We describe methods to develop an experimental model of diet-induced metabolic syndrome (MetS) in rabbits using a high-fat, high-sucrose diet. Animals developed central obesity, mild hypertension, pre-diabetes, and dyslipidemia, thus reproducing the main components of human MetS. This chronic model will allow acquisition of knowledge underlying mechanisms of disease progression.
In recent years, obesity and metabolic syndrome (MetS) have become a growing problem for public health and clinical practice, given their increased prevalence due to the rise of sedentary lifestyles and unhealthy eating habits. Thanks to animal models, basic research can investigate the mechanisms underlying pathological processes such as MetS. Here, we describe the methods used to develop an experimental rabbit model of diet-induced MetS and its assessment. After a period of acclimation, animals are fed a high-fat (10% hydrogenated coconut oil and 5% lard), high-sucrose (15% sucrose dissolved in water) diet for 28 weeks. During this period, several experimental procedures were performed to evaluate the different components of MetS: morphological and blood pressure measurements, glucose tolerance determination, and the analysis of several plasma markers. At the end of the experimental period, animals developed central obesity, mild hypertension, pre-diabetes, and dyslipidemia with low HDL, high LDL, and an increase of triglyceride (TG) levels, thus reproducing the main components of human MetS. This chronic model allows new perspectives for understanding the underlying mechanisms in the progression of the disease, the detection of preclinical and clinical markers that allow the identification of patients at risk, or even the testing of new therapeutic approaches for the treatment of this complex pathology.
Obesity and metabolic syndrome (MetS) have become a growing problem for public health and clinical practice, given their increased prevalence due to the rise of sedentary lifestyles and unhealthy eating habits1. There are several definitions of MetS, but most of them describe it as a cluster of cardiovascular and metabolic alterations such as abdominal obesity, reduced HDL and elevated LDL cholesterol, elevated triglycerides, glucose intolerance, and hypertension2,3,4. Diagnosis requires that three out of these five criteria are present.
Owing to animal models, basic research has been able to investigate the mechanisms underlying pathological processes such as MetS. Several animal models have been used, but it is of crucial importance that the model of choice reproduces the main clinical manifestations of the human pathology (Figure 1). With this aim, animal models considered similar to humans, mainly canine and swine, have been developed (see Verkest5 and Zhang & Lerman6 for review). However, canine models do not show all the components of MetS, given that the development of atherosclerosis or hyperglycemia in dogs by means of the diet is questionable5. Swine models present the most anatomical and physiological similarity with humans, and thus offer significant predictive power for elucidating the mechanisms underlying MetS, but their maintenance and the complexity of the experimental procedures make the use of this model very labor intensive and costly6.
On the other hand, rodent models (mouse and rat), diet-induced spontaneous and transgenic, have been extensively used in the literature for the study of obesity, hypertension, and MetS, and its pathological consequences in different organs and systems (see Wong et al.7 for review). Although the use of these models is more affordable than canine or swine, they have important drawbacks. Indeed, depending on the strain, animals develop some components of MetS, whereas others such as hypertension, hyperglycemia, and hyperinsulinemia are absent7. Furthermore, one of the main components of MetS, obesity, in some genetically modified strains, does not only depend on factors associated with the diet, rather it has been shown that some animals become obese with normal or even reduced food intake8. Finally, mice and rats show a natural deficiency in cholesteryl ester transfer protein (CETP) and use HDL as the major means of cholesterol transport, which makes them relatively resistant to the development of atherosclerosis. This is an important difference in lipid metabolism with humans, who express CETP and transport their cholesterol mainly in LDL9.
Conversely, the laboratory rabbit represents an intermediate stage between the larger animal and rodent experimental models. Thus, the rabbit can be easily submitted to different types of protocols with minimal requirements of personnel and maintenance, being more easily handled in experimental procedures than larger animal models. Furthermore, it has been reported that rabbits fed with a high-fat diet have similar hemodynamic and neurohumoral changes as obese humans8,10,11. Of note, regarding lipid metabolism, the rabbit has abundant CETP in plasma and their lipoprotein profile is LDL-rich12, which is also similar to humans. Additionally, rabbits develop hyperlipidemia quite rapidly given that, as herbivores, they are very sensitive to dietary fat13.
