were stained with standard hematoxylin-eosin (H&E) and for standard immunohistochemistry with an antiinsulin antibody (Guinea pig-anti-swine antiserum; Dako; Hamburg, Germany).
All data are given as mean ± standard deviation (SD).
Glucose metabolism in normoglycemic non-diabetic control GMP
Continuous interstitial glucose monitoring and glucose tolerance tests were performed in 3 adult, 11 to 17-month-old female non-diabetic GMP weighing 20 to 35 kg.
Real-time glucose monitoring in control GMP
Intravenous glucose tolerance test in control GMP
Glucose metabolism in diabetic STZ-GMP and PE-GMP
Like humans, the GMP were considered to be diabetic if they had a fasting blood glucose level of > 126 mg/dL (7 mmol/L) or a spontaneous blood glucose level of > 200 mg/dL (11.1 mmol/L). C-peptide values after stimulation with glucose did not exceed > 0.4 ng/mL.
Diabetes was induced in 5 GMP by total pancreatectomy. All PE-GMP survived the surgical procedure and became diabetic immediately postoperative. Two of the 5 PE-GMP, however, developed an ileus within 4-6 days postoperative and were removed from the study. Learning from this experience, we developed a more intensive postoperative care protocol for the remaining 3/5 PE-GMP: from day +1 to day +14, the remaining 3 PE-GMP were given 1 L sterofundin per infusionem, 2 g Novalgin and 20 mg Paspertin daily. Each animal was checked several times daily regarding general health, vitality, blood glucose levels, and gut noises. The following steps were also taken: Insulin and a 40% glucose solution (details below) were given daily, both in dependence on blood glucose levels, potassium (40 mval/d), Neostigmin (0.5 mg/d beginning on day +3 until start of intestinal activity), Tramal (0.7 mg/kg), and the antibiotic Tazobactam 2 × 4.5 g). The PE-GMP also received daily exercise therapy to improve their general health and vitality. A pancreas enzyme (Creon 25.000) was mixed with their dry feed. Under this intensive regimen the PE-GMP began to eat solid feed on their own on the 4th to 7th day postoperative and began to pass stool on the 6th to 8th postoperative day. Within 20 days after total pancreatectomy the PE-GMP exhibited good general health, moved about freely with no complications. In the ensuing time they were given daily exogenous insulin and exogenous pancreas enzyme. Under this protocol the PE-GMP survived without complications until the end of the observation period.
Real-time glucose monitoring
In dependence on morning (fasting) blood glucose levels, the GMP were fed dry feed containing insulin (Novomix) consisting of 30% insulin-aspart and 70% intermediary insulin). In the evening (without determining blood glucose levels), they were given the long-acting insulin Lantus, the dose depending on body weight. Following this regimen, the diabetic GMP were maintained without complications at blood glucose levels between 200 and 400 mg/dL over several months. Hypoglycemia was not observed under this protocol.
Persons, qualifications and time needed to induce the two diabetes models in the Goettingen minipig and care for the diabetic animals prior to grafting the isolated islets of Langerhans.
Number of persons
diabetes induction with STZ
1 scientist or surgeon
1 animal caretaker
diabetes induction with PE
1 medical assistant
management of the
1 animal caretaker
2 × 30 minutes/day
management of the PE diabetes (early phase)
Up to 4 hours/day
management of the PE diabetes (late phase)
1 animal caretaker
2 × 30 minutes/day
The present study shows that both the STZ-GMP and PE-GMP models of diabetes induction produced diabetic GMP. The RTGM and IVGTT test procedures reliably measured the diabetic metabolism of the GMP.
All GMP treated with STZ became diabetic within 24 hours; this confirms the data in the literature regarding diabetes induction in GMP using STZ . With regard to diabetes induction using total pancreatectomy and the contradictory data in the literature the following can be said: a) none of our PE-GMP would have survived the procedure without intensive postoperative care, and b) only the intensive drug regimen including insulin application ensured the long-term survival of the PE-GMP - in our animals for 28 days. Due to the total absence of endogenous insulin the application of exogenous insulin seems to be a critical point to ensure long term survival in PE-GMP when compared to the literature . In our experience both diabetes-induction methods are suited for long-term studies. Before beginning such a study researchers should intensively discuss the pros and cons of each model: The PE-GMP model ensures that no endogenous insulin or C-peptide will be produced since the cells that release them are surgically removed, a very important advantage for evaluation of the usually still marginal transplant function. In discussing the drawbacks of the PE-GMP model, a distinction must be made between the surgical procedure, postoperative care and physiology. Regarding the surgical procedure, it entails a great expenditure in time, technical resources and personnel, and is therefore very expensive. It requires a surgical team experienced in total pancreatectomy. The postoperative care is time intensive and involves tasks that must be performed several times daily until the animal has fully recovered from surgery. The STZ-GMP model, in contrast, can be produced relatively easily at low cost and the critical phase of intensive medical care rapidly gives way to the phase of routine care.
