Ali S Alfazari

Ali S Alfazari

United Arab Emirates University, United Arab Emirates

Title: Hepatic Tissue Bioenergetics is Preserved when Treated in vitro with Atorvastatin


Dr. Ali S Alfazari has completed his undergraduate medical degree at the United Arab Emirates University in 1999. He then pursued a formal clinical residency program in internal medicine and then gastroenterology at Dalhousie University, Halifax, NS and University of Ottawa, Ottawa, ON respectively. Dr. Alfazari is an assistant professor of medicine at the United Arab Emirates University’s Department of Medicine and attending physician in the Department of Medicine at Tawam Hospital, Al Ain, United Arab Emirates. His research interests are clinical toxicology and cancer biology.


The anti-hyperlipidemic agent, Atorvastatin (a 3-hydroxy-3-methylglutaryl coenzyme-A reductase inhibitor), is commonly prescribed for its potent cholesterol lowering effects. However, elevated transaminases and potential hepatotoxicity are known adverse effects. This study investigated the in vitro effect of this agent on hepatic tissue respiration, ATP content, caspase activity, urea synthesis and histology. Liver fragments from Taylor Outbred and C57Bl/6 mice were incubated at 37°C in Krebs-Henseleit buffer continuously gassed with 95% O2: 5% CO2 in the presence and absence of atorvastatin. Phosphorescence O2 analyzer that measured dissolved [O2] as a function of time was used to monitor cellular mitochondrial O2 consumption. The caspase-3 substrate N-acetyl-asp-glu-val-asp-7-amino-4-methylcoumarin was used to monitor caspase activity. The rates of hepatocyte respiration (μM O2 min-1 mg-1) in untreated samples were 0.15 ± 0.07 (n = 31). The corresponding rates for samples treated with 50 nM (therapeutic concentration), 150 nM or 1.0 μM atorvastatin for ≤13 h were 0.13 ± 0.05 (n = 19), p = 0.521. The contents of hepatocyte ATP (pmol-1 mg-1) in untreated samples were 40.3 ± 14.0 and in samples treated with 1.0 μM atorvastatin for ≤4.5 h were 48.7 ± 23.9 (p = 0.7754). The concentrations of urea (mg/dL mg-1, produced over 50 min) for untreated samples were 0.061 ± 0.020 (n = 6) and for samples treated with 1.0 μM atorvastatin for ≤6 h were 0.072 ± 0.022 (n = 6), p = 0.3866. Steadily, hepatocyte caspase activity and histology were unaffected by treatments with up to 1.0 μM atorvastatin for ≤6 h. Thus, the studied murine model showed preserved hepatocyte function and structure in the presence of high concentrations of atorvastatin.