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  • Molecular and biochemical modifications of liver glutamine synthetase elicited by daytime restricted feeding.

Molecular and biochemical modifications of liver glutamine synthetase elicited by daytime restricted feeding.

Liver international : official journal of the International Association for the Study of the Liver (2014-11-05)
Olivia Vázquez-Martínez, Dalia De Ita-Pérez, Marlen Valdés-Fuentes, Alejandra Flores-Vidrio, Gabriela Vera-Rivera, María I Miranda, Isabel Méndez, Mauricio Díaz-Muñoz
ABSTRACT

The circadian clock system in the liver plays important roles in regulating metabolism and energy homeostasis. Restricted feeding schedules (RFS) become an entraining stimulus that promotes adaptations that form part of an alternative circadian clock known as the food entrained oscillator (FEO). The aim of this study was to evaluate the daily variations of glutamine synthetase (GS) in liver under a daytime RFS. Hepatic GS properties were analysed at 3-h intervals over a 24-h period in adult male Wistar rats maintained in a 12:12 h light–dark cycle. RFS group: food access for 2-h in light phase, during 3 weeks. AL group: feeding ad libitum. Fa group: acute fast (21 h). Fa–Re group: acute fast followed by refed 2 h.mRNA expression was measured by RT-qPCR, protein presence by Western-blot and immunohistochemistry, enzyme activity by a spectrophotometric assay, and glutamine by high pressure liquid chromatography. Restricted feeding schedule induced circadian rhythmicity inmRNA levels of GS and the loss of the rhythmic pattern in mitochondrial GS activity. GS activity in liver homogenates displayed a robust rhythmic pattern in AL that was not modified by RFS. The presence of GS and its zonal distribution did not show rhythmic pattern in both groups. However, acute Fa and Fa–Re diminished GS protein and activity in liver homogenates. Hepatic glutamine concentrations showed a 24-h rhythmic pattern in both groups, in an antiphasic pattern. In conclusion, daytime RFS influences the liver GS system at different levels, that could be part of rheostatic adaptations associated to the FEO, and highlight the plasticity of this system.

MATERIALS
Product Number
Brand
Product Description

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Anti-Glutamine Synthetase Antibody, clone GS-6, clone GS-6, Chemicon®, from mouse
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L-Glutamine, Pharmaceutical Secondary Standard; Certified Reference Material
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L-Glutamine, γ-irradiated, BioXtra, suitable for cell culture
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L-Glutamine, meets USP testing specifications, suitable for cell culture, 99.0-101.0%, from non-animal source
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