Physiologically the main scientific advantage of the PE-GMP model, namely the complete elimination of host insulin production, also entails considerable drawbacks: Here again a distinction must be made between surgery-related problems and physiological factors. Regarding the former the following can be said: The massive surgical intervention severely compromises the homeostasis of the organism so that the diabetic GMP has major problems with wound healing and is slow to recuperate other bodily functions. Physiologically disadvantageous are the lack of both the anti-insulin hormone glucagon and the exocrine pancreas enzymes essential for digestion. STZ-GMP offer the advantage of ease of diabetes induction (application of central venous catheter) and no prolonged postoperative recuperation phase. Injection of STZ selectively destroys beta cells, leaving the glucagon producing alpha cells intact and thus lessening the risk of hypoglycemia. The exocrine pancreas function also remains intact, and feeding and digestion proceed without complications. The drawback of the STZ-GMP model is the incomplete destruction of beta cells, as confirmed in the present study by the histological detection of residual beta cells and the STZ-GMPs' partial response to a glucose and arginine bolus in IVGTT. For transplantation of islets of Langerhans, therefore, especially if there is inadequate transplant volume, the PE-GMP model is the superior recipient model. For research in the field of metabolic surgery (such as gastric bypass) the STZ-GMS model is better. The goals of metabolic surgery for improvement of glucose homeostasis are to change the incretin glucagon-like peptide 1 and glucose-dependent insulinotropic polypeptide so as to slow the passage of food and to improve insulin release and/or stimulate the generation of beta cells. These goals would be thwarted by prior abdominal surgery for removal of the pancreas.
The continual weight loss in diabetic GMP can be explained by impaired glucose tolerance and is also seen in type 1 diabetics. The clearly greater weight loss in PE-GMP can be attributed to the severity of the surgical intervention and the postoperative drop in food consumption. The control GMP did not gain weight during the observation period, which was expected since they were fully grown adults.
Intravenous glucose tolerance test
The IVGTT we used with subsequent hyperglycemic clamp is a generally accepted procedure for verification of diabetic disorders . We too could show that this test for monitoring blood glucose, C-peptide and insulin levels can reliably identify diabetes in GMP. The various data however must always be regarded in relation to one another. A simple rise in glucose tolerance above the diabetic threshold is not diagnostic. Independent of C-peptide levels, residual function of the endocrine pancreas may be at play. Unlike blood glucose and C-peptide values, insulin levels in the diabetic GMP lay below the measurement threshold of the methods we used (ELISA). In non-diabetic GMP, by contrast, insulin showed a course comparable to that of C-peptide in IVGTT.
Real-time glucose monitoring
The RTGM we used is a system developed for the diagnosis and control of diabetes. To our knowledge, its use in swine has only been reported by us ; the present data confirm and add to our previous results. Once again only measurements are used where the correlation of interstitial glucose and serum glucose levels was > 90%. The data obtained with RTGM permit two conclusions: 1) RTGM can be successfully applied preclinically in swine as shown in the correlation between our RTGM measurements and the event -- feeding or insulin injection -- influencing glucose homeostasis. 2) RTGM measurements mirror the metabolic state and thus provided valuable evidence regarding the organism's current glucose tolerance. An improvement in glucose tolerance with a slight increase in blood glucose levels after feeding, for example, or a rapid postprandial decline in blood glucose levels are made readily apparent over the long-term.
RTGM's ability to measure long-term trends is a basic difference to IVGTT, which allows only relatively brief monitoring for 120 min after glucose bolus. The major drawback to RTGM in swine though is its limited measurement range of 40-400 mg/dL. This range is ideal for human diabetics, since an interstitial glucose level below 40 mg/dL is accompanied by somnolence, if not coma. By nature GMP have lower blood glucose levels than humans, levels which cannot be detected by the device we employed. For future GMP studies a modified RTGM system is urgently needed, one that accommodates the greater natural range of swine.
