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Vertical sleeve gastrectomy improves liver and hypothalamic functions in obese mice
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Vertical sleeve gastrectomy (VSG) is an effective surgery to treat obesity and diabetes. However, the direct effect of VSG on metabolic functions is not fully understood. We aimed to investigate if alterations in hypothalamic neurons were linked with perturbations in liver metabolism after VSG in an energy intake-controlled obese mouse model. C57BL/6 and hrNPY-GFP reporter mice received HFD for 12 weeks and were then divided into three groups: Sham (ad lib), Sham (pair-fed) with VSG and VSG. Food intake was measured daily, and blood glucose levels were measured before and after the study. Energy expenditure and body composition were determined. Serum parameters, liver lipid and glycogen contents were measured and gene/protein expression were analyzed. Hypothalamic POMC, AgRP/NPY and tyrosine hydroxylase-expressing neurons were counted. The following results were obtained. VSG reduced body weight gain and adiposity induced by HFD, increased energy expenditure independent of energy intake. Fed and fasted blood glucose levels were reduced in the VSG group. While serum active GLP-1 level was increased, the active ghrelin and triglycerides levels were decreased along with improved insulin resistance in VSG group. Liver lipid accumulation, glycogen content and gluconeogenic gene expression were reduced in the VSG group. In the hypothalamus, TH-expressing neuron population was decreased, and the POMC-expressing neuron population was increased in the VSG group. In conclusion, our data suggest that VSG improves metabolic symptoms by increasing energy expenditure and lowering lipid and glycogen contents in the liver. These physiological alterations are possibly related to changes in hypothalamic neuron populations.
Title: Vertical sleeve gastrectomy improves liver and hypothalamic functions in obese mice
Description:
Vertical sleeve gastrectomy (VSG) is an effective surgery to treat obesity and diabetes.
However, the direct effect of VSG on metabolic functions is not fully understood.
We aimed to investigate if alterations in hypothalamic neurons were linked with perturbations in liver metabolism after VSG in an energy intake-controlled obese mouse model.
C57BL/6 and hrNPY-GFP reporter mice received HFD for 12 weeks and were then divided into three groups: Sham (ad lib), Sham (pair-fed) with VSG and VSG.
Food intake was measured daily, and blood glucose levels were measured before and after the study.
Energy expenditure and body composition were determined.
Serum parameters, liver lipid and glycogen contents were measured and gene/protein expression were analyzed.
Hypothalamic POMC, AgRP/NPY and tyrosine hydroxylase-expressing neurons were counted.
The following results were obtained.
VSG reduced body weight gain and adiposity induced by HFD, increased energy expenditure independent of energy intake.
Fed and fasted blood glucose levels were reduced in the VSG group.
While serum active GLP-1 level was increased, the active ghrelin and triglycerides levels were decreased along with improved insulin resistance in VSG group.
Liver lipid accumulation, glycogen content and gluconeogenic gene expression were reduced in the VSG group.
In the hypothalamus, TH-expressing neuron population was decreased, and the POMC-expressing neuron population was increased in the VSG group.
In conclusion, our data suggest that VSG improves metabolic symptoms by increasing energy expenditure and lowering lipid and glycogen contents in the liver.
These physiological alterations are possibly related to changes in hypothalamic neuron populations.
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