Opioid Analgesia in P450 gene cluster knockout mice: A search for analgesia-relevant isoforms

Cytochrome P450 monooxygenases (P450s), which are well-known drug-metabolizing enzymes, are thought to play a signal trans-duction role in m opioid analgesia and may serve as high-affinity ³H-cimetidine (³HCIM) binding sites in the brain. ³HCIM binding sites may also be related to opioid or nonopioid analgesia. However, of the more than 100 murine P450 enzymes, the specific isoform(s) responsible for either function have not been identified. Presently, three lines of constitutive P450 gene cluster knockout (KO) mice with full-length deletions of 14 Cyp2c, 9 Cyp2d, and 7 Cyp3a genes were studied for deficiencies in ³HCIM binding and for opioid analgesia. Liver and brain homogenates from all three genotypes showed normal ³HCIM binding values, indicating that gene products of Cyp2d, Cyp3a, and Cyp2c are not ³HCIM-binding proteins. Cyp2d KO and Cyp3a KO mice showed normal anti-nociceptive responses to a moderate systemic dose of morphine (20 mg/kg, s.c.), thereby excluding 16 P450 isoforms as mediators of opioid analgesia. In contrast, Cyp2c KO mice showed a 41% reduction in analgesic responses following systemically (s.c.) administered morphine. However, the significance of brain Cyp2c gene products in opioid analgesia is uncertain because little or no analgesic deficits were noted in Cyp2c KO mice following intra-cerebroventricular or intrathecalmorphine administration, respectively. These results show that the gene products of Cyp2d and Cyp3a do not contribute to μ opioid analgesia in the central nervous system. A possible role for Cyp2c gene products in opioid analgesia requires further consideration.