Both the STZ-GMP and PE-GMP models reliably induce diabetes in GMP and are thus suited for research into specific questions regarding type 1 and type 2 diabetes and/or for preclinical evaluation. To our knowledge we are the first to show that with appropriate postoperative care the PE-GMP can be kept without complications for prolonged periods (week to months), during which, for example, preparations for successful transplantation, e.g. the isolation and in vitro culture of several islets of Langerhans transplants, can be made.
The authors thank Mr. A. Reichert, Mr. J. Weinberger and Mr. P. Heuler for their excellent technical help; and Mrs. L. Stevenson-Knebel for her assistance in preparing the manuscript. This study was financed in part by funds from the EU (BARP+ #NMP3-CT-2003-505614). This publication was funded by the German Research Foundation (DFG) and the University of Wuerzburg in the funding programme Open Access Publishing
- Blaak E: Sex differences in the control of glucose homeostasis. Curr Opin Clin Nutr Metab Care. 2008, 11: 500-504. 10.1097/MCO.0b013e32830467d3.View ArticlePubMedGoogle Scholar
- Dumonteil E, Philippe J: Insulin gene: organisation, expression and regulation. Diabetes Metab. 1996, 22: 164-173.PubMedGoogle Scholar
- Turner RC, Hattersley AT, Shaw JT, Levy JC: Type II diabetes: clinical aspects of molecular biological studies. Diabetes. 1995, 44: 1-10. 10.2337/diabetes.44.1.1.View ArticlePubMedGoogle Scholar
- Permutt MA, Chiu K, Ferrer J, Glaser B, Inoue H, Nestorowicz A, Stanley CA, Tanizawa Y: Genetics of type II diabetes. Recent Prog Horm Res. 1998, 53: 201-216.PubMedGoogle Scholar
- Malecki MT: Genetics of type 2 diabetes mellitus. Diab Res Clin Pract. 2005, 68 (Suppl 1): 10-21.View ArticleGoogle Scholar
- Buchwald H, Estok R, Fahrbach K, Banel D, Jensen MD, Pories WJ, Bantle JP, Sledge I: Weight and type 2 diabetes after bariatric surgery: systematic review and metaanalysis. Am J Med. 2009, 122: 248-256. 10.1016/j.amjmed.2008.09.041.View ArticlePubMedGoogle Scholar
- Knip M, Kukko M, Kulala P, Veijola R, Simell O, Akerblom HK, Ilonen J: Humoral beta-cell autoimmunity in relation to HLA-defined disease susceptibility in preclinical and clinical type 1 diabetes. Am J Med Genet. 2002, 115: 48-54. 10.1002/ajmg.10343.View ArticlePubMedGoogle Scholar
- Larsson K, Elding-Larsson H, Cederwall E, Kockum K, Neiderud J, Sjöblad S, Lindberg B, Lernmark B, Cilio C, Ivarsson SA, Lernmark A: Genetic and perinatal factors as risk for childhood type 1 diabetes. Diabetes Metab Res Rev. 2004, 20: 429-437. 10.1002/dmrr.506.View ArticlePubMedGoogle Scholar
- Bretzel RG, Eckhard M, Bendel MD: Pancreatic islet and stem cell transplantation: new strategies in cell therapy of diabetes mellitus. Panminerva Med. 2004, 46: 25-42.PubMedGoogle Scholar
- Bretzel RG, Jahr H, Eckhard M, Martin I, Winter D, Brendel MD: Islet cell transplantation today. Langenbecks Arch Surg. 2007, 392: 239-253. 10.1007/s00423-007-0183-4.View ArticlePubMedGoogle Scholar
- Saliba J, Wattacheril J, Abumrad NN: Endocrine and metabolic response to gastric bypass. Curr Opin Clin Nutr Metab Care. 2009, 12: 515-521. 10.1097/MCO.0b013e32832e1b14.PubMed CentralView ArticlePubMedGoogle Scholar
- Frachetti KJ, Goldfine AB: Bariatric surgery for diabetes management. Curr Opin Endocrinol Diabetes Obes. 2009, 16: 119-124. 10.1097/MED.0b013e32832912e7.View ArticlePubMedGoogle Scholar
- Rajab A, Buss J, Diakoff E, Hadley GA, Osei K, Ferguson RM: Comparison of the Portal Vein and Kidney Subcapsule as Site for Primate Islet Autotransplantation. Cell Transplant. 2008, 17: 1015-1023. 10.3727/096368908786991533.View ArticlePubMedGoogle Scholar
