“…After cDNA synthesis, PCR amplification was carried out using appropriate sense and antisense primers specific for rat b-actin (a housekeeping gene), IL-1b, IL-6, TNF-a, KC, MIP-1b, MCP-1, TLR-4, CD14, and Myd88 in a final volume of 20 ll containing 1 ll of cDNA, 19 PCR buffer, 0.2 lM of each sense and antisense primer, 0.2 mM of dNTPs, and 1 U of Taq DNA polymerase (Promega). The information on specific primers and PCR conditions for b-actin, IL-1b, IL-6, TNF-a, KC, MIP-1b, TLR-4, and CD14 is described in Lasala et al [19] and Surriga et al [30]. The sense and antisense primers for rat Myd88 were 5 0 -TGT-CCC-AAA-GGA-AAC-ACA-CA-3 0 and 5 0 -CCC-CTG-ACA-TGC-CTA-TCA-CT-3 0 , respectively, and the sense and antisense primers for rat MCP-1 were 5 0 -ATG-ATC-CCA-ATG-AGT-CGG-3 0 and 5 0 -ACA-GAA-GTG-CTT-GAG-GTG-3 0 , respectively.…”