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. 2013 Nov 17;2013:161496. doi: 10.1155/2013/161496

Table 3.

Ethanol metabolism to acetaldehyde in the cytosolic fraction of uterine horn tissue from rats receiving an alcohol containing liquid diet.

Experimentala Acetaldehyde (nmol/mg protein)
Control EtOH-treated
Ethanol only 1.39 ± 0.03 1.78 ± 0.05
Ethanol + NAD 1.67 ± 0.04b 0.43 ± 0.03g
Ethanol + NAD + HX 1.76 ± 0.13c,e 0.32 ± 0.01g,h
Ethanol + NAD + HX + allopurinol 0.13 ± 0.01c,d,f 0.27 ± 0.06g,i,j

aIncubation mixtures containing cytosolic fraction (1.4–1.6 mg protein/mL), 0.14 M ethanol, and, when indicated, 0.25 mM hypoxanthine (HX) and 0.3 mM NAD+ in STKM buffer were conducted for 1 h at 37°C. Acetaldehyde was measured in the head space of each sample after adding 1 mL NaCl saturated solution. See Section 2 for details. Each result is the mean of three separate lots of pooled uterine tissue samples.

b P < 0.01 when compared to “Ethanol only” (Control).

c P < 0.001 when compared to “Ethanol only” (Control).

d P < 0.001 when compared to “Ethanol + NAD + HX” (Control).

e P > 0.05 when compared to “Ethanol + NAD” (Control).

f P < 0.001 when compared to “Ethanol + NAD” (Control).

g P < 0.001 when compared to “Ethanol only” (EtOH-treated).

h P < 0.05 when compared to “Ethanol + NAD” (EtOH-treated).

i P > 0.05 when compared to “Ethanol + NAD + HX” (EtOH-treated).

j P < 0.01 when compared to “Ethanol + NAD” (EtOH-treated).