Introduction
In the last years, the obesity has reached epidemic proportions globally. It is considered a public health problem in the worldwide1. Overweight is an important risk factor for chronic non-communicable diseases (CNCDs) such as diabetes mellitus, hypertension, cardio vascular disease and cancer. It is caused by several factors, such as genetic predisposition, inadequate eating habits and sedentary lifestyle2.
According to the World Health Organization (WHO) obesity can be understood as a grievance of multivariate origin and is result of positive energy balance that favors the accumulation of fat, related to risks to health due to its relationship to metabolic complications such as hypertension, hypercholesterolemia, hypertriglyceridemia and diabetes3.
In some studies of action mechanisms in obesity that induce physiological disorders is used animal model in research environment. In this context, it is mainly used rodents which have the ability to develop obesity through genetic changes or by consumption of a palatable and high calorie diet. Thus, the animal model develops the disease more similar way to the genesis of obesity in humans.
To study the action mechanisms present in obesity that inducing physiological disorders, can be used animal model in research environment. In this context, it is used mainly rodents, who develop obesity through genetic changes.
The laboratory rat due to the physiological, anatomical and metabolic similarity with the human, has been used as an animal model for the study of many diseases. Scientists have also started to create mice as model because they have interesting phenotypes. Mice are considered excellent for the study of genetic therefore have a relatively short cycle and are genetically similar to humans as well as easy to handle5.
Thus, the aim of the present study is to perform an integrative review of the major animal disease models in rodents used for obesity.
Methods
In this review were included experimental studies that use animal models of disease to obesity. Were considered studies published in scientific journals between the years 2010-2016, in Portuguese, English or Spanish. Exclusion criteria were: (1) studies that did not include the eligibility criteria described above; (2) Systematic reviews; (3) Case study; (4) Case study; (5) Retrospective studies and (6) Observational Studies;
The searches for experimental studies were conducted by CAPES Portal database. The survey was conducted from March to July 2016 with the DeCS / MeSH descriptors: Obesity; animal Models; Diet; Rodents.
For extracting data were first evaluated the titles and abstracts of all articles identified by the search strategy. All abstracts that did not provide enough information on the inclusion and exclusion criteria were selected to read in full. In the second stage, were assessed the full papers to select those in accordance with the eligibility criteria.
The extraction of data was accomplished through standardized forms that included: article title, author and year of publication; animals used (species, sample number, age and sex); study design, rating scale, the study duration; type diet and results of intervention If there was any inconsistency in the analysis, the original documents were recovered and investigated again. The outcomes of interest were: lineage; age; sex; tracking time and type of diet. Data were analyzed using descriptive statistics.
Results
In this work, 108 articles were found from the electronic search in the database. Of these, 19 articles were included in this review, according to the selection criteria described in the methodology. Table 1 contains the selected articles for review in accordance with the outcomes used for this study. The main data found in these works were shown in Table 2.
TABLE 1 Selected articles according to the type, age and sex of animals, follow-up time and type of diet used between the years 2010-2016 (n = 19).
AUTORS | TYPE OF ANIMAL | AGE | SEX | FOLLOW-UP TIME | TYPE OF DIET |
Privi-tera10 | Rats SD | 21 days | Male | 13 weeks | High Fat 60% |
Watanabe11 | Mice C57BL | 6 a 7 weeks | Male | 96 days | High Fat 60% |
Calli-garis12 | Mice C57BL | 5 weeks | Male | 16 months | High Fat 60% |
Krüger13 | Mice C57BL | 10-12 weeks | Male | 10 weeks | High Fat |
Walewski14 | Rats wistar Mice C57BL | 18 weeks | Female | 20 weeks | High Fat 60% |
Borengasse15 | Rats SD | 60 days | Male and Female | 12 weeks | High Carb72%, High Fat 40-45% |
Lalanza16 | Rats SD | 21 days | Male and Female | 8 weeks | Cafeteria |
Shao17 | Mice C57BL | 8 weeks | Male | 12 weeks | High Fat 40% |
Tillman18 | Mice C57BL | ND | Male | 14 weeks | High Carb, High Fat 45%; 67% |
Guan1 | Rats SD | ND | Male | 90 days | High Fat, High Carb |
Mc pherson2 | Mice C57BL | 5 weeks | Male | 9 weeks | High Fat 21% |
Qian21 | Rats SD | ND | Male | 12 weeks | High Fat |
Quiñones22 | Rats SD | 6 weeks | Male | 10 weeks | High Fat 60%, Low Fat 10% |
Roberts-tole23 | Mice C57BL | 6 weeks | Male | 16- 22 weeks | High Fat 60%, Hight.Carb 70% |
Zhuhua24 | Mice ICR | 8 weeks | Male | 12 weeks | High Fat, High Carb |
Note: Some studies worked with one or more types of species of animals. ND: non determined.
TABLE 2 Distribution of variables by categories of scientific articles published on animal models of disease to obesity between the years 2010-2016 (n = 19).
