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. 2013 Nov 3;2013:263846. doi: 10.1155/2013/263846

Figure 4.

Figure 4

The treatment with JWH-133 increased NO bioavailability in the corpus cavernosum of ApoE−/− mice. Relaxation produced by increasing cumulative concentrations of acetylcholine (a) in cavernosal strip from wild type mice and untreated and JWH-133-treated ApoE−/− mice. ((b)-(c)) Constriction induced by cumulative concentrations of phenylephrine in the presence (c) or absence (b) of NOS inhibitor (L-NAME) in cavernosal strip. (d) Normalized curve response of phenylephrine in the presence of L-NAME by phenylephrine response at 10−6 mol/L. *P < 0.05, **P < 0.01, and ***P < 0.001 (two-way ANOVA followed by the Bonferroni multiple comparison test). Each point represents the mean ± SEM (n = 7 to 10). n.s.: nonsignificant.