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. 1998 Nov;5(6):790–798. doi: 10.1128/cdli.5.6.790-798.1998

TABLE 3.

Effects of ethanol, acetaldehyde, and acetate on IL-1α, IL-1β, TNF-α, and TGF-β production in clone 43 cellsa

Treatment Production (pg/ml) of cytokineb:
IL-1α IL-1β TNF-α TGF-β
None 0 0 0 0
LPS (1 μg/ml) 302 ± 100 799 ± 147 535 ± 135 0
Ethanol
  25 mM 175 ± 43 165 ± 37 179 ± 81 75 ± 31
  75 mM 101 ± 31 85 ± 37 50 ± 71 25 ± 43
 150 mM 37 ± 10 57 ± 14 78 ± 34 250 ± 84
Acetaldehyde
  25 mM 168 ± 37 159 ± 50 180 ± 90 62 ± 20
  75 mM 99 ± 22 130 ± 50 157 ± 68 101 ± 30
 150 mM 40 ± 13 52 ± 20 73 ± 29 239 ± 70
Acetate
  25 mM 164 ± 40 153 ± 37 173 ± 70 39 ± 10
  75 mM 99 ± 24 79 ± 30 134 ± 80 110 ± 30
 150 mM 39 ± 13 59 ± 20 85 ± 30 210 ± 73
a

Some clone 43 cells were maintained in culture, while others were treated with various concentrations (25, 75, and 150 mM) of ethanol, acetaldehyde, and acetate for 16 h, washed in PBS, and stimulated with LPS (1 μg/ml) for 16 h. Cytokine determinations were performed with the culture supernatant by a direct-binding enzyme-linked immunosorbent assay. 

b

Data represent the means ± standard errors from three separate experiments.