Lycopene supplementation reduces TNF-alpha via RAGE in the kidney of obese rats
dc.contributor.author | Pierine, D. T. [UNESP] | |
dc.contributor.author | Navarro, M. E. L. [UNESP] | |
dc.contributor.author | Minatel, I. O. [UNESP] | |
dc.contributor.author | Luvizotto, R. A. M. [UNESP] | |
dc.contributor.author | Nascimento, A. F. [UNESP] | |
dc.contributor.author | Ferreira, A. L. A. [UNESP] | |
dc.contributor.author | Yeum, K-J | |
dc.contributor.author | Correa, C. R. [UNESP] | |
dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
dc.contributor.institution | Tufts University | |
dc.contributor.institution | Konkuk University | |
dc.date.accessioned | 2015-11-03T15:27:43Z | |
dc.date.available | 2015-11-03T15:27:43Z | |
dc.date.issued | 2014-11-01 | |
dc.description.abstract | The kidney is a target organ for injuries caused by advanced glycation end products (AGEs) in obesity. The receptor of AGEs (RAGE) is proinflammatory and appears to have a role in the pathogenesis of renal disease due to obesity.OBJECTIVE: The aim was to verify the effect of obesity on renal damage and the effect of lycopene on these complicationsDESIGN AND METHODS: Male Wistar rats were randomly assigned to receive a control diet (C, n = 7) or a high-fat diet plus sucrose (HD+S, n = 14) for 6 weeks. After this period, the HD+S animals were randomized into two groups: HD+S (n = 7) and HD+S supplemented with lycopene (HD+S+L, n = 7). The animals received maize oil (C and HD+S) or lycopene (HD+S+L) for a 6-week period.RESULTS: The HD+S and HD+S+L animals demonstrated insulin resistance (OGTT glucose after 150 min; C: 117.6 +/- 3.9 < HD+S: 138.1 +/- 5.1 = HD+S+L: 137.8 +/- 5.2 mg dl(-1); P = 0.01); however, no changes were seen in fasting glucose, plasma lipids, blood pressure or renal function. Renal concentrations of RAGE and TNF-alpha increased in the HD+S group and lycopene supplementation restored these to control group values (RAGE: C: 3.1 +/- 0.3 = DH+S+L: 3.1 +/- 0.3 < DH+S: 3.6 +/- 0.4 mu g g(-1); P = 0.014; TNF-alpha: C: 227.8 +/- 2.7 = DH+S+L: 227.4 +/- 2.2 < DH+S: 238.7 +/- 3.0 pg/ml; P = 0.014).CONCLUSIONS: Lycopene may be beneficial in the prevention and treatment of oxidative stress and inflammation in the kidney due to obesity. | en |
dc.description.affiliation | Jean Mayer Human Nutrition Research Center on Aging, Tufts University, Boston, MA, USA | |
dc.description.affiliation | Food and Nutrition Major, Division of Food Bioscience, College of Biomedical and Health Sciences, Konkuk University, Glocal Campus, Seoul, South Korea. | |
dc.description.affiliationUnesp | Pathology Department, Botucatu Medical School—São Paulo State University—UNESP, Botucatu, Brazil | |
dc.description.affiliationUnesp | Internal Medicine Department, Botucatu Medical School—São Paulo State University—UNESP, Botucatu, Brazil. | |
dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description.sponsorship | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) | |
dc.description.sponsorshipId | FAPESP: 2010/06100-9 | |
dc.description.sponsorshipId | FAPESP: 2011/14132-0 | |
dc.description.sponsorshipId | CAPES: 022/11 | |
dc.description.sponsorshipId | CAPES: BEX: 9847/11-1 | |
dc.format.extent | 1-6 | |
dc.identifier | http://www.nature.com/nutd/journal/v4/n11/full/nutd201439a.html | |
dc.identifier.citation | Nutrition & Diabetes. London: Nature Publishing Group, v. 4, p. 1-6, 2014. | |
dc.identifier.doi | 10.1038/nutd.2014.39 | |
dc.identifier.issn | 2044-4052 | |
dc.identifier.lattes | 2940051650846541 | |
dc.identifier.uri | http://hdl.handle.net/11449/129909 | |
dc.identifier.wos | WOS:000348501900001 | |
dc.language.iso | eng | |
dc.publisher | Nature Publishing Group | |
dc.relation.ispartof | Nutrition & Diabetes | |
dc.relation.ispartofjcr | 2.742 | |
dc.relation.ispartofsjr | 1,628 | |
dc.rights.accessRights | Acesso restrito | |
dc.source | Web of Science | |
dc.title | Lycopene supplementation reduces TNF-alpha via RAGE in the kidney of obese rats | en |
dc.type | Artigo | |
dcterms.rightsHolder | Nature Publishing Group | |
unesp.author.lattes | 2940051650846541[6] | |
unesp.author.orcid | 0000-0002-9922-2871[3] | |
unesp.author.orcid | 0000-0002-5267-1127[6] | |
unesp.campus | Universidade Estadual Paulista (Unesp), Faculdade de Medicina, Botucatu | pt |