Figure 1: Comparison of MetS animal models. See Verkest5, Zhang and Lerman6, and Wong et al.7 for review. "" indicates an advantage and "" indicates a disadvantage. *controversial, depends on the study, **as pointed out by Carroll et al.8, some genetically modified strains become obese independently of food intake. CEPT: cholesteryl ester transfer protein. GTT: glucose tolerance test. Please click here to view a larger version of this figure.
In order to elucidate the basic mechanisms underlying the pathological remodeling produced by MetS in the different organs and systems, and to gain understanding of this complex pathology, the choice of an experimental model that reproduces the main components of human MetS is essential. The rabbit can provide many advantages given its similarity with human physiology and the affordability of use in chronic protocols and measurements. In this line, few diet-induced rabbit models using high-fat and high-sucrose diet have been used14,15,16,17,18,19 (Table 1), and a characterization of the different components of MetS is of great importance when relating a phenotype with organ remodeling. Thus, this article's main objective is to describe the methods to develop a model of diet-induced MetS in rabbits that allows the study of its pathophysiology and impact in organ remodeling.
Study | Diet | Duration | Breed | MetS components | |||
Ob | HT | HG | Dl | ||||
Yin et al. (2002)14 | · 10% fat | 24 weeks | · Male NZW | – | |||
· 37% sucrose | · 2 kg | ||||||
Zhao et al. (2007)15 | · 10% fat | 36 weeks | · Male JW | ||||
· 30% sucrose | · 16 weeks | ||||||
Helfestein et al. (2011)16 | · 10% fat | 24 weeks | · Male NZW | – | |||
· 40% sucrose | · 12 weeks | ||||||
· 0.5-0.1 cholesterol | |||||||
Ning et al. (2015)17 | · 10% fat | 8-16 weeks | · Male WHHL | – | |||
· 30% fructose* | · 12 weeks | ||||||
Liu et al. (2016)18 | · 10% fat | 48 weeks | · Male NZW | – | |||
· 30% sucrose | · 12 weeks | ||||||
Arias-Mutis et al. (2017)19 | · 15% fat | 28 weeks | · Male NZW |
Table 1: Diet-induced MetS rabbit models using high-fat, high-sucrose diet. The symbol "" indicates absence, "" presence, and "-" not evaluated. *restricted. WHHL, Watanabe heritable hiperlipidemic rabbits. JW, Japanese white rabbits. Ob, obesity. HT, hypertension. HG, hyperglycemia. Dl, dyslipidemia.
Animal care and the experimental protocols used in this study complied with EU directive 2010/63 on the protection of animals used for scientific purposes, and were approved by the Institutional Animal Care and Use Committee (2015/VSC/PEA/00049).
NOTE: The protocol consists of the chronic administration of a high-fat, high-sucrose diet for 28 weeks, and the assessment of the main components of MetS. We used 11 adult male New Zealand White (NZW) rabbits weighing 4.39 ± 0.14 (s.d.) kg, which were 20 – 22 weeks old at the beginning of the experimental protocol. They were housed in a room with humidity (50 ± 5%) and temperature (20 ± 1.5 °C) controlled conditions with a 12-h light cycle. The words "chow" and "diet" may be used interchangeably in the protocol steps.
1. Diet Administration
2. Morphological Assessment
3. Fasting Glycemia and Intravenous Glucose Tolerance Test (IVGTT)
NOTE: It is advisable to start the procedures the same time of day (i.e., 2 – 3 PM).
4. Blood Pressure
5. Plasma Measurements
NOTE: It is advisable to start the procedures the same time of day (i.e., 2 – 3 PM).
