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Brite/beige adipocytes: a potential tool against obesity and diabetes?

Grant number: 18/18815-4
Support type:Scholarships abroad - Research Internship - Doctorate (Direct)
Effective date (Start): February 01, 2019
Effective date (End): January 31, 2020
Field of knowledge:Biological Sciences - Physiology - Physiology of Organs and Systems
Principal researcher:Sandro Massao Hirabara
Grantee:Tamires Duarte Afonso Serdan
Supervisor abroad: Barbara Cannon
Home Institution: Centro de Ciências Biológicas e da Saúde. Universidade Cruzeiro do Sul (UNICSUL). São Paulo , SP, Brazil
Research place: Stockholm University, Sweden  
Associated to the scholarship:16/14529-1 - Metabolism of the brown adipose tissue in animal models of insulin resistance: Goto-Kakizaki and obese Wistar rats, BP.DD

Abstract

Energy balance is defined by two components: energy intake and energy expenditure. Even minor but chronic perturbations in either of these two components can lead to an increase (obesity) or decrease in body weight. Obesity is not only a significant problem in itself but is also a major inducer of type 2 diabetes, cardiovascular disease and certain forms of cancer. At present there is no satisfactory treatment for obesity and in reality little understanding of the cause of obesity, except for the self-evident statement that it arises from an imbalance between energy intake and energy expenditure. The presence of two distinct types of adipose tissue, which have opposing functions, has been known for decades. White adipose tissue (WAT) is the main tissue of energy storage, while brown adipose tissue (BAT) dissipates energy as heat and is required for non-shivering thermoregulation. Within classical white adipose tissue depots, a particular type of adipocytes sometimes occurs. These adipocytes manifest several classical brown adipocyte characteristics, most notably the presence of UCP1 (uncoupling protein-1) and through this the ability to dissipate energy, to burn away (extra) food and thus to counteract the development of obesity. The identification of a novel type of adipocytes, i.e. the brite/beige adipocytes, that possess the ability to increase energy expenditure and that are localized within the white adipose depots themselves, has provided a basis for studying new opportunities, both for counteracting the development of obesity and perhaps even for diminishing it in already obese persons. However, these cells do not express all the genes found in classical brown adipocytes, and they display a distinctive ontogeny and specific anatomical location. Thus, this particular adipose cell-type cannot be classified as either brown or white. It is the goal of the studies described here to gain insight into the functional significance of the distinct populations of brite/beige adipocytes, seeking to elucidate the functional significance of distinct populations of brite/beige adipocytes; the functional significance of particular brite/beige adipocyte-selective genes; the potential therapeutic benefit of brite/beige adipocytes. We will investigate the following parameters: 1) Functional characterization of brite adipocytes by evaluating the thermogenic UCP1-dependent activity and energy substrate utilization, 2) Gene-specific expression and regulation in beige/brite and brown adipocytes, and 3)  Potential therapeutic benefit of brite/beige adipocytes in systemic glucose and lipid metabolism and insulin sensitivity. Considering the vast medical implications of the obesity epidemic, even modest amelioration of energy balance may be of significance. The studies of brite/beige adipocytes proposed here could represent one means of developing methods to accomplish such amelioration. (AU)

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Scientific publications
(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)
SERDAN, TAMIRES DUARTE AFONSO; MASI, LAUREANE NUNES; PEREIRA, JOICE NAIARA BERTAGLIA; RODRIGUES, LUIZ EDUARDO; ALECRIM, AMANDA LINS; SCERVINO, MARIA VITORIA MARTINS; DINIZ, VINICIUS LEONARDO SOUSA; DOS SANTOS, ALEF ARAGAO CARNEIRO; SOUSA FILHO, CELSO PEREIRA BATISTA; ALBA-LOUREIRO, TATIANA CAROLINA; MARZUCA-NASSR, GABRIEL NASRI; BAZOTTE, ROBERTO BARBOSA; GORJAO, RENATA; PITHON-CURI, TANIA CRISTINA; CURI, RUI; HIRABARA, SANDRO MASSAO. Impaired brown adipose tissue is differentially modulated in insulin-resistant obese wistar and type 2 diabetic Goto-Kakizaki rats. BIOMEDICINE & PHARMACOTHERAPY, v. 142, OCT 2021. Web of Science Citations: 0.

Please report errors in scientific publications list by writing to: cdi@fapesp.br.