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Thalidomide Prevents Alcoholic Liver Injury in Rats Through Inhibition of Kupffer Cell Sensitization
© Enomoto et al; licensee BioMed Central Ltd 2004
Published: 14 January 2004
Increasing lines of evidence show that activation of Kupffer cells plays a pivotal role in initiation and progression of alcoholic liver disease. Kupffer cell activation is evoked by endotoxin (lipopolysaccharide, LPS), which leads to rapid elevation of intracellular calcium accompanied by release of a variety of mediators including cytokines, eicosanoids and reactive radical species. Among them, TNF-alpha is a critical factor in the pathogenesis of alcoholic liver disease.
Thalidomide (alpha-N-phthalimidoglutarimide) was initially used as a sedative and antiemetic during pregnancy but was withdrawn from the market due to its teratogenic effects. Before it was banned, thalidomide was recognized to reduce dramatically symptoms associated with erythema nodosum leprosum, a complication of Hansen's disease. Subsequently, it was shown that thalidomide suppresses TNF-alpha production by macrophages and other cell types such as activated T cells [1, 2], which was attributed to a mechanism of thalidomide action .
Accordingly, the purpose of this study was to determine whether thalidomide could prevent alcohol-induced liver injury. Here we report that thalidomide prevents liver damage caused by chronic ethanol exposure through not only suppression of TNF-alpha production but abrogation of Kupffer cell sensitization to LPS.
Animals and Treatments
In this study, a model of alcoholic liver injury based on the sensitization of Kupffer cells, in which rats are given ethanol (5 g/kg body wt) once every 24 hours , was used. This model achieves inflammatory and necrotic changes in the liver only in 8 weeks, which mimics features of clinical alcohol liver injury . Liver damage was evaluated after 8 weeks of ethanol since histological manifestations are preceded by sensitization of Kupffer cells to LPS treatment, and Kupffer cell sensitization to LPS was evaluated at 4 weeks. Female Wistar rats weighing 200–250 g were fed on a liquid diet (Oriental, Tokyo, Japan). Two groups of rats received an oral dose of thalidomide (5 mg/kg body wt) only or concurrently with ethanol . Gut permeability was measured in isolated segments of ileum from translocation of horseradish peroxidase as described previously .
Kupffer Cell Preparation Culture, Measurement of [Ca2+]i, and TNF-alpha Production
Kupffer cells were isolated by collagenase digestion and [Ca2+]i was measured using a microspectrofluorometer with fura-2, and TNF-alpha in the culture media was measured using an enzyme-linked immunosorbent assay (ELISA) kit (Genzyme, Cambridge, MA).
All results were expressed as mean – S.E.M. Statistical differences between means were determined using analysis of variance (ANOVA) or ANOVA on ranks or Bonferroni's post-hoc test or Student's t test as appropriate. p < 0.05 was selected prior to the study to reflect significance.
Effect of Thalidomide on Alcoholic Liver Injury
Effect of thalidomide on ethanol-induced liver injury
101 – 12
30 – 6
Thalido (5 mg/kg) 8 weeks
62 – 3
38 – 6
Ethanol (5 g/kg) 8 weeks
162 – 7*
91 – 7*
Ethanol + Thalidomide 8 weeks
126 – 15**
37 – 3**
Effect of Thalidomide on Ethanol plus LPS-Induced Liver Injury
Effect of thalidomide on ethanol plus LPS-induced liver injury.
846 – 227
483 – 167
Thalido 4 weeks + LPS
307 – 15
239 – 15
Ethanol 4 weeks + LPS
2091 – 295*
1200 – 375*
Ethanol + Thalido 4 weeks + LPS
379 – 231**
219 – 179**
Effect of Thalidomide and Ethanol on LPS-Induced Increases in [Ca2+]iand TNF-alpha Production in Isolated Kupffer Cells
Effect of ethanol and thalidomide on LPS-induced increases in intracellular Ca2+ and TNF-alpha production in isolated Kupffer cells.
LPS (100 ng/ml)
85 – 4
559 – 71
Thalido 4 weeks + LPS
92 – 6
578 – 77
Ethanol 4 weeks + LPS
227 – 26*
1104 – 110*
Ethanol + Thalido 4 weeks + LPS
83 – 4**
625 – 72**
Effect of Ethanol and Thalidomide on CD14 Expression in the Liver
Because CD14, a functional LPS/LBP receptor, is critical for signaling pathways leading to expression of cytokines, eicosanoids and radical species in Kupffer cells, we measured CD14 with Western blotting (data not shown). Liver from control rats expressed the 55 kD CD14. Thalidomide did not change the amount of CD14 protein; however, the band was far more intense in liver from rats treated with ethanol chronically. Furthermore, the ethanol-induced increase in CD14 protein levels was abrogated completely with co-administration of thalidomide for 4 weeks.
