Front. Endocrinol., 27 May 2016
Sec. Systems Endocrinology

Normocaloric Diet Restores Weight Gain and Insulin Sensitivity in Obese Mice

imageGiovanni Enrico Lombardo1, imageBiagio Arcidiacono1, imageRoberta Francesca De Rose1, imageSaverio Massimo Lepore1, imageNicola Costa1, imageTiziana Montalcini2, imageAntonio Brunetti1*, imageDiego Russo1*, imageGiovambattista De Sarro1 and imageMarilena Celano1
  • 1Department of Health Sciences, University “Magna Graecia” of Catanzaro, Catanzaro, Italy
  • 2Department of Medical and Surgical Sciences, University “Magna Graecia” of Catanzaro, Catanzaro, Italy

An increased incidence of obesity is registered worldwide, and its association with insulin resistance and type 2 diabetes is closely related with increased morbidity and mortality for cardiovascular diseases. A major clinical problem in the management of obesity is the non-adherence or low adherence of patients to a hypocaloric dietetic restriction. In this study, we evaluated in obese mice the effects of shifting from high-calorie foods to normal diet on insulin sensitivity. Male C57BL/6JOlaHsd mice (n = 20) were fed with high fat diet (HFD) for a 24-week period. Afterward, body weight, energy, and food intake were measured in all animals, together with parameters of insulin sensitivity by homeostatic model assessment of insulin resistance and plasma glucose levels in response to insulin administration. Moreover, in half of these mice, Glut4 mRNA levels were measured in muscle at the end of the high fat treatment, whereas the rest of the animals (n = 10) were shifted to normocaloric diet (NCD) for 10 weeks, after which the same analyses were carried out. A significant reduction of body weight was found after the transition from high to normal fat diet, and this decrease correlated well with an improvement in insulin sensitivity. In fact, we found a reduction in serum insulin levels and the recovery of insulin responsiveness in terms of glucose disposal measured by insulin tolerance test and Glut4 mRNA and protein expression. These results indicate that obesity-related insulin resistance may be rescued by shifting from HFD to NCD.


Modern lifestyle is often characterized by sedentary activities and overeating. As a consequence, in the last decades, this has been responsible for the increased incidence and prevalence of obesity and obesity-induced comorbidities, such as insulin resistance and metabolic syndrome (1, 2) that may contribute to type 2 diabetes mellitus (T2DM) and cardiovascular disease (3). Several studies have demonstrated that a healthy lifestyle can lead to weight loss and improve insulin sensitivity (47). In this regard, a crucial role is played by the nutrient composition of the diet, both in terms of total caloric intake and the variety of its components, with particular attention to the different types of fatty acids (8, 9). Unfortunately, most of anti-obesity interventions are often limited by the difficulty to maintain a low-calorie dietary regimen, especially when long-term treatments are required (10, 11). Thus, few anti-obesity programs have been found to be helpful.

To date, several animal models have been used to evaluate the effects of various dietetic regimens on body weight and metabolic parameters. A validated experimental model is represented by mice fed with a high fat diet (HFD), which develop obesity, insulin resistance, and dyslipidemia (813).

In the present study, we evaluated the effects of the transition from HFD to normocaloric diet (NCD) (regular food with no additive agents or nutraceutical compounds) on body weight and insulin responsiveness in C57BL/6JOlaHsd mice, a strain of mice genetically prone to develop obesity and insulin resistance (14).

Materials and Methods

Animals and Study Design

Five-week-old male C57BL/6JOlaHsd mice (n = 20), NCD and HFD, were purchased from Harlan Laboratories S.r.l (Udine, Italy). Mice were housed in individual cages and maintained on 12-h light/dark cycle at 21 ± 1°C and 50 ± 5% humidity with free access to water and food ad libitum. Animals were fed with HFD containing 60.3% kcal fat, 21.3% kcal carbohydrate, and 18.4% kcal protein (HFD group) for 24 weeks. After this period, 10 mice were euthanized by cervical dislocation and the other 10 were fed with NCD only (Teklad Global 18% kcal fat, 58% kcal carbohydrate, and 24% kcal protein) (NCD group) for the subsequent 10 weeks. A schematic representation of the study design is shown in Figure 1. Body weight, girth waist, and food intake were recorded at weekly interval for all animals (15). Liver, skeletal muscle, and abdominal fat were excised, weighted, and stored in liquid nitrogen. This study was performed following the Italian (D.M. 116/92) and ECC regulations (O.J. of E.C.L 358/1 12/18/1986), in accordance with the guide for the care and use of laboratory animals and approved by the local ethical committee.


