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World J Hepatol. Apr 27, 2014; 6(4): 188-198
Published online Apr 27, 2014. doi: 10.4254/wjh.v6.i4.188
Published online Apr 27, 2014. doi: 10.4254/wjh.v6.i4.188
Ref. | Focus | Model | RSV dose | RSV exposure(wk) | Histology/LW | TG/CH content | LiverAMPK activation | Suggested RSV actions/mechanisms |
Baur et al[37] (2006) | Longevity | Middle-aged DIO mice | 22.4 mg/kg BW = 0.04% in diet | 27 | +/+ | ND | + | Elevated PGC-1α deacetylation as marker of enzymatic SIRT1 activity. Phosphorylation of ACC |
Ahn et al[65] (2008) | NAFLD/NASH | DIO mice (1% CH in diet) | 1.25 g/kg diet | 8 | +/+ Decrease in NASH | +/- | ND | Reduced hepatic expression of FAS, PPARγ, CD36. Increased PPARα expression |
Kang et al[46] (2010) | Insulin signaling | DIO mice | 30 mg/kg BW | 2 | +/ND | ND | - | Increased Akt phosphorylation, improving insulin signaling |
Labbé et al[109] (2011) | NAFLD, metabolic profile, longevity | Werner syndrome mice | 0.04% RSV in diet | Life-long ( ≤ 22.5 mo) | +/ND | ND | - | Decreased FAS expression Decreased HCC prevalence |
Tauriainen et al[115] (2011) | Obesity, NAFLD | DIO mice | 2 or 4 g/kg diet | 15 | +/ND | ND | ND | Increased SIRT1 expression in liver tissue. High-dose most effective |
Cho et al[111] (2012) | NAFLD | DIO mice (1% CH in diet) | 7 mg/kg BW or 30 mg/kg BW | 10 | +/ND | +/+ | ND | Suppressed FAS activity. Activation of FA β-oxidation in liver. The lower dose is more efficient than the higher dose |
Zhou et al[108] (2012) | Overall transcriptomic and metabolic profiling | DIO mice | 0.04% or 0.02% RSV + quercetin 0.02% | 26 | +/ND | -/+ | ND | Modulation of inflammation and FA β-oxidation. Combination with quercetin was more effective than RSV alone |
Jeon et al[51] (2012) | Cognitive deficit | DIO mice | 200 mg/kg BW | 20 | +/ND | ND | ND | Attenuation of hepatic lipid peroxidation and macrophage infiltration |
Shiozaki et al[97] (2012) | Longevity | SAMP10 mice | 0.04% RSV | 20 | +/ND | ND | ND | Inhibition of ACC. Improved mitochon-drial number, redox status and activity |
Gao et al[114] (2013) | NAFLD | T0901317-treated mice | 200 mg/kg BW | < 1 | +/+ | +/ND | + | Inhibition of ACC. Unchanged expression SREBP-1c and related genes |
Li et al[110] (2013) | NAFLD | HFS mice | 50 mg/kg BW | 3 | +/ND Decrease in NASH | ND | ND | Inhibition of NF-κB-induced inflamma-tion and MDA-induced oxidative stress. Protection against NASH fibrosis |
Bujanda et al[49] (2008) | NAFLD | Fasting/feeding special diet, rats | 10 mg daily | 4 | +/- | ND | ND | Hepatic TNF-α decrease. Improved oxidant/antioxidant markers (MDA, NOS, SOD, e.g., catalase) |
Shang et al[74] (2008) | NAFLD | HFD rats | 100 mg/kg BW | 10 | +/+ | +/- | + | Suppressed SREBP-1c and FAS gene expression |
Poulsen et al[76] (2012) | NAFLD | HFD rats | 100 mg daily | 8 | +/- | +/ND | - | Increased UCP2 expression Increased mitochondrial number |
Gomez-Zorita et al[103] (2012) | NAFLD | Obese Zucker rats | 15 mg/kg BW or 45 mg/kg BW | 6 | +/+ | +/? | ND | Increased CPT-1α and ACO No effect on activity of lipogenic enzymes |
Bagul et al[94] (2012) | Oxidative stress | High fructose fed rats | 10 mg/kg BW | 8 | +/ND | ND | ND | Attenuation of hepatic oxidative stress, e.g., with increased level of NRF2 |
Franco et al[96] (2013) | Oxidative stress and NAFLD | Obese ‘early weaned’ rats | 30 mg/kg BW | 4 | +/ND | +/ND | ND | Decreased markers of oxidative stress |
Xin et al[66] (2013) | NAFLD | HFS rats | 50 or 100 mg/kg BW | 13 | +/ND | +/+ | ND | Decreased hepatic LDLr and SRB1 mRNA and protein express |
Cho et al[67] (2008) | Hyperlipidemia | HFD hamsters | 0.25 g/kg diet | 8 | +/+ | +/+ | ND | Decreased HMG-CoA expression and modulated lipoprotein expression |
Burgess et al[110] (2011) | Metabolic syndrome | HFD mini-swine | 100 mg/kg daily | 11 | (+)/ND | ND | ND | Improved insulin sensitivity |
- Citation: Heebøll S, Thomsen KL, Pedersen SB, Vilstrup H, George J, Grønbæk H. Effects of resveratrol in experimental and clinical non-alcoholic fatty liver disease. World J Hepatol 2014; 6(4): 188-198
- URL: https://www.wjgnet.com/1948-5182/full/v6/i4/188.htm
- DOI: https://dx.doi.org/10.4254/wjh.v6.i4.188