MetS represents a cluster of metabolic and cardiovascular abnormalities whose study can be facilitated by the use of experimental models. Indeed, to elucidate the mechanisms underlying the pathological remodeling produced by MetS, the choice of an experimental model that appropriately resembles the human condition and is suitable for research is of crucial importance. Here, we present the methods to induce MetS in rabbit using a diet high in saturated fat and sucrose, and a detailed characterization for its evaluation. The use of diet instead of a genetically modified animal model is of great importance since diet affects whole-body metabolism19, thus resembling closely what happens in human MetS. We used a factorial (mixed model) ANOVA with two factors, one repeated measures or "within" factor (time: pre, week 14 and week 28, depending of the analysis) and one "between" factor (group: control and MetS) for statistical analysis. Significance was accepted when p <0.05.
The high-fat, high-sucrose diet is well tolerated by the animals. An acclimation period of 4 weeks is necessary for the correct transition from the previous feeding regime to the high-fat, high-sucrose diet. Animals in control group are fed 120 g chow, which has been shown to be appropriate for the maintenance of the adult rabbit8. Rabbits in the MetS group increased progressively in weight until the end of the experimental protocol (Table 2). Animals should gain 50 – 100 g per week. It is important that rabbits are housed individually in cages with enough space, light, and environmental enrichment (Figure 2C), and a daily check of the animals is performed. Also on a daily basis, chow and drink intake must be supervised and registered, in order to achieve weight gain and detect possible health problems, since rabbits are easily stressed and the response may be to stop nourishment consumption. In addition, since high-fat pellets tend to be very unstable and lose consistency very easily, turning into powder which rabbits do not eat, it is of critical importance to prepare the daily portions of chow very carefully (Figure 2A). In Figure 3A, we can observe the behavior of energy intake and its fluctuations, ranging from 250 to 815 kCal in the MetS group. In Figure 3B, the relative contribution of the different sources of energy (chow and drink) is depicted. There are critical periods in weeks 14 and 28 because, given the stress produced by experimental procedures, rabbits might decrease chow and water intake. The daily quantification allows the rapid identification of this problem, which can be avoided by introducing control chow (80% high-fat, 20% control) and decreasing the sucrose solution from 15% to 10%, or even 5%, during 2-3 days until animals recover their normal intake values. Animals also developed central obesity as shown by the increase in weight, abdominal perimeter and BMI (Table 2), which is closely related with the risk factors that define MetS3.
Figure 2: Diet administration. In panel A, control chow (top) and high-fat chow (below) are depicted, showing the differences between the two due to the added fat. In order to avoid the powder that makes high-fat pellets less palatable, it is necessary to use a strainer to separate high-fat pellet powder (Panel A, bottom). In panel B, we can observe the materials needed to make the drinking solution (left), and how it is advisable to make a stock solution to distribute in the water dispenser. Lastly, the welfare of the animals is very important, and they must be housed individually in cages (C) with enough space and light and, if possible, environmental enrichment (i.e., platforms, toys, etc.). Please click here to view a larger version of this figure.
Figure 3: Energy intake. The evolution of weekly intake during the 28 weeks of the experimental period is depicted in panel A for control and MetS. The relative intake (in percentage) of kCal from high-fat chow and the drinking solution of MetS animals is shown in panel B. Control (n = 5), MetS (n = 6). Error bars: SD. Modified from Arias-Mutis et al.19 Please click here to view a larger version of this figure.
Pre-diet | Week 14 | Week 28 | ||||
Control | MetS | Control | MetS | Control | MetS | |
Weight (Kg) | 4.35(0.15) | 4.43(0.14) | 4.49(0.12) | 5.42(0.17) | 4.51(0.13) | 5.75(0.6) |
Length (cm) | 52.4(1.6) | 53.6(1.7) | 52.5(0.8) | 54.4(1.7) | 53.7(0.7) | 54.6(0.8) |
Height (cm) | 25.9(0.7) | 25.5(1.1) | 25.9(2.2) | 26.1(5.3) | 26.0(1.0) | 26.1(1.5) |
Abdom. perimeter (cm) | 39.8(1.7) | 40.5(1.4) | 38.5(1.5) | 47.5(2.2) | 38.1(1.0) | 49.7(3.5) |
Tibial length (cm) | 16.4(0.8) | 16.3(0.7) | 16.7(0.3) | 16.7(0.4) | 17.4(0.4) | 16.8(0.6) |
BMI (Kg/m2) | 32.8(1.9) | 32.9(2.6) | 32.8(1.2) | 36.8(1.9) | 32.6(2.1) | 39.3(6.0) |
Table 2: Morphological characteristics. We found differences when comparing control vs. MetS at weeks 14 and 28 in weight (main effect p = 0.003, η2 = 0.6; pairwise comparisons at week 14 p <0.001 and week 28 p <0.001), abdominal perimeter (main effect p<0.001, η2 = 0.9 pairwise comparisons at week 14 p <0.001 and week 28 p <0.001), and BMI (main effect p = 0.016, η2 = 0.5; pairwise comparisons at week 14 p <0.001 and week 28 p <0.001). Control (n = 5) and MetS (n = 6). Values are expressed as Mean (SD). Modified from Arias-Mutis et al.19.
