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. 2015 Oct 2;11(4):571–580. doi: 10.1007/s11302-015-9475-2

Table 1.

The effects of guanosine on LPS-induced inflammatory response were independent of the adenosinergic system

Treatment TNF-α levels (% of control) IL-1β levels (% of control)
LPS 280 ± 18a 190 ± 12a
GUO + LPS 112 ± 12b 110 ± 10b
ADO 100 + LPS 271 ± 15a 182 ± 12a
ADO 1000 + LPS 277 ± 21a 185 ± 15a
CAF 100 + LPS 283 ± 22a 180 ± 14a
CAF 1000 + LPS 268 ± 22a 178 ± 15a
GUO + CAF 100 + LPS 115 ± 14b 107 ± 10b
GUO + CAF 1000 + LPS 114 ± 12b 115 ± 15b

Cells were incubated in serum-free DMEM/F12 with adenosine (100 and 1000 μM) or 100 μM guanosine (GUO) and caffeine (100 and 1000 μM) for 1 h before being treated with 10 μg/mL LPS for 3 h. TNF-α and IL-1β levels were measured as described in the “Materials and methods” section. Data represent the mean ± S.E.M. of three independent experiments that were performed in triplicate. Differences between groups were statistically analyzed using two-way ANOVA, followed by Tukey’s test. Values of P < 0.05 were considered significant

aDifferences from control conditions

bDifferences from LPS