Figure 1. Study design. A schematic representation of the study protocol and experimental plan is shown.

Biochemical Analysis

Blood samples were collected after 12 h of fasting. Serum was separated by centrifugation at 1700 g for 10 min at room temperature and stored at −20°C, until use. Total cholesterol and triglycerides were measured using commercial reagents (Siemens Healthcare Diagnostics, Milano, Italy) and an automated biochemistry analyzer (Dimension EXL, Siemens Healthcare Diagnostics). Insulin levels were measured using ELISA kit (Rat/Mouse Insulin ELISA Kit, EMD Millipore Corporation, Darmstadt, Germany), according to the manufacturers’ instructions.

Insulin Tolerance Test

Insulin tolerance test (ITT) was performed in both HFD and NCD groups, as previously described (16). Animals were fasted for 12 h, weighed, and injected intraperitoneally with insulin (1 U/kg body weight Regular®, Novorapid, Novonordisk, Roma, Italy). Blood glucose levels were measured after 0, 15, 30, 60, and 90 min using an automatic glucometer (Glucocard, Menarini Diagnostics, Firenze, Italy).

Expression of Glucose Transporter Type 4

Total RNA was isolated from quadriceps skeletal muscle using TRIzol reagent (Life Technologies, Monza, Italy), following the manufacturer’s recommended protocol and quantified with a NanoDrop Spectrophotometer (Thermo Fisher Scientific, Inc., Waltham, MA, USA). RNA levels were normalized against 18S ribosomal RNA in each sample, and cDNAs were synthesized from 1 μg of total RNA using the High Capacity cDNA Reverse Transcription Kit (Life Technologies). Primers for mouse Glut4 and ribosomal protein S9 (RPS9) were designed according to sequences from the GenBank database. Relative quantification was made using a real-time thermocycler (Eppendorf Mastercycler ep realplex, Milano, Italy). In a 20-μl final volume, 1 μl of cDNA solution was mixed with SYBR Green RealMasterMix (Eppendorf) and 0.2 μM of each sense and antisense primers. SYBR Green fluorescence was measured, and relative quantification was made against either RPS9 or Gapdh cDNAs, used as internal standards. All PCR reactions were carried out in triplicates. Glut4 protein expression was measured in quadriceps muscle from six to eight mice of each group, using a rabbit anti-Glut4 polyclonal antibody as previously described (17).

Statistical Analysis

Results are expressed as mean ± SD. The independent t-test was used to evaluate intergroup differences. All statistical analyses were performed using GraphPad Prism version 5.0 statistical software (GraphPad Software Inc., San Diego, CA, USA). p values lower than 0.05 were considered statistically significant.


Effects of Normocaloric Diet on Body Weight and Biochemical Parameters

Twenty mice were fed with HFD (HFD group) for 24 weeks, reaching a weight of approximately 43 g, with fasting plasma glucose levels between 90.5 and 117.7 mg/dL, which were consistent with a condition of impaired fasting glucose. After the 24-week period, half of the mice were fed with NCD for the following 10 weeks (NCD group). A significant decrease of body weight was observed in the NCD group compared to the HFD group (27%, p < 0.001), as a result of the decrease in energy intake due to the less caloric supply derived from the NCD rather than the different food intake (Figure 2). In the NCD group, we also observed a decrease in liver size, fat depots, and girth waist (Table 1). Moreover, shifting to NCD resulted in a significant decrease in plasma glucose levels (p < 0.05) and serum insulin levels (p < 0.01), as well as triglycerides (p < 0.05) and total cholesterol (p < 0.05) (Figure 3).