Regarding fasting blood glucose, the response to the IVGTT plays a key role in the characterization of glucose homeostasis21. We observe mild hyperglycemia at week 14, which reaches a plateau and maintains similar values at week 28 (Figure 4A). The area under the curve (AUC) also increases in the MetS group (Figure 4B). Even though cut-off values to identify type II diabetes in rabbits based on fasting blood glucose have not yet been recognized19, with this experimental protocol, rabbits submitted to 28 weeks of high-fat, high-sucrose feeding developed pre-diabetes with impaired fasting glucose and glucose intolerance.
Figure 4: Blood glucose regulation. The results of the IVGTT in control and MetS animals at weeks 14 and 28 are shown in panel A. The quantification of the area under the curve (AUC) from 0 to 180 min is depicted in panel B with a box and whiskers plot. This parameter increased in MetS animals in weeks 14 and 28 versus controls (main effect p = 0.001, η2 = 0.5; pairwise comparisons at week 14 p = 0.001 and week 28 p = 0.002). Control (n = 5), MetS (n = 6). Modified from Arias-Mutis et al.19 Please click here to view a larger version of this figure.
Hypertension is closely and directly related to the severity of obesity. Rabbits fed a high-fat, high-sucrose diet for 28 weeks showed an increase in systolic, diastolic, and mean blood pressure already at week 14, and this increase in blood pressure is maintained at week 28 (Figure 5C – E). Given the close relationship between blood pressure and BMI22, it is of great importance to ensure that animals gain weight progressively to obtain a significant increase in blood pressure.
Figure 5: Modifications in blood pressure. Panel A depicts the catheter inserted in the auricular artery. Of note, given that the vein and the auricular artery run through the dentition of the ear very closely, it is of crucial importance to differentiate them. Before cannulation, it is advisable to warm up the ear and, after topical anesthesia, to tap gently the area where the vascular package runs. The artery has a thicker vascular wall and a lighter color than the vein, and blood pulses can be observed. Panel B shows the experimental setup with the pressure transducer, which is connected to an amplifier and records continuously the signal (BP recording). Panels C and D show box and whiskers plots of systolic and diastolic blood pressure at week 14 and 28 in both experimental groups. Mean arterial pressure (MAP) is presented in panel E. We found differences when comparing control vs. MetS at weeks 14 and 28 in systolic (main effect p = 0.003, η2 = 0.4; pairwise comparisons at week 14 p = 0.029 and week 28 p = 0.013), diastolic (main effect p = 0.027, η2 = 0.3; pairwise comparisons at week 14 p = 0.036 and week 28 p = 0.001) and MAP (main effect p = 0.006, η2 = 0.4; pairwise comparisons at week 14 p = 0.027 and week 28 p = 0.001). Control (n = 5), MetS (n = 6). Modified from Arias-Mutis et al.19 Please click here to view a larger version of this figure.
Finally, to assess the development of MetS, an evaluation of changes in plasma biochemical markers is needed. In this chronic model, we observed an alteration in the lipid profile as early as week 14, and this alteration remained stable until week 28, without further increases in the differences. Modifications in plasma lipid profile are characterized by an increase in triglycerides and LDL, a decrease in HDL, and no changes in total cholesterol in MetS animals versus controls at both time points (weeks 14 and 28) (Table 3).
