4.7 Article

A rapid juvenile murine model of nonalcoholic steatohepatitis (NASH): Chronic intermittent hypoxia exacerbates Western diet-induced NASH

期刊

LIFE SCIENCES
卷 276, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.lfs.2021.119403

关键词

Chronic intermittent hypoxia; NAFLD; NASH; Western diet; Juvenile murine model

资金

  1. Natural Science Foundation of Hebei Province [H2019423136]
  2. Science and Technology Research Fund Project of Hebei Colleges, and Universities [ZD2020142]
  3. Science and Technology Project of Hebei Education Department [QN2017110]
  4. Graduate Innovation Fund of Hebei University of Chinese Medicine [XCXZZBS2020003, XCXZZSS2020004]

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This study established a rapid juvenile murine NASH model and found that the combination of CIH and a western-style diet can fully display key pathologic features of NASH.
Aims: Many dietary NASH models require a long duration to establish (4?6 months). Chronic intermittent hypoxia (CIH), a cardinal hallmark of obstructive sleep apnea (OSA), may accelerate the progression of pediatric nonalcoholic fatty liver disease (NAFLD). However, diet-induced obese (DIO) mice exposed to CIH have not been perceived as a fast or reliable tool in NASH research. This study was designed to establish a rapid juvenile murine NASH model, and determine whether the combination of CIH and a western-style diet (hypercaloric fatty diet plus high fructose) can fully display key pathologic features of NASH. Methods: C57BL/6 N mice (3 weeks old) fed a control diet or western diet (WD) were exposed to CIH (9% nadir of inspired oxygen levels) or room air for 6 and 12 weeks. Key findings: The Control/CIH group mainly exhibited hyperinsulinemia and insulin resistance (IR). In contrast, mice fed a WD developed weight gain after 3 weeks, microvesicular steatosis in 6 weeks, and indices of metabolic disorders at 12 weeks. Furthermore, CIH exposure accelerated WD- induced macromicrovesicular steatosis (liver triglycerides and de novo lipogenesis), liver injury (ballooned hepatocytes and liver enzymes), lobular/portal inflammation (inflammatory cytokines and macrophage recruitment), and fibrogenesis (hydroxyproline content and TGF-? protein). Notably, only the WD/CIH group exhibited elevated hepatic MDA content, protein levels of NOX4, ?-SMA and collagen I, as well as reduced Nrf2 and HO-1 protein expression. Significance: WD/CIH treatment rapidly mimics the histological characteristics of pediatric NASH with metabolic dysfunction and fibrosis, representing an appropriate experimental model for NASH research.

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