Andre Leopoldo

Dr. Andre Leopoldo

orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2008 in Archives of Endocrinology and Metabolism
Verified
Journal Article
Open access
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ANAndré F. Nascimento
André F. Nascimento
MSMário M. Sugizaki
Mário M. Sugizaki
ALAndre Leopoldo
Andre Leopoldo
ALAna P. Lima-Leopoldo
Ana P. Lima-Leopoldo
RLRenata A. M. Luvizotto
Renata A. M. Luvizotto
ACAntonio Cicogna
Antonio Cicogna
The present study was carried to develop and analyze the consequences of hypercaloric pellet-diet cycle that promotes obesity in rats. Male Wistar rats were randomly distributed into two groups that received either normal diet (ND; n =32; 3,5 Kcal/g) or a hypercaloric diet (HD; n =32; 4,6 Kcal/g). The ND group received commercial Labina rat feeding while the HD animals received a cycle of five hypercaloric diets over a 14-week period. The effects of the diets were analyzed in terms of body weight, body composition, hormone-metabolite levels, systolic arterial pressure and glucose tolerance at the 5% significance level. The hypercaloric pellet diet cycle promoted an increase in body weight and fat, systolic arterial pressure and a high serum level of glucose, triacylglycerol, insulin and leptin. The HD group also presented an impaired glucose tolerance. In conclusion, the results of this study show that the hypercaloric pellet-diet cycle promoted obesity in Wistar rats and displayed several characteristics that are commonly associated with human obesity, such as high arterial pressure, insulin resistance, hyperglycaemia, hyperinsulinaemia, hyperleptinaemia and dyslipidaemia.

1 October 2010 in Canadian Journal of Cardiology
Verified
Journal Article
Closed access
ALAndre Leopoldo
Andre Leopoldo
MSMário Matheus Sugizaki
Mário Matheus Sugizaki
ALAna Paula Lima-Leopoldo
Ana Paula Lima-Leopoldo
ANAndré Ferreira Do Nascimento
André Ferreira Do Nascimento
RLRenata de Azevedo Melo Luvizotto
Renata de Azevedo Melo Luvizotto
ACAntonio Cicogna
Antonio Cicogna

1 January 2016 in Brazilian Journal of Medical and Biological Research
Verified
Journal Article
Open access
ALAndre Leopoldo
Andre Leopoldo
ALA.P. Lima-Leopoldo
A.P. Lima-Leopoldo
ANA.F. Nascimento
A.F. Nascimento
RLR.A.M. Luvizotto
R.A.M. Luvizotto
MSM.M. Sugizaki
M.M. Sugizaki
ACAntonio Cicogna
Antonio Cicogna
In experimental studies, several parameters, such as body weight, body mass index, adiposity index, and dual-energy X-ray absorptiometry, have commonly been used to demonstrate increased adiposity and investigate the mechanisms underlying obesity and sedentary lifestyles. However, these investigations have not classified the degree of adiposity nor defined adiposity categories for rats, such as normal, overweight, and obese. The aim of the study was to characterize the degree of adiposity in rats fed a high-fat diet using cluster analysis and to create adiposity intervals in an experimental model of obesity. Thirty-day-old male Wistar rats were fed a normal (n=41) or a high-fat (n=43) diet for 15 weeks. Obesity was defined based on the adiposity index; and the degree of adiposity was evaluated using cluster analysis. Cluster analysis allowed the rats to be classified into two groups (overweight and obese). The obese group displayed significantly higher total body fat and a higher adiposity index compared with those of the overweight group. No differences in systolic blood pressure or nonesterified fatty acid, glucose, total cholesterol, or triglyceride levels were observed between the obese and overweight groups. The adiposity index of the obese group was positively correlated with final body weight, total body fat, and leptin levels. Despite the classification of sedentary rats into overweight and obese groups, it was not possible to identify differences in the comorbidities between the two groups.

1 June 2011 in Life Sciences
Verified
Journal Article
Closed access
ANAndré F. Nascimento
André F. Nascimento
RLRenata A.M. Luvizotto
Renata A.M. Luvizotto
ALAndre Leopoldo
Andre Leopoldo
ALAna P. Lima-Leopoldo
Ana P. Lima-Leopoldo
FSFabio Seiva
Fabio Seiva
ACAntonio Cicogna
Antonio Cicogna

11 August 2018 in Nutrients
Verified
Journal Article
Open access
PDF file
AMAmanda Martins Matias
Amanda Martins Matias
WEWagner Müller Estevam
Wagner Müller Estevam
PCPriscila Murucci Coelho
Priscila Murucci Coelho
DHDouglas Haese
Douglas Haese
JKJéssika Butcovsky Botto Sarter Kobi
Jéssika Butcovsky Botto Sarter Kobi
ALAndre Leopoldo
Andre Leopoldo
Background: Dietary interventions in rodents can induce an excess of adipose tissue and metabolic disorders that resemble human obesity. Nevertheless, these approaches are not standardized, and the phenotypes may vary distinctly among studies. The aim of this study was to investigate the effects of different dietary interventions on nutritional, metabolic, biochemical, hormonal, and cardiovascular profiles, as well as to add to development and characterization of an experimental model of obesity. Methods: Male Wistar rats were randomized into four groups: control diet (C), high-sugar (HS), high-fat (HF), or high-sugar and high-fat (HFHS). Weekly measurements of body weight, adiposity, area under the curve (AUC) for glucose, blood pressure (BP) and serum triglycerides, total cholesterol level, and leptin were performed. Results: HF and HFHS models were led to obesity by increases in adipose tissue deposition and the adiposity index. All hypercaloric diets presented systolic BP increases. In addition, the AUC for glucose was greater in HF and HFHS than in C, and only the HF group presented hyperleptinemia. Conclusions: HF and HFHS diet approaches promote obesity and comorbidities, and thus represent a useful tool for studying human obesity-related disorders. By contrast, the HS model did not prove to be a good model of obesity.

1 February 2011 in Journal of Cellular Physiology
Verified
Journal Article
Closed access
PDF file
ALAndre Leopoldo
Andre Leopoldo
ALAna Paula Lima‐Leopoldo
Ana Paula Lima‐Leopoldo
MSMário Mateus Sugizaki
Mário Mateus Sugizaki
ANAndré Ferreira Do Nascimento
André Ferreira Do Nascimento
DCDijon Henrique Salomé de Campos
Dijon Henrique Salomé de Campos
ACAntonio Cicogna
Antonio Cicogna