Figure 2. Effects on body weight, food, and energy intake in mice fed with high fat diet (HFD) for 24 weeks and with normocaloric diet (NCD) for other 10 weeks. A significant reduction of body weight and energy intake was observed in NCD mice (A,B), whereas no significant difference was detected in food intake (C). Body weight over the time is shown in the inset. Values are expressed as mean ± SD. *p < 0.001.


Table 1. Weight and waist in HFD and NCD mice.


Figure 3. Biochemical parameters. Blood samples were collected as indicated in Section “Materials and Methods.” After 10 weeks of feeding with a normocaloric diet (NCD), mice showed a significant reduction of plasma glucose levels and serum insulin levels, as well as a reduction in both triglycerides and total cholesterol when compared to the HFD. Values are expressed as mean ± SD. *p < 0.05.

Effects on Insulin Sensitivity

Next, we evaluated the effects of NCD on insulin sensitivity. ITT performed in mice before and after NCD showed a better response to insulin in terms of changes in blood glucose concentrations in the NCD group than in the HFD group. In fact, the glucose-lowering effect of exogenous insulin was enhanced in NCD mice during ITT and was reduced in HFD mice (Figure 4). From a mechanistic point of view, the improvement in insulin sensitivity in mice in response to NCD was dependent, at least in part, on an increase in Glut4 expression induced in skeletal muscle following the transition from HFD to NCD. To show such a molecular link between restoration of insulin sensitivity and NCD, total RNA was extracted from skeletal muscle of animals before and after shifting to NCD, after insulin stimulation, and Glut4 mRNA and protein levels were measured. As shown in Figure 5, both insulin-stimulated Glut4 mRNA and protein expression were significantly increased in skeletal muscle of NCD mice as compared with that of HFD mice (p < 0.05).


Figure 4. Insulin sensitivity. HFD and NCD mice fasted for 12 h were injected intraperitoneally with insulin (1 U/kg). Blood glucose levels were measured with a glucometer, as reported in Section “Materials and Methods.” Values are expressed as mean ± SD. *p < 0.05.


Figure 5. Expression of Glut4. Glut4 mRNA levels were measured by qRT-PCR in skeletal muscle from HFD and NCD mice, after insulin stimulation. Results are the mean ± SD for six animals per group. *p < 0.05 versus HFD mice. A representative Western blot (WB) of Glut4 in quadriceps muscle from six to eight mice of each group is shown in duplicate in the autoradiogram. Gapdh, control of protein loading.


Obesity is a chronic disorder that can cause other health problems, such as diabetes, hypertension, hepatic steatosis, obstructive sleep apnea, and atherosclerosis (18). The association of obesity with T2DM is well established, due to the negative influence of excessive body fat on peripheral insulin action and hepatic function, leading to insulin resistance (19). Treatment of obesity includes hypocaloric diet, exercise, and lifestyle modifications, with dietary manipulation still representing the first-line therapeutic approach for this common disorder (20, 21). However, it is still debated which is the more appropriated dietetic regimen to obtain a weight loss, which may be at the same time rapid, well tolerated, and sustainable for a long period of time. Although the importance of calorie restriction in this condition is well recognized, also for the positive psychological benefit for the patient and the family, there is no doubt that a major problem in treating obesity is still represented by the relatively low level of adherence of affected subjects to low/very low-calorie diets (2224). Thus, many dietary strategies have been proposed to overcome such obstacles, but the results are not satisfactory enough in most of obese patients (25, 26). In these individuals, we hypothesized that shifting to normocaloric balanced diet, formulated to avoid excess fat, rather than hypocaloric diet – which would obtain a better compliance especially in view of long-term treatment – might be sufficient, in addition to physical exercise and lifestyle change, to get more satisfactory results in terms of weight loss and consequent improvement in obesity-related insulin resistance. This hypothesis is well supported by the present finding in our mouse model of obesity and obesity-induced insulin resistance. In fact, shifting from HFD to NCD for 10 weeks, caused a significant reduction of body weight mainly due to the reduction of visceral fat, together with the overall reduction of triglycerides, total cholesterol, and, most importantly, restoration of insulin sensitivity, as reflected by the decline in fasting insulin levels. A similar approach treating obese mice with NCD has also been used in a few other studies where, however, some nutraceutical compounds or other ingredients were added to regular food (2730). This is slightly different than what we did in our study, in which NCD itself, without any additive agent, was able to improve insulin sensitivity and Glut4 expression.

