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. 2010 Jun;160(3):657–668. doi: 10.1111/j.1476-5381.2010.00769.x

Figure 7.

Figure 7

Pharmacological inhibition or genetic deletion of cannabinoid-1 (CB1) receptors attenuated the cisplatin-induced increased expression of reactive oxygen species-generating NADPH oxidase enzymes [NOX4(RENOX), NOX2(gp91phox)] and the inducible nitric oxide synthase (iNOS) in kidneys of mice. Cisplatin induced marked increases in expression of renal NOX4, NOX2 and iNOS mRNA 72 h following its administration to mice (A–D). These increases were attenuated by AM281 or SR141716 treatment (A and C), and also in CB1 knockout (CB1−/−) mice compared with CB1+/+ littermates (B and D). Results are mean ± SEM of 9–10 experiments per group. *P < 0.01 versus vehicle in C57BL/6 mice (A and C) or versus CB1+/+ mice treated with vehicle (B and D); #P < 0.05 versus cisplatin in C57BL/6 or CB1+/+ mice (A/C and B/D respectively).