Effects of Ethanol and Thalidomide on Gut Permeability
Effect of ethanol and thalidomide treatment on gut permeability.
63 – 6
Thalido 4 weeks
68 – 12
Ethanol 4 weeks
591 – 90*
Ethanol + Thalido 4 weeks
543 – 161*
Effect of Thalidomide on LPS-Induced TNF-alpha mRNA Expression and TNF-alpha Production in Cultured Kupffer Cells
Effect of thalidomide on LPS-induced TNF-alpha mRNA expression and TNF-alpha production in cultured Kupffer cells.
(A) TNF-alpha and beta-actin mRNA expression
TNF-alpha/beta-actin(%1 h LPS)
LPS (100 ng/ml) 1 hour
LPS + Thalido (5 micromolar) 1 hour
LPS 3 hours
LPS + Thalido 3 hours
(B) TNF-alpha production
LPS (100 ng/ml)
501 – 19
LPS + Thalido (5 micromolar)
268 – 4*
Effect of Thalidomide and TNF-alpha on Expression of CD14 in Cultured Kupffer Cells
To explore the mechanism by which thalidomide abrogated Kupffer cell sensitization to LPS caused by chronic ethanol, we determined the effect of TNF-alpha on CD14 expression in Kupffer cells obtained from normal rats in vitro (data not shown). Treatment with TNF-alpha (10 ng/ml) for 24 hours resulted in enhancement of CD14 expression in Kupffer cells. Inclusion of thalidomide (5 micromolar) in the culture media reduced CD14 expression to a level comparable to the control.
Effect of Thalidomide and TNF-alpha on LPS-Induced TNF-alpha Production by Cultured Kupffer Cells
Effect of thalidomide and TNF-alpha on LPS-induced TNF-alpha production by cultured Kupffer cells.
LPS (100 ng/ml)
726 – 82
TNF-alpha (10 ng/ml)+ LPS
936 – 186*
Thalidomide (5 micromolar) + TNF-alpha + LPS
439 – 105**
The results of this study showed that thalidomide prevented liver injury caused by chronic ethanol treatment (Table 1). To investigate the mechanism of inhibitory effects of thalidomide against ethanol-induced liver injury, we determined if thalidomide directly acted on Kupffer cells thereby reducing TNF-alpha production. As shown in Table 6, thalidomide did not affect the levels of TNF-alpha mRNA in Kupffer cells after 1 hour of challenged with LPS, however, reduced later the amounts of TNF-alpha mRNA. Consequently, the LPS-induced TNF-alpha synthesis by Kupffer cells was inhibited by thalidomide. This result agrees with an earlier work showing that thalidomide abrogated LPS-induced TNF-alpha production from macrophages [1, 2]. It was reported that thalidomide decreases TNF-alpha production by accelerating the degradation of its mRNA .
TNF-alpha has a pleiotropic cytokine and regulatory mechanisms of TNF-alpha production in macrophages and its intracellular signaling have been studied extensively . It was suggested that TNF-alpha acts on macrophages/monocytes to promote its own synthesis and secretion . The fact that thalidomide destabilizes TNF-alpha mRNA provides a good basis for the use of thalidomide to treat alcohol-induced liver injury because a recent work by Kishore et al. revealed stabilization of TNF-alpha mRNA by chronic ethanol . We hypothesized that an autocrine stimulation by TNF-alpha is involved in the ethanol-induced Kupffer cell sensitization and that thalidomide interferes with this pathway, leading to abrogation of Kupffer cell sensitization.
This scenario is supported by the facts that pretreatment with TNF-alpha led to an increased TNF-alpha synthesis in response to LPS and enhancement of CD14 expression in Kupffer cells, and that inclusion of thalidomide in the culture media inhibited this TNF-alpha-induced autocrine activation of TNF-alpha synthesis (Table 6). Furthermore, thalidomide blocked completely the TNF-alpha-induced upregulation of CD14 in Kupffer cells in vitro.
The precise mechanisms of the thalidomide actions remain to be pursued, however, the results of this study suggest that thalidomide prevents liver injury caused by chronic ethanol consumption through destabilization of TNF-alpha mRNA and abolishing Kupffer cell sensitization to LPS. Though currently its side effects preclude the use of thalidomide in clinical settings and require rigors of the drug distribution program and prescription decision, efforts to synthesize thalidomide analogues lacking teratogenic effects but having more potent efficacy are underway . Given that thalidomide has unique mechanisms of actions, there appears to be a strong possibility that this type of drug will prove beneficial to patients with severe alcoholic liver injury.
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