[¹¹C]metoclopramide PET imaging provides a sensitive and translational tool to explore P-glycoprotein (P-gp) function at the blood-brain barrier (BBB). Patients with neurological diseases are often treated with cytochrome (CYP) modulators which may impact the plasma and brain kinetics of [¹¹C]metoclopramide. The impact of the CYP inducer carbamazepine or the CYP inhibitor ritonavir on the brain and plasma kinetics of [¹¹C]metoclopramide was investigated in rats. Data obtained in a control group were compared with groups that were either orally pretreated with carbamazepine (45 mg/kg twice a day for 7 days before PET) or ritonavir (20 mg/kg, 3 h before PET) (n = 4 per condition). Kinetic modelling was performed to estimate the brain penetration (V_T) of [¹¹C]metoclopramide. CYP induction or inhibition had negligible impact on the plasma kinetics and metabolism of [¹¹C]metoclopramide. Moreover, carbamazepine neither impacted the brain kinetics nor V_T of [¹¹C]metoclopramide (p > 0.05). However, ritonavir significantly increased V_T (p < 0.001), apparently behaving as an inhibitor of P-gp at the BBB. Our data suggest that treatment with potent CYP inducers such as carbamazepine does not bias the estimation of P-gp function at the BBB with [¹¹C]metoclopramide PET. This supports further use of [¹¹C]metoclopramide for studies in animals and patients treated with CYP inducers.