Glut4 is the major insulin-dependent glucose transporter in muscle. Abnormalities at this level are a hallmark of peripheral insulin resistance (31). In the present study, the improvement in insulin sensitivity associated with increased Glut4 mRNA expression in NCD mice provides a possible mechanistic explanation as to how the normal calorie diet can improve insulin responsiveness and supports the hypothesis that rescue from insulin resistance and diabetes can be reached without the adoption of a low-calorie diet. If confirmed in obese humans, such an approach, in association with adequate and individualized physical exercise programs, might be able to contribute to counteract the long-term failure of the current therapeutic approaches adopted in these individuals, and this would confirm further the appropriateness of mouse models for studying human obesity. However, on the other hand, it is also known that marked interspecies differences exist between human and mouse with respect to behavioral control of food uptake, tissue energy disposal and storage, weight, and weight loss, which emphasize the influence of non-genetic environmental factors and genetic modifiers in determining the phenotypic variations observed in humans and animal models of obesity. Thus, caution is required in generalizing these findings. As a limitation of the present work, the fact is that mice of different ages were compared in our study.

In conclusion, numerous anti-obesity initiatives have been adopted up to now, which include lifestyle changes, drug treatments, and surgery. However, because of the limited efficacy and the occurrence of adverse events in affected treated patients, alternative and complementary therapies for weight loss have been investigated, including acupuncture, dietary supplements, etc. Our findings in the current work provide valuable information about the efficacy of shifting to NCD in restoring weight and insulin sensitivity in HFD-induced obese mice. Similar studies in obese humans would reveal whether this strategy, probably better accepted by patients, may be successful in correcting weight gain and obesity-related insulin resistance.

Author Contributions

GEL contributed to animal testing and drafting of the manuscript; RFDR elaborated figures and tables and contributed to the analysis of the results; SML contributed to animal testing and drafting of the manuscript; BA performed the molecular analysis; NC performed the operation on the animals and supervised the animals’ maintenance during the treatment period; TM and GDS reviewed the final version of the manuscript; AB contributed to the conception of the idea and critically reviewed the manuscript; DR contributed to the conception of the idea, drafted the manuscript, and critically reviewed the final manuscript; and MC contributed to animal testing, analysis of the results, and editing of the manuscript. All authors read and approved the submitted version.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.


We thank Professor D. Britti and Dr. F. Trimboli for assistance in the management of animals.


1. Lieberman LS. Dietary, evolutionary, and modernizing influences on the prevalence of type 2 diabetes. Annu Rev Nutr (2003) 23:345–77. doi:10.1146/annurev.nutr.23.011702.073212

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Forbes JM, Cowan SP, Andrikopoulos S, Morley AL, Ward LC, Walker KZ, et al. Glucose homeostasis can be differentially modulated by varying individual components of a western diet. J Nutr Biochem (2013) 24:1251–7. doi:10.1016/j.jnutbio.2012.09.009

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Kahn SE, Hull RL, Utzschneider KM. Mechanisms linking obesity to insulin resistance and type 2 diabetes. Nature (2006) 444:840–6. doi:10.1038/nature05482

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Paolisso G, Gambardella A, Amato L, Tortoriello R, D’Amore A, Varricchio M, et al. Opposite effects of short- and long-term fatty acid infusion on insulin secretion in healthy subjects. Diabetologia (1995) 38:1295–9. doi:10.1007/BF00401761

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Hotamisligil GS. Molecular mechanisms of insulin resistance and the role of the adipocyte. Int J Obes Relat Metab Disord (2000) 24:S23–7. doi:10.1038/sj.ijo.0801497

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Shulman GI. Cellular mechanisms of insulin resistance. J Clin Invest (2000) 106:171–6. doi:10.1172/JCI10583

