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Hepatic Acat2 overexpression promotes systemic cholesterol metabolism and adipose lipid metabolism in mice
by
Ma, Zhimin
, Ma, Yue
, Shu, Hui
, Liu, Zhiwei
, Huang, Zhengyun
, Kuang, Shihuan
, Jia, Zhihao
, Feng, Yu
, Zhang, Chi
, Zhang, Jie
, Liu, Xiangpeng
, Chen, Xiyue
, Zhang, Yong
in
Acetyltransferase
/ Adipocytes
/ Adipose tissue
/ Animals
/ Body composition
/ Body fat
/ Body weight
/ Body weight gain
/ Calorimetry
/ Cholesterol
/ Coenzyme A
/ Energy expenditure
/ Energy metabolism
/ Gene expression
/ Glucose - metabolism
/ Glucose tolerance
/ High fat diet
/ Human Physiology
/ Hypercholesterolemia
/ Internal Medicine
/ Lipid metabolism
/ Lipid Metabolism - genetics
/ Liver
/ Liver - metabolism
/ Medicine
/ Medicine & Public Health
/ Metabolic Diseases
/ Metabolic pathways
/ Metabolic rate
/ Metabolism
/ Metabolomics
/ Mice
/ Obesity
/ Obesity - genetics
/ Obesity - metabolism
/ Rodents
/ Thiolase
2023
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Hepatic Acat2 overexpression promotes systemic cholesterol metabolism and adipose lipid metabolism in mice
by
Ma, Zhimin
, Ma, Yue
, Shu, Hui
, Liu, Zhiwei
, Huang, Zhengyun
, Kuang, Shihuan
, Jia, Zhihao
, Feng, Yu
, Zhang, Chi
, Zhang, Jie
, Liu, Xiangpeng
, Chen, Xiyue
, Zhang, Yong
in
Acetyltransferase
/ Adipocytes
/ Adipose tissue
/ Animals
/ Body composition
/ Body fat
/ Body weight
/ Body weight gain
/ Calorimetry
/ Cholesterol
/ Coenzyme A
/ Energy expenditure
/ Energy metabolism
/ Gene expression
/ Glucose - metabolism
/ Glucose tolerance
/ High fat diet
/ Human Physiology
/ Hypercholesterolemia
/ Internal Medicine
/ Lipid metabolism
/ Lipid Metabolism - genetics
/ Liver
/ Liver - metabolism
/ Medicine
/ Medicine & Public Health
/ Metabolic Diseases
/ Metabolic pathways
/ Metabolic rate
/ Metabolism
/ Metabolomics
/ Mice
/ Obesity
/ Obesity - genetics
/ Obesity - metabolism
/ Rodents
/ Thiolase
2023
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Hepatic Acat2 overexpression promotes systemic cholesterol metabolism and adipose lipid metabolism in mice
by
Ma, Zhimin
, Ma, Yue
, Shu, Hui
, Liu, Zhiwei
, Huang, Zhengyun
, Kuang, Shihuan
, Jia, Zhihao
, Feng, Yu
, Zhang, Chi
, Zhang, Jie
, Liu, Xiangpeng
, Chen, Xiyue
, Zhang, Yong
in
Acetyltransferase
/ Adipocytes
/ Adipose tissue
/ Animals
/ Body composition
/ Body fat
/ Body weight
/ Body weight gain
/ Calorimetry
/ Cholesterol
/ Coenzyme A
/ Energy expenditure
/ Energy metabolism
/ Gene expression
/ Glucose - metabolism
/ Glucose tolerance
/ High fat diet
/ Human Physiology
/ Hypercholesterolemia
/ Internal Medicine
/ Lipid metabolism
/ Lipid Metabolism - genetics
/ Liver
/ Liver - metabolism
/ Medicine
/ Medicine & Public Health
/ Metabolic Diseases
/ Metabolic pathways
/ Metabolic rate
/ Metabolism
/ Metabolomics
/ Mice
/ Obesity
/ Obesity - genetics
/ Obesity - metabolism
/ Rodents
/ Thiolase
2023
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Hepatic Acat2 overexpression promotes systemic cholesterol metabolism and adipose lipid metabolism in mice
Journal Article
Hepatic Acat2 overexpression promotes systemic cholesterol metabolism and adipose lipid metabolism in mice
2023
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Overview
Aims/hypothesis
Acetyl coenzyme A acetyltransferase (ACAT), also known as acetoacetyl-CoA thiolase, catalyses the formation of acetoacetyl-CoA from acetyl-CoA and forms part of the isoprenoid biosynthesis pathway. Thus, ACAT plays a central role in cholesterol metabolism in a variety of cells. Here, we aimed to assess the effect of hepatic
Acat2
overexpression on cholesterol metabolism and systemic energy metabolism.
Methods
We generated liver-targeted adeno-associated virus 9 (AAV9) to achieve hepatic
Acat2
overexpression in mice. Mice were injected with AAV9 through the tail vein and subjected to morphological, physiological (body composition, indirect calorimetry, treadmill, GTT, blood biochemistry, cardiac ultrasonography and ECG), histochemical, gene expression and metabolomic analysis under normal diet or feeding with high-fat diet to investigate the role of ACAT2 in the liver.
Results
Hepatic
Acat2
overexpression reduced body weight and total fat mass, elevated the metabolic rate, improved glucose tolerance and lowered the serum cholesterol level of mice. In addition, the overexpression of
Acat2
inhibited fatty acid, glucose and ketone metabolic pathways but promoted cholesterol metabolism and changed the bile acid pool and composition of the liver. Hepatic
Acat2
overexpression also decreased the size of white adipocytes and promoted lipid metabolism in white adipose tissue. Furthermore, hepatic
Acat2
overexpression protected mice from high-fat-diet-induced weight gain and metabolic defects
Conclusions/interpretation
Our study identifies an essential role for ACAT2 in cholesterol metabolism and systemic energy expenditure and provides key insights into the metabolic benefits of hepatic
Acat2
overexpression. Thus, adenoviral
Acat2
overexpression in the liver may be a potential therapeutic tool in the treatment of obesity and hypercholesterolaemia.
Graphical abstract
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