Week 14 | Week 28 | |||
Control | MetS | Control | MetS | |
Total cholesterol (mg·dL-1) | 20.4(2.3) | 24.0(9.1) | 27.4(15.7) | 21.2(4.4) |
HDL (mg·dL-1) | 9.1(4.2) | 4.3(1.7) | 11.2(4.2) | 5.1(2.9) |
LDL (mg·dL-1) | 3.8(1.1) | 8.7(4.5) | 4.0(1.2) | 13.8(9.3) |
Triglycerides (mg·dL-1) | 71.2(58.8) | 118.0(40.7) | 30.2(11.4) | 76.8(28.2) |
Table 3: Assessment of plasma biochemistry. We found differences when comparing control vs. MetS at weeks 14 and 28 in HDL (main effect p = 0.008, η2 = 0.3; pairwise comparisons at week 14 p = 0.006 and week 28 p = 0.037), LDL (main effect p = 0.040, η2 = 0.2; pairwise comparisons at week 14 p = 0.028 and week 28 p = 0.034), and triglycerides (main effect p = 0.002, η2 = 0.4; pairwise comparisons at week 14 p = 0.004 and week 28 p = 0.001). Control (n = 5) and MetS (n = 6). Values are expressed as Mean (SD). Modified from Arias-Mutis et al.19
The establishment of an appropriate experimental model can provide a more consistent and reliable method to study the development of MetS, and it is also necessary to understand the basic mechanisms that underlie the organs and systems remodeling. Here, we describe the methods used to develop a relevant experimental model of diet-induced MetS and how to assess the main components of this cluster of metabolic and cardiovascular abnormalities that characterize this model: central obesity, hypertension, glucose intolerance, and dyslipidemia with low HDL, high LDL, and an increase of TG levels.
A major strength of the model is the ability to study the condition that precedes the clinical manifestation of the pathology. Indeed, regarding metabolic changes, in 28 weeks animals did not develop type II diabetes and were in a state of prediabetes (Figure 4). Similarly, plasma biochemical markers showed an evident alteration in the lipid profile with an increase in LDL and TG, a decrease in HDL, but no changes in total cholesterol (Table 3), which is a key factor in the development of atherosclerosis. Even though we can observe an increase in systolic, diastolic, and MAP at week 28 (Figure 5), this can be considered mild hypertension. Overall, the effects in those metabolic and cardiovascular markers are modest, but this model can enable the research of the state before the manifested (and in most cases irreversible) pathology, thus allowing the identification of preclinical and clinical markers that might allow the detection of patients at risk.
Furthermore, unlike other MetS animal models (mouse, rat, and dog), spontaneous or transgenic rabbits models can develop all the components of the MetS. Interestingly, it has been reported that the combination of the different components of MetS can amplify cardiovascular risk. Indeed, the pathological remodeling produced by hypertension is aggravated when more components of MetS appear23. This experimental model could allow the study of the underlying mechanisms, and the effect of the different components combined. Furthermore, given that diet affects whole-body metabolism, the use of a diet-induced model has important significance, closely emulating what happens in human MetS19.
The last, but not least important strength, is the balance between the relevance and impact on translational research and the economic cost. On one side we find the swine models, very similar to humans, but very expensive in terms of time, resources, and economic cost. On the other side, we have rodent models, which are easy to implement with very little cost, but have a lower generalization power. The rabbit model represents the middle point, as it is flexible enough for many different types of studies while avoiding some of the drawbacks of large animal models, and shows similar hemodynamic and neurohumoral changes observed in human MetS8,10,19.
The following limitations of the methods described should be considered. With respect to central obesity and body fat distribution, the use of magnetic resonance imaging would be the gold standard, if available, otherwise use the quantification of visceral fat at the end of the 28 weeks. Other non-invasive methods for longitudinal studies, such as X-ray computed tomography, would be more adequate24. We measured abdominal circumference and BMI instead (Table 2), which have also been used in several studies in rabbits as a measure of central obesity25,11,26. Tibial length measurement could also be more precise using echography or a leg radiography. In order to establish if the cause of glucose intolerance in this chronic model is insulin resistance or decreased insulin production, insulin resistance should be determined using an insulin tolerance test or determining fasting insulin levels.
