Table 1.

Primers for PCR amplification of each studied gene.

Gene	Sense Primer	Anti-Sense Primer	Annealing ta (°C)
atgl	5′-GAGCTTCGCGTCACCAAC-3′	5′-CACATCTCTCGGAGGACCA-3′	60.0
hsl	5′-GGTGACACTCGCAGAAGACAATA-3′	5′-GCCGCCGTGCTGTCTCT-3′	60.0
lpl	5′-CAGCTGGGCCTAACTTTGAG-3′	5′-CCTCTCTGCAATCACACGAA-3′	61.5
fasn	5′-AGCCCCTCAAGTGCACAGTG-3′	5′-TGCCAATGTGTTTTCCCTGA-3′	60.0
β-actin	5′-ACGAGGCCCAGAGCAAGAG-3′	5′ -GGTGTGGTGCCAGATCTTCTC-3′	60.0
srebf1	5´- GCTGTTGGCATCCTGCTATC-3′	5′-TAGCTGGAAGTGACGGTGGT-3′	60.0
cebpβ	5′-CAAGCTGAGCGACGAGTACA-3′	5′-CAGCTGCTCCACCTTCTTCT-3′	67.5
bcl2	5′-AGTACCTGAACCGGCATCTG-3′	5′-GGGGCCATATAGTTCCACAAA-3′	60.0

atgl = adipose triglyceride lipase; hsl = hormone sensitive lipase; lpl = lipoprotein lipase; fasn= fatty acid synthase; srebf1 = sterol regulatory element-binding factor 1; cebpβ = CCAAT-enhancer- binding protein β; bcl2 = B cell leukemia/lymphoma 2.