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. Author manuscript; available in PMC: 2009 Mar 1.
Published in final edited form as: Pharmacol Res. 2008 Feb 2;57(3):223–233. doi: 10.1016/j.phrs.2008.01.007

Table 2.

The mRNA levels (mean±SE) of the genes under analysis measured by RT-PCR amplification are reported. Each RT-PCR was repeated at least four times. The semiquantitative analysis of mRNA levels was carried out by the “Gel Doc 2000 UV System” (Bio-Rad, Hercules, CA). The measured mRNA levels were normalised with respect to HPRT (housekeeping gene) and gene expression values were expressed as arbitrary units ± SE.

Gene Sham CCI 3 days CCI/JNJ16259685 3 days CCI 7 days CCI/JNJ16259685 7 days
bax/HPRT 0.17±0.03 0.68±0.13* 0.67±0.20* 0.21±0.02 0.18±0.02
bcl-2/HPRT 0.43±0.05 0.36±0.04 1.25±0.18*° 0.71±0.04* 1.34±0.27*°
GFAP/HPRT 5.21±0.31 13.02±0.60* 19.79±0.35° 11.04±1.21* 5.83±0.18°
APAF-1/HPRT 0.63±0.11 1.62±0.32* 0.53±0.02° 0.98±0.13* 0.69±0.10°
caspase-7/HPRT 1.02±0.06 1.64±0.08* 0.84±0.04° 0.83±0.09 1.30±0.06*
*

p<0.05 vs the corresponding sham,

°

p<0.05 vs the CCI JNJ16259685 untreated rats, as analysed by ANOVA, followed by Student-Neuman-Keuls test. JNJ16259685 did not affect behavioural analysis in sham rats. For this reason we did not perform other experiments on JNJ16259685 treatment in sham rats.