- van der Windt DJ, Echeverri GJ, Ijzermans JNM, Cooper DKC: The Choice of the Anatomical Site for Islet Transplantation. Cell Transplant. 2008, 17: 1005-1014. 10.3727/096368908786991515.View ArticlePubMedGoogle Scholar
- Cui H, Tucker-Burden C, Cauffiel SM, Barry AK, Iwakoshi NN, Weber CJ, Safley SA: Lang-term metabolic control of autoimmune diabetes in spontaneously diabetic nonobese diabetic mice by nonvascularized microencapsulated adult porcine islets. Transplantation. 2009, 88: 160-169. 10.1097/TP.0b013e3181abbfc1.View ArticlePubMedGoogle Scholar
- Kobayashi T, Arefanian H, Harb G, Tredget EB, Rajotte RV, Korbutt GS, Rayat GR: Prolonged survival of microencapsulated neonatal porcine islet xenografts in immune competent mice without antirejection therapy. Cell Transplant. 2008, 17: 1243-1256. 10.3727/096368908787236602.View ArticlePubMedGoogle Scholar
- Truong W, Hancock WW, Anderson CC, Merani S, Shapiro AM: Coinhibitory T-cell signalling in islet allograft rejection and tolerance. Cell Transplant. 2006, 15: 105-119.View ArticlePubMedGoogle Scholar
- Aguirre V, Stylopoulos N, Grinbaum R, Kaplan LM: An endoluminal sleeve induces substantial weight loss and normalizes glucose homeostasis in rats with diet-induced obesity. Obesity. 2008, 16: 2585-2592. 10.1038/oby.2008.502.PubMed CentralView ArticlePubMedGoogle Scholar
- Gäbel H, Bitter-Suermann H, Henriksson C, Säve-Söderbergh J, Lundholm K, Brynger H: Streptozotocin Diabetes in Juvenile Pigs. Evaluation of an Experimental Model. Horm Metab Res. 1985, 17: 275-280. 10.1055/s-2007-1013518.View ArticlePubMedGoogle Scholar
- Grüssner R, Nakhleh R, Grüssner A, Tomadze G, Diem P, Sutherland D: Streptozotocin-induced diabetes mellitus in pigs. Horm Metab Res. 1993, 25: 199-203. 10.1055/s-2007-1002076.View ArticlePubMedGoogle Scholar
- Wilson D, Dhall DP, Simeonovic CJ, Lafferty KJ: Induction and management of diabetes mellitus in the pig. Aust J Exp Biol Med Sci. 1986, 64: 489-500. 10.1038/icb.1986.53.View ArticlePubMedGoogle Scholar
- Kobayashi K, Kobayashi N, Okitsu T, Yong C, Fukazawa T, Ikeda H, Kosaka Y, Narushima M, Arata T, Tanaka N: Development of a porcine model of type 1 diabetes by total pancreatectomy and establishment of a glucose tolerance evaluation method. Artif Organs. 2004, 28: 1035-1042. 10.1111/j.1525-1594.2004.00002.x.View ArticlePubMedGoogle Scholar
- Edamura K, Itakura S, Nasu K, Iwami Y, Ogawa H, Sasaki N, Ohgawara H: Xenotransplantation of Porcine Pancreatic Endocrine Cells to Total Pancreatectomized Dogs. J Vet Med Sci. 2003, 65: 549-556. 10.1292/jvms.65.549.View ArticlePubMedGoogle Scholar
- Morsiani E, Fogli L, Lanza G, Lebow LT, Demetriou AA, Rozga J: Long-Term Insulin Independence Following Repeated Islet Transplantation in Totally Pancreatectomized Diabetic Pigs. Cell Transplant. 2002, 11: 55-66.PubMedGoogle Scholar
- Strauss A, Tiurbe C, Chodnevskaja I, Thiede A, Timm S, Ulrichs K, Moskalenko V: Use of the continuous glucose monitoring system in Goettingen Minipigs, with a special focus on the evaluation of insulin-dependent diabetes. Transplant Proc. 2008, 40: 536-539. 10.1016/j.transproceed.2008.02.003.View ArticlePubMedGoogle Scholar
- Rakotoambinina B, Timsit J, Deschamps I, Laborde K, Gautier D, Jos J, Boitard C, Robert JJ: Insulin responses to intravenous glucose, intravenous arginine and a hyperglycaemic clamp in ICA-positive subjects with different degrees of glucose tolerance. Diabetes Metab. 1997, 23: 43-50.PubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.