Intraperitoneal administration of follistatin promotes adipocyte browning in high-fat diet-induced obese mice

Autor: Xiaoyun He, Fei Liang, Wentao Xu, Junyu Liu, Chuanhai Zhang, Wenya Xie, Haoyu Li, Kunlun Huang
Jazyk: angličtina
Rok vydání: 2019
Předmět:
0301 basic medicine
Physiology
Adipose tissue
White adipose tissue
Biochemistry
Fats
chemistry.chemical_compound
0302 clinical medicine
Glucose Metabolism
Animal Cells
Adipocyte
Brown adipose tissue
Medicine and Health Sciences
Adipocytes
Medicine
Routes of Administration
Connective Tissue Cells
Glucose tolerance test
Multidisciplinary
biology
medicine.diagnostic_test
Animal Models
Lipids
Blood Sugar
Body Fluids
Blood
medicine.anatomical_structure
Physiological Parameters
Experimental Organism Systems
Adipose Tissue
Connective Tissue
030220 oncology & carcinogenesis
Brown Adipose Tissue
Carbohydrate Metabolism
Anatomy
Cellular Types
hormones
hormone substitutes
and hormone antagonists

Research Article
medicine.medical_specialty
Science
Mouse Models
Carbohydrate metabolism
Research and Analysis Methods
03 medical and health sciences
Model Organisms
Internal medicine
Obesity
Pharmacology
business.industry
Body Weight
Biology and Life Sciences
Cell Biology
Biological Tissue
Metabolism
030104 developmental biology
Endocrinology
Subcutaneous Injections
chemistry
Animal Studies
biology.protein
business
Thermogenesis
Follistatin
Zdroj: PLoS ONE, Vol 14, Iss 7, p e0220310 (2019)
PLoS ONE
ISSN: 1932-6203
Popis: With rapid economic development, the prevalence of obesity has increased remarkably worldwide. Obesity can induce a variety of metabolic diseases, such as atherosclerosis, diabetes, hypertension and coronary heart disease, which significantly endanger the health and welfare of individuals. Brown and beige fat tissues play an important role in thermogenesis in mammals. Recent studies have shown that follistatin (FST) can potentially induce the browning of white adipose tissue (WAT). In this study, high-fat diet-induced obese mice were injected with follistatin for one week to explore the effects of follistatin on browning and metabolism and to determine the mechanism. The results showed that follistatin suppressed obesity caused by a high-fat diet and increased insulin sensitivity, energy expenditure, and subcutaneous fat browning. The beneficial effects remained even after a period of withdrawal. Follistatin promoted secretion of irisin from subcutaneous fat via the AMPK-PGC1α-irisin signal pathway, which induces browning of WAT, and activated the insulin pathway in beige fat thereby promoting metabolism.
Databáze: OpenAIRE