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. 2020 May 5;7(1):e000381. doi: 10.1136/bmjgast-2020-000381

Table 2.

Effect of chronic resveratrol (resv) treatment on the metabolic profiles of NASH mice

Ctrl (n=5) NASH (n=9) NASH-resv (n=9) NASH-resv-EX527 (n=9)
(Triglyceride, TG, mg/dL) 55±4.8 209±28* 124±17 167±9
(Fasting glucose) (mg/dL) 99±8 189±21* 118±16 158±13
(Fasting insulin) (ng/mL) 1.4±0.09 5.8±0.68* 3.4±0.78 4.7±0.42
HOMA-IR index 2.4±0.1 18.8±2.1* 6.9±1.3 12.8±0.8
(Aspartate aminotransferase) (AST, U/L) 52.3±4.9 145.7±5.2* 98.5±11.4 114.8±10.3
(Alanine aminotransferase) (ALT, U/L) 49.1±7.1 120.3±20.1* 84.4±9.6†† 114.5±1.6
Hepatic hydroxyproline content (μg/mg liver weight) 0.19±0.02 0.79±0.07* 0.35±0.02 0.64±0.03

Ctrl/NASH/NASH-resv: mice receiving 12 week of high-fat diet (HFD)+MCD diet or normal chow (NC) feeding and vehicle or resv (resveratrol, 30 mg/kg/day) treatment for 6 week from the 7th to 12th weeks of HFD+MCD feeding; NASH-resv+EX527: NASH mice are concomitant receiving resveratrol and EX-527 (SIRT1 inhibitor) treatment. HOMA-IR: homeostasis model assessment-insulin-resistance, calculated as ((fasting glucose)×(fasting insulin))/58.32.

*p<0.05 vs Ctrl group.

p<0.05 vs NASH group.

HOMA-IR, homeostasis model assessment-insulin-resistance; MCD, methionine and choline deficient; NASH, non-alcoholic steatohepatitis.