VARIABLE | TOTAL |
Year of Publication | |
2010-2011 | 05 |
2012-2013 | 03 |
2014-2015 | 11 |
Animal Species | |
Mice | 10 |
Rats | 10 |
Age of animals | |
21 days | 02 |
4 a 8 weeks | 11 |
≥ 8 weeks | 02 |
ND | 04 |
Sex of Animals | |
Male | 16 |
Female | 01 |
Ambos | 02 |
Follow-up time | |
6 a 10 weeks | 05 |
11 a 16 weeks >16 weeks | 09 05 |
Type of diet | |
High Fat | 18 |
High Carb | 06 |
Cafeteria | 01 |
Note: For some variables, the roles worked with more than one animal and diet option. ND: non determined.
Discussion
A suitable animal model with rodents should allow the study of biological phenomena, animal behavior, induced pathological process or spontaneous. This model should be similar to the human characteristics in several respects. It is from the physiological and genetic similarities between both, that studies in animal models provide the understanding of diseases in humans4.
From the animal model it is possible to obtain information faster and better control of the disease such as obesity and its comorbidities. The searches for replies on the physiological dysfunctions in diseases induced by promoted animal model of obesity are increasingly intense. It is observed in the number of papers published in the last 3 years (2013-2015) which was higher for the years 2010-2012 according to this review.
In the reports evaluated in our review, the use of rat in experiments6,8-10,14-16,21,22 and mice7,11-14,17,18,20,23,24 are identical. However, in a survey conducted by Fagundes and Taha25 the rats were most used in experimental studies than the mouse. But it notes that the use of mice in the study of obesity has grown in recent years.
The insertion of mice as laboratory animals is due mainly to the size, very prolific, have a short gestation period and easily of taming5. Mice require small space for its establishment, and consume a smaller amount of food. Thus their maintenance is cheap compared to the mouse. Mice have little blood volume, which sometimes does not allow the realization of biochemical tests. On the other hand, some researchers choose to use the mouse.
In the most studies the found age range was 4 to 18 weeks. It is interesting to note that the puberty of rat occurs 30 days after his birth and the mice is between 30 to 40 days. The sexual maturation of both occurs around sixty days. Factors such as age and different maturation cycles, and diseases related to the lifetime can interfere in the outcome of research5.
Most of the selected works in this review used male animals, probably this preference may be related to own existing biological structure between the sexes6-13,15-24. Male have hormonal factors that are related to body growth, which reflected in higher body weight23. While these hormones in female are related to the lower growth of body and increased of fat storage26. The amount of hormone is related to metabolic alterations such as leptin and adiponectin, it is higher in female, thus influencing in the food and energy intake, as well as weight gain interfering26.
Different studies in the literature use C57BL / 6J mice and consider the follow-up time greater than 15 weeks to obesity induced by high fat diet27,28. However, in another study with Swiss mice found that it took only about 10 weeks to induce obesity by means of a high-fat diet, in this case with the same percentage of lipids described above29.
In our revision, it was found that 47,3% of the analyzed studies used the follow-up time from 11 to 16 weeks and 26.3% worked with the follow-up time from 6 to 10 weeks , and 26,3% have taken follow-up time next greater than 16 weeks. Thus, it was possible to verify the existence of variation of the follow-up times used in the studies. There was a major highlight in studies with follow-up time that exceeded 11 to 16 weeks.
With respect to the diets evaluated in the articles the most representative was Hight Fat using fat sources such as lard oil and soybean, but it considers different concentrations of lipids in the preparation. In diets with ratio of 40% to 60% of lipids, obesity induction occurred in all groups, regardless of the strains of rodents6,9-12,15,17,18,22-24. In experiments with diets containing 60% lipids, mice obtained in addition to weight gain and epididymal fat, hyperglycemia and insulin resistance11,12,23.
In simple carbohydrate calorie diet (High Carb) with a mean proportion of 60% based on sucrose, fructose and corn starch, the animals had increased weight, body fat, triglycerides, hyperglycemia and hypertension18. In a study with the cafeteria diet (bacon, biscuit, pâté and milk sugar) the levels of triglycerides and glucose were altered and liver was increased16.
The effect of diets in rodents has been studied since 1988, showing that feeding high-fat, simple carbohydrates and poor in fiber produce obesity and is associated to moderate intolerance factors glucose, insulin resistance, dysfunction of the islets of Langerhans and type 2 diabetes in rodents. Therefore, the standard HF diet can be used for studies on the mechanisms of obesity and as a tool for the development of new therapeutic interventions29,30.
Conclusions
This literature review indicates that both rats and mice were used in the same proportion in experimental studies in obesity model, were observed variations in age to the beginning of the experiment soon after weaning. The follow-up time of the studies, in general, proved to be long. Furthermore, the High Fat diet was the most used in the studies analyzed. Given the above, this study demonstrates the importance of animal models of disease in the scientific field, in spite of intense ethical discussions on the use of laboratory animals for experimental research.