CrossRef Full Text | Google Scholar

7. Zraika S, Dunlop M, Proietto J, Andrikopoulos S. Effects of free fatty acids on insulin secretion in obesity. Obes Rev (2002) 3:103–12. doi:10.1046/j.1467-789X.2002.00062.x

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Riccardi G, Giacco R, Rivellese AA. Dietary fat, insulin sensitivity and the metabolic syndrome. Clin Nutr (2004) 23:447–56. doi:10.1016/j.clnu.2004.02.006

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Andrikopoulos S. Obesity and type 2 diabetes: slow down! – can metabolic deceleration protect the islet beta cell from excess nutrient-induced damage? Mol Cell Endocrinol (2010) 316:140–6. doi:10.1016/j.mce.2009.09.031

CrossRef Full Text | Google Scholar

10. Moreno B, Bellido D, Sajoux I, Goday A, Saavedra D, Crujeiras AB. Comparison of very low-calorie ketogenic diet with a standard low-calorie diet in the treatment of obesity. Endocrine (2014) 47:793–805. doi:10.1007/s12020-014-0192-3

CrossRef Full Text | Google Scholar

11. Basciani S, Costantini D, Contini S, Persichetti A, Watanabe M, Mariani S, et al. Safety and efficacy of a multiphase dietetic protocol with meal replacements including a step with very low calorie diet. Endocrine (2015) 48:863–70. doi:10.1007/s12020-014-0355-2

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Andrikopoulos S, Massa CM, Aston-Mourney K, Funkat A, Fam BC, Hull RL, et al. Differential effect of inbred mouse strain (C57BL/6, DBA/2, 129T2) on insulin secretory function in response to a high fat diet. J Endocrinol (2005) 187:45–53. doi:10.1677/joe.1.06333

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Zaman MQ, Leray V, Le Bloc’h J, Thorin C, Ouguerram K, Nguyen P. Lipid profile and insulin sensitivity in rats fed with high-fat or high-fructose diets. Br J Nutr (2011) 106:S206–10. doi:10.1017/S0007114511004454

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Nishikawa S, Yasoshima A, Doi K, Nakayama H, Uetsuka K. Involvement of sex, strain and age factors in high fat diet-induced obesity in C57BL/6J and BALB/cA mice. Exp Anim (2007) 56:263–72. doi:10.1538/expanim.56.263

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Lepore SM, Morittu VM, Celano M, Trimboli F, Oliverio M, Procopio A, et al. Oral administration of oleuropein and its semisynthetic peracetylated derivative prevents hepatic steatosis, hyperinsulinemia, and weight gain in mice fed with high fat cafeteria diet. Int J Endocrinol (2015) 2015:431–53. doi:10.1155/2015/431453

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Foti D, Chiefari E, Fedele M, Iuliano R, Brunetti L, Paonessa F, et al. Lack of the architectural factor HMGA1 causes insulin resistance and diabetes in humans and mice. Nat Med (2005) 11:765–73. doi:10.1038/nm1254

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Chiefari E, Paonessa F, Iiritano S, Le Pera I, Palmieri D, Brunetti G, et al. The cAMP-HMGA1-RBP4 system: a novel biochemical pathway for modulating glucose homeostasis. BMC Biol (2009) 7:24. doi:10.1186/1741-7007-7-24

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Baeza-Raja B, Sachs BD, Li P, Christian F, Vagena E, Davalos D, et al. p75 neurotrophin receptor regulates energy balance in obesity. Cell Rep (2016) 14:255–68. doi:10.1016/j.celrep.2015.12.028

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Chang JW, Chen HL, Su HJ, Lee CC. Abdominal obesity and insulin resistance in people exposed to moderate-to-high levels of dioxin. PLoS One (2016) 11:e0145818. doi:10.1371/journal.pone

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Haslam DW, James WP. Obesity. Lancet (2005) 366:1197–209. doi:10.1016/S0140-6736(05)67483-1

