[HTML][HTML] Chloroquine ameliorates carbon tetrachloride-induced acute liver injury in mice via the concomitant inhibition of inflammation and induction of apoptosis
This is the first study to investigate the hepatoprotective effect of CQ on acute liver injury
caused by carbon tetrachloride (CCl4) in a murine model and the underlying molecular
mechanisms. Ninety-six mice were randomly divided into the control (n= 8), CQ (n= 8), CCl4
(n= 40), and CCl4+ CQ (n= 40) treatment groups. In the CCl4 group, mice were
intraperitoneally (ip) injected with 0.3% CCl4 (10 mL/kg, dissolved in olive oil); in the CCl4+
CQ group, mice were ip injected with CQ at 50 mg/kg at 2, 24, and 48 h before CCl4 …
caused by carbon tetrachloride (CCl4) in a murine model and the underlying molecular
mechanisms. Ninety-six mice were randomly divided into the control (n= 8), CQ (n= 8), CCl4
(n= 40), and CCl4+ CQ (n= 40) treatment groups. In the CCl4 group, mice were
intraperitoneally (ip) injected with 0.3% CCl4 (10 mL/kg, dissolved in olive oil); in the CCl4+
CQ group, mice were ip injected with CQ at 50 mg/kg at 2, 24, and 48 h before CCl4 …
Abstract
This is the first study to investigate the hepatoprotective effect of CQ on acute liver injury caused by carbon tetrachloride (CCl4) in a murine model and the underlying molecular mechanisms. Ninety-six mice were randomly divided into the control (n = 8), CQ (n = 8), CCl4 (n = 40), and CCl4 + CQ (n = 40) treatment groups. In the CCl4 group, mice were intraperitoneally (i.p) injected with 0.3% CCl4 (10 mL/kg, dissolved in olive oil); in the CCl4 + CQ group, mice were i.p injected with CQ at 50 mg/kg at 2, 24, and 48 h before CCl4 administration. The mice in the control and CQ groups were administered with an equal vehicle or CQ (50 mg/kg). Mice were killed at 2, 6, 12, 24, 48 h post CCl4 treatment and their livers were harvested for analysis. The results showed that CQ pre-treatment markedly inhibited CCl4-induced acute liver injury, which was evidenced by decreased serum transaminase, aspartate transaminase and lower histological scores of liver injury. CQ pretreatment downregulated the CCl4-induced hepatic tissue expression of high-mobility group box 1 (HMGB1) and the levels of serum HMGB1 as well as IL-6 and TNF-α. Furthermore, CQ pre-treatment inhibited autophagy, downregulated NF-kB expression, upregulated p53 expression, increased the ratio of Bax/Bcl-2, and increased the activation of caspase-3 in hepatic tissue. This is the first study to demonstrate that CQ ameliorates CCl4-induced acute liver injury via the inhibition of HMGB1-mediated inflammatory responses and the stimulation of pro-apoptotic pathways to modulate the apoptotic and inflammatory responses associated with progress of liver damage.
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