GLUT4 content decreases along with insulin resistance and high levels of inflammatory markers in rats with metabolic syndrome


Autoria(s): Leguisamo, Natalia M.; Lehnen, Alexandre M.; Machado, Ubiratan Fabres; Okamoto, Maristela Mitiko; Markoski, Melissa M.; Pinto, Graziela H.; Schaan, Beatriz D.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

12/10/2013

12/10/2013

2012

Resumo

Background: Metabolic syndrome is characterized by insulin resistance, which is closely related to GLUT4 content in insulin-sensitive tissues. Thus, we evaluated the GLUT4 expression, insulin resistance and inflammation, characteristics of the metabolic syndrome, in an experimental model. Methods: Spontaneously hypertensive neonate rats (18/group) were treated with monosodium glutamate (MetS) during 9 days, and compared with Wistar-Kyoto (C) and saline-treated SHR (H). Blood pressure (BP) and lipid levels, C-reactive protein (CRP), interleukin 6 (IL-6), TNF-alpha and adiponectin were evaluated. GLUT4 protein was analysed in the heart, white adipose tissue and gastrocnemius. Studies were performed at 3 (3-mo), 6 (6-mo) and 9 (9-mo) months of age. Results: MetS rats were more insulin resistant (p<0.001, all ages) and had higher BP (3-mo: p<0.001, 6-mo: p = 0.001, 9-mo: p = 0.015) as compared to C. At 6 months, CRP, IL-6 and TNF-alpha were higher (p<0.001, all comparisons) in MetS rats vs H, but adiponectin was lower in MetS at 9 months (MetS: 32 +/- 2, H: 42 +/- 2, C: 45 +/- 2 pg/mL; p<0.001). GLUT4 protein was reduced in MetS as compared to C rats at 3, 6 and 9-mo, respectively (Heart: 54%, 50% and 57%; Gastrocnemius: 37%, 56% and 50%; Adipose tissue: 69%, 61% and 69%). Conclusions: MSG-treated SHR presented all metabolic syndrome characteristics, as well as reduced GLUT4 content, which must play a key role in the impaired glycemic homeostasis of the metabolic syndrome.

Rio Grande do Sul State Foundation for Research (Fapergs)

Rio Grande do Sul State Foundation for Research (Fapergs)

FAPESP (Sao Paulo State Foundation for Research)

Sao Paulo State Foundation for Research (Fapesp)

CNPq

CNPq

Capes [113/2007]

CAPES

Department of Biochemistry at UFRGS

Department of Biochemistry at UFRGS

Identificador

CARDIOVASCULAR DIABETOLOGY, LONDON, v. 11, pp. 135-138, AUG 16, 2012

1475-2840

http://www.producao.usp.br/handle/BDPI/34187

10.1186/1475-2840-11-100

http://dx.doi.org/10.1186/1475-2840-11-100

Idioma(s)

eng

Publicador

BIOMED CENTRAL LTD

LONDON

Relação

CARDIOVASCULAR DIABETOLOGY

Direitos

openAccess

Copyright BIOMED CENTRAL LTD

Palavras-Chave #MONOSODIUM GLUTAMATE #SPONTANEOUSLY HYPERTENSIVE RATS #GLUCOSE TRANSPORTER 4 #SPONTANEOUSLY HYPERTENSIVE-RATS #MONOSODIUM-L-GLUTAMATE #NECROSIS-FACTOR-ALPHA #HIGH-FAT DIET #GLUCOSE-TRANSPORTER GLUT-4 #BROWN ADIPOSE-TISSUE #TREATED OBESE MICE #SKELETAL-MUSCLE #NEUROENDOCRINE REGULATION #NEONATAL TREATMENT #CARDIAC & CARDIOVASCULAR SYSTEMS #ENDOCRINOLOGY & METABOLISM
Tipo

article

original article

publishedVersion