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Donini LM, Cuzzolaro M, Gnessi L, Lubrano C, Migliaccio S, Aversa A, et al. Obesity treatment: results after 4 years of a nutritional and psycho-physical rehabilitation program in an outpatient setting. Eat Weight Disord (2014) 19:249–60. doi:10.1007/s40519-014-0107-6

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Barte JC, ter Bogt NC, Bogers RP, Teixeira PJ, Blissmer B, Mori TA, et al. Maintenance of weight loss after lifestyle interventions for overweight and obesity, a systematic review. Obes Rev (2010) 11:899–906. doi:10.1111/j.1467-789X.2010.00740.x

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Wadden TA, Fujioka K, Toubro S, Gantz I, Erondu NE, Chen M, et al. A randomized trial of lifestyle modification and taranabant for maintaining weight loss achieved with a low-calorie diet. Obesity (2010) 18:2301–10. doi:10.1038/oby.2010.67

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Grams J, Garvey WT. Weight loss and the prevention and treatment of type 2 diabetes using lifestyle therapy, pharmacotherapy, and bariatric surgery: mechanisms of action. Curr Obes Rep (2015) 4:287–302. doi:10.1007/s13679-015-0155-x

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Melotto S. Clinical pharmacology of eating and not eating. Curr Opin Pharmacol (2014) 14:1–5. doi:10.1016/j.coph.2013.09.015

CrossRef Full Text | Google Scholar

26. Munsters MJ, Saris WH. Body weight regulation and obesity: dietary strategies to improve the metabolic profile. Annu Rev Food Sci Technol (2014) 5:39–51. doi:10.1146/annurev-food-030212-182557

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Li P, Lu M, Nguyen MT, Bae EJ, Chapman J, Feng D, et al. Functional heterogeneity of CD11c-positive adipose tissue macrophages in diet-induced obese mice. J Biol Chem (2010) 285(20):15333–45. doi:10.1074/jbc.M110.100263

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Guo J, Jou W, Gavrilova O, Hall KD. Persistent diet-induced obesity in male C57BL/6 mice resulting from temporary obesigenic diets. PLoS One (2009) 4(4):e5370. doi:10.1371/journal.pone.0005370

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Dossi CG, Tapia GS, Espinosa A, Videla LA, D’Espessailles A. Reversal of high-fat diet-induced hepatic steatosis by n-3 LCPUFA: role of PPAR-α and SREBP-1c. J Nutr Biochem (2014) 25(9):977–84. doi:10.1016/j.jnutbio.2014.04.011

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Panchenko PE, Voisin S, Jouin M, Jouneau L, Prézelin A, Lecoutre S, et al. Expression of epigenetic machinery genes is sensitive to maternal obesity and weight loss in relation to fetal growth in mice. Clin Epigenetics (2016) 8:22. doi:10.1186/s13148-016-0188

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Al-Shaqha WM, Khan M, Salam N, Azzi A, Chaudhary AA. Anti-diabetic potential of Catharanthus roseus Linn. and its effect on the glucose transport gene (GLUT-2 and GLUT-4) in streptozotocin induced diabetic wistar rats. BMC Complement Altern Med (2015) 15:379. doi:10.1186/s12906-015-0899-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: insulin resistance, obesity, Glut4, diet, glucose

Citation: Lombardo GE, Arcidiacono B, De Rose RF, Lepore SM, Costa N, Montalcini T, Brunetti A, Russo D, De Sarro G and Celano M (2016) Normocaloric Diet Restores Weight Gain and Insulin Sensitivity in Obese Mice. Front. Endocrinol. 7:49. doi: 10.3389/fendo.2016.00049

Received: 24 March 2016; Accepted: 09 May 2016;
Published: 27 May 2016

Edited by:

Nicholas Michael Morton, University of Edinburgh, Scotland

Reviewed by:

Maximilian Zeyda, Medical University of Vienna, Austria
Matthew Brook, University of Edinburgh, UK

Copyright: © 2016 Lombardo, Arcidiacono, De Rose, Lepore, Costa, Montalcini, Brunetti, Russo, De Sarro and Celano. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Antonio Brunetti, brunetti@unicz.it;
Diego Russo, d.russo@unicz.it