[11C]Carfentanil binds preferentially to μ -Opioid receptor subtype 1 compared to subtype 2

Abstract

The positron emission tomography (PET) ligand [11C]carfentanil is a selective agonist for μ-opioid receptors and has been used for studying m-opioid receptors in the human brain. However, it is unknown if [11C]carfentanil binding differentiates between subtype receptors μ 1 and μ 2. In this study, we investigated whether μ 1 and μ 2 can be studied separately through receptor subtype- selective inhibition of [11C]carfentanil by pharmacologic intervention. [11C]Carfentanil binding characteristics on rat brain sections were assessed either alone or in the presence of the m-receptor inhibitor cyprodime or the μ1-specific inhibitor naloxonazine. [11C]Carfentanil binding in the living rat brain was similarly studied by small animal PET/computed tomography during baseline conditions or following displacement by cyprodime or naloxonazine. Autoradiography binding studies on rat brain sections demonstrated that [11C]carfentanil has higher affinity and binding potential for μ 1 than for μ2. [11C]Carfentanil binding to μ 2 in vivo could not be detected following specific blocking of μ1, as predicted from the low binding potential for μ2 as measured in vitro. [11C]Carfentanil binding is preferential for 1 compared to μ 2 in vitro and in vivo. Clinical studies employing [11C]carfentanil are therefore likely biased to measure μ1 rather than μ2.