Finally, in order to improve the model, several measures could be taken. We could probably have obtained a faster increase in glycaemia with the combination of brief periods of alloxan injection and the high fat, high sucrose diet, but then the phenotype could not be attributed only to the diet. Age could play also an important role, since we worked with young adult rabbits (4.5 months old when animals arrived in the animal facilities, 12.5 – 13 months old by the end of the experimental protocol) and MetS often occurs at older age27. Unfortunately, older rabbits were not commercially available. It would be interesting to test this model in older animals and observe if the phenotype is aggravated.
The methods presented here for the development of this experimental model of MetS in laboratory rabbits should provide a valuable tool for studies aiming to elucidate the basic mechanisms underlying the pathological remodeling produced by MetS in the different organs and systems, and to gain understanding of this complex pathology. Finally, since NZW rabbits are sedentary animals, this diet-induced model can be useful to study how the different components of the pathology evolve in a similar way than occurs in human MetS, and could allow new perspectives for understanding the pathophysiological mechanisms involved in the progression of the disease, the identification of preclinical and clinical markers to identify patients at risk, or even the testing of new therapeutic approaches for the treatment of this complex pathology.
The authors have nothing to disclose.
This work was supported by Generalitat Valenciana (GV2015-062), Universitat de València (UV-INV-PRECOMP14-206372) to MZ, Generalitat Valenciana (PROMETEOII/2014/037) and Instituto de Salud Carlos III-FEDER funds (CIBERCV CB16/11/0486) to FJC.
Veterinary scale | SOEHNLE | 7858 | Scale https://www.soehnle-professional.com/en/productgroup/details/103/veterinary-scale |
Shovel for aluminum feed | COPELE | 10308 | Shovel for aluminum feed http://copele.com/es/herramientas/48-pala-para-pienso-de-aluminio.html |
Balance | PCE Ibérica | PCE-TB 15 | Balance http://www.pce-iberica.es/medidor-detalles-tecnicos/balanzas/balanza-compacta-pce-bdm.htm |
Strainer (20 cm diam.) | ZWILLING | 39643-020-0 | Strainer https://es.zwilling-shop.com/Menaje-del-hogar/Menaje-de-cocina/Menaje-especial/Accesorios/Colador-20-cm-ZWILLING-39643-020-0.html |
Bowl | ZWILLING | 40850-751-0 | Scale https://www.soehnle-professional.com/en/productgroup/details/103/veterinary-scale |
Funnel | BT Ingenieros | not available | Funnel http://www.bt-ingenieros.com/fluidos-y-combustibles/961-juego-de-4-embudos-de-plastico.html?gclid=EAIaIQobChMIuInui_y-1QIVASjTCh28Zwf-EAQYBSABEgK7xPD_BwE |
Introcan Certo 22G blue | B Braun | 4251318 | Peripheral intravenous catheter http://www.bbraun-vetcare.es/producto/introcan- |
Propofol Lipuro 10 mg/ml vial 20 ml | B Braun | 3544761VET | General intravenous anesthetic http://www.bbraun-vetcare.es/producto/propofol-lipuro-1- |
FisioVet serum solution 500ml | B Braun | 472779 | Scale https://www.soehnle-professional.com/en/productgroup/details/103/veterinary-scale |
Askina Film Vet 1,25cm x 5m | B Braun | OCT13501 | Plastic Plaster http://www.bbraun-vetcare.es/producto/askina-film-vet |
Askina Film Vet 2,50cm x 5m | B Braun | OCT13502 | Plastic Plaster http://www.bbraun-vetcare.es/producto/askina-film-vet |
Injekt siringe 10ml luer | B Braun | 4606108V | Injection-aspiration syringe of two single-use bodies http://www.bbraun-vetcare.es/producto/injekt- |
