4.4 Article

Irisin induces white adipose tissue browning in mice as assessed by magnetic resonance imaging

期刊

EXPERIMENTAL BIOLOGY AND MEDICINE
卷 246, 期 14, 页码 1597-1606

出版社

SAGE PUBLICATIONS LTD
DOI: 10.1177/15353702211006049

关键词

Obesity; adipocytes; white; uncoupling protein 1; metabolic diseases

资金

  1. National Natural Science Foundation of China [81501523, 81871412]
  2. Fundamental Research Funds for the Central Universities [2242019k30035]
  3. Research Funds for 333 project in Jiangsu province [LGY2017100]

向作者/读者索取更多资源

This study tracked and evaluated the effect of low-dose irisin on the browning of white adipose tissue in mice using MRI noninvasively in vivo. Results showed that irisin treatment led to a significant reduction in WAT volume and fat fraction, as well as improving metabolic disorders in diet-induced obese mice.
This study aimed to track and evaluate the effect of low-dose irisin on the browning of white adipose tissue (WAT) in mice using magnetic resonance imaging (MRI) noninvasively in vivo. Mature white adipocytes extracted from mice were cultured, induced and characterized before being treated by irisin. The volume and fat fraction of WAT were quantified using MRI in normal chow diet and high fat mice after injection of irisin. The browning of cultured white adipocytes and WAT in mice were validated by immunohistochemistry and western blotting for uncoupling protein 1 (UCP1) and deiodinase type II (DIO2). The serum indexes were examined with high fat diet after irisin intervention. UCP1 and DIO2 in adipocytes showed increases responding to the irisin treatment. The size of white adipocytes in mice receiving irisin intervention was reduced. MRI measured volumes and fat fraction of WAT were significantly lower after Irisin treatment. Blood glucose and cholesterol levels were reduced in high fat diet mice after irisin treatment. Irisin intervention exerted browning of WAT, resulting reduction of volume and fat fraction of WAT as measured by MRI. Furthermore, it improved the condition of mice with diet-induced obesity and related metabolic disorders.

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