Fabiana Maria Coimbra de Carvalho
Federal University of Rio Grande do Norte
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Publication
Featured researches published by Fabiana Maria Coimbra de Carvalho.
Journal of Enzyme Inhibition and Medicinal Chemistry | 2016
Alexandre Coelho Serquiz; Richele J.A. Machado; Raphael Paschoal Serquiz; Vanessa Cristina Oliveira de Lima; Fabiana Maria Coimbra de Carvalho; Marcella A. A. Carneiro; Bruna Leal Lima Maciel; Adriana Ferreira Uchôa; Elizeu A. Santos; Ana Heloneida de Araújo Morais
Abstract Ingestion of peanuts may have a beneficial effect on weight control, possibly due to the satietogenic action of trypsin inhibitors. The aim of this study was to isolate a new trypsin inhibitor in a typical Brazilian peanut sweet (paçoca) and evaluate its effect in biochemical parameters, weight gain and food intake in male Wistar rats. The trypsin inhibitor in peanut paçoca (AHTI) was isolated. Experimental diets were prepared with AIN-93G supplemented with AHTI. Animals had their weight and food intake monitored. Animals were anesthetized, euthanized, and their bloods collected by cardiac puncture for dosage of cholecystokinin (CCK) and other biochemical parameters. Supplementation with AHTI significantly decreased fasting glucose, body weight gain, and food intake. These effects may be attributed to increased satiety, once supplemented animals showed no evidence of impaired nutritional status and also because AHTI increased CCK production. Thus, our results indicate that AHTI, besides reducing fasting glucose, can reduce weight gain via food intake reduction.
Nutrients | 2016
Fabiana Maria Coimbra de Carvalho; Vanessa Cristina Oliveira de Lima; Izael de Sousa Costa; Amanda Fernandes de Medeiros; Alexandre Coelho Serquiz; Maíra C. J. S. Lima; Raphael Paschoal Serquiz; Bruna Leal Lima Maciel; Adriana Ferreira Uchôa; Elizeu A. Santos; Ana Heloneida de Araújo Morais
Trypsin inhibitors are studied in a variety of models for their anti-obesity and anti-inflammatory bioactive properties. Our group has previously demonstrated the satietogenic effect of tamarind seed trypsin inhibitors (TTI) in eutrophic mouse models and anti-inflammatory effects of other trypsin inhibitors. In this study, we evaluated TTI effect upon satiety, biochemical and inflammatory parameters in an experimental model of metabolic syndrome (MetS). Three groups of n = 5 male Wistar rats with obesity-based MetS received for 10 days one of the following: (1) Cafeteria diet; (2) Cafeteria diet + TTI (25 mg/kg); and (3) Standard diet. TTI reduced food intake in animals with MetS. Nevertheless, weight gain was not different between studied groups. Dyslipidemia parameters were not different with the use of TTI, only the group receiving standard diet showed lower very low density lipoprotein (VLDL) and triglycerides (TG) (Kruskal–Wallis, p < 0.05). Interleukin-6 (IL-6) production did not differ between groups. Interestingly, tumor necrosis factor-alpha (TNF-α) was lower in animals receiving TTI. Our results corroborate the satietogenic effect of TTI in a MetS model. Furthermore, we showed that TTI added to a cafeteria diet may decrease inflammation regardless of weight loss. This puts TTI as a candidate for studies to test its effectiveness as an adjuvant in MetS treatment.
Journal of Enzyme Inhibition and Medicinal Chemistry | 2018
Amanda Fernandes de Medeiros; Izael de Sousa Costa; Fabiana Maria Coimbra de Carvalho; Sumika Kiyota; Beatriz Blenda Pinheiro de Souza; Daniel Nogoceke Sifuentes; Raphael Paschoal Serquiz; Bruna Leal Lima Maciel; Adriana Ferreira Uchôa; Elizeu A. Santos; Ana Heloneida de Araújo Morais
Abstract A trypsin inhibitor isolated from tamarind seed (TTI) has satietogenic effects in animals, increasing the cholecystokinin (CCK) in eutrophy and reducing leptin in obesity. We purified TTI (pTTI), characterised, and observed its effect upon CCK and leptin in obese Wistar rats. By HPLC, and after amplification of resolution, two protein fractions were observed: Fr1 and Fr2, with average mass of [M + 14H]+ = 19,594,690 Da and [M + 13H]+ = 19,578,266 Da, respectively. The protein fractions showed 54 and 53 amino acid residues with the same sequence. pTTI presented resistance to temperature and pH variations; IC50 was 2.7 × 10−10 mol.L−1 and Ki was 2.9 × 10−11 mol.L−1. The 2-DE revealed spots with isoelectric points between pH 5 and 6, and one near pH 8. pTTI action on leptin decrease was confirmed. We conclude that pTTI is a Kunitz trypsin inhibitor with possible biotechnological health-related application.