Seca 201 | seca | seca 201 | Ergonomic tape for measuring perimeters https://www.seca.com/es_es/productos/todos-los-productos/detalles-del-producto/seca201.html#referred |
Sterican 21Gx1" – 0,8x25mm verde | B Braun | 4657543 | Single Use Hypodermic Needle http://www.bbraun-vetcare.es/producto/agujas-hipodermicas-sterican- |
CONTOURNEXT-Meter | BAYER | 84413470 | Blood glucose analysis system http://www.contournextstore.com/en/contour-next-meter-2 |
CONTOUR NEXT test strips | BAYER | 83624788 | Blood glucose test strips http://www.contournextstore.com/en/contour-next-test-strips-100-ct-package |
MICROLET NEXT LANCING DEVICE | BAYER | 6702 | Lancing device http://www.contournextstore.com/en/new-microlet-next-lancing-device |
MICROLET 2 Colored Lancets | BAYER | 81264857 | Ultra-thin sterile lancet for capillary puncture http://www.contournextstore.com/en/microlet2-colored-lancets-100s |
Injekt 20ml luer siringe | B Braun | 4606205V | Scale https://www.soehnle-professional.com/en/productgroup/details/103/veterinary-scale |
Askina Mullkompressen 7,5×7,5cm – sterile | B Braun | 9031219N | Sterile gauze packets in envelopes http://www.bbraun-vetcare.es/producto/askina-mullkompressen-esteril |
Emla lidocaine/prilocaine | AstraZeneca | not available | Local anesthetics https://www.astrazeneca.es/areas-terapeuticas/neurociencias.html |
Introcan Certo 18G short | B Braun | 4251342 | Peripheral intravenous catheter http://www.bbraun-vetcare.es/producto/introcan- |
Introcan Certo 20G | B Braun | 4251326 | Peripheral intravenous catheter http://www.bbraun-vetcare.es/producto/introcan- |
Blood Pressure Transducers-MA1 72-4497 | Harvard Apparatus | 724497 | Transducer for monitoring blood pressure http://www.harvardapparatus.com/physiology/physiological-measurements/transducers/pressure-transducers/research-grade-pressure-transducers.html |
PowerLab 2/26 | AD Instruments | ML826 | Amplifier https://www.adinstruments.com/products/powerlab |
LabChart ver. 6 | AD Instruments | not available | Acquisition software https://www.adinstruments.com/products/labchart |
Animal Bio Amp | AD Instruments | FE136 | Amplifier https://www.adinstruments.com/products/bio-amps#product-FE136 |
K2EDTA 7.2mg | BD | 367861 | Blood collection tubes http://catalog.bd.com/nexus-ecat/getProductDetail?productId=367861 |
Centrifuge | SciQuip | 2-16KL | Centrifuge http://www.sigma-centrifuges.co.uk/store/products/refrigerated-sigma-2-16k-centrifuge/ |
Eppendorf Reference 2, 100 – 1000 μL | Eppendorf | 4920000083 | Pipette https://online-shop.eppendorf.es/ES-es/Pipeteo-44563/Pipetas-44564/Eppendorf-Reference2-PF-42806.html |
Eppendorf Safe-Lock Tubes, 0.5 mL | Eppendorf | 30121023 | Tubes https://online-shop.eppendorf.es/ES-es/Puntas-tubos-y-placas-44512/Tubos-44515/Eppendorf-Safe-Lock-Tubes-PF-8863.html |
NZW rabbits (16-18 weeks old) | Granja San Bernardo | not available | New Zealand White rabbits http://www.granjasanbernardo.com/en/welcome/ |
Sucrose | Sigma | S0389-5KG | Sucrose for drinking solution http://www.sigmaaldrich.com/catalog/product/sigma/s0389?lang=es®ion=ES |
Rabbit maintenance control diet | Ssniff | V2333-000 | Control diet http://www.ssniff.com/ |
Rabbit high-fat diet | Ssniff | S9052-E020 | High-fat diet http://www.ssniff.com/ |
Rabbit rack and drinker | Sodispan | not available | Rack for rabbits https://www.sodispan.com/jaulas-y-racks/racks-conejo-y-cobaya/ |
Rabbit restrainer | Zoonlab | 3045601 | http://www.zoonlab.de/en/index.html |