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. 2012 Apr 22;2012:479348. doi: 10.1155/2012/479348

Table 4.

Effects of chronic ethanol consumption on hepatic expression of proceramide genes-biosynthetic pathways.

Protein Control Ethanol P value
CerS1 0.542 ± 0.162 1.145 ± 0.228 0.025
CerS2 3634 ± 509.2 3982 ± 450
CerS4 160.2 ± 36.36 172.7 ± 22.86
CerS5 1.62 ± 0.22 3.62 ± 0.27 <0.0001
CerS6 15.70 ± 3.59 33.52 ± 5.48 0.0071
SPTLC-1 121.4 ± 9.29 253.3 ± 26.26 0.0001
SPTLC-2 2615 ± 444.8 3187 ± 309.5
SMPD-1 685.7 ± 133.9 1214 ± 244.8 0.036
SMPD-3 765.4 ± 140.5 1353 ± 216.6 0.019
CERD2 6.524 ± 2.439 1.887 ± 0.3439 0.04
CERD3 5.583 ± 1.458 6.896 ± 1.853
UGCG 282.6 ± 68.27 609.9 ± 174.5 0.0006
GM3Syn 56.21 ± 7.80 72.32 ± 6.981 0.006

RNA extracted from normal or chronic alcoholic livers (N = 8/group) was reverse transcribed, and the cDNAs were used to measure gene expression by qPCR analysis with gene-specific primer pairs in a duplex qPCR reaction, in which the genes of interest were co-amplified with HPRT for normalization (see Section 2 and Table 1). Table represents relative levels of gene expression for Ceramide synthases (CERS), UDP glucose ceramide glycosyltransferase (UGCG), ceramidases (CERD), GM3-synthase, serine palmitoyl transferase subunits (SPTLC), sphingomyelinases (SMPD). Intergroup comparisons were made using Student's t-tests and significant P values are shown over the graphs.