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. 2017 Nov 2;174(23):4263–4276. doi: 10.1111/bph.14019

Figure 2.

Figure 2

Cannabinoid acids induce PPARγ transcriptional activity and PPARγ degradation. (A–C) HEK‐293T cells were transiently transfected with PPARγ‐GAL4 plus GAL4‐luc and incubated with increasing concentrations of the indicated neutral and cannabinoid acids for 6 h (n = 5). (D) Transfected HEK‐293T cells were stimulated with two phytoextracts derived from the Cannabis variety MONIEK before and after decarboxylation (n = 5). (E) STHdh Q7/Q7 cells were treated with Δ9‐THCA, Δ9‐THC and rosiglitazone (RGZ) for 6 h, and the steady‐state levels of endogenous PPARγ and β‐actin detected by Western blots (n = 5). (F) STHdh Q7/Q7 cells were transiently transfected with PPARγ‐GAL4 plus GAL4‐luc and incubated with increasing concentrations of Δ9‐THCA or Δ9‐THC for 6 h (n = 5). * P < 0.05, significantly different from untreated cells.