Revista Brasileira De Fruticultura | 2014
Ágnes Denise de Lima Bezerra; Claudia Renata Montenegro Barbosa; Fabiana Maria Coimbra de Carvalho; Alexandre Coelho Serquiz; Ana Heloneida de Araújo Morais
A healthy and diversified eating is essential for the maintenance of physical and mental health, and despite the current trend that appreciates the convenience of eating, it is noted that the population is increasingly consuming fruit, both in natura and / or juices. However, the use of certain fresh fruits is accompanied by the consumption of the seeds, peels or other parts may contain antinutritional factors, molecules and / or compounds that may adversely affect the bioavailability and / or digestibility of nutrients, such as inhibitors of trypsin. Such inhibitors may impair the utilization of proteins in food, but recent studies have been published also demonstrating the beneficial effects of the same. This study aimed to evaluate the trypsin inhibitors in aqueous extracts of fruits: guava (Psidium guajava L) varieties Kumagai (white) and Paluma (red), yellow passion fruit (Passiflora edulis f.) and watermelon (Citrullus vulgaris Schrad). Tests were done in order to detect the presence of antitryptic activity and the dosage of soluble proteins. Trypsin inhibitory activity was detected in all extracts tested, as well as soluble proteins. Thus, inhibition can be explained by the presence of an inhibitor protein, because it was possible, in seed extracts, in SDS-PAGE, to visualize a wide range of protein bands. It is noteworthy that in the study, the protein bands that coincide with the molecular masses of the trypsin inhibitors did not appear in a majority, showing that seed extracts are likely to have protein inhibitor, however sparingly, justifying the low antitryptic activity (1, 36 to 15.15 IU / mg of dry weight), also shown by the extracts of the pulp. Therefore, having the recommended consumption of fruits including guava, passion fruit and watermelon in sight, possibly this inhibitory activity is more related to benefits than to hazards, regarding ones health. However, it is important to emphasize a careful consumption of large quantities of seeds present in these fruits.
Nutrire | 2012
Fabiana Maria Coimbra de Carvalho; Amanda Fernandes de Medeiros; Maria G. F. Rocha; Richele J.A. Machado; Alexandre Coelho Serquiz; Ágnes Denise de Lima Bezerra; Elizeu A. Santos; Ana Heloneida de Araújo Morais
Saúde (Santa Maria) | 2018
Ana Heloneida de Araújo Morais; Izael de Sousa Costa; Fabiana Maria Coimbra de Carvalho
Revista Brasileira de Nutrição Esportiva | 2018
Leonardo Oliveira de Assis; Hygor Bruno de Moura Andrade; Fabiana Maria Coimbra de Carvalho; Raphael Paschoal Serquiz; Alexandre Coelho Serquiz
Revista Brasileira de Inovação Tecnológica em Saúde <br /> ISSN: 2236-1103 | 2018
Vanessa Cristina Oliveira de Lima; Priscila Fabíola dos Santos Silva; Nínive Rayane de Medeiros Alves; Danielle Alves de Oliveira Pereira; Júlia Braga dos Santos Figueredo; Izael de Sousa Costa; Fabiana Maria Coimbra de Carvalho; Elizeu A. Santos; Ana Heloneida de Araújo Morais
Revista Brasileira de Neurologia | 2017
Glenya Estevam de Medeiros; Bárbara Oliveira Rosas; Amanda de Souza Nunes Lessa; Fabiana Maria Coimbra de Carvalho; Daliana Caldas Pessoa da Silva; Juliana Bianca Maia Franco; Alexandre Coelho Serquiz
DEMETRA: Alimentação, Nutrição & Saúde | 2017
Ana Paula Araújo de Souza; Lorena Maria Araújo Marinheiro Nascimento; Vanessa Cristina Oliveira de Lima; Fabiana Maria Coimbra de Carvalho; Elizeu A. Santos; Ana Heloneida de Araújo Morais
Collaboration
Dive into the Fabiana Maria Coimbra de Carvalho's collaboration.
Ana Heloneida de Araújo Morais
Federal University of Rio Grande do Norte
View shared research outputsVanessa Cristina Oliveira de Lima
Federal University of Rio Grande do Norte
View shared research outputs